I just started Tecfidera after being diagnosed 17 yrs ago. I know I've been lucky with little problems in that time. (3 mri scans...yes its active). Is there anyone out there with a similar experience?
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Has anyone debated meds for years?
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I was diagnosed 14 years ago and stayed away from meds altogether until 9 months ago when I started Copaxone. I only started it because I started having a hard time walking and my neuro said it might prevent future relapses. I finally decided to try. You are so lucky to start Tecfidera! I can't wait to get coverage for that. Cheers
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Tom,
That's a long time. Do you think you would take BG12?
Do you go back and get MRI's during the 25 yrs? (I've had 3 in 17 yrs and lesions have increased but doc says they are more surface ones...vs. deep ones).
I didn't read anything or think about meds until now. My hands and feet had tingling....then some sensation loss and numbness. That was scary. My feet are better now and hands are about 70% better.
I'm not fully on board that meds will do anymore than exercise and diet...but docs disagree!
I am curious as I am not sure there are a lot of people out there in this situation.
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