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OMG and meds
Diagnosed OMG six months ago. My only symptoms are double/blurry vision. I’ve been taking Mestinon but it was affecting my asthma. I switched to Huperzine A with some success but still get DV when I’m tired. My neurologist wants to add cellcept. The side effects sound scary and it sounds like it takes a long time to even see improvement. I’d appreciate hearing your thoughts on cellcept!😊
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1 Reply
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I was diagnosed with seropositive MG in 2013. Since then my only symptoms have also been double/blurry vision with no ptosis so I am also very interested in the responses to your post. I tried Mestinon but it didn’t help. I have not tried any of the drugs, such as Celcept, because of the side effects. I am constantly weighing the fact of which is worse double vision or medication side effects. It also seems, from what I’ve read in forums, that double vision is one of the most difficult symptoms to treat successfully, another reason I haven’t tried the stronger meds. I cannot take Prednisone. I look forward to reading the replies and any help offered. I also have MS, diagnosed 30 years ago, but I haven’t had a true exacerbation in over a decade.
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