Hello all again, its been a while since ive last posted anything. I have been diagnoised with highly active MS and last week i had a treatment meeting, the neurologist and MS team have gone through 3 treatment options and cladribine was one i could poissble starting next month. I just want some feedback about The DMD that anyone may know about it? Or if anyone is on it? I know its recently came out but just thought ill ask.
Thankyou for looking🙂
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