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    You are here : Home » Get Involved » MSRC Interactive » Tysabri® User Diaries » Stuart S's Tysabri Diary

    Stuart S's Tysabri Diary

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    Stuart S.

    Name: Stuart S.
     
    Diagnosed - 1998
    First Symptom may have been as early as when I was 17
     
    You can read about me, by clicking here,then scrolling a bit down on the page.

    If too small to read, copy and paste into an email or word document and enlarge the font, like I so often need to do.
      
    Previous medications:
    Avonex - approx 1 year - too long ago to remember -- wasn't enough to do alone, was having relapses every few months
    Avonex with Copaxone -  approx  2 years - who remembers? -- Was still having relapses, was thought I needed something stronger.
    Rebif with Copaxone  - approx 1-1/2 years  - was doing great with this combo therapy but when I had to stop working, the new insurance plan told me to choose one of the two meds to continue
    Copaxone alone - approx 6 months  -- developed the symptom of not being able to breath so what do you think I did? I stopped using it.
    Rebif alone -  5 years +/-  -- this was great at first but in the last year plus, found to be not as effective
    Tysabri - since Dec 2009

    An MS patients' views of his current Drug therapy for Multiple Sclerosis and about Quality of Life 
     
    My First Infusion - blogged
    My first infusion day 2 - update
     
    My Primary Symptoms: Fatigue, Pain, Vertigo, and sensory tingles
     
    I can be contacted at : [email protected]

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