Evening all, Just joined this site. My wife is about to start treatment for RR MS that was diagnosed last week. From the options presented we have decided on Tecfidera. Although we are aware of the side effects from the material already out there, I was wondering if anyone has any recent experience (good or bad) to share on this? If the comment is likely to be really bad can I ask that this is sent privately (if this is possible?) as I would rather not scare others. As a demographic, my wife is late 30s and only started showing acute symptoms in late March 2018.
Hi :) I'm 23 and have been on Tec for just over a year now. Its been a pretty mooth ride for me luckily minus hot flushes/upset tummy if I don't eat enough with my doses. Other than this I have gotten back to my normal self like I was pre first episode and hopefully at my next MRI at the end of September I will see no new activity. Good luck to you and your wife, I hope she has as easy a time as I have.