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        <title>MedWorm Tags: everyday</title>
        <description>MedWorm provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest medical blog items that have been tagged with 'everyday'.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=%22everyday%22&t=%22everyday%22&r=Exact&o=d&f=tag]]></link>
        <lastBuildDate>Sat, 03 Sep 2011 02:05:29 +0100</lastBuildDate>
        <item>
            <title>SXSW 2012 Psychology Picks: Need Your Vote!</title>
            <link>http://www.medworm.com/index.php?rid=5181897&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F09%2F01%2Fsxsw-2012-psychology-picks-need-your-vote%2F</link>
            <description>Time is running out to vote for some of your favorite SXSW 2012 Interactive panel ideas through the SXSW panel picker (Friday at midnight is the deadline). Yes, you need to register a free account in order to vote, but it takes only a minute to do so.
I&amp;#8217;ve organized a panel again for consideration, as have some other psychologists and professionals. I&amp;#8217;ve highlighted three panels I&amp;#8217;d like you to vote a big thumbs-up on, if you have a minute today. While people&amp;#8217;s votes only constitute 30 percent of how a panel idea is chosen to present at SXSW Interactive, it&amp;#8217;s an important part of the process that helps the organizers make the tough decisions.
The panel I&amp;#8217;ve proposed is about online therapy. But not your everyday kind of online therapy&amp;#8230;

Click on th...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5181897</comments>
            <pubDate>Thu, 01 Sep 2011 12:14:46 +0100</pubDate>
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            <title>Why A Hurricane Filled Me With Gratitude</title>
            <link>http://www.medworm.com/index.php?rid=5181901&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F08%2F30%2Fwhy-a-hurricane-filled-me-with-gratitude%2F</link>
            <description>Like much of the East Coast, New York City was hit by Hurricane Irene. On Saturday, we checked our flashlights, loaded up on food, filled the bathtub, and hoped for the best.
We were extremely lucky. The hurricane didn’t affect us much &amp;#8212; we didn’t even lose power. And I’m very, very grateful for that.
The hurricane was a good reminder about gratitude.

For one thing, it reminded me that I have so much to be grateful for that it seems a bit preposterous that I need to remind myself to be grateful &amp;#8212; but I do. When life is taking its ordinary course, it’s so easy to take everyday life for granted.
Also, the hurricane made me much more mindful of how much I love my apartment and my city, and how safe and secure I generally feel. It&amp;#8217;s a sad foible of human nature that ...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5181901</comments>
            <pubDate>Tue, 30 Aug 2011 19:53:47 +0100</pubDate>
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        <item>
            <title>The MS ‘Honeymoon’</title>
            <link>http://www.medworm.com/index.php?rid=5107744&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fthe-ms-honeymoon%2F</link>
            <description>Diagnostics are better. Primary care doctors are more aware. Patients are seeking knowledge. The general population of people newly diagnosed with MS seems to be getting a bit younger. Truth be known, it’s likely that they are being diagnosed earlier in the course of multiple sclerosis, and that’s a good thing!
Medications appear to be more effective early in the course of MS. That’s not just to say they seem to “work” better at keeping attacks down. The meds seem to slow the progression to the point where we may have some extra “good years” before (if) our MS decides to get progressive.
Herein lay my thoughts for today: The MS Honeymoon.
Many, if not most, of us can think back to some physical “oddities” which we experienced well prior to diagnosis. It wasn’t until a f...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5107744</comments>
            <pubDate>Mon, 08 Aug 2011 19:40:34 +0100</pubDate>
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        <item>
            <title>Standing Up With Multiple Sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=5086380&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fstanding-up-with-multiple-sclerosis%2F</link>
            <description>It’s not uncommon for me to use alliterations and metaphor when I write about MS. Today, however, I write about the actual difficulties of “standing up” when you have multiple sclerosis.
Difficulties with the vertical posture come in many colors, shades, and tones for those of us on different places on the MS rainbow.
When I was first diagnosed, and trying to keep my jet-set, full-time employment, my boss in Germany told me of a dear friend of his with MS. Your man had apparently had MS for years and the only way you might notice anything is that he couldn’t stand for very long at a cocktail party. If that is the “infrared” end of the MS standing spectrum, “ultraviolet” would be those who cannot stand at all.
I recognize that there are many in our Life With MS Blog communit...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086380</comments>
            <pubDate>Mon, 01 Aug 2011 21:00:32 +0100</pubDate>
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        <item>
            <title>New Study Questions MS Drug ‘Value’</title>
            <link>http://www.medworm.com/index.php?rid=5077888&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fnew-study-questions-ms-drug-value%2F</link>
            <description>This study will surely be a part of my decision-making process.
We all know that MS meds work better for some than others, that some MS meds work for each of us while others may not, and we know that we really don’t know if a drug was working unless we stop and see our disease kick back into pre-therapy mode. This study, however, makes me believe that it’s time for the price of MS medications to come down — WAY DOWN — and I think that it’s time that we get some regulators involved.
Many MS meds have been on the market for nearly 20 years now. Those first drugs have well been paid for and their investors handsomely rewarded. It’s time that we start realizing that. While I’m not diminishing the importance of multiple sclerosis disease-modifying drugs, it is not good for Manyone...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5077888</comments>
            <pubDate>Thu, 28 Jul 2011 16:28:12 +0100</pubDate>
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        <item>
            <title>July Check-In: How’s Your MS Today?</title>
            <link>http://www.medworm.com/index.php?rid=5028750&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fjuly-check-in-hows-your-ms-today%2F</link>
            <description>Time once again for our monthly open blog where we ask the question, “How’s your MS today?”
After catching up (or trying) on all of your comments while I was away on holidays I’d venture to say that this may be a busy month for comments on this topic. I wrote some of those posts in advance and some during my trip. I didn’t have time to check in very often so I was surprised to see so many comments on many of the posts.
As to how my MS is; I can’t really tell…
I’m recovering from a sinus infection and we all know how that can muck with MS. In fact, I now remember that my diagnosing MRI showed a big, ol’ nasty sinus infection. The radiologist who read the films even mentioned it in his report: “major sinus infection in three cavities, multiple plaque lesions on brain and ...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5028750</comments>
            <pubDate>Wed, 13 Jul 2011 19:16:47 +0100</pubDate>
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        <item>
            <title>Multiple Sclerosis and the Question of Disability Insurance</title>
            <link>http://www.medworm.com/index.php?rid=5028752&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fmultiple-sclerosis-and-the-question-of-disability-insurance%2F</link>
            <description>I’m not sure if the advancement of a post-holidays head cold into a sinus infection (and the associated MS issues related to a fever) had any part of my sensitivity to comments that circulated here on the Life With MS Blog and our Facebook Page but I thought that it might be time we discuss disability insurance and SSDI again.
In this day and age of starkly divided political views many see “leaving work” because of MS as yet another way in which too many people are grasping at a government entitlement and suckling from the public teat. Others see SSDI as an insurance plan into which they have paid and, like any other insurance policy, when they need it they expect it to be there for them.
There are many, many problems with the entire “disability” system (for lack of better termin...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5028752</comments>
            <pubDate>Mon, 11 Jul 2011 19:26:57 +0100</pubDate>
            <guid isPermaLink="false">5028752</guid>        </item>
        <item>
            <title>Multiple Sclerosis Falls: Secondary Damages</title>
            <link>http://www.medworm.com/index.php?rid=5008473&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fmultiple-sclerosis-falls-secondary-damages%2F</link>
            <description>Supportive, light-weight shoes, a sturdy cane (“stick” in Ireland), cool ocean breezes and keen mindfulness allowed for some “hiking” on my recent holidays in Ireland. We kept to well worn paths and all, but it was nice to get out into nature even if it was only a few feet of the roads.
Preparations for these jaunts included cool showers, a fistful of meds and the ever-watchful eye of Caryn as we trod step by spongy, peat supported step… And I’m proud to say that I was one of the few in our group who did not fall during our trekking! Chalk that one up to another lesson of living with MS.
So many times, however, we know that we do fall and as I’ve commented before we may meet the canvas more often when we are feeling at the upper end of the MS spectrum.
The injuries resulting ...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5008473</comments>
            <pubDate>Fri, 08 Jul 2011 15:18:28 +0100</pubDate>
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        <item>
            <title>Life Can Become Very Weird Living With Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=5008472&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Flife-can-become-very-weird-living-with-chronic-pain%2F</link>
            <description>I know. You’re thinking life is weird already but let me say, if you’re newly diagnosed, “You ain’t seen nothin’ yet!”
If you are one of us who live with connective tissue or rheumatoid disease you may see a certain set of weirdness. If you suffer from back pain or had a previous injury, you’re not excluded, either. It’s amazing what life can do to twist, shape and torment us. If our diseases or injuries don’t do enough in that department then there are always the medications to take up the slack and pile it on. Get your sense of humor ready and if you don’t have one, well, blessings upon you my friend because you’re going to need one.
The other day I was fitted for a sacroiliac belt to aid my sacroiliac joints to stay put. All that was missing at the fitting was Scar...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5008472</comments>
            <pubDate>Thu, 07 Jul 2011 20:13:33 +0100</pubDate>
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        <item>
            <title>How MS Treatments (And Our Expectations) Have Changed</title>
            <link>http://www.medworm.com/index.php?rid=4984585&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fhow-ms-treatments-and-our-expectations-have-changed%2F</link>
            <description>The old adage is that “Nothing is more constant than change” and there is little truer to someone living with MS. Symptoms change, doctor change, medications change…MS changes. A person living with MS 20 years ago, stranded on an island and newly returned to their home, wouldn’t even recognize the face of Multiple Sclerosis in the world today.
Where once there were no meds (or maybe a very competitive lottery to get into a drug trial) there are now 6 approved therapies and scores in the final testing phases. Those once told to “go home and get your affairs in order” are now assisted in living a more fulfilling and meaningful life. Exercise — once the terror of MS docs — is now not only recommended, it is encouraged. Woman who were once counseled to really think about having...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4984585</comments>
            <pubDate>Wed, 29 Jun 2011 13:04:54 +0100</pubDate>
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        <item>
            <title>Riding Around In A Very Personal Journey With MS</title>
            <link>http://www.medworm.com/index.php?rid=4976059&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Friding-around-in-a-very-personal-journey-with-ms%2F</link>
            <description>A bus full of commuters passes you on a busy street. A car idles, waiting for a traffic light to change. The azure-blue, summer sky is unzipped by the contrail of a jumbo jet filled with hundreds of souls… and they all have a story.
Have you ever been in an airplane on approach or departure; close enough to the ground to see the ant-like scene below as it gets on with the workaday world? Have you ever thought of the lives going on inside that plane far, far above your head? Have you ever felt yourself cut-off from the world as if you were in a personal space capsule catapulting through time, space and dimension and nobody gets it?
Caryn and I have just experienced a very personal grief (and I trust our community to please leave it at that) during which we felt as if the world was going b...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4976059</comments>
            <pubDate>Mon, 27 Jun 2011 17:48:56 +0100</pubDate>
            <guid isPermaLink="false">4976059</guid>        </item>
        <item>
            <title>Where Do You Find True Grit?</title>
            <link>http://www.medworm.com/index.php?rid=4968705&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fwhere-do-you-find-true-grit%2F</link>
            <description>It’s often inspiring how life leads us along, licking our wounds which it also inflicted upon us; we love it, we hate it. These last few weeks I have been immersed in the past. I live in a home that is 120 years old and often wonder about those who lived here before we did. Did they love? Did they find joy and survival, together or individually? Did they have physical pain? Surely, they must have because they were without NSAIDs, biologics, acid inhibitors, a local drug store, or a supermarket.
I often run across some little remnant of the past presence of one who lived here, like finding an oyster shell working its way out of the foundation outdoors or the aqua blue marine paint that dripped from the brush of an “ancient” mariner who used to live here, many years ago, still trailing...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4968705</comments>
            <pubDate>Fri, 24 Jun 2011 13:08:46 +0100</pubDate>
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        <item>
            <title>Progressing With Progressive MS</title>
            <link>http://www.medworm.com/index.php?rid=4968706&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fprogressing-with-progressive-ms%2F</link>
            <description>Most of us with MS know terms like RRMS (relapsing remitting), SPMS (secondary progressive), and PPMS (primary progressive) when it comes to our disease. Less often heard variations are “chronic progressive&amp;#8221; or &amp;#8220;worsening progressive,” and I even heard someone refer to their MS as “acute, progressive chronic MS.&amp;#8221; Not sure where he had heard that one.
While we all want to find a “normal” group of people with MS to which we can identify and belong, it really isn’t all that important as to which group we fall (save for those of us whose doctors are sticklers for medications).
What is important is that, as our disease may move from a relapsing-remitting phase – which is often medically described as “inflammatory disease” – to a stage of slow (or not), stea...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4968706</comments>
            <pubDate>Fri, 24 Jun 2011 13:04:58 +0100</pubDate>
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        <item>
            <title>The Little Things We Can Still Do for Ourselves</title>
            <link>http://www.medworm.com/index.php?rid=4960209&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fthe-little-things-we-can-still-do-for-ourselves%2F</link>
            <description>Like many of my generation and those who came before, I feel now like I may have spent too much time in my “former life” chasing the elusive brass ring. It wasn’t enough to be recognized wherever I went, professionally. Not enough to have the house in town and an apartment in the city. Even my dear Jaguar was a few years older than I would have liked.
Now, please don’t get me wrong! I was very appreciative of the things I had attained, but they did not make me happy — Things seldom make us happy.
Because of the way I have learned to live my life post-MS, I feel much more attuned with what happiness rarely is and I find it mostly on the inside. That being said, there are still a few little things that I do that make me very happy indeed.
Last week, while in New York I treated myse...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4960209</comments>
            <pubDate>Wed, 22 Jun 2011 15:36:22 +0100</pubDate>
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        <item>
            <title>How Would You Like Your MS Society to Use Social Media?</title>
            <link>http://www.medworm.com/index.php?rid=4934587&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fhow-would-you-like-your-ms-society-to-use-social-media%2F</link>
            <description>I am off this morning to meetings in New York City with a newly formed group of advisors to the National MS Society on the topic of social media. Like many organizations, the NMSS is aware that online communities have changed the way that people with MS connect with one another and the whole-wide world around us.
The event is to include several roundtable sessions with some of my fellow bloggers and online community leaders on the topic of multiple sclerosis.
Lisa Emerich of Brass &amp; Ivory and Carnival of MS Bloggers , Marc Stecker who many of you will know as the Wheelchair kamikaze and Ashley Ringstaff of MS World will all be in attendance for the day-long summit along with several national and chapter leaders from the Society.
I am, of course, humbled to be in such lauded company and...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4934587</comments>
            <pubDate>Wed, 15 Jun 2011 21:08:54 +0100</pubDate>
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        <item>
            <title>A Glass of Wine, a Nibble of Cheese, and Some MS Art</title>
            <link>http://www.medworm.com/index.php?rid=4934588&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fa-glass-of-wine-a-nibble-of-cheese-and-some-ms-art%2F</link>
            <description>One of the down sides to my increased schedule of travel schedule, writing deadlines and other obligations (oh, and how our favorite disease is handcuffing me in the heat and humidity) is that I don’t get to do all of the things that I would like to do. It’s something we all have to deal with on some level; right?
Well I want to make sure that I share this event – which I’ll, unfortunately, have to miss due to the above listed set of cascading events – with all of you who are within driving distance of Seattle. But in doing so, I hope that it might be a little bit of a spark for those of you who are not.

Next weekend, the 18th &amp; 19th, the Multiple Sclerosis Center of Swedish Neuroscience Institute, in association with the Bellevue Arts Museum, is presenting their second annu...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4934588</comments>
            <pubDate>Mon, 13 Jun 2011 20:30:04 +0100</pubDate>
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        <item>
            <title>A restless night</title>
            <link>http://www.medworm.com/index.php?rid=4953296&amp;cid=t_200519_136_f&amp;fid=39016&amp;url=http%3A%2F%2Fturquoisegates.blogspot.com%2F2011%2F06%2Frestless-night.html</link>
            <description>My smallest one is down and out with a stomach bug and kept us up for a large portion of the night with his stomach pain and fever. I look at his 3-year-old face and I remember the first time he was put in my arms, his quizzical look and blinking baby eyes.Nothing else much going on at the Thul house today. Just trying to keep the sick one happy and the rest of us healthy! (Source: Turquoise Gates)</description>
            <author>Turquoise Gates</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4953296</comments>
            <pubDate>Sat, 11 Jun 2011 15:09:00 +0100</pubDate>
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        <item>
            <title>A Life With Chronic Pain? Don’t Panic!</title>
            <link>http://www.medworm.com/index.php?rid=4921623&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fa-life-with-chronic-pain-dont-panic%2F</link>
            <description>When we are struck with a life of chronic pain, we are terrified, feel forsaken and usually panic. Those who don’t panic are usually in denial and get around to panic later when the fear of the unknown sweeps over them. Today, as usual, I searched my heart and mind to find the helpful ideas which have and do help me everyday of my life. Please, let me list them for you in the hope that you will also find courage, calm and control in your life if you are also facing this monster each day.

