I saw a year ago someone had posted they had been taking BG12 for about 2 years. They were doing a trial. I just wanted to see what anyone who did the trial tesing, for BG 12, thinks about it today. I have MS (optical nueritus) and thinking about switching to the BG12 but nervous. Been on Avonex but I really dont like it. Makes me feel awful.
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I, too take Avonex, and it aggravates my psoriasis tremendously. I understand BG12 was originally FOR psoriasis, so I am seriously thinking of making the change. 2 pills a day over an IM weekly shot sounds good, too.Originally posted by zachblake View Post
I should have researched this more before posting, but since I didn't
, does anyone know if this particular drug does ANYTHING in regards to symptoms, unlike the DMDs we are currently taking? I realize the key is slowing progression, but it sure would be great if there was something else that could improve our quality of life in the meantime!
Tawanda
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Diagnosed with Multiple Sclerosis 2004; First sign of trouble: 1994
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