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Re: tysabri just wondering.....reply to Sherri's post

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Just typing out loud, but have you been tried on Avonex?Love and hope,n, from out near San FranciscoSubject: tysabri just wondering.....To: MSersLife Date: Thursday, September 29, 2011, 6:12 AM

I am curious how many people opt to not take any of the handful of treatments available. Fail on Rebif, fail with Copaxone, now although Tysabri has done some very positive things for me it is also doing some not very positive things for me too-liver enzymes, infections, starting to have flairs again.... The next drug in line for me is form of Chemo-starts with A (too lazy to look it up right now) but I am feeling like the medicine is poisoning me basically and what good does it do to save my brain and kill my liver. Some days I want to say if u quote one more statistic to me grrr but with Tysabri the info is changing all the time. 10 months ago when I started it I felt like i had made a choice based on informed decision but the info/stats risks are way different that I was told then kinda too late to exactly change my mind. Reality is my ms is agressive and my choices were limited but as things evolve I am really considering no drugs and seeing

where i go from there. Any thoughts, do others do this, how is it going? ty Sherri

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