Gain Control. I know, you feel like your body has betrayed you and after all the great things you did for it, too. Stop asking yourself why this happened to you and look forward. Of course, it might help you to know if it’s genetic, for the sake of your children, but for now, you have to deal with eac...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4921623</comments>
            <pubDate>Fri, 10 Jun 2011 13:20:44 +0100</pubDate>
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        <item>
            <title>Everyday Life With Chronic Back Pain</title>
            <link>http://www.medworm.com/index.php?rid=4893703&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Feveryday-life-with-chronic-back-pain%2F</link>
            <description>As many of you who have been reading this blog for some time know, I live with sacroiliac joint pain and have for more than twenty years. Those particular joints are the two upon which you place your derriere, hold your two lower cheeks together and keep your legs from falling off. The pain from them often extends into the pubic area, the hips, and the lumbar spine and down the legs. Pain in these regions can have an affect on your bowel and bladder habits as well. Recently, the inflammation of those large joints has, for me, been worse than ever. I share this with you to explain why I have low back pain on the brain today, as well as on my backside.
Since I have a brain that tickles easily, I have been remembering an event of many years ago when I was in nursing school. One of my nursing ...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4893703</comments>
            <pubDate>Thu, 02 Jun 2011 22:12:47 +0100</pubDate>
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        <item>
            <title>Helping Others Is Good For Your Health: An Interview with Stephen G. Post, PhD</title>
            <link>http://www.medworm.com/index.php?rid=4876421&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F05%2F28%2Fhelping-others-is-good-for-your-health-an-interview-with-stephen-g-post-phd%2F</link>
            <description>Mahatma Gandhi once said that &amp;#8220;The best way to find yourself is to lose yourself in the service of others.&amp;#8221; I have benefited from that advice, for sure, especially in the months that I was crawling out of a very severe depression.
An expert on the perks that come with helping others is bestselling author Stephen G. Post, author of The Hidden Gifts of Helping: How the Power of Giving, Compassion, and Hope Can Get us Through Hard Times (Jossey-Bass, 2011). He is Professor of Preventive Medicine, Heard of the Division of Medicine in Society, and Director of the Center for Medical Humanities, Compassionate Care and Bioethics at Stony Brook University. Visit him on his website at www.stephengpost.com/hiddengifts.
I have the privilege of conducting an exclusive interview with him for...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4876421</comments>
            <pubDate>Sat, 28 May 2011 10:07:20 +0100</pubDate>
            <guid isPermaLink="false">4876421</guid>        </item>
        <item>
            <title>Understanding Research Methodology 2: Systematic Empiricism</title>
            <link>http://www.medworm.com/index.php?rid=4676871&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F04%2F04%2Funderstanding-research-methodology-2-systematic-empiricism%2F</link>
            <description>Scientific research relies on the use of empirical data for acquiring knowledge.  Empiricism means making use of observation and experience.  Science goes beyond the use of the empiricism normally used in everyday life, however.  Scientific research employs systematic empiricism.
Observation itself is necessary in acquiring scientific knowledge, but unstructured observation of the natural world will not lead to an increased understanding of the world.
“Write down every observation you make from the time you get up in the morning to the time you go to bed on a given day. When you finish, you will have a great number of facts, but you will not have a greater understanding of the world.” (Stanovich &amp; Stanovich, 2003, p. 12)

Empiricism becomes systematic empiricism when it is stru...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4676871</comments>
            <pubDate>Mon, 04 Apr 2011 09:54:10 +0100</pubDate>
            <guid isPermaLink="false">4676871</guid>        </item>
        <item>
            <title>Understanding Research Methodology</title>
            <link>http://www.medworm.com/index.php?rid=4615186&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F03%2F21%2Funderstanding-research-methodology%2F</link>
            <description>In order to fully appreciate and apply the knowledge that has been acquired through the scientific process, it is imperative to have a basic understanding of scientific research methodology.
Methodology: scientific techniques used to collect and evaluate data.
This is the first in a series of articles that will shed light on scientific research methods.  It is important to understand that all research methods play an important role in leading us to tentative conclusions concerning how things work in the observable universe.  But, it also important to realize different types of research should be interpreted and applied in a different manner.
As an example, the primary goal of correlation research is prediction, while the primary goal of experimental research is explanation/understanding....</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4615186</comments>
            <pubDate>Mon, 21 Mar 2011 11:43:47 +0100</pubDate>
            <guid isPermaLink="false">4615186</guid>        </item>
        <item>
            <title>Think Like a Skeptic, Part 2</title>
            <link>http://www.medworm.com/index.php?rid=4527772&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F02%2F27%2Fthink-like-a-skeptic-part-2%2F</link>
            <description>I was a presenter at the JP Fitness Summit in Kansas City in 2009, where I spoke about the importance of exercising skepticism in your life, whether you&amp;#8217;re a fitness expert or anyone else. You can read my first article on the topic here.
Here are some additional notes from my lecture at that event. I hope to be able to help readers understand the importance of relying on logic and how to do this more often in everyday life, and, in essence, how to think like a skeptic.
The Concise English Oxford Dictionary defines &amp;#8220;logic&amp;#8221; as the science of reasoning, proof, thinking or inference. In the structure of a logical argument, one or more premises leads to a conclusion (a conclusion that could be true even if the argument is invalid).
To sharpen critical thinking skills, it is im...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4527772</comments>
            <pubDate>Sun, 27 Feb 2011 19:06:22 +0100</pubDate>
            <guid isPermaLink="false">4527772</guid>        </item>
        <item>
            <title>3 Top Sources of Psychology Myths</title>
            <link>http://www.medworm.com/index.php?rid=4525054&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F02%2F26%2F3-top-sources-of-psychology-myths%2F</link>
            <description>In a recent interview I asked Scott Lilienfeld, the author of 50 Great Myths of Popular Psychology, about the sources of psychology myths.  Here&amp;#8217;s what he has to say about where psychology myths come from:
The primary source is the huge, burgeoning pop psychology industry: self-help books, the internet, films, TV shows, magazines, and the like. But many of these myths also spring from the allure of our everyday experience; many of these myths seem persuasive because they accord with our common sense intuitions. But these intuitions are often erroneous. The public can defend themselves against shams by becoming armed with accurate knowledge.
Many other fields &amp;#8212; not just psychology &amp;#8212; are subject to myths disseminated by the media.
So what are some of the top sources of psy...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4525054</comments>
            <pubDate>Sat, 26 Feb 2011 12:19:26 +0100</pubDate>
            <guid isPermaLink="false">4525054</guid>        </item>
        <item>
            <title>6 Steps to Living a Good, Happy and Long Life</title>
            <link>http://www.medworm.com/index.php?rid=4522146&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F02%2F25%2F6-steps-to-living-a-good-happy-and-long-life%2F</link>
            <description>Compassion. Gratitude. Conscientiousness. Being humble. A little stress to keep you energized and motivated. Using common sense. Hanging out with the people that are doing healthy things. Having a stable relationship.
You might think the secret to a long and happy life was hidden in a book or could be found by following that famous media guru, Oprah. The truth is, a long life and happiness are not obtained by doing extraordinary things or looking for that magical &amp;#8220;dream job&amp;#8221; (or dream spouse, for that matter).
Research has shown &amp;#8212; most recently by psychologists Friedman and Martin in The Longevity Project (2010) &amp;#8212; that getting to a long life is really just a combination of simple, everyday things and an approach to life that some might say emphasizes a sense of resi...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4522146</comments>
            <pubDate>Fri, 25 Feb 2011 15:46:57 +0100</pubDate>
            <guid isPermaLink="false">4522146</guid>        </item>
        <item>
            <title>When God seems far away</title>
            <link>http://www.medworm.com/index.php?rid=4489931&amp;cid=t_200519_136_f&amp;fid=39016&amp;url=http%3A%2F%2Fturquoisegates.blogspot.com%2F2011%2F02%2Fwhen-god-seems-far-away.html</link>
            <description>I remember the moment clearly, when last He showed His face. It was only the second time in my life I felt like I had seen Him. Both times I was wrung out, wasted, worn, weary. The first time by the confounding decisions I faced as a single woman. This day, by the suffering of life...Amy's illness, the newly worsened drudgery of my days as a mom, failures at school and work, at home as wife and mother and housekeeper.So I flung myself like a rag doll across my bed, and my inner two year old showed herself in the hot tears and loud sobs. I heard the kids edging toward the closed door of the bedroom, but the sobs kept coming. And WHY? It wasn't as though someone had died or anything truly terrible had happened. I was undone by a whole list of small problems, that's all.Where are you? I sobbe...</description>
            <author>Turquoise Gates</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4489931</comments>
            <pubDate>Thu, 17 Feb 2011 10:09:00 +0100</pubDate>
            <guid isPermaLink="false">4489931</guid>        </item>
        <item>
            <title>Is Life With Chronic Pain a Reality Show or a Cartoon?</title>
            <link>http://www.medworm.com/index.php?rid=4464607&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fis-life-with-chronic-pain-a-reality-or-a-cartoon%2F</link>
            <description>As most of you already know I have been having a terrible time with some funky new virus this year. I feel like a turtle that got tipped and can’t get upright again. That could explain why the room keeps spinning. Some spirit with a sense of humor keeps rocking my shell and occasionally gives it a spin.
On Saturday, I went into urgent care. It was cold and slow. The people were very kind but I had to wear my gloves and jacket to keep from shaking my teeth out of my mouth while shivering. I had a chest X-ray, was given an antibiotic and left there being told I would eventually be okay. The diagnosis was viral with bronchitis. Since, like many of you, I already had a satchel full of problems, all things were complicated. We got out into the parking lot and I could hardly wait to get home a...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4464607</comments>
            <pubDate>Sat, 12 Feb 2011 00:46:51 +0100</pubDate>
            <guid isPermaLink="false">4464607</guid>        </item>
        <item>
            <title>Is Life With Chronic Pain a Reality or a Cartoon?</title>
            <link>http://www.medworm.com/index.php?rid=4460063&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fis-life-with-chronic-pain-a-reality-or-a-cartoon%2F</link>
            <description>As most of you already know I have been having a terrible time with some funky new virus this year. I feel like a turtle that got tipped and can’t get upright again. That could explain why the room keeps spinning. Some spirit with a sense of humor keeps rocking my shell and occasionally gives it a spin.
On Saturday, I went into urgent care. It was cold and slow. The people were very kind but I had to wear my gloves and jacket to keep from shaking my teeth out of my mouth while shivering. I had a chest X-ray, was given an antibiotic and left there being told I would eventually be okay. The diagnosis was viral with bronchitis. Since, like many of you, I already had a satchel full of problems, all things were complicated. We got out into the parking lot and I could hardly wait to get home a...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4460063</comments>
            <pubDate>Thu, 10 Feb 2011 22:13:54 +0100</pubDate>
            <guid isPermaLink="false">4460063</guid>        </item>
        <item>
            <title>10 Blogs to Spark Your Creativity</title>
            <link>http://www.medworm.com/index.php?rid=4433136&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F02%2F03%2F10-blogs-to-spark-your-creativity%2F</link>
            <description>Recently, I&amp;#8217;ve talked quite a bit about connecting to our creative selves. (Yes, everyone is creative!)
One way to access our creativity, I believe, is through inspiration from other amazing minds.
In honor of that, I wanted to share 10 blogs that help me get creative (this is by no means an exhaustive list), find tons of right answers and most importantly, get super-excited about the world and all there is to see.
In no particular order, they are:
1. Scoutie Girl. 
This blog features interesting independent craft and design work. As their about page states, “Simply put, Scoutie Girl is the blog with a penchant for the passionately handmade.” The posts are always a lovely surprise. Topics include creative living and mindful spending.

2. Susannah Conway 
Susannah is a writer and ...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4433136</comments>
            <pubDate>Thu, 03 Feb 2011 19:53:54 +0100</pubDate>
            <guid isPermaLink="false">4433136</guid>        </item>
        <item>
            <title>Best of Our Blogs: February 1, 2011</title>
            <link>http://www.medworm.com/index.php?rid=4424280&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F02%2F01%2Fbest-of-our-blogs-february-1-2011%2F</link>
            <description>I have to say in some ways, 2011 has been uneventful. Maybe I was in need of a little mundane in my life after 2011 kick me in the butt. But while boredom is welcomed (Thank goodness for the sun! There&amp;#8217;s no seasonal affective disorder on my end.), it can also be a sign of stagnation.
Maybe we&amp;#8217;re getting too comfortable in our relationships and in our jobs and have started to take for granted the everyday moments in our lives. If that sounds like you, keep reading.
This week&amp;#8217;s post are all about rethinking your life, transforming ordinary moments into extraordinary ones, analyzing your relationships and your body language. Basically, they are five posts to re-energize your 2011.
If you&amp;#8217;ve been feeling run-down, down and out, tired of the lack of sunlight, I think you...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4424280</comments>
            <pubDate>Wed, 02 Feb 2011 00:14:25 +0100</pubDate>
            <guid isPermaLink="false">4424280</guid>        </item>
        <item>
            <title>A Video on Creativity in Daily Life</title>
            <link>http://www.medworm.com/index.php?rid=4424282&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F02%2F01%2Fa-video-on-creativity-in-daily-life%2F</link>
            <description>A few days ago, my boyfriend sent me a link to a video he said I absolutely had to watch. He first saw it in a seminar at work.
The short video introduces viewers to Dewitt Jones, a National Geographic photographer, who shares some of his thoughts on creativity and, essentially, everyday life.
In the video, he talks about a key lesson he’s learned: There are amazing things for all of us to see every single day. Whether we actually see these remarkable things depends on our perspective, or as Jones says, on our ability to be creative.
We all have the ability to be creative, he says.
I&amp;#8217;ve talked before about creativity and about connecting to my own creativity on my body image blog, Weightless. (Many fantastic bloggers talked about it too.) I’ve said that creativity is inside all o...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4424282</comments>
            <pubDate>Tue, 01 Feb 2011 13:02:05 +0100</pubDate>
            <guid isPermaLink="false">4424282</guid>        </item>
        <item>
            <title>The official beginning</title>
            <link>http://www.medworm.com/index.php?rid=4405998&amp;cid=t_200519_136_f&amp;fid=39016&amp;url=http%3A%2F%2Fturquoisegates.blogspot.com%2F2011%2F01%2Fofficial-beginning.html</link>
            <description>We called ourselves &quot;Thul Homeschool&quot;.But it felt sort of unofficial.Until our first field trip, and getting back into the swing this January,post cancer scans and epilepsy monitoring unit and holidays and snowstorms.We topped off a trip to the local museum with a trip to the local Culvers.Sticky, and sweet, and the perfect crowning treat for our first&amp;nbsp;Field Trip with a capital F and T!Susan was along, just for fun.Caleb's newest, &quot;I'm a boy and I'll be weird just to be weird&quot; face.Topped off with a small Wednesday miracle, an &quot;A&quot; and a &quot;4&quot; from Amelia,courtesy of Wikki Stix, raved about by mothers of special needs kids on Amazon.We've recently switched to natural rubber pacifiers, which I added to thespecial needs shop I have created in Amazon as well. I'll have to tell the story...b...</description>
            <author>Turquoise Gates</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4405998</comments>
            <pubDate>Thu, 27 Jan 2011 13:32:00 +0100</pubDate>
            <guid isPermaLink="false">4405998</guid>        </item>
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            <title>Medical Ethics: Why They Should Matter To Patients</title>
            <link>http://www.medworm.com/index.php?rid=4394446&amp;cid=t_200519_87_f&amp;fid=39187&amp;url=http%3A%2F%2Fgetbetterhealth.com%2Fmedical-ethics-why-they-should-matter-to-patients%2F2011.01.24</link>
            <description>Medical ethics has properly gained a foothold in the public square. There is a national conversation about euthanasia, stem cell research, fertilization and embryo implantation techniques, end-of-life care, prenatal diagnosis of serious diseases, defining death to facilitate organ donation, cloning and financial conflicts of interest. Nearly every day, we read (or click) on a headline highlighting one of these or similar ethical controversies. These great issues hover over us.
We physicians face ethical dilemmas every day in the mundane world of our medical practices. They won’t appear in your newspapers or pop up on your smartphones, but they are real and they are important. Here is a sampling from the everyday ethical smorgasbord that your doctor faces. How would you act under the fol...</description>
            <author>Better Health</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4394446</comments>
            <pubDate>Mon, 24 Jan 2011 16:00:00 +0100</pubDate>
            <guid isPermaLink="false">4394446</guid>        </item>
        <item>
            <title>More Skeptic Insights</title>
            <link>http://www.medworm.com/index.php?rid=4382798&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F01%2F21%2Fmore-skeptic-insights%2F</link>
            <description>In Kentucky, skeptics meeting are occurring on a regular basis.  Skeptics can thank Laurie Tarr for many of these meetings.  Tarr is the co-founder and co-director of Louisville Area Skeptics.  Recently, I had a chance to talk skepticism with Tarr.
What is the mission statement of the Louisville Area Skeptics?  Why are you a skeptic?
I created the Louisville Area Skeptics as an opportunity for people from Louisville and the surrounding areas to meet and share their love of science, their interest in critical thinking, and their skeptical worldview through social events and informal science presentations by professional scientists. I&amp;#8217;ve been a skeptic since I was a young teenager and discovered the writings of Carl Sagan. Being a skeptic is a way for me to use science to evaluate ...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4382798</comments>
            <pubDate>Fri, 21 Jan 2011 19:35:39 +0100</pubDate>
            <guid isPermaLink="false">4382798</guid>        </item>
        <item>
            <title>Let a Child Teach You About a Life of Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=4343245&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Flet-a-child-teach-you-about-a-life-of-chronic-pain%2F</link>
            <description>The children in our lives bring us many gifts throughout all seasons. They may be your children, your grandchildren, or a friend or neighbor&amp;#8217;s child; all seem capable of performing this fete. They bring us the gift of laughter, the gift of acceptance and most of all, the gift of insight. Today, I would like to share with you some of the gifts the children in my life have taught me over the years, if I may?

Anything is possible. Unless someone tells you otherwise, there is nothing you cannot accomplish. Just do it.
You may not always succeed in doing something well, but you must try.
Giving up is not an option. With all of life’s possibilities, why should it be?
Santa, as well as Mary Poppins, has a bag that holds anything you want to be in it. Size and weight are not issues; but y...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4343245</comments>
            <pubDate>Thu, 13 Jan 2011 21:13:25 +0100</pubDate>
            <guid isPermaLink="false">4343245</guid>        </item>
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            <title>9 Ways to Ward Off Your Worries</title>
            <link>http://www.medworm.com/index.php?rid=4331058&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F01%2F10%2F9-ways-to-ward-off-your-worries%2F</link>
            <description>Worrying is like a magnifying glass: It enlarges everything.
It empowers anxiety. It gives anxiety legs, fuel and a superhero costume.
You get the picture: Worrying gives us a false sense of control.
I&amp;#8217;m a worrywart, who feels like she has to worry. (Don&amp;#8217;t all worrywarts?) Because if I&amp;#8217;m not concerned about one thing or another, that means I have no choice but to relax.
And relaxing feels strange — not always, but most of the time.
Relaxing means that the grip on control is loosened.
For many people, worrying is living. You can&amp;#8217;t help but worry. You have an endless list of “what ifs?” What if I lose my job? What if I get into a car accident right now? What if dinner is disgusting? What if the weather is bad? What if I miss my flight?

