Friday, October 15, 2010

Always something

So this week was full of fun and games in WWMS ( wonderful world of MS). I have been taking Copaxone for close to three years. I had a small stunt with Rebif for a few months that didnt work out so hot. Anywhoo they found two new lesions in the past 4 months and now I have to add IV steriods once per month. Fucking great.
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2 comments:

  1. StarlaNovember 20, 2010 at 10:59 AM

    Have you considered Tysabri? I was on Copaxone for 6 months after my diagnosis and in that time frame I developed numberous lesions in my brain and spinal cord. It was not aggressive enough for me but everyone is different. I hope you find something that works for you.

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  2. NRN2BNovember 20, 2010 at 2:38 PM

    Hey starla I think I am not advanced enough for tysabri.. Im not sure though.

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