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    How it started

    I think I began to have some transitory issues in my early 20's. Fatigue, pain and nerve issues but assumed it was normal wear and tear. A guy I was dating had himself tested for AIDS during an extreme bout of fatigue at I had at 24years of age. I got better and we went our separate ways.

    That was about 1994 and no one considered MS least of all me. My mother died at age 35 of cancer so I kind of always thought something was wrong and I may not be built to last. I am 45 now and have secondary progressive multiple sclerosis.

    #2
    Well, glad that you have found the group/website. When were you actually diagnosed?
    RRMS Dx: 3/23/15
    (Optic Neuritis Dx 2/27/15; Feb/2014 right leg numbness--at the time diagnosed as Sciatica, but probably first episode)
    Started Tysabri 5/22/15: (Infusions: 5/22/15, 6/18/15, 7/16/15)

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      #3
      Diagnosed

      I was diagnosed in 2008. I went to many different doctors for different issues over the years. I could not drive anymore unfortunately.

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        #4
        I had the great good fortune to have 12 quite good years, as promised, dmd or not. It was all there in a musty, dusty old book I found in my Aunty's second hand shop before I was diagnosed, from the early 1900s.
        The book recommended knitting as a therapy, but offered no hope of a cure. Funnily enough, a century later, still kind of the same.
        I knew I had MS, but I had hope, 'cos ten years still walking, well that meant it was benign.
        Those days are over. Took the drugs, and it was no picnic early on, because I felt pretty darn good, and that Beta made me feel horrible.
        And now, obviously progressive diseases progress.

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