Concern after concern pop...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4331058</comments>
            <pubDate>Mon, 10 Jan 2011 14:11:05 +0100</pubDate>
            <guid isPermaLink="false">4331058</guid>        </item>
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            <title>2011: The Power of Positive Being</title>
            <link>http://www.medworm.com/index.php?rid=4302887&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2011%2F01%2F01%2F2011-the-power-of-positive-being%2F</link>
            <description>Be kind whenever possible. It is always possible.
~Dalai Lama 
Last year I began the Proof Positive blog here at Psych Central. The goal was to review the best research in positive psychology and offer applications from this research for everyday use. All of the techniques for promoting wellbeing and happiness were drawn from the research literature, and I experimented with each of them. Some had more power that others, and some were more difficult to maintain. But overall there was a clear, strong, positive shift not only in my way of thinking, but also in the degree of positive experiences noted, encountered, and received.
This is not to say that the miserable things that come with being human stopped happening, or the sorrows and grief from losses weren’t there; they certainly were. B...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4302887</comments>
            <pubDate>Sat, 01 Jan 2011 15:01:17 +0100</pubDate>
            <guid isPermaLink="false">4302887</guid>        </item>
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            <title>Taking back the sacred</title>
            <link>http://www.medworm.com/index.php?rid=4253408&amp;cid=t_200519_136_f&amp;fid=39016&amp;url=http%3A%2F%2Fturquoisegates.blogspot.com%2F2010%2F12%2Ftaking-back-sacred.html</link>
            <description>Remember the Sabbath day, to keep it holy [set apart].Six days shall you labor, and do your work,but the seventh day is a Sabbath dedicated to the Lord your God.Exodus 20:9-10We hustle and bustle at Christmastime, and I read others lament it but don't feel the same. I am snug in my house, shopping online with my fingers and eyes instead of walking through stores, my driver's license unused in my purse for a month now. Every year, a season of no driving reminds me that I depend on others and God and not just my strong two legs and the arms strong for my labor (Proverbs 31:17).But maybe God hears all of our cries, and sometimes takes back the sacred with a display of power that stalls every earthly plan and maroons people to sit silent for a whole 24 hours. A whole day set apart to marvel at...</description>
            <author>Turquoise Gates</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4253408</comments>
            <pubDate>Sun, 12 Dec 2010 17:43:00 +0100</pubDate>
            <guid isPermaLink="false">4253408</guid>        </item>
        <item>
            <title>Living water</title>
            <link>http://www.medworm.com/index.php?rid=4251241&amp;cid=t_200519_136_f&amp;fid=39016&amp;url=http%3A%2F%2Fturquoisegates.blogspot.com%2F2010%2F12%2Fliving-water.html</link>
            <description>I wasn't born with a demonstrative bone in my body. From Scandinavian and Native American heritage, I come from people who are generally quiet...until you get to know them a bit. But you might not know that if you just met me now. I played softball with some outspoken girls in high school and hockey with a bunch of wild women in college and learned to shout, and hug people I didn't know that well, and give high fives and slap the ice when something really cool happened. Started attending a more flamboyant, rock-band type of church in 2000 and learned there to lift&amp;nbsp;hands in prayer (Psalm 134:2 and I Timothy 2:8). Cancer has been refining me since 2008 and teaching me what is important and whats not...and often social mores mean less to me than showing someone I love them or telling the...</description>
            <author>Turquoise Gates</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4251241</comments>
            <pubDate>Sat, 11 Dec 2010 11:09:00 +0100</pubDate>
            <guid isPermaLink="false">4251241</guid>        </item>
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            <title>What Doctors Can Learn from Nordstrom's &amp; Apply to Patient Care</title>
            <link>http://www.medworm.com/index.php?rid=4190414&amp;cid=t_200519_134_f&amp;fid=35187&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FDiabetesDaily%2F%7E3%2FlDIQlozEock%2Ffor-yearsnordstroms-employee-handbookwas-a.php</link>
            <description>Nordstrom's is known for their exemplary customer service and&amp;nbsp;successful business model. For years,&amp;nbsp;Nordstroms Employee Handbook&amp;nbsp;was a single 5×8 gray card containing these 75 words:Welcome to NordstromWere glad to have you with our Company. Our number one goal is to provide outstanding customer service. Set both your personal and professional goals high. We have great confidence in your ability to achieve them.Nordstrom Rules: Rule #1: Use best judgment in all situations. There will be no additional rules.Please feel free to ask your department manager, store manager, or division general manager any question at any time.The Result?During this time, Nordstrom had&amp;nbsp;the highest sales per square foot performance in the retail industry&amp;nbsp; by almost&amp;nbsp;double.Th...</description>
            <author>Diabetes Daily</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4190414</comments>
            <pubDate>Sun, 21 Nov 2010 19:34:04 +0100</pubDate>
            <guid isPermaLink="false">4190414</guid>        </item>
        <item>
            <title>What Not to Say to a Depressed Person</title>
            <link>http://www.medworm.com/index.php?rid=4164556&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F11%2F13%2Fwhat-not-to-say-to-a-depressed-person%2F</link>
            <description>I&amp;#8217;m always on the lookout for articles that touch on ways to communicate to a friend or family member who is depressed because, well, it&amp;#8217;s a delicate issue and one that deserves some education. I found this quiz on Everyday Health on what you should and should not say to a loved one struggling with depression.
1. Snap out of it!
Your loved one hasn&amp;#8217;t left the house in what seems like days. Should you tell him to pull himself up by his bootstraps and just snap out of it?
Don&amp;#8217;t say it.
You may be tempted to tell someone who&amp;#8217;s depressed to stop moping around and just shake it off. But depression is not something patients can turn on and off, and they&amp;#8217;re not able to respond to such pleas. Instead, tell your loved one that you&amp;#8217;re available to help them ...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4164556</comments>
            <pubDate>Sat, 13 Nov 2010 21:16:54 +0100</pubDate>
            <guid isPermaLink="false">4164556</guid>        </item>
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            <title>Up And Down The Ladder… Job Changes</title>
            <link>http://www.medworm.com/index.php?rid=4098463&amp;cid=t_200519_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FNHui_6K0h3g%2F</link>
            <description>Hired someone new and exciting? Promoted a rising star? Finally solved that hard-to-fill spot? Share the news with us and we’ll share with it others. That’s right. Send us your announcements and we’ll find a home for them. Don’t be shy. Everyone wants to know who is coming and going, especially with all the layoffs. Despite the downsizing, there is movement. Here are some of the latest changes. Recognize anyone?
And here is something that’s become a regular feature. Send us a photo and we will spotlight a different person each week. This time around, we note that the Biomedical Research Alliance of New York hired Carmela Houston-Henry as business development director. Prior to joining BRANY, she was
a senior manager for corporate clinical research at Bracco Diagnostics, and also ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4098463</comments>
            <pubDate>Fri, 22 Oct 2010 12:26:00 +0100</pubDate>
            <guid isPermaLink="false">4098463</guid>        </item>
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            <title>Introducing an Epidemic of Addiction</title>
            <link>http://www.medworm.com/index.php?rid=3920900&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F08%2F31%2Fintroducing-an-epidemic-of-addiction%2F</link>
            <description>I&amp;#8217;m pleased today to introduce our newest blog, Epidemic of Addiction, with Dr. Jeffrey Junig. Addictions to substances &amp;#8212; like alcohol, cocaine, opioids, prescription drugs and other kinds of drugs &amp;#8212; remain a serious problem in modern society. It&amp;#8217;s a telling sign that society pays little attention to drug addicts, believing that theirs is a self-made bed in which to lie upon.
But like any mental illness, addiction is not something a person ever asks for. Addiction often creeps up on a person as they&amp;#8217;re living their everyday lives, starting out not so much as a problem at first. It can quickly snowball, though, and become a problem before a person ever realizes it.

As Dr. Junig says in his introduction, &amp;#8220;This blog will explore the psychology of addictive...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3920900</comments>
            <pubDate>Tue, 31 Aug 2010 17:27:03 +0100</pubDate>
            <guid isPermaLink="false">3920900</guid>        </item>
        <item>
            <title>Best of Our Blogs: August 31, 2010</title>
            <link>http://www.medworm.com/index.php?rid=3920901&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F08%2F31%2Fbest-of-our-blogs-august-31-2010%2F</link>
            <description>Here is it. The last day of August. When you think back to the last three months of summer, how do you feel?
Did you get to do everything you wanted to do? Read every book you wanted to read? Spend a few days relaxing and doing nothing too?
Sometimes we get sucked into this &amp;#8220;I need to accomplish everything and be perfect&amp;#8221; hole. And when we&amp;#8217;re there, we don&amp;#8217;t know how we winded up where we are or why we wanted to be there in the first place.
There&amp;#8217;s a theme in this week&amp;#8217;s top posts that have to do with perfectionism and also truth. I think we all strive to seek truth, what&amp;#8217;s true for us and how to accept ourselves and be comfortable with who we are. Yet, there&amp;#8217;s this crazy sense of push and pull between who we are (what&amp;#8217;s true) and who w...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3920901</comments>
            <pubDate>Tue, 31 Aug 2010 11:57:48 +0100</pubDate>
            <guid isPermaLink="false">3920901</guid>        </item>
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            <title>Real Mental Health is HealthyPlace?</title>
            <link>http://www.medworm.com/index.php?rid=3833454&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F08%2F07%2Freal-mental-health-is-healthyplace%2F</link>
            <description>Who runs Real Mental Health? Who owns Healthy Place.com? Are they one and the same?
These are interesting questions to ask, because you can&amp;#8217;t find such information on their websites. What makes it even more interesting is what recently happened to the Real Mental Health website that demonstrates a behind-the-scenes connection between these two sites &amp;#8212; a connection not acknowledged anywhere on either site.
Real Mental Health is a small mental health community built upon a third-party social networking suite of tools. The website used to reside at realmentalhealth.com. But at the end of May, the site suddenly went away without notice to its members. That&amp;#8217;s when the intrigue began.
 
It came back a week later at a different URL (realmentalhealthsite.com), with little explana...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3833454</comments>
            <pubDate>Sat, 07 Aug 2010 11:56:00 +0100</pubDate>
            <guid isPermaLink="false">3833454</guid>        </item>
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            <title>God’s Petrie Dish</title>
            <link>http://www.medworm.com/index.php?rid=3827248&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fgods-petrie-dish%2F</link>
            <description>I’m sure you feel like I do
Sometimes when life’s too much;
Pain happens once too often,
Downhill without a clutch.
I’m the little smear
On the surface of God’s dish
Growing in the medium
With all that squish and swish.
Is my life an experiment,
Of some mad scientist?
Or is this whole thing planned
Like a novel with a twist?
Problems upon problems
Begin to weigh me down
My body, mind, and spirit spent
I’m certain I will drown.
I can feel the water o’er me
As I come up for air
Struggling I resurface paddling,
I’m driven by despair.
I’ve learned what will support me
I know what brings me down,
But I don’t do either,
Just lie there on the ground.
I know I will get up,
When I pull myself erect
And after hunting high and low
Will find my self-respect.
I know it’s here somepl...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3827248</comments>
            <pubDate>Thu, 05 Aug 2010 21:18:53 +0100</pubDate>
            <guid isPermaLink="false">3827248</guid>        </item>
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            <title>People Say the STUPIDIST Things (About MS)</title>
            <link>http://www.medworm.com/index.php?rid=3648685&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fpeople-say-the-stupidist-things-about-ms%2F</link>
            <description>While , &amp;#8220;But you look so good…” may be intended as a compliment (or at least a deflector) coming from someone talking about your multiple sclerosis, there are other things that people say that is downright mean.  Whether or not it is intended, people can say some pretty hurtful things about (or actually TO) those of us living with MS.
While I must admit that the most offensive thing anyone has ever said to me was along the line of, “You don’t really need that cane; do you?”; in a recent article in the National MS Society’s Momentum magazine I read evidence of some pretty awful stuff that people can say.
Sure, we could chalk some of it up to ignorance, some comments up to fear and some a deflection device for their own &amp;#8220;stuff&amp;#8221;.  Some of it, however, is nothin...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3648685</comments>
            <pubDate>Thu, 10 Jun 2010 14:26:29 +0100</pubDate>
            <guid isPermaLink="false">3648685</guid>        </item>
        <item>
            <title>MS and a Moment of Silence</title>
            <link>http://www.medworm.com/index.php?rid=3641160&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fms-and-a-moment-of-silence%2F</link>
            <description>Multiple sclerosis has created a lot of “noise” in my life.  Either real or perceived or figurative; a lot goes on in the head of someone living with MS.  I think the sheer volume of &amp;#8220;stuff&amp;#8221; I think about has quadrupled since diagnosis.
I mean, seriously, who else has to think about all of the &amp;#8220;what if’s&amp;#8221; and &amp;#8220;then I would’s&amp;#8221; and &amp;#8220;how will I’s&amp;#8221; and &amp;#8220;am I able to’s&amp;#8221; that go with just about every part of our lives as MS progresses?!
Whether it’s sleepless nights during/post attack, as my brain tries to reroute signals or the constant self-talk to get me through-over-around-(sometimes) under obstacles (both real and imagined) it seems that I’ve never a quiet moment.
Well, this weekend I got one… well, several.
I a...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3641160</comments>
            <pubDate>Mon, 07 Jun 2010 19:26:45 +0100</pubDate>
            <guid isPermaLink="false">3641160</guid>        </item>
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            <title>New Beginnings in Your Heart and Head</title>
            <link>http://www.medworm.com/index.php?rid=3629763&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fnew-beginnings-in-your-heart-and-head%2F</link>
            <description>There is a great tendency to be discouraged when you have pain everyday. It’s like a slippery slide in our Oregon rain. If you just sit there on that slick slope, you’re going to slide down and probably land in the gooey mud. Sliding through this life is easy. You don’t really have to do anything in particular. Just embrace your depression, know life today and again tomorrow, will be terrible and there you have it; the slow descent into a life of hellish pain and suffering. It’s an interesting fact about suffering that it is not all in the physical realm. Suffering is highly contagious and can infect our hearts, out minds and our attitudes…big time. It spews and oozes over into our social lives, our family lives and our financial existence.
All of us know what it is to wallow, we...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3629763</comments>
            <pubDate>Thu, 03 Jun 2010 22:06:31 +0100</pubDate>
            <guid isPermaLink="false">3629763</guid>        </item>
        <item>
            <title>How Important is “Stuff” in A Life of Chronic Pain?</title>
            <link>http://www.medworm.com/index.php?rid=3607677&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fhow-important-is-stuff-in-a-life-of-chronic-pain%2F</link>
            <description>Do you ever wonder what you’ll leave behind? With Memorial Day approaching and the recent loss of my sweet mother-in-law, I’ve had a lot of time this week to think about the debris we leave behind. We all know we leave a trail of possessions and financial resources when we die but we lay that trail while we are alive, don’t we?  
We humans leave bits of our skin as we shed it every day, according to the vacuum cleaner salesmen. Most of us find our hair falling out; some more than others. We have tons of garbage rotting in dumps all over the country, some even out on barges in the ocean. We see discarded disposable diapers lying in parking lots and wonder at the term, disposable. It’s strange to realize many of these bits of debris and garbage will be around long after we are not....</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3607677</comments>
            <pubDate>Thu, 27 May 2010 19:28:49 +0100</pubDate>
            <guid isPermaLink="false">3607677</guid>        </item>
        <item>
            <title>Something You Can Do For World MS Day</title>
            <link>http://www.medworm.com/index.php?rid=3603716&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fsomething-you-can-do-for-world-ms-day%2F</link>
            <description>Today, May the 26th, 2010 has been proclaimed World MS Day by Multiple Sclerosis International Federation. This is the second of such observances.

