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ARCHIVE # 4: 554 ARTICLES (NOV -SEPT 2006) |
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My Educational Video on MS and MS Trials| Visitors Since 03/2006 |
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| Click here to read messages from our MySpace Friends HERE'S A FEW OF OUR 1,404 MySpace FRIENDS |
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 Click to view 1280 MS Walk photos! | ||||||||||||||||||||||||||||||||||||||||
| "Join a trial at Barrow & receive all medication & study based procedures at no charge!" | ||||||||||||||||||||||||||||||||||||||||
Stan Swartz, CEO, The MD Health Channel "WE PRODUCED THE FOLLOWING 9 VIDEOS FOR YOU!" Simply click the "video" buttons below: . |
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| Previious Posts | ||||||||||||||||||||||||||||||||||||||||
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| MS NEWS ARCHIVES: by week | ||||||||||||||||||||||||||||||||||||||||
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Monday, October 02, 2006
Samantha: OUR HERO FOR HER DEVOTION TO HER MOM...PLUS THE HELP SHE GIVES 100'S OF OTHERS THROUGH HER MySpace GROUP: "MS SUCKS"
"My name is Samantha and i am 15 years old.
My mom was diagnosed with MS about 11 years ago.
I give my mom her shots every-other night
Although life is harder for my mom than most, she loves life and does as much as she can. Our whole family participates in the annual MS walk in San Diego every year. My mom enjoys walking, and working out; even with her disease. She is a person who refuses to break down, and sometimes acts as if she doesnt have a disability at all.
I never realized how many people have, or know other who have MS until i became more involved with MS groups and events. I think it is really important that people with MS know that there are others out there going through the same things, and that no one is alone" - Samantha
My mom was diagnosed with MS about 11 years ago.
I give my mom her shots every-other night
Although life is harder for my mom than most, she loves life and does as much as she can. Our whole family participates in the annual MS walk in San Diego every year. My mom enjoys walking, and working out; even with her disease. She is a person who refuses to break down, and sometimes acts as if she doesnt have a disability at all.
I never realized how many people have, or know other who have MS until i became more involved with MS groups and events. I think it is really important that people with MS know that there are others out there going through the same things, and that no one is alone" - Samantha