I have spms from rrms diagnosis started in 2005,&2020 have been on dalfamapride is that a MS med
If you have the money, get out of this lousy country and get real help, like stem ell therapy. Do not stay here in hopes of the"medications" making you better. How valuable is a healthy person to the "healthcare" industry " in a country that seeks profit over everything? They have no financial incentive to cure you or greatly diminish your symptoms. Get out if you can. At least look at the website of The Stem Cell Institute. Located in Panama City, Panama.
Does anyone go through this also or know how to make the symptoms decrease
I am having trouble with the optical neuritious my eyes stray not staying straight ahead more frequently than before and my pupils don't dialate like they should staying really big or small people that don't know why often think I'm on drugs it's really embarrassing and I don't know what to do about it
At the moment I am just taking vitamin d helped more than any meds for years but now they are waiting on MRIs to come back to start another treatment therapy but the main concern I hv is the optical nueritous
Dalfamapride is a drug to help walking/mobility. Are you on a DMT?