When I wrote about the day last year, I noted several of us who would have liked to do something in respect to the day, but didn’t know what, where or how.
Today, not necessarily in direct connection with World MS Day, I have something we can all do (in a matter of 5 minutes) which might make us feel like we’ve added to the body of knowledge, as it were.
Last week, I was forwarded a link to a short (like 5-question short) survey about MS and the Internet by the National MS Society. The results of which will be published in the fall edition of “Momentum”, the Society’s quarterly magazine.
There is no personal information required in th...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3603716</comments>
            <pubDate>Thu, 27 May 2010 02:34:12 +0100</pubDate>
            <guid isPermaLink="false">3603716</guid>        </item>
        <item>
            <title>MS Tremor of Intent</title>
            <link>http://www.medworm.com/index.php?rid=3595766&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fms-tremor-of-intent%2F</link>
            <description>Multiple sclerosis tremors can be couched in a few categories; Resting Tremor (more common in Parkinson’s than MS), Postural Tremor (sitting or standing, but not lying down), Nystagmus Tremor (those crazy eye jerking tremors).
“Intention Tremor”, however, is the tremor symptom which occurs most commonly in people living with multiple sclerosis.
This form of shaking happens when our brains try to tell a body part to move and the “static-y” signal gets mucked up on the way down the central nervous system.  I oft liken this to hearing every other word on a phone conversation or listening to AM radio as you drive past high-power electric lines.
While I have resting tremor at the end of the day, intention tremor used to be one of my oddest symptoms.
It only occurred in my left arm an...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3595766</comments>
            <pubDate>Mon, 24 May 2010 18:43:37 +0100</pubDate>
            <guid isPermaLink="false">3595766</guid>        </item>
        <item>
            <title>It’s the Little Things</title>
            <link>http://www.medworm.com/index.php?rid=3595903&amp;cid=t_200519_151_f&amp;fid=35818&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FRecoveryIsSexycom%2F%7E3%2FhIvc2vinbtU%2F</link>
            <description>It&amp;#8217;s the little things: Everyday gratitude as a booster shot for romantic relationships
In early recovery from alcoholism, addiction, co-dependency or gambling one can be so relieved at finally finding a solution that one may over-commit to the new activity. With all the attendance at meetings, coffee with other members, 12th Step work one tends to do so at the expense of quality time with family and friends.
The Big Book of Alcoholics Anonymous talks about this in chapter 8, ‘To Wives’. 
Additionally, the legacy of self-centeredness can run well into sobriety excluding again family and friends. As one gets further into recovery one tends to realize an element of gratitude for the people as well as making amends where necessary.
Expressing gratitude is one way of making amends an...</description>
            <author>Recovery Is Sexy.com</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3595903</comments>
            <pubDate>Mon, 24 May 2010 15:04:00 +0100</pubDate>
            <guid isPermaLink="false">3595903</guid>        </item>
        <item>
            <title>Alternative Scenes in a Life of Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3588963&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Falternatives-scenes-in-a-life-of-chronic-pain%2F</link>
            <description>Quite often when you rent a movie, on the main menu they give you an opportunity to view deleted scenes, humorous flubs and alternative endings. I find it interesting and have often thought how wonderful it would be to be able to delete many of my past and present &amp;#8220;scenes&amp;#8221; in a life with chronic pain. I could fill a DVD with humorous misadventures and examples of screwing up and most certainly, it would be a good thing to write alternative adventures, whether they are beginnings or endings. So much of our daily life with chronic pain is far too boring to be an interesting movie. I can see it now in my mind’s eye. The main character is limping to the bathroom. She or he is struggling to get into a hot shower, camera pans to foggy windows. He grumbles into his clothes as life p...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3588963</comments>
            <pubDate>Fri, 21 May 2010 21:03:33 +0100</pubDate>
            <guid isPermaLink="false">3588963</guid>        </item>
        <item>
            <title>MS and Menopause</title>
            <link>http://www.medworm.com/index.php?rid=3588964&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fms-and-menopause%2F</link>
            <description>MS affects so many parts of our daily life. I wonder how much of our daily lives affect our multiple sclerosis…
There is proof that diet and exercise can help improve symptoms of MS and a growing body of evidence that what we do may change, on at least some small level, the course of our actual disease. Even if it’s written off as “a healthy body recovers faster”, that’s at least something!
Of course some things happen to our bodies, over which we have little to no control, which can have significant effect on our symptoms and disease.
Infection/fever and pregnancy come to mind.
My diagnosing MRI revealed a massive sinus infection; the fever from which made the flair so much worse (bad enough to make me go to the doctor).
The issue of pregnancy and its confounding effect on a wo...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3588964</comments>
            <pubDate>Fri, 21 May 2010 19:27:37 +0100</pubDate>
            <guid isPermaLink="false">3588964</guid>        </item>
        <item>
            <title>Things We’ve Learned From MS</title>
            <link>http://www.medworm.com/index.php?rid=3573825&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fthings-weve-learned-from-ms%2F</link>
            <description>Please do not get me wrong; I HATE multiple sclerosis!  The content of this posting does not, in ANY WAY, hint that I’m ok with having this disease.  Like every circumstance in my life, however, I believe it is my task to learn something from and advance myself because of the experience.
That said, I have learned much from living with MS.
This weekend friends from Europe called to let us know they were arriving (in hours).  We knew they would be coming sometime this month, but weren’t exactly sure (as they have been driving around the western states on holidays).
A quick phone call from a national forest in California and we were in full planning mode!
On Saturday, just hours before a welcoming party, I suffered a couple of back-to-back self-inflicted injuries which lay me down for ...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3573825</comments>
            <pubDate>Mon, 17 May 2010 19:23:36 +0100</pubDate>
            <guid isPermaLink="false">3573825</guid>        </item>
        <item>
            <title>MAY I Ask: How’s Your MS Today?</title>
            <link>http://www.medworm.com/index.php?rid=3566720&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fmay-i-ask-how%25e2%2580%2599s-your-ms-today%2F</link>
            <description>MS changes: Day-to-day, week-to-week, month-to-month.
Every month, we try to take time in the first couple of weeks with the intent to allow for a bit of reflection and self-analysis about the current state or your Multiple Sclerosis.
Feel free to leave a comment about your current successes and/or difficulties.  Ask questions of one another, or propose a topic for future blog discussions.  This monthly conversation has been going on for over 4 years now, and I don’t see a reason to stop now!
As for my MS today?
You may have noted a lack of posts this week until today.  I was working in Portland, OR from last Sunday and, quite frankly between the travel and the work I found my limits… about 100yds behind me!
My next 6 weeks have me traveling a considerable amount (7 trips, 5 states ...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3566720</comments>
            <pubDate>Fri, 14 May 2010 17:50:04 +0100</pubDate>
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            <title>Finding Your Limits in a Life With Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3564106&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Ffinding-your-limits-in-a-life-with-chronic-pain%2F</link>
            <description>There are few subjects we haven’t covered in the four years of this blog’s existence but there are certain themes which keep recurring as we wind our way through life with this “load” of chronic pain on our backs. We aren’t inanimate objects, groceries on a shelf going stale, produce in a bin rotting away with each hour; no, we’re human beings with lives, families and homes. We have chores, jobs, and other responsibilities to fulfill each day. Many of us have stopped working for remuneration but we still have work to do. We live, surrounded by a world that sheds, grows, blows dust, sheds skin, gets hungry, and often needs fixing.
The constant issue which keeps arising in our lives is how much to do, how far to go and what is safe for us. How do you find your limits? How do you ...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3564106</comments>
            <pubDate>Fri, 14 May 2010 01:50:00 +0100</pubDate>
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            <title>Stem Cells for Crohn’s Disease</title>
            <link>http://www.medworm.com/index.php?rid=3545542&amp;cid=t_200519_129_f&amp;fid=36036&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Fkelly-building-a-crohns-disease-community%2Fstem-cells-for-crohns-disease%2F</link>
            <description>Since I am now in the midst of a huge flare up, I have been researching new and upcoming therapies for Crohn’s and thought that I would share what I have found out. One of the most exciting areas of research right now is stem-cell research.  There are a couple of different investigations with stem cells for Crohn’s disease going on right now that I found very interesting and hopeful. All of the stem cell therapies are still in the clinical trial phase and are not available to the public yet.
The first area of research is studying the effects of injecting adult stem cells into the patient. I actually almost joined this clinical trial back in 2007, but decided to wait since I was getting better at that time and had just started my new job here in the states. I kind of wish that I did joi...</description>
            <author>Life with Crohn's</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3545542</comments>
            <pubDate>Sat, 08 May 2010 03:46:42 +0100</pubDate>
            <guid isPermaLink="false">3545542</guid>        </item>
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            <title>Spring Cleaning in a Life With Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3542732&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fspring-cleaning-in-a-life-with-chronic-pain%2F</link>
            <description> 

 
Those of us who live with chronic pain have looked forward to spring. Slowly, it’s seeping into our lives and we look forward to a respite from the cold, the snow, the wet and the wind. It’s been a long hard winter for so many among us and continues to cause problems today in many areas of the United States. We feel the weather changes in our bodies and we have to use energy we don’t have to cope with all of the surprises and clean-up of severe weather. Life is just more difficult when it’s dreary, cold and wet.
There is, however, a down-side to spring’s arrival as fresh light reveals dust, dirt and swinging cobwebs. Somehow it’s easier in the darkness of winter to throw that magazine onto a pile of other magazines. They should be with their friends.  At our house we ...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3542732</comments>
            <pubDate>Thu, 06 May 2010 20:36:17 +0100</pubDate>
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            <title>Multiple Sclerosis Home Modifications</title>
            <link>http://www.medworm.com/index.php?rid=3542733&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fmultiple-sclerosis-home-modifications%2F</link>
            <description>MS, by definition, is a degenerative disease of the central nervous system.  That term “degenerative” has always bothered me but, it’s true.  For most of us, it keeps getting a little worse – taking (at least) a little bit more from us – as we get older.
I mentioned (or “teased” as they say in the broadcast business) the idea of modifications we may need to make to our homes in my recent post about a fall and have moved forward with plans to install a second handrail on the steps to our home office.
As we look to an eventual move back to Ireland, there are many considerations to keep in mind when buying a new home. Most of us won’t go as far (unless it’s mandatory) as moving out of our homes because of our MS.  Many of us, however, have considered the need to make ou...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3542733</comments>
            <pubDate>Thu, 06 May 2010 19:33:23 +0100</pubDate>
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            <title>When MS Meets Social Media</title>
            <link>http://www.medworm.com/index.php?rid=3526861&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fwhen-ms-meets-social-media%2F</link>
            <description>One thing that can surely be said about the World Wide Web; it’s, well world-wide, 24/7.
It is now, as I write this post, 5:30 a.m. local time and I’ve been up for nigh 2 hours already.  I was using the wonderful world of the Internet to link into a social media meeting in Switzerland (not travel accepted, no “secret” information exchanged, no harm, no foul);  I said my piece and relayed your comments and half an hour later – I’m ready to go back to sleep!
The topic of social media has, obviously, been on my mind for some time now and your comments have helped, but have also left me wondering about the medium…
Technically, Life With MS comments are “screened”, as we try to weed out spam and personal attacks.  “Un-screened” social media is something like Facebook;...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3526861</comments>
            <pubDate>Mon, 03 May 2010 15:05:49 +0100</pubDate>
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            <title>Your Opinion MATTERS (to Pharma AND to Me!)</title>
            <link>http://www.medworm.com/index.php?rid=3519582&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fyour-opinion-matters-to-pharma-and-to-me%2F</link>
            <description>Our earlier post about ethics has really stirred up a conversation!  I knew I could count on our multiple sclerosis community for thoughtful debate on this as a specific topic.  You always come through!
If you hadn’t noticed in my comment to Jane D I have decided that I will not be attending the group mentioned.
The broader question, really, is what we want from the pharmaceutical companies (other than the obvious).  We’ve had a bit of a conversation about this before and your comments were, again, thoughtful.  I’d like to open that up again.
For your information (if not disclosure) I am going to Skype into part of their discussion to give my/our opinions.  This way, not only will I not be accepting travel, I’m actually going to have to look presentable for a video conference ...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3519582</comments>
            <pubDate>Thu, 29 Apr 2010 18:32:59 +0100</pubDate>
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            <title>The Art of Living With MS</title>
            <link>http://www.medworm.com/index.php?rid=3515517&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fthe-art-of-living-with-ms%2F</link>
            <description>“Nature abhors a vacuum”, Rabelas said; and so do I!
Multiple sclerosis has carved our big gaping chunks from our lives; be it our career, family, activity or some other joy-giving entity.  MS leaves holes; some large some now so.  How to fill them?
That question was one of the first to enter my mind once the initial slide abated (read about 6 months post Dx).  It’s still one with which I struggle and suspect that many others do as well.
For me, writing, gardening, and volunteer work with the National MS Society (along with the extra time everything seems to take with MS) have filled much of the time I used to spend working; but not all of it.  I’ve learned that many people with MS have turned to art (in many forms) to not only fill the void of available time but to help either...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515517</comments>
            <pubDate>Wed, 28 Apr 2010 19:13:50 +0100</pubDate>
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            <title>Vertigo and MS</title>
            <link>http://www.medworm.com/index.php?rid=3508326&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fms-and-vertigo%2F</link>
            <description>A couple of short spells of dizziness this weekend brought back memories of my first discernable MS attack.
Dizziness is a fairly common symptom of multiple sclerosis.  Many of us will feel the occasional light headed-ness, a slight bit of disorientation, and a sense of being off-balance when placing one foot in front of the other.  Vertigo, however, is a much more severe and significantly rarer (but far from unknown) symptom of MS. 
This past weekend I experienced a bit of the former while walking through a parking lot.  Luckily, Caryn was at my side and the episodes passed after a couple of moments.  Being that we were walking to a live-aboard friend’s boat for an early evening supper made me leery of the evening’s prospects but everything turned out fine (better than that; we h...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3508326</comments>
            <pubDate>Mon, 26 Apr 2010 20:58:11 +0100</pubDate>
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            <title>Off the Internet for 24 Hours</title>
            <link>http://www.medworm.com/index.php?rid=3501563&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F04%2F24%2Foff-the-internet-for-24-hours%2F</link>
            <description>What happens when you take 200 journalism students and cut them off from the Internet for 24 hours?
It&amp;#8217;s something I might call &amp;#8220;information anxiety,&amp;#8221; because the students expressed a great deal of anxiety in the narratives they provided the researchers after the experiment was over. (But I would be quick to add, I&amp;#8217;d never consider this a &amp;#8216;disorder&amp;#8217; &amp;#8212; just a simple, predictable result of removing an important set of tools we&amp;#8217;ve come to rely on from our everyday world.)

“Students expressed tremendous anxiety about being cut-off from information,” observed Ph.D. student Raymond McCaffrey, a former writer and editor at The Washington Post, and a current researcher on the study.
“One student said he realized that he suddenly ‘had less in...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3501563</comments>
            <pubDate>Sat, 24 Apr 2010 12:34:08 +0100</pubDate>
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            <title>Ethics, Big Pharma, and Life With MS</title>
            <link>http://www.medworm.com/index.php?rid=3499196&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fethics-big-pharma-and-ms%2F</link>
            <description>When it comes to living a life with Multiple Sclerosis, the Life With MS Blog community has made mine much more bearable.  This blog, however, is not about me.  As I stated over 4 years ago, in our first posting, “It’s all about you!”
So today, I’d like to bring up an important question.  I need to know what you want from this blogger; it’s a bit of an ethical dilemma for me.
As our community has grown, so has our visibility to the greater MS world.  It is not simply patients and their loved ones who visit this blog.  More and more, I am approached by the members of the broader MS community; service organizations, other bloggers, care providers, medicos, pharmaceutical companies, etc…
In the past, it has been pretty easy to stay above the fray, as it were. I simply used wh...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3499196</comments>
            <pubDate>Fri, 23 Apr 2010 15:18:07 +0100</pubDate>
            <guid isPermaLink="false">3499196</guid>        </item>
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            <title>MS &amp; Self-Compassion</title>
            <link>http://www.medworm.com/index.php?rid=3499197&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fms-and-compassion%2F</link>
            <description>Do you ever feel like you maybe don’t give yourself enough credit for doing as much as you do…MS and all?
I had a very busy work weekend (which ran into Tuesday).  I had every intention of waking up on Wednesday, banging out a blog for posting and getting on with a productive day.
And now, it’s Thursday!
I really have no idea where yesterday went.
By the evening I was beating myself up pretty good over what didn’t get done; including (but FAR from limited to) that blog…
But this morning, even though I don’t feel 100%, I think I’ll get a little more done.  Certainly, I’ll not get everything done I want.  In fact I hope to get everything done I need and will call that a successful day.  But, here I am writing this blog so things are at least a bit better than yesterday.
P...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3499197</comments>
            <pubDate>Thu, 22 Apr 2010 20:32:31 +0100</pubDate>
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            <title>Brain Games Don’t Help Your Brain</title>
            <link>http://www.medworm.com/index.php?rid=3490679&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F04%2F21%2Fbrain-games-dont-help-your-brain%2F</link>
            <description>A red flag always goes up in my mind when I see an entire industry sprout up around something that doesn&amp;#8217;t have a lot of research backing. That&amp;#8217;s been the problem with these so-called &amp;#8220;brain games&amp;#8221; &amp;#8212; you know, those video or online games that supposedly improve your memory or thinking. 
Makers of these games like to point to studies of people who were older (usually seniors), had existing memory or cognitive problems or other issues who engaged in specific tasks and then were shown to have some improvement in memory or cognition. Few studies have been done on these games with everyday folks like you and I. And fewer still studies have been done on the specific games being marketed to consumers (often the studies use tasks that the games then try and replicate,...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3490679</comments>
            <pubDate>Wed, 21 Apr 2010 15:43:08 +0100</pubDate>
            <guid isPermaLink="false">3490679</guid>        </item>
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            <title>Is It MS?</title>
            <link>http://www.medworm.com/index.php?rid=3479789&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fis-it-ms%2F</link>
            <description>A couple of years ago, my local chapter of the National MS Society spearheaded a media campaign under the header “Why Here?” having to do with an increased prevalence of MS in America’s Pacific Northwest (approximately 1:500)
Numerous billboards around the area were the impetus for many, MANY in depth conversations about MS in the community.
This year the chapter has launched “Is It MS?” and while there are many conversations, the tone of the conversations has changed a bit.
“Why Here?” seemed to open the door to questions and discussion about our disease without threatening.  When people found out about my multiple sclerosis, they would mention that they had heard that MS was a big issue here, etc.
“Is It MS?”, however has started far few conversations from the general...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3479789</comments>
            <pubDate>Fri, 16 Apr 2010 21:25:09 +0100</pubDate>
            <guid isPermaLink="false">3479789</guid>        </item>
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            <title>The Morning in My Life With Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3475946&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fthe-morning-in-my-life-with-chronic-pain%2F</link>
            <description>Before I open my eyes each morning, upon awakening, I feel pain. 
Each day it is the same, that moment never changes because my body has not changed. The area of pain may move, and does, as I take inventory each morning. “Arms, legs…  still intact. Hips in pain as well as the backside. Neck, sore yet functional, etc.”
When I am asleep I dream the dreams of the healthy which are shattered on awakening.
Each day, I am disappointed. I must be a slow learner because I have not accepted the pitiful side of my fate by now; or perhaps I am just a believer in efforts, faith and possibilities.
When I open my eyes, I usually have the front or the rear view of a furry grey Miniature Schnauzer who has cuddled closely to me with the morning chill, trying to horn in on my heating pad. Both ends...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3475946</comments>
            <pubDate>Thu, 15 Apr 2010 19:46:19 +0100</pubDate>
            <guid isPermaLink="false">3475946</guid>        </item>
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            <title>April Check: How’s YOUR MS Today?</title>
            <link>http://www.medworm.com/index.php?rid=3471922&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fapril-check-how%25e2%2580%2599s-your-ms-today%2F</link>
            <description> 
Every month, Life With MS opens up the conversation about Multiple Sclerosis to your thoughts.
Usually, I try to post this blog the first Wednesday of the month, but last Wednesday was when I heard about the CCSVI webcast and wanted to get that information out to everyone straight away!  In fact, that webcast takes place today (4/14) at 9:00am PDT. I’ve submitted my question.  I hope you did as well!
So, this is a little late this month, but; How is YOUR MS today?
I’ll not cover up the fact that my MS has been hanging around this past fortnight a bit more predominantly than I’d like.
Between the “post-Novantrone” anemia, a 2-hr live TV program, Walk MS in Seattle and my recent fall, I guess you could say that I’ve had my share of MS this month already!
But enough about m...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3471922</comments>
            <pubDate>Wed, 14 Apr 2010 18:26:54 +0100</pubDate>
            <guid isPermaLink="false">3471922</guid>        </item>
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            <title>Chronic Pain Blog to Change</title>
            <link>http://www.medworm.com/index.php?rid=3463725&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fchronic-pain-blog-to-change%2F</link>
            <description>After much contemplation, I have decided to write a new blog only once a week instead of the two fresh entries I have been writing since August 2006. Those of you who read this blog frequently know I fight an uphill battle each day with my health which is the source of inspiration for this. I’m trying to decide what to share with all of you. The bad news is that I’m running out of steam with all the current problems I’m having and the blog has become more and more popular and demands more responses from me. I’m thrilled at the popularity of this blog and stubbornly try to answer each entry from all of you. I will continue to do so.
As many of you know, there are many days your energy only goes so far and then, that’s it. I thought about shortening the blogs or making them less su...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3463725</comments>
            <pubDate>Mon, 12 Apr 2010 22:25:51 +0100</pubDate>
            <guid isPermaLink="false">3463725</guid>        </item>
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            <title>MS and Falling</title>
            <link>http://www.medworm.com/index.php?rid=3463726&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fms-and-falling%2F</link>
            <description>We likely all studied Newton’s theory of Gravity in school; “F = GmM/r^2” is how the renowned scientist mapped out the force (F) of attraction between two objects (m, M) which draw them together.  I’ll have to remember that equation the next time I find myself in a crumpled heap at the bottom of the stairs…
I’m sporting a wicked bruise on my left arm this week; a result of such a fall.
A momentary shift in focus from placing my foot on the bottom step in preparation for a routine assent, as Sadie hurried past in an heretofore unannounced race, and I was inhaling the scent of recently-vacuumed carpet…up close!
On my way down the up staircase, my forearm met the end of the handrail with the “F” of “m” meets “M” leaving a 7” deep muscled bruise which is now that u...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3463726</comments>
            <pubDate>Mon, 12 Apr 2010 22:08:51 +0100</pubDate>
            <guid isPermaLink="false">3463726</guid>        </item>
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            <title>Is it Ever Too Late to Take Back Your Life?</title>
            <link>http://www.medworm.com/index.php?rid=3454051&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fis-it-ever-too-late-to-take-back-your-life%2F</link>
            <description>Roll up the cuffs on your pants; take off your shoes because it’s going to get deep in here. We’re going to ask ourselves questions like, “What is the meaning of life?” as well as “What does life mean to you?” and “Is it possible to be happy living a life with chronic pain?”
What is the meaning of life to you? I know there are as many answers to that question as there are individuals asking it. To some of us it has changed over the years as we have changed. We age, we decline, we become more educated, we get sick, and we get rich or poor and our goals in life change. Nobody stays the same, ever. The glitch in the answers to life seems to come in at that change part. When we live with someone else and we change, they have to adapt, or adjust to that change or there can be su...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3454051</comments>
            <pubDate>Thu, 08 Apr 2010 22:00:01 +0100</pubDate>
            <guid isPermaLink="false">3454051</guid>        </item>
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            <title>Adapting to a Life of Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3443859&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fadapting-to-a-life-of-chronic-pain%2F</link>
            <description>I may look the same as everyone else, but inside, I feel differently because I always have pain. It doesn’t come and go, like an errant neighbor; no, it stays, more like an inconsiderate relative who moved in without waiting for an invitation. When a cataclysmic event occurs in your life, like the advent of chronic pain, it changes you. Not only do you have the physical part of it to deal with, but because you still walk, hopefully, talk and breathe, you have to find a new and often inventive way to do everything. Life’s personal responsibilities remain, our family duties continue and the mere simple tasks of daily life call out to us; therefore you find new ways to do old, everyday jobs.
Over the years on this blog I have discussed with all of you the many ways to ease life while at t...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3443859</comments>
            <pubDate>Wed, 07 Apr 2010 00:33:52 +0100</pubDate>
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            <title>New Webcast/Telecast: MS and Employment</title>
            <link>http://www.medworm.com/index.php?rid=3440935&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fnew-webcasttelecast-ms-and-employment%2F</link>
            <description>Multiple Sclerosis is a disease which affects our lives in so many different ways; employment being one of them.
Many of us have, for much of our adult lives, associated our identities with our careers.  Many of us derive great satisfaction and meaning from the work we do or from the independence our work (or at least our paycheck) affords.
Many of us living with Multiple Sclerosis are struggling to say employed.
Tomorrow (Tuesday, April 6th) night, I’ll be hosting a 2-hour live telecast/webcast entitled “Staying In The Employment Game”.
The program will air live, with a studio audience at 8:00pm (PDT) on the stations of the University of Washington.  If you don’t live in the Seattle area, you can watch live via webcast on either the University website or Research Channel on the ...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3440935</comments>
            <pubDate>Mon, 05 Apr 2010 18:59:00 +0100</pubDate>
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            <title>When MS Wrings You Out</title>
            <link>http://www.medworm.com/index.php?rid=3435144&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fwhen-ms-wrings-you-out%2F</link>
            <description>MS is a condition which, no matter how well we plan, takes us by surprise now and again.  Go to bed “fine” wake up with part of our body not responding to a call to action.  A simple battle with the circulating bug du jour and a fever sits you down like a crumpled boxer in his corner. Vertigo, which can make a turn of the head into a cyclone-spiral to the floor…
MS can really wring one out…with little warning!
I’m currently on a planned slide into anemia after my treatment on Monday.  I’ve been able to pretty much plan a lighter schedule (ok, who am I kidding?) knowing that I’d be far from 100%.  Still there are things which should get done by me.  It’s just taking a little extra effort.
So, it got me to thinking about those times when our requirements wander beyond t...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3435144</comments>
            <pubDate>Fri, 02 Apr 2010 18:18:02 +0100</pubDate>
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        <item>
            <title>What Excellent MS Care Looks Like!</title>
            <link>http://www.medworm.com/index.php?rid=3429326&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fwhat-excellent-ms-care-looks-like%2F</link>
            <description> 
&amp;#8216;Hello, I’m Trevis and I’ll be your veins today!&amp;#8217;
My parents&amp;#8217; (or was it my grandparents&amp;#8217;?) generation is the one which coined the phrase, “We were poor; we just didn’t know it because everyone else was too…”
Well, I had always thought I was getting excellent service/treatment at infusion centers… until I really had excellent service/treatment!
On Monday I went in for my last dose of Novantrone, as I posted that day.  The overall experience I had was leaps and bounds beyond any infusion center I’ve ever encountered.
I’ve always considered myself pretty well informed, as a patient.  In the first 5 minutes of conversation with my chemo nurse, I was told everything I already knew about the treatment. You may think that was a waste of time.  Thin...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429326</comments>
            <pubDate>Wed, 31 Mar 2010 19:51:53 +0100</pubDate>
            <guid isPermaLink="false">3429326</guid>        </item>
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            <title>The Mental POWER Prague Film Festival</title>
            <link>http://www.medworm.com/index.php?rid=3424908&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F03%2F31%2Fthe-mental-power-prague-film-festival%2F</link>
            <description>Our friends organizing the mental POWER Prague film festival wanted me to let you know that they&amp;#8217;ve extended the submission deadline for films. What is this film festival? (Keep in mind that mental disorders are thought of differently in different cultures, and are referred to with different terminology, so please don&amp;#8217;t take offense at the specific language used below.)

