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Tysabri Recovery Series - Infusion #21

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Uploaded by on Jun 4, 2008

Continuing recovery with the new MS drug Tysabri

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Uploader Comments (vbeachy)

  • im in a wheelchair is it worthwhile taking tysabri?

  • In a word: ABSOLUTELY! It is amazing how much freedom I recovered when I started walking!

  • Hello I just started tysabri 1 week ago and your videos are inspiring. I continue to drag my left leg but am hoping for the best. Thanks for your inspiring comments

    Lisa

    SPMS

  • I hope Tysabri does for you what it did for me! Thanks, Lisa!

  • hey vern,

    my name is elise and i started tysabri 6 months ago. ive been watching all you videos for about a year now. they inspired me to not be afraid to start using tysabri myself. i feel a major difference since ive switched over from betaseron. i can now jog and i no longer have to look to my family for support when doing everyday activities. My daughter has just been diagnosed with rhuematiod arthritis(autoimmune) and i am helping her with walking. i just wanted to say thanks. plz cmmt me.

  • Thanks Elise! I am so glad you feel better on Tysabri. I tried running two days ago and my balance is just not "there" yet. Please keep me informed on how you are doing!

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  • Hi Bear;

    I was SPMS with remissions when I started taking Tysabri.

    Of course I believe in God. I think prayers and Tysabri are the reasons I can now walk!

  • Vern, I feel I know you very well by watching all your videos on tysabri. I have had MS for twenty two years. I'm still walking, just a little slower because of my right leg. I wanted to know that when you started tysabri was your MS relapsing/remitting? I turned secondary-progressive four years ago. I'm still doing well. My doctor says tysabri is my next step. God Bless you (that's if you believe in God.) Keep on informing all of us. You're great! bbear318

  • Thanks Wendell! I will do that, brain fog is much better with Tysabri.

  • Hi Vern! You look & sound great. You've answered questions about you liver & PML concerns by stating that TYSABRI has gotten you out of the wheelchair. Which is terrific.

    You've talked about how shingles made the left side of your face numb.

    I've heard stories from others on TYSABRI that their VISION really improved OR that their "brain fog" disappeared. Did you have any VISION or BRAIN FOG prior to taking TYSABRI?

    If you did...on your next infusion....would you care to comment, please? TIA

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