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	<title>Comments on: Creatine helps people with &#8216;Muscular Dystrophies&#8217; ?</title>
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	<link>http://www.creatinejournal.com/creatine-supplement-creatine-helps-people-with-muscular-dystrophies/</link>
	<description>A Creatine Journal</description>
	<lastBuildDate>Sat, 07 Nov 2009 02:01:01 -0500</lastBuildDate>
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		<title>By: world of warcraft eu</title>
		<link>http://www.creatinejournal.com/creatine-supplement-creatine-helps-people-with-muscular-dystrophies/comment-page-1/#comment-33913</link>
		<dc:creator>world of warcraft eu</dc:creator>
		<pubDate>Wed, 21 Oct 2009 02:29:15 +0000</pubDate>
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		<description>Thank you!</description>
		<content:encoded><![CDATA[<p>Thank you!</p>
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		<title>By: furniture</title>
		<link>http://www.creatinejournal.com/creatine-supplement-creatine-helps-people-with-muscular-dystrophies/comment-page-1/#comment-33542</link>
		<dc:creator>furniture</dc:creator>
		<pubDate>Mon, 05 Oct 2009 07:10:44 +0000</pubDate>
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		<description>I agree, creatine does help build muscle tissues but i don’t know too much about muscular dystrophie either.</description>
		<content:encoded><![CDATA[<p>I agree, creatine does help build muscle tissues but i don’t know too much about muscular dystrophie either.</p>
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		<title>By: Needshelpwithscholarships</title>
		<link>http://www.creatinejournal.com/creatine-supplement-creatine-helps-people-with-muscular-dystrophies/comment-page-1/#comment-31880</link>
		<dc:creator>Needshelpwithscholarships</dc:creator>
		<pubDate>Tue, 11 Aug 2009 01:21:05 +0000</pubDate>
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		<description>Im a high school gradaute. Im planning to attend college in the spring. I do have Muscular Dystrophy. I wanted to know if anyone out there would have information on anything about scholarships grants etc for students with muscular dystrophy. email me at. kaykay1324@yahoo.com thank you</description>
		<content:encoded><![CDATA[<p>Im a high school gradaute. Im planning to attend college in the spring. I do have Muscular Dystrophy. I wanted to know if anyone out there would have information on anything about scholarships grants etc for students with muscular dystrophy. email me at. <a href="mailto:kaykay1324@yahoo.com">kaykay1324@yahoo.com</a> thank you</p>
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		<title>By: michael jordan shoes</title>
		<link>http://www.creatinejournal.com/creatine-supplement-creatine-helps-people-with-muscular-dystrophies/comment-page-1/#comment-30147</link>
		<dc:creator>michael jordan shoes</dc:creator>
		<pubDate>Thu, 25 Jun 2009 04:01:20 +0000</pubDate>
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		<description>For further information about the Warhammer CD-key and Warhammer Timecard, Please keep an eye on air jordon shoes. For more  information please keep an eye on cheap jordon shoes .</description>
		<content:encoded><![CDATA[<p>For further information about the Warhammer CD-key and Warhammer Timecard, Please keep an eye on air jordon shoes. For more  information please keep an eye on cheap jordon shoes .</p>
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		<title>By: Sam Abu</title>
		<link>http://www.creatinejournal.com/creatine-supplement-creatine-helps-people-with-muscular-dystrophies/comment-page-1/#comment-24019</link>
		<dc:creator>Sam Abu</dc:creator>
		<pubDate>Sun, 12 Oct 2008 06:31:01 +0000</pubDate>
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		<description>hi my name is sam and i have muscular dystrophy and its getting really hard to handle i am very thankful that i am not on a wheelchair yet because i am sixteen and usually by this age i should be on a wheelchair but recently i feel weaker and its harder for me to get up and i have never taken any medicine to help or slow the symptoms of muscular dystrophy can someone please email me at lilsam92forever@yahoo.com if they information about any medicine that can help or organizations that can aid muscular dystrophy people like me thanks alot
Sam Abu</description>
		<content:encoded><![CDATA[<p>hi my name is sam and i have muscular dystrophy and its getting really hard to handle i am very thankful that i am not on a wheelchair yet because i am sixteen and usually by this age i should be on a wheelchair but recently i feel weaker and its harder for me to get up and i have never taken any medicine to help or slow the symptoms of muscular dystrophy can someone please email me at <a href="mailto:lilsam92forever@yahoo.com">lilsam92forever@yahoo.com</a> if they information about any medicine that can help or organizations that can aid muscular dystrophy people like me thanks alot<br />
Sam Abu</p>
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	<item>
		<title>By: Shane</title>
		<link>http://www.creatinejournal.com/creatine-supplement-creatine-helps-people-with-muscular-dystrophies/comment-page-1/#comment-3215</link>
		<dc:creator>Shane</dc:creator>
		<pubDate>Sat, 14 Apr 2007 08:50:28 +0000</pubDate>
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		<description>I have beckers muscular dytrophy and have been considering doing my own &quot;Creatine Therapy&quot;  thanks for posting this.  I will need to do more research about Creatine of course and its effects any info you have about this or knowledge of where to get info about Creatine and muscular dystrophy.

