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.