I am new, I have just officially been diagnosed after of almost 2 long years of testing. The doctors wanted to make sure because there are 3 other diseases that mimic MS in first nation people. I also have a whole host of other things that going on with me which is probably why it took so long. I have just started on Tecfidera and as with all the other meds I am nervous but here I go. By the looks of the scans I have had MS for years but until certain symptoms started cropping up like it was getting harder to walk and nerve pain and other things happening, I always put it down to the so this has to do all the other stuff. I went for brain scans and the results opened another door.
Thanks for listening/reading.