[It] is an international film festival of (non-)actors with a mental or combined handicap organized by HENDAVER, o.s. The festival shows feature films in which exclusively people with a mental and combined handicap act.
The main idea of the festival is to create the conditions for artistic self-fulfillment of handicapped people and thus to take part in their mental development. In addition to that, this activit...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3424908</comments>
            <pubDate>Wed, 31 Mar 2010 14:55:46 +0100</pubDate>
            <guid isPermaLink="false">3424908</guid>        </item>
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            <title>Novantrone - One Last Dose</title>
            <link>http://www.medworm.com/index.php?rid=3420632&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fnovantrone-one-last-dose%2F</link>
            <description>Well, today ends an era for my MS treatment. Today I max out my lifetime allowable dosage of Novantrone.
Much has changed since I began taking the drug. Most notable, my symptoms have changed dramatically for the better. Of course it should be noted that things had gotten pretty bad by the time we made the decision to use that drug.
I was about a year and a half post Dx and had experienced 6 additional attacks. I was walker-dependant for most things outside of the house and fighting every indication that I should purchase a scooter.
My disease had gotten aggressive so, my medical team and I decided we had to respond in kind; we got aggressive!
At the time, Novantrone was the only drug available for a “breakthrough disease”, meaning MS that was not responding to one of the (at that time...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3420632</comments>
            <pubDate>Tue, 30 Mar 2010 03:28:36 +0100</pubDate>
            <guid isPermaLink="false">3420632</guid>        </item>
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            <title>Am I Normal?</title>
            <link>http://www.medworm.com/index.php?rid=3416085&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F03%2F29%2Fam-i-normal%2F</link>
            <description>This is a common theme I hear echoed from a lot of people I meet.
&amp;#8220;Am I normal?&amp;#8221;
&amp;#8220;I can&amp;#8217;t wait to feel more normal again.&amp;#8221;
&amp;#8220;Must be nice being so normal&amp;#8230;&amp;#8221;
The problem is, I don&amp;#8217;t know what normal is.
I suppose for some of the people, they mean &amp;#8220;without the symptoms of my disorder.&amp;#8221; That makes sense, especially as some symptoms of some disorders can be pretty severe and debilitating toward living their everyday life. 
But then I realize that even people without a diagnosed condition still don&amp;#8217;t often feel &amp;#8220;normal.&amp;#8221; We live our lives, we have our stresses, we hate our bosses or the 9-to-5 routine, we get into arguments with our significant others. Is this &amp;#8220;normal?&amp;#8221; 

Some days you don&amp;#8217;t know...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3416085</comments>
            <pubDate>Mon, 29 Mar 2010 11:52:02 +0100</pubDate>
            <guid isPermaLink="false">3416085</guid>        </item>
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            <title>MS “Care Partners”</title>
            <link>http://www.medworm.com/index.php?rid=3411196&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fms-care-partners%2F</link>
            <description>There is a lot of Politically Correct language out there in the world of multiple sclerosis and disabilities in general.
One of the terms bantered about is “Care Partner”.  This replaces caregiver and other terms deemed by some to be demeaning and misunderstood.  I like “care partner” as it gives a sense that people are in the thing together and working in tandem.
I’ve thought that Caryn will be a good care partner to me if and when my MS progresses “that far”.  Then, a couple of weeks ago, I had something of an epiphany.  She already is my care partner…even when I don’t think I need care!
Those of us who live with this disease at any stage, be it in remission or in the midst of a full-on attack, rely on others in our everyday lives.  Caryn lives with my MS every si...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3411196</comments>
            <pubDate>Fri, 26 Mar 2010 19:25:13 +0100</pubDate>
            <guid isPermaLink="false">3411196</guid>        </item>
        <item>
            <title>Keeping it Simple In a Life of Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3408531&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fkeeping-it-simple-in-a-life-of-chronic-pain%2F</link>
            <description>Today’s challenge is enough;  the next flight of stairs, that next load of laundry or the next weed that needs pulling is all you need to be concerned with, for now.
Did you know you can wash one window at a time?
Simple foods can sustain you as readily as complicated dishes; such as veggies, fresh fruit, yogurt and a can of soup. Frozen dinners are often healthy, tasty and convenient. 
It’s easier, safer and wiser to fill your refrigerator with fresh food than to go out for fast food that is fraught with fat and needless calories. Keep food simple.
It’s okay to sit or lie down and rest after any chore. It’s legal, wise and renewing. The “goof off” police will not show up at your door.
Laughter and humor feel like sunshine on a cold, damp day.
Laughter is allowed even when yo...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3408531</comments>
            <pubDate>Thu, 25 Mar 2010 21:29:41 +0100</pubDate>
            <guid isPermaLink="false">3408531</guid>        </item>
        <item>
            <title>A Funny Surprise From Breast Cancer</title>
            <link>http://www.medworm.com/index.php?rid=3385512&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fa-funny-surprise-from-breast-cancer%2F</link>
            <description>There is one positive thing that I can honestly say came out of chemotherapy. It came up with my hairdresser today when she happened to notice that I have great eyebrows. I know it sounds funny, but hey, let me have this one thing. I have always had darker and thicker eyebrows than most women, but not quite as great as Brooke Shields.
I was constantly plucking and shaping them and then breast cancer hit. Chemotherapy thinned them out quite a bit, but it couldn’t quite get rid of them.
After my hair grew back, my eyebrows took on a new shape – and I couldn’t be happier.
So today, my hair dresser commented on how great my eyebrows looked. When I told her I did not have to pluck or shape them ever, I knew she was impressed.
We suffer so much through chemotherapy. Many of us struggle wit...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385512</comments>
            <pubDate>Fri, 19 Mar 2010 21:05:55 +0100</pubDate>
            <guid isPermaLink="false">3385512</guid>        </item>
        <item>
            <title>MS at Work: “Thrive to Survive”?</title>
            <link>http://www.medworm.com/index.php?rid=3385460&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fms-at-work-thrive-to-survive%2F</link>
            <description>Last week I was “workshopping” some of the topics for the upcoming “Staying in the Employment Game” MS TV program.  We sat, a group of about a dozen of us, talking about issues with staying employed after diagnosis.
My full-time work experience ended abruptly within 4 months of Dx.  Most of the people in our group were still employed with the same employers (if not in the exact same jobs) as they were when they learned of their multiple sclerosis.  For this reason, I wanted to learn more about the nuts and bolts of their experiences.
I was a little surprised at the universality of one of the sentiments I heard that night…
“I’ve gone from thrive to survive,” said one man; EVERYONE chimed in with the same feeling.  The conversation that ensued about promotion, income, sta...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385460</comments>
            <pubDate>Fri, 19 Mar 2010 20:46:28 +0100</pubDate>
            <guid isPermaLink="false">3385460</guid>        </item>
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            <title>4 Years of the “Life With MS” Blog</title>
            <link>http://www.medworm.com/index.php?rid=3378617&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2F4-years-of-the-life-with-ms-blog%2F</link>
            <description>Sometimes, life with MS can be an annoyance.  Sometimes, life with MS can be depressing.  Sometimes, life with MS can be frightening.  Sometimes, life with MS can be uncertain.  Sometimes, life with MS can be exhausting…
I hope, however, that you’ve found the Life With MS Blog to be, at least sometimes, a comfort!
This week marks the 4th anniversary of the Life With MS blog and I quite frankly cannot believe it’s been that long!  Well over 600 postings, thousands of comments, tens of thousands of regular readers and I sometimes feel as if we’re just getting started!
Many things have changed since that first posting in 2006; new website, new formats, new topics, new treatments… lots of new!  We’ve consistently seen new readers join our community.
We’ve also lost track of...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3378617</comments>
            <pubDate>Wed, 17 Mar 2010 19:12:00 +0100</pubDate>
            <guid isPermaLink="false">3378617</guid>        </item>
        <item>
            <title>Weakness in the Hands and the Price of Dishes</title>
            <link>http://www.medworm.com/index.php?rid=3374261&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fweakness-in-the-hands-and-the-price-of-dishes%2F</link>
            <description>I’m dropping things!
Pre-diagnosis, back in my 20’s, I simply thought I was clumsy.  I’d trip on exposed tree roots on a hike.  I’d slip and fall down the stairs.  Rugs (and cats) became my introduction to the floor more than once and oh, the glassware I’ve broken…
That was then; this is now and I’m still dropping things.
Over the past couple of weeks, I’ve noticed that I’m sweeping up more broken glass and porcelain than I have in a while.  Wine glasses (empty, thank goodness, up to this point) seem to have an additional gravitational pull these days.  Plates (not all empty, unfortunately) have simply flung from my hand as I turned.  The cost of toothbrushes I’ve had to replace is starting to need its own line in my budget.
The incidents are not coincidence.  I ...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3374261</comments>
            <pubDate>Tue, 16 Mar 2010 19:14:44 +0100</pubDate>
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            <title>MS and Social Media</title>
            <link>http://www.medworm.com/index.php?rid=3362491&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fms-and-social-media%2F</link>
            <description>The topic of MS and social media brings a joke to mind:
Man I: Did you hear about the latest tech news?
Man II: No.
Man I: YouTube, Twitter and Facebook have announced a merger.
Man II: Really; what are they going to call it?
Man I: YouTwitFace.
I was never a social media person; remember I didn’t even know what a blog was when I was asked to start this journey.  I must, however, admit that I’ve really enjoyed being able to catch up with long-lost pals through the medium.
Many people who are limited in their access to the “outside world” due to MS, find such sites and their communities at least a diversion and at best a real lifesaver.
I’ve noticed, especially when it comes to the “MS Underground”, that social media sites are full of people spouting opinions as facts and dec...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3362491</comments>
            <pubDate>Fri, 12 Mar 2010 21:34:18 +0100</pubDate>
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            <title>Creativity is a Miraculous Treatment in a Life of Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3359128&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fcreativity-is-a-miraculous-treatment-in-a-life-of-chronic-pain%2F</link>
            <description>I know you want to be healthy and as well as possible, of course you do. We have covered so many chronic pain treatments over the last few years. We’ve discussed medication, physical therapy and exercise, as well as alternative treatments. We’ve discussed diet and nutrition and the influence on our lives by other people. I always love to chat with all of you about pet therapy and it’s powerful, loving influence on our lives and health. Today, I’d like to talk about another kind of therapy and that is the importance of creative therapy. So grab a lollipop, a Popsicle or a Tootsie pop and read along with me.
Those of us who are around small children have the benefit of being reminded of the joys in creativity. When a small child sits down at the dining room table with a large pad and...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3359128</comments>
            <pubDate>Thu, 11 Mar 2010 22:05:05 +0100</pubDate>
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        <item>
            <title>Naturopathy and MS</title>
            <link>http://www.medworm.com/index.php?rid=3354467&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fnaturopathy-and-ms%2F</link>
            <description>Today, I am keeping one of my New Year’s Resolutions! I am packing myself off to see a new doctor for my MS (and for my whole health).  Today I’m off to see a Naturopath.

For well over 2 years, I’ve had the very good intentions of adding Naturopathy to my medical regimen.  For just as long, I’ve found reasons not to make the appointments.  It’s not like it was difficult; there is a wonderful clinic not 5 miles from my house with NDs who have a keen interest in multiple sclerosis (in fact, the clinic chief is recommended by my MS neurologist!)

I’m not using Naturopathy as an alternative to more standard “western medicine”.  Rather, I intend to augment and compliment my other MS treatments/procedures with the practice.

