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	<title>Comments on: The MS Blog Becomes the MS Website</title>
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	<description>Within every Multiple Sclerosis Patient there Lies an Indomitable Strength.</description>
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		<title>By: Jen</title>
		<link>http://www.msstrength.com/the-blog-becomes-the-website/comment-page-1/#comment-124</link>
		<dc:creator>Jen</dc:creator>
		<pubDate>Mon, 25 Aug 2008 01:52:22 +0000</pubDate>
		<guid isPermaLink="false">http://www.msfriend.com/?p=50#comment-124</guid>
		<description>Hi Nadja---

My MS journey was a walk in the park, too, in the beginning.  I also had mild MS (started very vaguely at around age 27) and I took no meds or even steroids until a little over 3 years ago.  But the bright side is that I am rebounding very well from my latest attack.  It takes me forever (6-12 weeks) to get through it, do the steroids, regain my sleep, and be somewhat normal again.  But I walk without a cane, I don&#039;t have tremendous fatigue (a bit of lead limbs at times), and I only take my injections and something for my shot nerves (no pun.) My biggest issue is my left leg being a bit unsteady at times, but it&#039;s manageable without a cane.  So I don&#039;t want you to think that MS is always a disability sentence.  It can go either way, and I thank my lucky stars for my pretty good overall case.  But I embrace that the road could turn down the line.</description>
		<content:encoded><![CDATA[<p>Hi Nadja&#8212;</p>
<p>My MS journey was a walk in the park, too, in the beginning.  I also had mild MS (started very vaguely at around age 27) and I took no meds or even steroids until a little over 3 years ago.  But the bright side is that I am rebounding very well from my latest attack.  It takes me forever (6-12 weeks) to get through it, do the steroids, regain my sleep, and be somewhat normal again.  But I walk without a cane, I don&#8217;t have tremendous fatigue (a bit of lead limbs at times), and I only take my injections and something for my shot nerves (no pun.) My biggest issue is my left leg being a bit unsteady at times, but it&#8217;s manageable without a cane.  So I don&#8217;t want you to think that MS is always a disability sentence.  It can go either way, and I thank my lucky stars for my pretty good overall case.  But I embrace that the road could turn down the line.</p>
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		<title>By: Nadja Tizer</title>
		<link>http://www.msstrength.com/the-blog-becomes-the-website/comment-page-1/#comment-123</link>
		<dc:creator>Nadja Tizer</dc:creator>
		<pubDate>Sun, 24 Aug 2008 23:19:56 +0000</pubDate>
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		<description>This sounds like a good idea but keep posting a few blogs.  I like visiting your site.  I also love reading your comments on my blog.  

I read what you wrote on blindbeard&#039;s blog about the &quot;benign&quot; MSer.  Don&#039;t throw things, but until I have another relapse, I am &quot;benign&quot; too.  My first exacerbation was a trip to hell so I pray that I remain &quot;benign&quot;. I know how lucky I am even with the symptoms I do experience at times.  Compared to your journey, mine is a stroll in the park.</description>
		<content:encoded><![CDATA[<p>This sounds like a good idea but keep posting a few blogs.  I like visiting your site.  I also love reading your comments on my blog.  </p>
<p>I read what you wrote on blindbeard&#8217;s blog about the &#8220;benign&#8221; MSer.  Don&#8217;t throw things, but until I have another relapse, I am &#8220;benign&#8221; too.  My first exacerbation was a trip to hell so I pray that I remain &#8220;benign&#8221;. I know how lucky I am even with the symptoms I do experience at times.  Compared to your journey, mine is a stroll in the park.</p>
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