Photo of National MS Society

National MS Society

www.myspace.com/mssociety

The Official National Multiple Sclerosis Society MySpace Page

View My:

  • National MS Society

  • Age: Private / Female
  • NEW YORK, NEW YORK, US
  • Last Login: Private

18071761||11110|http://c4.ac-images.myspacecdn.com/images02/12/m_6fbba2e5bfdd4bd2b2738267c71da29f.jpg

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Blurbs

About me:

The National MS Society is a collective of passionate individuals who want to do something about MS now—to move together toward a world free of multiple sclerosis. MS stops people from moving. We exist to make sure it doesn't.

Find Your Chapter

World MS Day Video To see more of our videos, please visit our YouTube channel - www.youtube.com/nationalmssociety.

Who I'd like to meet:

..Multiple Sclerosis's Profile | Create Your Badge
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Comments

Displaying 5 of 649 comments
  • JessJessica Garcia

    Jul 15 2009 11:47 PM

    Thank you for the add...I was added some time ago...but have just gotten around to show my appreciation. I started reading a book yesterday...that's kind of moved me to reach out to other people who are dealing with some of the struggles MS brings and might understand what I'm going through. I was diagnosed about 4 years ago...but I think lately it's been becoming a realization more than ever...can anybody relate?

    I guess I'm an optimistic person and have always been optimistic about life and still am...but as a result there are times that I don't deal with reality...wow...I think I'll stop there...can you say too much information :)
  • a.m Personal Trainer Ha…

    Jul 13 2009 10:27 PM

    THANKS FOR THRE INVITE.
  • *Mrs~Keller*

    Jul 13 2009 11:36 PM

    I was diagnosed in 2002,relapsing remitting ms. I was taking rebif, but it was not working, so I will be starting tysabri very soon...
  • Tracey

    Jul 14 2009 3:29 AM

    Thank for the add. Needing to converse with people like me that have RRMS and have had it without knowing until the damage has been done.
  • StaceyStacey Smith

    Jul 9 2009 5:53 AM

    Well, I was 32. I lost everything from my neck down for about 6 months, found lesions on my spain. Got everything back but my left side. I'm one of these people that has to work all the time. "NOW STOP" I'm sure there is some people out there that can say the same thing. So I went back, worked until I have some of my feel back, but not all. My doctor said that If I lose my site, then they would diag me with MS, and put me on the shots. By now I have lesions on my spinal cord and two on my brain.. I was putting into my drive way, and I lost both of my eyes. Everything went black. When I was able to put everything together one eye was going to the right, and the other was on the left. I went to the hospital and my doctor came in and said that I'm not going to die from this, and she gave me information about Copazone. I have been on it for a year now, I still have problems from the what was already damage . We all just all need to put yourself up and go on, don't give up you will make it....Stacey Smith