I’m sure that the battery of lab work will expos...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3354467</comments>
            <pubDate>Wed, 10 Mar 2010 23:45:45 +0100</pubDate>
            <guid isPermaLink="false">3354467</guid>        </item>
        <item>
            <title>Wisdom From the Ages in a Life of Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3350439&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fwisdom-from-the-ages-in-a-life-of-chronic-pain%2F</link>
            <description>If there’s one thing we need as we chug along with this life of pain everyday, it&amp;#8217;s wisdom. Many of our founding fathers were full of profundity and wisdom which sure could come in handy in today’s fast-paced world.
Thomas Jefferson said, “Take care of your change; dollars will take care of themselves.” Certainly, many of us have discovered the same truth applies to minutes. Take care of your minutes; your hours and yes days, will take care of themselves. If you have to scoot, push, pull or crawl toward that goal, surely, you and I can do it one minute at a time. My goodness, Jefferson and a handful of other independent thinkers founded a whole new country. They did it one act, one township and one battle at a time.
So often we look down this road of chronic pain and it appea...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3350439</comments>
            <pubDate>Tue, 09 Mar 2010 23:34:30 +0100</pubDate>
            <guid isPermaLink="false">3350439</guid>        </item>
        <item>
            <title>MS Awareness Week - Are You Ready?</title>
            <link>http://www.medworm.com/index.php?rid=3346595&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fms-awareness-week-are-you-ready%2F</link>
            <description>Even though World MS Day is still more than a month away (May 26th), this is MS Awareness Week in North America.
It’s time to dust off the talking points, break out the MS buttons and get ready to answer questions. There will be television adverts, billboards and radio PSAs this week which could afford each of us to speak about MS this week.
I know that here in Seattle, our chapter of the NMSS (which has just recently been expanded to support people living with MS in Alaska) has a new “Is It MS?” campaign which has been stirring up questions and conversations…and doctor’s appointments
It’s not like each and every one of us has to give a press conference or stand on an overpass waving an “I Have MS; Ask Me!” banner. But, I think we owe it to ourselves and to one another to b...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3346595</comments>
            <pubDate>Mon, 08 Mar 2010 21:16:24 +0100</pubDate>
            <guid isPermaLink="false">3346595</guid>        </item>
        <item>
            <title>Learning About Transcendental Meditation</title>
            <link>http://www.medworm.com/index.php?rid=3338252&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F03%2F06%2Flearning-about-transcendental-meditation%2F</link>
            <description>Discussion tab makes clear feuding editors battling for control about tone and focus. 
I don&amp;#8217;t know what to make of transcendental meditation personally, but I find studies like the recently published one interesting. I know people who use it and swear by its positive effects (but I also know people who use other techniques and methods and swear by them as well). I suspect some of the skepticism comes from the pseudo-religious nature of technique, or the fact that it costs money to learn it. But in my experience, many things worth learning cost money (look at my graduate education, for instance). My only concern is that if it is something that is &amp;#8220;simple, natural, effortless, and easily learned,&amp;#8221; why does it cost $1,500 and an entire day to learn?
I&amp;#8217;ve read enough t...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3338252</comments>
            <pubDate>Sat, 06 Mar 2010 13:32:15 +0100</pubDate>
            <guid isPermaLink="false">3338252</guid>        </item>
        <item>
            <title>No “Death With Dignity” for MS Patients</title>
            <link>http://www.medworm.com/index.php?rid=3338351&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fno-%25e2%2580%259cdeath-with-dignity%25e2%2580%259d-for-ms-patients%2F</link>
            <description>I am not a morbid person - a black sense of humor; that I’ll cop to – but a recent batch of comments on a previous post on the subject brought the topic back to my mind. I’ve been meaning to post something of a follow-up ever since my state passed a &amp;#8220;Death With Dignity&amp;#8221; Act, back in 2008.
It was a hard-fought battle between the two sides with impassioned pleas from proponents and opponents alike.  In the end, the measure passed overwhelmingly.
The thing is, the law was crafted with such tight restrictions as to make (some say “appropriately”) difficult to carry out.  In fact, a reading of the 10 pages of legalese which is the law makes it quite clear that a person in the final throws of MS would not be eligible for the relief intended by the law.
A person, in Washin...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3338351</comments>
            <pubDate>Fri, 05 Mar 2010 22:42:03 +0100</pubDate>
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        <item>
            <title>A Life of Chronic Pain and The Domino Effect</title>
            <link>http://www.medworm.com/index.php?rid=3335484&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fa-life-of-chronic-pain-and-the-domino-effect%2F</link>
            <description>In the last twenty years, since I’ve been living with chronic pain, I’ve met very few individuals who have only one problem. Most of them, like me, have numerous ones. Some of them are permanent and some come and go like unwelcome guests. I often have to be careful because some of my friends feel they are in crisis when they have some current issue arise and their life is in a spin, trying to deal with it. The size of the problem is not the real issue; it’s the jarring effect it has on the life of the individual as it disrupts, worries and often, hurts. Since I’m an old hand at this suffering gig, I often have to watch my level of empathy and keep it in check. It’s not their fault I’m a veteran in the game and they’re not. Thank God they’re not.
As I’ve mentioned so often...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3335484</comments>
            <pubDate>Thu, 04 Mar 2010 22:00:44 +0100</pubDate>
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        <item>
            <title>March Forth and Tell us How’s Your MS Today?</title>
            <link>http://www.medworm.com/index.php?rid=3327181&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fmarch-forth-and-tell-us-hows-your-ms-today%2F</link>
            <description>Tomorrow is the only day I know of which sounds like an order: “March Fourth!”
So, we do…with MS, we March Forth!
Every month we take a moment and assess our MS symptoms, treatments, coping mechanisms, triumphs and tribulations; our lives with MS.
Today, have a check-in moment with yourself and answer the question; “How is your MS today?”
My MS has been static the past several weeks.  I’m pretty glad as I have not been!  Maybe it’s because I’ve gotten used to the “stuff” MS has already taken away, but life with MS has been alright (relative) this past four weeks.  Anyway, I’ve had a lot going on (I’ve already traveled away from home 2 weeks on three trips this year…and it’s only the third month!) and I’m happy that I haven’t had any new stuff to deal with...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3327181</comments>
            <pubDate>Wed, 03 Mar 2010 16:34:58 +0100</pubDate>
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        <item>
            <title>Battling Breast Cancer With Memories</title>
            <link>http://www.medworm.com/index.php?rid=3327250&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fbattling-breast-cancer-with-memories%2F</link>
            <description>Cancer is a family affair. One life may be affected but all lives are disrupted. When you talk to someone who had a mother or sister or wife or daughter that battled breast cancer, it is plain that they felt the pain of that diagnosis and the fear of loss. It is at those times a family needs to remember all the happy days they had. I think of all the happy days in my family&amp;#8217;s life and am grateful that they outweigh the cancer days. Making memories becomes so important for those of us that survive cancer and realize how much those happy days we created before the diagnosis meant to us during the battle.

I think this is what is fueling my need for family pictures all over the house. For the past three months I have been buying frames and photo books and even have one wall in the hallw...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3327250</comments>
            <pubDate>Wed, 03 Mar 2010 15:34:14 +0100</pubDate>
            <guid isPermaLink="false">3327250</guid>        </item>
        <item>
            <title>A Life With Chronic Pain and My Enemies</title>
            <link>http://www.medworm.com/index.php?rid=3327180&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fa-life-with-chronic-pain-and-my-enemies%2F</link>
            <description>GRAVITY is always there, to trip us up, drag us down or rocket some object into our pathway. It is also an enemy to us as the pull of the earth draws all body parts downward. It’s truly amazing how quickly your face can hit the floor.
PAIN of course, that’s a given with the title of this blog. Pain everyday pokes, prods, tugs, needles, cramps and generally befuddles, bewilders and baffles a normal existence. Pain is the giant wrench in the engine of life as it attempts to chug along life’s track.
NEGATIVITY can rock your world, darken your day and cause the skies to open up. When you need every bit of positive fortitude within you to tackle a challenging life, this comes along to tie your hands, dim your wits and cause tears to stream down your face. It very soon can warp into it’s...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3327180</comments>
            <pubDate>Tue, 02 Mar 2010 22:38:12 +0100</pubDate>
            <guid isPermaLink="false">3327180</guid>        </item>
        <item>
            <title>How Are You Proactive With Your MS?</title>
            <link>http://www.medworm.com/index.php?rid=3322519&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fhow-are-you-proactive-with-your-ms%2F</link>
            <description>Let me begin this posting with a disclaimer.  I am not an expert at living with multiple sclerosis.  I am a student of living with my MS.
Last week we began an 8-week course of “Empowered Living for Couples”.  The program is offered by my local chapter of the National MS Society and taught (though she prefers “facilitated”) by my dear friend Maureen Manley.
For the next eight weeks, a group of 7 couples will take 2-hour journeys of discovery and (hopefully) learn skills for living our lives more aware.  I suspect the concept may be a little touchy-feely for some, but I’m looking at it as; anything that may help us live our lives better, in the company of this uninvited guest, is worth a go.
Part of our initial meeting divided us into two groups (the haves and the have nots) w...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3322519</comments>
            <pubDate>Tue, 02 Mar 2010 00:18:10 +0100</pubDate>
            <guid isPermaLink="false">3322519</guid>        </item>
        <item>
            <title>Legal…But lethal?</title>
            <link>http://www.medworm.com/index.php?rid=3316255&amp;cid=t_200519_151_f&amp;fid=35818&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FRecoveryIsSexycom%2F%7E3%2FmE0ay36XUKQ%2F</link>
            <description>Legal addiction?
Robbie Williams and Anna Nicole Smith have both been hooked on everyday medicines &amp;#8211; like millions of others&amp;#8230;
A drug addict used to be someone who bought illegal fixes from a shady character in a back alley. But with more and more people admitting addiction to prescription drugs, your &amp;#8216;dealer&amp;#8217; can be the person you least expect to harm your health &amp;#8211; your GP.
Former model Anna Nicole Smith died of an overdose of sleeping pills and eight other prescription drugs. And earlier this year Robbie Williams checked himself into rehab after allegedly becoming hooked on painkillers and antidepressants. Michael Jackson appears to have died from prescription medications administered by a doctor.
Many doctors agree that powerful tranquillisers, sleeping pill...</description>
            <author>Recovery Is Sexy.com</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3316255</comments>
            <pubDate>Sat, 27 Feb 2010 18:27:50 +0100</pubDate>
            <guid isPermaLink="false">3316255</guid>        </item>
        <item>
            <title>Time</title>
            <link>http://www.medworm.com/index.php?rid=3311834&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Ftime%2F</link>
            <description>The clock is non-judgmental
It doesn’t care at all
No thought it gives to me
As it stands within the hall.
The gold watch on my wrist
The alarm clock by the bed,
What care they for misery
Or what may lay ahead?
They only serve one purpose
And that’s to track my life,
Moment by moment, clock ticking
Time maps this life of strife.
The good days and the bad
They are the same in length
As you and I struggle to balance
Our pain against our strength.
I try to stop the pendulum
Save time for better days
But the treadmill of time keeps moving
It cares not if I’m ablaze.
When I was very young, time dragged
Christmas’s eons apart and
I measured life by birthdays
Not knowing what life would impart.
Why does wisdom come so late?
Why wasn’t I prepared?
Is everyone caught by surprise?
I didn...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311834</comments>
            <pubDate>Thu, 25 Feb 2010 23:09:10 +0100</pubDate>
            <guid isPermaLink="false">3311834</guid>        </item>
        <item>
            <title>Support the IBD Research and Awareness Act for Crohn’s and Ulcerative Colitis</title>
            <link>http://www.medworm.com/index.php?rid=3311835&amp;cid=t_200519_129_f&amp;fid=36036&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Fkelly-building-a-crohns-disease-community%2Fsupport-the-ibd-research-and-awareness-act-for-crohn%25e2%2580%2599s-and-ulcerative-colitis%2F</link>
            <description>Last year, an important Act, The IBD Research and Awareness Act, was introduced to the House and Senate to expand research for Crohn’s Disease and Ulcerative Colitis.  The legislation would enhance activities at the Centers for Disease Control and Prevention (CDC) for Crohn’s and Ulcerative Colitis, as well as, expand biomedical research for IBD (Irritable Bowel Disease).
You can help advocate for the passage of the IBD Research and Awareness Act with the help of the Crohn’s and Colitis Foundation of America (CCFA).  They have made this really great website where they make it easy for you to contact your legislators and ask them to cosponsor H.R. 2275 (House bill number) and S. 981 (Senate bill number).
It is very easy to do.  Just click here.
Then, scroll down to the ‘compose m...</description>
            <author>Life with Crohn's</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311835</comments>
            <pubDate>Thu, 25 Feb 2010 19:00:56 +0100</pubDate>
            <guid isPermaLink="false">3311835</guid>        </item>
        <item>
            <title>Latest CCSVI Results Raise a Question</title>
            <link>http://www.medworm.com/index.php?rid=3306982&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Flatest-ccsvi-results-raise-a-question%2F</link>
            <description>We’ve had a few postings here at Life with MS on the topic of CCSVI and they’ve all stirred a spirited debate. Well, as I was re-reading the latest research results something new stirred inside my brain.
Unlike Dr Zamboni’s original research findings, wherein none of the &amp;#8220;non-MS&amp;#8221; subjects showed signs of CCSVI, this (more extensive and single blinded) study showed over a quarter of non-MS patients also living with CCSVI.
While everyone is focusing on the 55%-62% (depending on which way you read the results) of people living with MS who show signs of CCSVI, I’d like to know more about the nearly 26% of &amp;#8220;healthy&amp;#8221; subjects who exhibit signs of something that was heretofore thought to be (nearly) exclusive of people living with multiple sclerosis.
Don’t get me...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3306982</comments>
            <pubDate>Wed, 24 Feb 2010 21:09:21 +0100</pubDate>
            <guid isPermaLink="false">3306982</guid>        </item>
        <item>
            <title>Fight Breast Cancer with Pomegranates</title>
            <link>http://www.medworm.com/index.php?rid=3307045&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Ffight-breast-cancer-with-pomegranates%2F</link>
            <description>I love a lot of different fruits. Oranges are my favorite, but I love strawberries and blueberries too, but pomegranates are a special treat. When I was a little girl, every now and then my mom would buy one, which was a big deal when you consider we were living in a little tiny mining town in northern Ontario at the time.  She gave my sister and me each half and sat us outside to pick through the juicy seeds.  I’m sure part of her plan was to keep us occupied for a very long time. Since then I lost my patience for that delightful fruit until this fall. I couldn’t get enough pomegranates, I ate pretty much one a week until early this year when they went out of season.
I also love pomegranate juice. I keep a little bottle in my fridge all year round. When I am out to dinner or a speci...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3307045</comments>
            <pubDate>Wed, 24 Feb 2010 19:51:32 +0100</pubDate>
            <guid isPermaLink="false">3307045</guid>        </item>
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            <title>Introducing ADHD In Focus</title>
            <link>http://www.medworm.com/index.php?rid=3306898&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F02%2F24%2Fintroducing-adhd-in-focus%2F</link>
            <description>Attention deficit disorder is a serious mental health issue that affects the lives not only of children and teens, but millions of adults as well. So we&amp;#8217;re pleased to announce the launch of our latest blog, ADHD In Focus, that will focus on topics in attention deficit disorder (ADHD).
ADHD In Focus is hosted by Kathryn Goetzke. Kathryn is the driving force behind the non-profit organization for depression called iFred (the International Foundation for Research and Education on Depression). iFred is dedicated to encouraging research on depression and reducing the stigma associated with the disease.
In addition to her incredible work on iFred, Kathryn is someone who actually battles attention deficit disorder, hence the reason she agreed to write for this blog. I’m proud to welcome h...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3306898</comments>
            <pubDate>Wed, 24 Feb 2010 17:57:35 +0100</pubDate>
            <guid isPermaLink="false">3306898</guid>        </item>
        <item>
            <title>Reward Yourself With a Treat</title>
            <link>http://www.medworm.com/index.php?rid=3302493&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Freward-yourself-with-a-treat%2F</link>
            <description>My dogs have taught me over the years, the importance of the reward. There’s nothing quite as inspirational to a pooch as the question, “Want a bone?” The only other motivator that comes close is a platter of juicy steak, but that’s a bit messy to pop into your pocket. Sure, you smell good and have every dog in town following you, but oh, the grease stains.