email me at     te.kokako@gmail.com</description>
		<content:encoded><![CDATA[<p>I have beckers muscular dytrophy and have been considering doing my own &#8220;Creatine Therapy&#8221;  thanks for posting this.  I will need to do more research about Creatine of course and its effects any info you have about this or knowledge of where to get info about Creatine and muscular dystrophy.</p>
<p>email me at     <a href="mailto:te.kokako@gmail.com">te.kokako@gmail.com</a></p>
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		<title>By: Tim McGuirk</title>
		<link>http://www.creatinejournal.com/creatine-supplement-creatine-helps-people-with-muscular-dystrophies/comment-page-1/#comment-2589</link>
		<dc:creator>Tim McGuirk</dc:creator>
		<pubDate>Sat, 10 Mar 2007 15:54:34 +0000</pubDate>
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		<description>I&#039;m 55 years old and I was born with muscular dystrophy, Charcot-Marie-Tooth disease.    I have a level (3) type of CMT.    My hands and legs have been relatively useless all my life because of the weaknesses I have had to live with.     I am an educated person with a masters in computer science, and I mention this to demonstrate that I have been trained to analyze problems and thus seek solutions.   

To conteract my weakness problems brought on with CMT I started doing exercises with weights back in 1976.    As I aged, the pain and weakness in my forearms and hands became more intense, and no one in the medical community could help.....doctors only shrugged their shoulders and told me to take asprin when the pain became overwhelming, no one had any answers.........the Muscular Dystrophy Association had no suggestions.
(Was it the disease or apathy?)

Last year by chance I came across an article about people with different types of muscular dytrophies possibly getting some relief by taking creatine.    I thought, &quot;hell, what do I have to lose.&quot;   So I began taking a teaspoon of creatine every morning......then exercising.

After three months the pain is now what I would consider, &quot;mild.&quot;     I have much more overall energy.........my stamina has improved greatly, and my strength has doubled.     Say what you will about creatine, but to me it is a big help in my life.    

I am my own test dummy for the experiments I&#039;ve undertaken to combat CMT muscular dystrophy, and I take no endorsements from any company or manufacturer......I am also cautious right now about recommending creatine for MD patients.     But as my own lab rat, I continue to study the daily effects of creatine and exercise on my own body and overall health.

In trying to do in my own individual way what so many government grant &amp; university sponsored research people and doctors, including those sponsored by the MDA, can NOT do.....I&#039;m at least TRYING to help with some helpful 
possibilities! 

My work is a bit on the selfish side........I have been blessed with two grandsons......born to my daughter......and those who know about the source roots of CMT muscular dystrophy know what that means.    At least I&#039;ll have some explanatory advice for my grandsons when the time comes.


Tim McGuirk
St. Louis, Missouri</description>
		<content:encoded><![CDATA[<p>I&#8217;m 55 years old and I was born with muscular dystrophy, Charcot-Marie-Tooth disease.    I have a level (3) type of CMT.    My hands and legs have been relatively useless all my life because of the weaknesses I have had to live with.     I am an educated person with a masters in computer science, and I mention this to demonstrate that I have been trained to analyze problems and thus seek solutions.   </p>
<p>To conteract my weakness problems brought on with CMT I started doing exercises with weights back in 1976.    As I aged, the pain and weakness in my forearms and hands became more intense, and no one in the medical community could help&#8230;..doctors only shrugged their shoulders and told me to take asprin when the pain became overwhelming, no one had any answers&#8230;&#8230;&#8230;the Muscular Dystrophy Association had no suggestions.<br />
(Was it the disease or apathy?)</p>
<p>Last year by chance I came across an article about people with different types of muscular dytrophies possibly getting some relief by taking creatine.    I thought, &#8220;hell, what do I have to lose.&#8221;   So I began taking a teaspoon of creatine every morning&#8230;&#8230;then exercising.</p>
<p>After three months the pain is now what I would consider, &#8220;mild.&#8221;     I have much more overall energy&#8230;&#8230;&#8230;my stamina has improved greatly, and my strength has doubled.     Say what you will about creatine, but to me it is a big help in my life.    </p>
<p>I am my own test dummy for the experiments I&#8217;ve undertaken to combat CMT muscular dystrophy, and I take no endorsements from any company or manufacturer&#8230;&#8230;I am also cautious right now about recommending creatine for MD patients.     But as my own lab rat, I continue to study the daily effects of creatine and exercise on my own body and overall health.</p>
<p>In trying to do in my own individual way what so many government grant &amp; university sponsored research people and doctors, including those sponsored by the MDA, can NOT do&#8230;..I&#8217;m at least TRYING to help with some helpful<br />
possibilities! </p>
<p>My work is a bit on the selfish side&#8230;&#8230;..I have been blessed with two grandsons&#8230;&#8230;born to my daughter&#8230;&#8230;and those who know about the source roots of CMT muscular dystrophy know what that means.    At least I&#8217;ll have some explanatory advice for my grandsons when the time comes.</p>
<p>Tim McGuirk<br />
St. Louis, Missouri</p>
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