Our Jack Russell, Annie, is aging and often has a recalcitrant, doubtful attitude about climbing the stairs in our home. I can hear her little nails tapping on the wood floor at the foot of the steps and often go to the head of the stairs and utter that question to her, “Want a bone?” That simple question gives her the “oomph” she needs to ascend the dreaded stairs. It reminds me that many of us who have chronic pain al...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3302493</comments>
            <pubDate>Tue, 23 Feb 2010 22:52:51 +0100</pubDate>
            <guid isPermaLink="false">3302493</guid>        </item>
        <item>
            <title>Breast Cancer and the Power of Napping</title>
            <link>http://www.medworm.com/index.php?rid=3298550&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fbreast-cancer-and-the-power-of-napping%2F</link>
            <description>There is new information out of the University of California at Berkley that indicates that napping during the day boosts cognitive power. I like this! I am a napper. I don&amp;#8217;t always get the opportunity for a short afternoon nap, but when I need it I take it. It might just be a few minutes before dinner or an evening class but it helps. When we go through chemotherapy or radiation one of the most distressing side effects is fatigue. Usually I worked in the morning and then went to Chemotherapy in the afternoon, returning to work the next day. This resulted in only a half day off from work. After a couple of months I would take the day after chemo off as I began to feel the cumulative effects of months of treatment. That would give me the whole day to rest.
I then learned that if I cou...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3298550</comments>
            <pubDate>Mon, 22 Feb 2010 22:16:14 +0100</pubDate>
            <guid isPermaLink="false">3298550</guid>        </item>
        <item>
            <title>Taking Inspiration from Other Breast Cancer Survivors</title>
            <link>http://www.medworm.com/index.php?rid=3290967&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Ftaking-inspiration-from-other-breast-cancer-survivors%2F</link>
            <description>There is a lot of transition in my life right now. I am working on new projects and my husband is refocusing his career while my boys are working on major plans of their own. During times like this, not necessarily bad times, but when I am not the one being able to predict how we will all end up, I feel agitated and overwhelmed. I am not one to back away from risk or change, but I do fantasize about going in my office covering myself with a blanket and sitting under the desk until everything works out. Sounds crazy, but I&amp;#8217;ve come a long way from when I used to imagine locking myself in the closet. I didn&amp;#8217;t have these feelings when I was diagnosed with breast cancer. I really am a fighter. Show me injustice and I&amp;#8217;ll speak up, pick on my friend and you pick on me. Take on o...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3290967</comments>
            <pubDate>Fri, 19 Feb 2010 20:22:33 +0100</pubDate>
            <guid isPermaLink="false">3290967</guid>        </item>
        <item>
            <title>Goodbye to our Behind the Scenes MS Advocate</title>
            <link>http://www.medworm.com/index.php?rid=3290901&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fgoodbye-to-our-behind-the-scenes-ms-advocate%2F</link>
            <description>Why is it, do you suppose ,that I had an easier time writing a farewell blog post to a fictional American president with MS than I am writing this goodbye?
For nearly four years this blog has been quietly (to most of you at least) nudged along in its existence to the place of recognition we currently hold.  Through diligent behind the scenes efforts one cannot search for an MS blog and not have our Life with MS pop up “above the fold” on the first page of a search engine’s results page.
New readers join us every day and partake (and sometimes participate) in our lively conversation, advice and experience because of her tireless work.
It may seem that I have been at the helm of this ship but I’ve had a little (one might say “pixy-like”) voice on my shoulder, whispering things l...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3290901</comments>
            <pubDate>Fri, 19 Feb 2010 19:21:15 +0100</pubDate>
            <guid isPermaLink="false">3290901</guid>        </item>
        <item>
            <title>Don’t Feed the Chronic Pain Monsters</title>
            <link>http://www.medworm.com/index.php?rid=3287889&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fdont-feed-the-chronic-pain-monsters%2F</link>
            <description>Please don’t feed the chronic pain monsters, it only encourages them. Never make them feel welcome or they will move in and make a complete mess of your life, your home and your mind.
Please don’t feed them anger and bitterness, it only makes them thrive and feel empowered, and you don’t want that.
The best way to deal with the monsters is to turn your back on them and get on with your life. It will frustrate them when they realize they aren’t winning, which is of course their goal.
They will throw an ugly tantrum, they’ll scream, and rant and rave; just find a peaceful place of safety and they will eventually go away.
Certainly they will come again, probably every day. These monsters are tenacious and stubborn. Once they dig in they hold on tightly, but if you firmly tell them, ...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3287889</comments>
            <pubDate>Thu, 18 Feb 2010 20:42:22 +0100</pubDate>
            <guid isPermaLink="false">3287889</guid>        </item>
        <item>
            <title>We Need Information Not Hype on CCSVI</title>
            <link>http://www.medworm.com/index.php?rid=3283722&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fwe-need-information-not-hype-on-ccsvi%2F</link>
            <description>CCSVI, CCSVI, CCSVI.  For the past three months, the world of multiple sclerosis world has been turned on its ear with discussions of chronic cerebrospinal venous insufficiency (CCSVI).
The concept broached by Italian medical doctor and professor, Dr. Paolo Zamboni, was a reexamination of several old theories (with significantly more sophisticated equipment) as to the relationship/correlation of tiny iron deposits in and around MS lesions.
While Dr. Zamboni and his team of researchers presented academic papers showing a unique similarity (dubbed CCSVI) in 100 percent of MS patients they studied, these publications called for further investigation within the peer-review system.  Dr. Zamboni’s specialty is the vascular system and hence began experimental treatment of these patients with ...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3283722</comments>
            <pubDate>Wed, 17 Feb 2010 21:32:44 +0100</pubDate>
            <guid isPermaLink="false">3283722</guid>        </item>
        <item>
            <title>Breakfast With Crohn’s Disease</title>
            <link>http://www.medworm.com/index.php?rid=3283721&amp;cid=t_200519_129_f&amp;fid=36036&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Fkelly-building-a-crohns-disease-community%2Fbreakfast-with-crohns-disease%2F</link>
            <description>I think that I have mentioned before that I have been experimenting with my diet for the last year in an effort to improve my Crohn&amp;#8217;s symptoms.  I have eliminated all dairy products and now use only Rice milk because it causes the least amount of trouble and tastes good.  I am also limiting the amount of gluten that I eat.  I still eat some items that have a little bit of gluten, but have for the most part deleted that out of my diet too.  I also don’t eat a lot of fiber because it seems to make matters worse.  Once you get rid of dairy, gluten and fiber, there are not a lot of choices left for breakfast.
For the last year, I have been eating Trix for breakfast.  I recently discovered Berry Berry Kix and have switched to that instead because it has a lot less sugar.  I don...</description>
            <author>Life with Crohn's</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3283721</comments>
            <pubDate>Wed, 17 Feb 2010 19:26:52 +0100</pubDate>
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        <item>
            <title>Beware of the Legal Drug Pushers, They’re Out There</title>
            <link>http://www.medworm.com/index.php?rid=3280093&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fbeware-of-the-legal-drug-pushers-theyre-out-there%2F</link>
            <description>Occasionally, in my experience as a nurse I have run into doctors who are very, shall we say, “loose” with the prescription pad. I don’t know why or what drives an educated physician who has practiced for a short time or long to decide to take the road of least resistance; but some do. You have to wonder why they would risk their professional trust, but occasionally some do. I’m sure there are a myriad of reasons but that’s not for me to say.
Part of the problem is the complete subjective nature of pain. When a patient enters a doctor’s office and states they have pain, it often is not as simple as it sounds. Sometimes it is a legitimate complaint, sometimes it is not. There are many ways this can be expressed to the doctor during an office call. I would presume there are as ma...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3280093</comments>
            <pubDate>Tue, 16 Feb 2010 22:26:57 +0100</pubDate>
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        <item>
            <title>What Do You Think About Your MS Society?</title>
            <link>http://www.medworm.com/index.php?rid=3280094&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fwhat-do-you-think-about-your-ms-society%2F</link>
            <description>As many of you are aware, I am an ambassador for my local chapter of the National MS Society (the US organization). There are “MS Societies” all over the world and, even here in America, each chapter runs things a little differently.
Of course I know that not everyone has the same relationship with their chapter of the society.  I also have come to the understanding that some are vehemently opposed to these organizations.
As I reviewed comments on the web about CCSVI I was taken aback to read that some of you were even calling for “war” against organizations (NMSS being one) who were conspiring to “keep us sick.”
I do not think that this is a pervasive attitude but I thought it was time to check in on this topic.
I’m not a member who thinks these societies are above reproach...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3280094</comments>
            <pubDate>Tue, 16 Feb 2010 22:06:12 +0100</pubDate>
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        <item>
            <title>Too Quiet on the Breast Cancer Front</title>
            <link>http://www.medworm.com/index.php?rid=3269852&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Ftoo-quiet-on-the-breast-cancer-front%2F</link>
            <description>I have been in the breast cancer business for six and a half years. I call it “the business” because of how it affects my life, not because of the science or medicine. In all that time I have held to the hope of a cure for breast cancer. Not a treatment, not just a drug to eliminate risk; a real cure. In the past four years I have read and written about research studies and findings and breakthroughs. I have even blogged about British scientists that said there would be a cure in two years – that was in 2009. Things are very quiet right now about breast cancer and the quiet is deafening.
We are in a war. The war against cancer. Remember, Nixon declared war on cancer and no one to my knowledge has declared a truce. When you are in a war you need to know what is happening on the front ...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3269852</comments>
            <pubDate>Fri, 12 Feb 2010 19:38:40 +0100</pubDate>
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        <item>
            <title>Staying Employed with Multiple Sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=3262760&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fstaying-employed-with-multiple-sclerosis%2F</link>
            <description>A topic which seems to thread itself into the tapestry of nearly all of our conversations at our Life with MS blog is employment.
In these economic times, finding and/or keeping a job is difficult for “typical” people.  For we of the compromised myelin, the idea of finding new employment is daunting, while the thought of losing our jobs (and oft, thus our health insurance) is downright frightening!
There are so many questions we have about MS and employment: Who do we tell and when?  How much do we disclose?  What are reasonable accommodations to request?  What does discrimination look like?  When do we say when?
There is no shortage of questions…the problem is: Who do we ask?
That one, I can answer!
I am in the process of writing a two-hour television program/webcast which I’...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3262760</comments>
            <pubDate>Wed, 10 Feb 2010 23:12:11 +0100</pubDate>
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        <item>
            <title>Is Your DNA Your Destiny in a Life with Chronic Pain?</title>
            <link>http://www.medworm.com/index.php?rid=3262758&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fis-your-dna-your-destiny-in-a-life-with-chronic-pain%2F</link>
            <description>For many of us who have daily pain due to disease, we are very familiar with the role genetics play in our lives. Do we have to allow fear to enter our lives and our futures if we had close relatives, such as mothers or fathers, who suffered similar diseases? Most of us have been taught in college that your DNA is more or less set in bedrock and determines your future. I have a relative who has been obsessed for many years in finding health information on all our relatives, living and dead. At a family gathering she corners a relative or two and questions them about their health in minute detail.  I believe she does this out of sincere concern for the future health of her children and grandchildren but also out of fear for herself. Sadly, I often sense a feeling of hopelessness in her man...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3262758</comments>
            <pubDate>Wed, 10 Feb 2010 22:10:55 +0100</pubDate>
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        <item>
            <title>Why Am I Keeping this Wig After I Survived Cancer?</title>
            <link>http://www.medworm.com/index.php?rid=3262847&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fwhy-am-i-keeping-this-wig-after-i-survived-cancer%2F</link>
            <description>Like a lot of women I know I have fat pants in my closet. You know, the ones you kept from when you were at your heaviest so you can remind yourself how much weight you lost. They are usually one or two sizes bigger than you are now. Only some of us keep them because every now and then our weight creeps back up and we actually need a pair of bigger pants. We refuse to pay for fat clothes because we are convinced the weight will come off again. Some of us never even tell anyone but sisters and close girlfriends about our fat pants. Certainly my husband doesn&amp;#8217;t know. When he comes with me to doctor&amp;#8217;s offices I don&amp;#8217;t even let my husband see the nurse weigh me or check my height; I don&amp;#8217;t want to ruin his image of me as tall and thin, which isn&amp;#8217;t easy to accomplish...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3262847</comments>
            <pubDate>Wed, 10 Feb 2010 21:29:19 +0100</pubDate>
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        <item>
            <title>New Information from the FDA on Tysabri</title>
            <link>http://www.medworm.com/index.php?rid=3254586&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fnew-information-from-the-fda-on-tysabri%2F</link>
            <description>As if progressive multifocal leukoencephalopathy (PML) wasn’t a big enough word to get out of our mouths and a big enough concept around which to get our brains…now there’s immune reconstitution inflammatory syndrome (IRIS)!
This morning, the US Food and Drug Administration (FDA) has posted notice to the neurologic community (and thus they believe to patients) that the risk of developing PML increases with the number of doses one receives.  In the same MedWatch bulletin the FDA mentions another adverse event which is, “characterized by a severe inflammatory response” and can create serious issues for people even after return of the immune system to normal function.
As of last week, the number of confirmed cases of PML for patients using Tysabri as their MS disease modifying ther...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3254586</comments>
            <pubDate>Mon, 08 Feb 2010 21:42:05 +0100</pubDate>
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        <item>
            <title>Size Doesn’t Matter in a Life with Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3243920&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fsize-doesnt-matter-in-a-life-with-chronic-pain%2F</link>
            <description>I’m constantly amazed at the power of the human spirit. I’ve met so many wonderful people in my nursing career and on this blog. The degree, the size or the intensity of the pain is not nearly as important as the size of the courage that is called on to meet it.
When you think about life it is sometimes the little things that get you down; the splinter in a finger, the blister on a heel or the flea on the dog. If you’re in the right frame of mind, little things can “do you in” as much as the larger incidents. We all have learned the power of the insistent “little things” as they persist in nagging and niggling at our self-control. How many times can you be stuck by the tiniest pin before you react? How many red, raw areas beneath surgical tape does it take to make you miserab...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3243920</comments>
            <pubDate>Thu, 04 Feb 2010 22:12:42 +0100</pubDate>
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        <item>
            <title>Choices You Can Make in a Life of Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3235973&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fchoices-you-can-make-in-a-life-of-chronic-pain%2F</link>
            <description>Either I accept my limitations and challenge them
Or I use them as an excuse to lose my life, without putting up a fight.
Either I lie here and feel the full weight of my self-pity
Or I rise up and do just one thing that is productive.
Either I sit here during this commercial
Or I arise off my seat and perform one quick chore.
I either water that pot of African violets
Or I watch them wither and die.
I either walk down the stairs to let the dog out to pee
Or face the consequences with paper towels in hand.
I either snatch a small fragment of time to be productive
Or I achieve nothing, willingly and without guilt. What’s with all this guilt, anyway?
Either I consider the act of resting to be healing and do it without guilt
Or consider it wasteful and of little importance. I’m the judge ...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3235973</comments>
            <pubDate>Tue, 02 Feb 2010 22:12:53 +0100</pubDate>
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        <item>
            <title>Weighing In on CCSVI and the Liberation Treatment</title>
            <link>http://www.medworm.com/index.php?rid=3231679&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fweighing-in-on-ccsvi-and-the-liberation-treatment%2F</link>
            <description>Before I launch into this topic for a second (and more informed) time, let me remind us all that just because I write this blog, it does not mean I have all the answers…not even a plurality of them, really.
Earlier in the month we posted my preliminary thoughts on the subject of Dr. Paulo Zamboni’s research into chronic cerebrospinal venous insufficiency (CCSVI) and what he calls the Liberation Treatment.  At that time, I stated a skepticism which I felt healthy but others equated to some form of conspiracy, in which I was a player.
I am not.
After reading the published papers of Dr. Zamboni, et al, I could sum up my thoughts in just four words: “I don’t get it.”
I don’t get it, and that’s why I’m excited to know that there is further research into the premise.
While the t...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3231679</comments>
            <pubDate>Mon, 01 Feb 2010 22:59:33 +0100</pubDate>
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        <item>
            <title>Do We Ever Get Too Old or Ill for Dignity?</title>
            <link>http://www.medworm.com/index.php?rid=3220648&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fdo-we-ever-get-too-old-or-ill-for-dignity%2F</link>
            <description>“A rose by any other name would smell as sweet.” It’s an old quote, and often used but do you think it’s true? Yesterday we received a brief update on Lolly, my husband’s Mom. As many of you know, she is quite elderly and receiving help at home in an effort to allow her to stay in her own comfortable environ with her beloved pets. Her case manager sends us updates from time to time and in each one she refers to Lolly as “Mother” or “Mom.” I confess, this affectation really bothers me. As far as I know Lolly only has one living child and I’m married to him.
It reminds me of an incident, many years ago, when my family took my Dad out to dinner for his birthday. We were all stretched out along a large table at our favorite Italian restaurant, classic red and white checked ...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3220648</comments>
            <pubDate>Fri, 29 Jan 2010 03:13:50 +0100</pubDate>
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        <item>
            <title>What Did You Learn from Breast Cancer?</title>
            <link>http://www.medworm.com/index.php?rid=3216802&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fwhat-did-you-learn-from-breast-cancer%2F</link>
            <description>I had to stand in a long line to pay for my groceries this weekend. Once I finished reading all the covers of the gossip magazines which updated me on the important stuff in the world, I decided to entertain myself by making a mental list of all the things that I learned from having breast cancer. I thought I would share it with you.
Breast cancer taught me:
That it&amp;#8217;s not what you have but who you are that matters.
That healthy people get cancer.
That good people get cancer.
That if life was fair no one would get cancer.
That you need to be grateful for the good times.
That a real friend is one who calls just to chat when you have cancer.
That one great sister is better than twenty good doctors.
That there is always something to smile about.
That people will tell you your wig looks g...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3216802</comments>
            <pubDate>Wed, 27 Jan 2010 20:41:52 +0100</pubDate>
            <guid isPermaLink="false">3216802</guid>        </item>
        <item>
            <title>Is My Pain Crohn’s or Something Else?</title>
            <link>http://www.medworm.com/index.php?rid=3216729&amp;cid=t_200519_129_f&amp;fid=36036&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Fkelly-building-a-crohns-disease-community%2Fis-my-pain-crohns-or-something-else%2F</link>
            <description>The mystery pain that I had back in Feb 2008 has returned.  Back then, I thought that I had a kidney stone, but the doctors were not so sure.  At the time, I had a lot of pain that felt very similar to a kidney stone – came and went, sharp sometimes and dull achy pain other times.  I did have a stone that was in my kidney but the urologists told me that I shouldn’t have pain with it there – it would only hurt when it made its way to the urethra.   My general doctor thought that it was the stone causing the pain so I never really had a clear answer since no one agreed.
Since then, I have had bouts of pain that felt similar but not as severe and they would last only a few days.  Well, I started having pain again on Jan 16th and it got really severe this time.  I was hurting near...</description>
            <author>Life with Crohn's</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3216729</comments>
            <pubDate>Wed, 27 Jan 2010 18:23:51 +0100</pubDate>
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        <item>
            <title>Bring It on Life and I’ll Just Write a Blog About it!</title>
            <link>http://www.medworm.com/index.php?rid=3212459&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fbring-it-on-life-and-ill-just-write-a-blog-about-it%2F</link>
            <description>Our children and grandchildren have a lot more literature than we did while growing up. We had all of those scary fairy tales about witches burning children, babies rocking out of trees with their cradles falling and wolves with drooling jowls dressing up like Grandma. I also remember one trouble making little guy called Chicken Little who came around in a near panic exclaiming, “The sky is falling. The sky is falling.”
Well, Mr. Little, I have news for you. The figurative sky fell and we survived. I’m not sure if you thought it was just going to fall on you or if it was going to fall on everyone but voila, here we are with dust and debris all over the tops of our heads yet we’re still alive. We’re fortunate in so many ways. We’ve had a painful reminder in Haiti of thousands of...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212459</comments>
            <pubDate>Tue, 26 Jan 2010 22:53:46 +0100</pubDate>
            <guid isPermaLink="false">3212459</guid>        </item>
        <item>
            <title>Multiple Sclerosis and Headaches</title>
            <link>http://www.medworm.com/index.php?rid=3200554&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fmultiple-sclerosis-and-headaches%2F</link>
            <description>I’ve read your comments enough times to realize that we’re likely over due for a discussion about headaches, particularly migraine headaches and multiple sclerosis.
Many have made statements, in comments left on other general topics, of experiencing migraine headaches along with their other MS symptoms.  Some state that they’ve experienced these most of their lives while others have only gotten these monster headaches after they experienced MS symptoms or were diagnosed.
The topic of migraine is a difficult one for medical science to explain in general.  Terms such as “cluster headaches,” “sick-headaches,” “ocular migraine” and “vascular headaches” are bantered about the medical community within a cloud of certain mystery.
Even the National MS Society states that ...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3200554</comments>
            <pubDate>Fri, 22 Jan 2010 22:19:35 +0100</pubDate>
            <guid isPermaLink="false">3200554</guid>        </item>
        <item>
            <title>Buying Shoes to Get Through Chemo</title>
            <link>http://www.medworm.com/index.php?rid=3200629&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fbuying-shoes-to-get-through-chemo%2F</link>
            <description>I have decided that I need a pair of red patent leather high heel pumps with a platform. I saw them somewhere a couple of weeks ago and they keep creeping into my thoughts. I have a real weakness for shoes. This doesn&amp;#8217;t make me unique as a woman, shoes have a real appeal for most of us. These shoes are pretty sensational though, they are shiny and the perfect shade of tomato red and have at least a four inch heel. I picture them with a skinny pair of jeans (I was envisioning when I was skinnier). Truthfully I didn&amp;#8217;t buy them because I sensed they would end up with the rest of my collection of shoes, many of which are still new and in the box. OK, I confess, I am obsessed with shoes and have a very weird relationship with them. They make me happy!
Before I had the second surgery...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3200629</comments>
            <pubDate>Fri, 22 Jan 2010 21:02:09 +0100</pubDate>
            <guid isPermaLink="false">3200629</guid>        </item>
        <item>
            <title>Who is Your Mama in a Life of Chronic Pain?</title>
            <link>http://www.medworm.com/index.php?rid=3197793&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fwho-is-your-mama-in-a-life-of-chronic-pain%2F</link>
            <description>When I was a child of eleven years of age, I had to go to bed for a year due to rheumatic fever. I was never a particularly healthy kid and had strep throat more times than I can remember, before and after that time. Naturally, it worried my parents and my mother, who had trouble expressing her feelings, did so by being very protective of me. My father was an adorable and loving man who wept when I was diagnosed and over the years, each time I became ill, he brought me milkshakes, usually strawberry, and of course, the latest comic books. As I recall my favorites were always the Archie comics and another character named Lulu. Even then I decided you could only watch so much TV. The thing I hated the most, besides being cut off from my friends at school and church, was this most miserable l...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3197793</comments>
            <pubDate>Thu, 21 Jan 2010 21:48:00 +0100</pubDate>
            <guid isPermaLink="false">3197793</guid>        </item>
        <item>
            <title>Really Weird MS Symptoms</title>
            <link>http://www.medworm.com/index.php?rid=3189288&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Freally-weird-ms-symptoms%2F</link>
            <description>If multiple sclerosis symptoms are nothing else, especially to the newly diagnosed, they are weird!  Sure, symptoms can be frightening, challenging, difficult and even debilitating… but how many times have I caught myself saying, “Hmmmm, that’s weird!”
Often we are told, “That’s doesn’t sound like MS,” or something of the kind, by our medical professionals only to find out (oft, via the pages of this blog) that we are not alone in our experience of something not in the medical text books.  It is one of the aspects of the Life with MS blog of which I am most proud!
I have a real doozie to share, with a discussion of MS symptoms from the X-Files.
The middle of last week, I developed a cold.  You know that feeling when you wake, somewhere between the back of your nose and t...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3189288</comments>
            <pubDate>Wed, 20 Jan 2010 17:14:22 +0100</pubDate>
            <guid isPermaLink="false">3189288</guid>        </item>
        <item>
            <title>Do You Have any Triggers for an MS Attack?</title>
            <link>http://www.medworm.com/index.php?rid=3178899&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fdo-you-have-any-triggers-for-an-ms-attack%2F</link>
            <description>Over the years, we’ve come to understand that medical science is a ways behind those of us living with multiple sclerosis when it comes to the experience of our disease.  The biggest of these lags comes to mind in the form of multiple sclerosis pain.  Most of us can remember a day when leading minds didn’t believe that pain could be a symptom of a disease which also caused numbness.
Now, of course, most scientists agree with what we have known all along: MS can hurt!
Current thinking about the progression of disability, by way of exacerbation (or attack), is fragmented at best.
I thought we might have a discussion headed into the weekend about “triggers” for our multiple sclerosis.
Many people will convey a memory of great stress before their first big attacks (which, if the dise...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3178899</comments>
            <pubDate>Fri, 15 Jan 2010 20:51:03 +0100</pubDate>
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            <title>Committing to Better Health</title>
            <link>http://www.medworm.com/index.php?rid=3178952&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fcommitting-to-better-health%2F</link>
            <description>Well it&amp;#8217;s my first week back on Weight Watchers and I lost five pounds. I love the program, I always have. There is no reason that I can&amp;#8217;t follow the principles of Weight Watchers for the rest of my life except that food gets in the way. Not the good food, but things like potato chips and chocolate. You know that is why Weight Watchers should really work for me because it allows even these things a little at a time.
Health takes commitment. It&amp;#8217;s easy for me to commit to my family and friends, but I fall down when I commit to me. This is a new decade and I think I really have to make it about me. It is a little cliché, but so true that if you don&amp;#8217;t take care of yourself you can&amp;#8217;t take care of anyone else. I let myself get run down before Christmas. I ran throu...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
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            <pubDate>Fri, 15 Jan 2010 17:20:26 +0100</pubDate>
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            <title>A New Decade Begins: How’s Your MS Today?</title>
            <link>http://www.medworm.com/index.php?rid=3172104&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fa-new-decade-begins-hows-your-ms-today%2F</link>
            <description>We try to take the second week of each month and post the query: How’s your MS today?  It’s a chance for you to check in with yourself and with other members of this community and it’s a chance for me to be true to something I stated in our very first blog nearly four years ago, “It’s all about you!”
This monthly open forum allows for new threads of conversation as well as an opportunity to take stock of where we are with our multiple sclerosis relative to the previous months.  I have found it a very helpful part of my health care plan!
As for me and my MS&amp;#8230; two day-long flights and bouts of eight hour time change induced jet lag have made me quite very aware of how different my body reacts as compared to just four years ago (my last extended trip to Ireland was just pri...</description>
            <author>Life with MS</author>
            <type>blogs</type>
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            <pubDate>Wed, 13 Jan 2010 17:46:04 +0100</pubDate>
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            <title>Discovering Who You Really Are After Cancer</title>
            <link>http://www.medworm.com/index.php?rid=3172163&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fdiscovering-who-you-really-are-after-cancer%2F</link>
            <description>“In a world where you can be anything&amp;#8230; be yourself”
I saw this wonderful quote today. It is brilliant! Imagine really choosing to be who you are and knowing that&amp;#8217;s enough. If breast cancer teaches us anything it teaches us how to be our self. Cancer affects who we are, not who we are trying to be, and it takes our real selves to live through it. That person deserves to be heard. Think of the times you gave up your voice. When you wanted to question your doctor&amp;#8217;s decisions but didn&amp;#8217;t, or when you were in a hospital bed and needed something but didn&amp;#8217;t want to cause any trouble. If you don&amp;#8217;t listen to your voice, no one else will either.
It hasn&amp;#8217;t been easy being me. I have always had a deep rooted need to be who others need me to be. And you know...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
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            <pubDate>Wed, 13 Jan 2010 17:09:46 +0100</pubDate>
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            <title>The Road of Chronic Pain is Not a Smooth Ride</title>
            <link>http://www.medworm.com/index.php?rid=3167281&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fthe-road-of-chronic-pain-is-not-a-smooth-ride%2F</link>
            <description>Bumpy rides are right up there in my book of horrors. When you have to sit on your problem all day long, any bumps along the way can hurt, often to the point of nausea. Sometimes I think about our great, great grandparents and find it amazing they lived as long as they did without the medications we have; riding around on horses or in covered wagons and having to perform all their own chores without the aid of machinery. Small wonder 35 years of age was considered old. Besides the physicality of those bumps in a life with chronic pain, there are other pits, ditches and potholes we need to watch out for along this path of life we’re on.
SELF-PITY is the first pothole that comes to mind. I have a relative who suffered an injury last year. I called to see how she was feeling and she said, w...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
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            <pubDate>Tue, 12 Jan 2010 22:53:17 +0100</pubDate>
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            <title>Lasting Side Effects from MS Meds</title>
            <link>http://www.medworm.com/index.php?rid=3163916&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Flasting-side-effects-from-ms-meds%2F</link>
            <description>I can’t remember what I was doing the other day, but the way I moved my arm coupled with the angle of the light showed two very deep groves from the back of my hand, running serpentine around my forearm before they fade into the muscle near my elbow.  I’ve seen these collapsed veins before; the result of treatment with Novantrone for my progressive multiple sclerosis. But that day, again in that certain light, they looked deeper, older and more prominent than I’ve seen in a while.
As I made this morning’s coffee, I saw them again and I thought they (and other lasting side effects) might be a good topic for today’s blog.
Though Novantrone is “baby chemo,” it is still a pretty potent and dangerous drug.  Anyone that has watched their chemo nurse &amp;#8220;suit-up&amp;#8221; before h...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3163916</comments>
            <pubDate>Mon, 11 Jan 2010 19:33:22 +0100</pubDate>
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            <title>A Controversial New Cure for Multiple Sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=3156577&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fa-controversial-new-cure-for-multiple-sclerosis%2F</link>
            <description>By this time, you may be wondering if I’ve taken my finger off the pulse of MS research.  It’s been over two months since Canadian television broadcast a “breaking story” about Italian Dr. Paulo Zamboni and his vascular “cure” for multiple sclerosis.  Where have I been on the topic?
This subject intrigues me greatly, I’ll admit.  It also frightens me more than minutely and I am still gathering information.  That said, I wanted to open up the lines of communication about the topic today.
A brief history for those who may not have heard the news:
In 2008, Dr. Zamboni and his research colleagues began publishing findings  referencing something called chronic cerebrospinal venous insufficiency (CCSVI).   In other words, constriction of the blood vessels leaving the brain a...</description>
            <author>Life with MS</author>
            <type>blogs</type>
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            <pubDate>Fri, 08 Jan 2010 21:34:11 +0100</pubDate>
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            <title>The Ongoing Battle with Breast Cancer</title>
            <link>http://www.medworm.com/index.php?rid=3156628&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fthe-ongoing-battle-with-breast-cancer%2F</link>
            <description>I am getting back on track. I have found some great supplements which includes a foul tasting green powder full of vegetables. Thanks to all of you for responding to my lament on my blog about my bad habits; I received some great advice and tips and I am really feeling motivated. I have even decided to follow Weight Watchers to make sure I am eating good food and the right portions.
The doctor&amp;#8217;s decision that I switch from Tamoxifen to Femera is still a little concerning to me.  I figure if I really get on track and in good physical condition then I will be able to note any changes Femera wreaks on my body more quickly. I haven&amp;#8217;t really experienced any adverse symptoms from Tamoxifen except Sister insists it is what is making me fat and makes it more difficult for me to lose w...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
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            <pubDate>Fri, 08 Jan 2010 17:37:56 +0100</pubDate>
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            <title>What Secrets Lie in a Life of Chronic Pain</title>
            <link>http://www.medworm.com/index.php?rid=3153513&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fwhat-secrets-lie-in-a-life-of-chronic-pain%2F</link>
            <description>This whole business of online sharing is very public. Those of us who share on this blog often hold back a bit because of the glaring nature of our words staying here forever. We hide behind first names, try to watch our language, although that isn’t always easy to do, and often hold onto our emotions to be civil. In short, we make a noble attempt to behave like ladies and gents. All the while, we know, within each of us we are so much more than just our pain.
We all have homes to run, many have jobs to hold down just to survive and many have children with needs, tears, laughter and love to share. We worry about money, family problems and mortgages, just like everyone else. The difference is that we have this “albatross” to carry, each and every day on top of the usual stresses of li...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
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            <pubDate>Thu, 07 Jan 2010 22:16:06 +0100</pubDate>
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            <title>Crohn’s Book Club: January Edition</title>
            <link>http://www.medworm.com/index.php?rid=3149202&amp;cid=t_200519_129_f&amp;fid=36036&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Fkelly-building-a-crohns-disease-community%2Fcrohns-book-club-january-edition%2F</link>
            <description>Happy 2010!  I can’t believe that we are in 2010 already,  time really flies.
I should not have written in my last blog about how well I was doing because I got sick that very same night!   I picked up a stomach bug and on top of that had a sinus infection.  I am now taking antibiotics.   So, I have started my New Year off with a blast; sick as a dog.  But, it is getting better now.  I just need to work on gaining the weight back that I lost from being sick.  I was already getting kind of low with my weight and then I lost another three or four pounds on top of that because I’m sick.  I may try drinking Ensure for weight gain again to see if it still bothers me or not.
For those of you new to this Crohn’s blog we decided not long ago that we would create a book club since ...</description>
            <author>Life with Crohn's</author>
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            <pubDate>Wed, 06 Jan 2010 21:24:40 +0100</pubDate>
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            <title>Back to the Front Lines in the Battle Against Breast Cancer</title>
            <link>http://www.medworm.com/index.php?rid=3149274&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fback-to-the-front-lines-in-the-battle-against-breast-cancer%2F</link>
            <description>I&amp;#8217;m at four month visits with my oncologist now. After five years of trotting off to the same office, I still look forward to visiting my old support network that saw me through chemotherapy. It appears though that after five years, the old support staff has changed. The oncology nurses that hooked me up to the drip bags have all moved on to other jobs and I didn&amp;#8217;t recognize anyone in the chemo clinic this visit. Maybe that&amp;#8217;s a good thing. Nothing to link me to the chemo period.
This visit I met with my doctor&amp;#8217;s physician assistant. She checked me out and told me everything looked good, gave me my prescription for a chest x-ray and sent me to the chemo clinic for a blood sample. Before she finished though she advised me that I was finishing with Tamoxifen this month...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
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            <pubDate>Wed, 06 Jan 2010 19:37:25 +0100</pubDate>
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            <title>How to Stay Warm During the Cold Winter Months</title>
            <link>http://www.medworm.com/index.php?rid=3146110&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fhow-to-stay-warm-during-the-cold-winter-months%2F</link>
            <description>I had something else in mind for today but after receiving so many notes from all of you who are reacting to the extreme cold, I thought we’d talk about some practical matters. It may be a bit repetitious because some of us have been chatting about these things, but for other, it will be new information. I often think by gathering all of our experiences together we often come up with some very helpful information. I’d like to chat about current problems and challenges so we can all help each other by pooling our information.
FACING THE COLD. One of the greatest challenges those of us with rheumatoid disease face is the effect of weather changes on our bodies. There is little doubt that barometric changes affect us and the effect that both heat and cold can have on us. The most common c...</description>
            <author>Life with Chronic Pain</author>
            <type>blogs</type>
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            <pubDate>Tue, 05 Jan 2010 22:15:38 +0100</pubDate>
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            <title>A New Year and a New Outlook on Life with MS</title>
            <link>http://www.medworm.com/index.php?rid=3142706&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fa-new-year-and-a-new-outlook-on-life-with-ms%2F</link>
            <description>A very happy New Year to all!
We are finishing up our trip at a most fabulous 16th century castle (with free Internet), so I thought I’d jot a few thoughts before we make our way back to Dublin and onward to Seattle.
This year, with the help of a bunch of Irish youngsters, I’ve decided to experience the joys of life…even if it’s a life with multiple sclerosis.
I’ve had the wonderful opportunity to lodge at this castle on a number of occasions and every time, I am taken by its beauty and grandeur.  I walk the grounds (study Hazelwood at my side) and see the game kept on the grounds, the statuary and the old, old beauty.  Every time, I enjoy it as I did the first time.
This, however, is the holidays and thus in Ireland the wedding season.  We arrived in the middle of many weddin...</description>
            <author>Life with MS</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3142706</comments>
            <pubDate>Mon, 04 Jan 2010 20:44:56 +0100</pubDate>
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            <title>Surviving Breast Cancer to Celebrate Another Year</title>
            <link>http://www.medworm.com/index.php?rid=3142785&amp;cid=t_200519_136_f&amp;fid=36032&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-breast-cancer%2Fsurviving-breast-cancer-to-celebrate-another-year%2F</link>
            <description>Happy New Year! What are you going to do with this new year, this new decade? A new year is like a clean sheet of paper just waiting to be written on and you get to choose the story that gets written. Breast cancer may have impacted the last decade of your life, or maybe you&amp;#8217;re still not quite through the battle but the new decade is marching in so get ready for great things.
That is the one problem I have had with being a survivor, the idea that something great is going to happen to make up for the fact that I had breast cancer. Each birthday, each new year is supposed to be this milestone or a marker for something special I&amp;#8217;m supposed to do. The wisdom I have gained these past years though informs me that something great does happen each time one of these milestones is reache...</description>
            <author>Life with Breast Cancer</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3142785</comments>
            <pubDate>Mon, 04 Jan 2010 18:54:56 +0100</pubDate>
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            <title>This Emotional Life Begins Tonight</title>
            <link>http://www.medworm.com/index.php?rid=3139080&amp;cid=t_200519_109_f&amp;fid=34750&amp;url=http%3A%2F%2Fpsychcentral.com%2Fblog%2Farchives%2F2010%2F01%2F04%2Fthis-emotional-life-begins-tonight%2F</link>
            <description>Can I every really be happy?
Is it true that money can&amp;#8217;t buy happiness?
Will more friends help make me feel more happy?
What is happiness anyway?
This Emotional Life is a two-year outreach campaign anchored by a PBS series, in partnership with Microsoft co-founder Paul Allen, (airing January 4 – 6, 2010 &amp;#8212; that&amp;#8217;s starting tonight!) that examines the science behind our emotions, the challenges to our well-being, and the keys to happier lives. 
This is a groundbreaking endeavor that is focused on emotional well-being and happiness, and designed to help people foster stronger social relationships. Spearheaded by Allen&amp;#8217;s Vulcan Productions, the project includes a three-part, nationally broadcast series on PBS, a dynamic website, a national outreach campaign, and educat...</description>
            <author>World of Psychology</author>
            <type>blogs</type>
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            <pubDate>Mon, 04 Jan 2010 12:55:50 +0100</pubDate>
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            <title>How is Your Crohn’s Today? Christmas and New Year Edition</title>
            <link>http://www.medworm.com/index.php?rid=3133711&amp;cid=t_200519_129_f&amp;fid=36036&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Fkelly-building-a-crohns-disease-community%2Fhow-is-your-crohns-today-christmas-and-new-year-edition%2F</link>
            <description>Merry Christmas everyone!  I hope that you were able to have a pain free Christmas and I also wish you a Happy and Blessed 2010.  Since we haven’t had a “How is your Crohn’s Today” blog in a while (I think since August), maybe we should have one now and you can tell us how your Christmas was.  In case you are new to our Crohn’s blog, I try to have a blog once a month where we all write in and tell how we are doing (physically and emotionally) with our Crohn&amp;#8217;s disease and pretty much just share as much as you want.
I am doing really well.  I am always afraid to make that statement because I feel like whenever I do, things go bad, but I’ll risk it today.  I have recently reduced my prednisone to 8mg a day and am hoping to keep going down little by little.  So far, not...</description>
            <author>Life with Crohn's</author>
            <type>blogs</type>
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            <pubDate>Wed, 30 Dec 2009 22:06:03 +0100</pubDate>
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            <title>Holiday Blog Contest Winner: How MS Has Affected My Family</title>
            <link>http://www.medworm.com/index.php?rid=3133713&amp;cid=t_200519_129_f&amp;fid=36038&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Ftrevis-life-with-multiple-sclerosis-ms%2Fholiday-blog-contest-winner-how-ms-has-affected-my-family%2F</link>
            <description>Today’s holiday guest blog comes to us from Airial of Portsmouth, New Hampshire.
We had more submissions to this topic than any of our others which I’ll admit surprised me a bit.  Maybe it’s because this is a place where many of us take time to be alone with our thoughts and others who may share them…or at least have experienced many of them firsthand.  It was very difficult to choose which one of these entries to publish.  Perhaps we should somehow make all submitted entries to this contest available on Everyday Health because I think we could all benefit from them.
Airial writes as to how MS has affected her family at its very inception…or, in this case it’s very conception.
How MS Has Affected My Family by Arial Sillanpaa
It was a chilly New England Tuesday when I was dia...</description>
            <author>Life with MS</author>
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            <pubDate>Mon, 28 Dec 2009 18:02:29 +0100</pubDate>
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            <title>Wishing All of You a Memorable Christmas Song</title>
            <link>http://www.medworm.com/index.php?rid=3118982&amp;cid=t_200519_129_f&amp;fid=36035&amp;url=http%3A%2F%2Fwww.everydayhealth.com%2Fblog%2Flife-with-chronic-pain%2Fwishing-all-of-you-a-memorable-christmas-song%2F</link>
            <description>We may be maimed, sore and hurting but our hearts and minds are, for the most part, intact; that is if you don’t use too strict a sliding scale of rationality. When assessing ourselves, I think we’re allowed to be a little “loosey Goosey”, don’t you? Our Christmas celebrations may change, our festivities become more simplistic and our pockets more lean but we still have our memories, our friends and families who love us and whom we can love in return. I sometimes wonder if it’s better to love or to be loved. I guess you’re a winner both ways.
One good thing about being older is all the memories of Christmas past. I’m old enough to especially remember all the wonderful, silly and often beautiful songs of past years. It’s funny how some of them stay with you even though you...</description>
            <author>Life with Chronic Pain</author>
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            <pubDate>Wed, 23 Dec 2009 21:45:22 +0100</pubDate>
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