Any Aubagio feedback?

Hi snowgoose! Sorry for the delay in replying to your comment! I do hope you get some feedback from other community members about their experiences with Aubagio. While you are waiting on that feedback, I thought I would share this comparison of common treatments for MS symptoms and how they rank, compared to each other (including Aubagio) -- https://multiplesclerosis.net/treatment/comparison-reviews-of-drug-efficacy-safety/. One side effect that may be one to watch out for is hair loss. It doesn't happen to every person and it does taper off, but it can be a very emotional side effect to experience if you aren't prepared for it. That may not be much of a reassurance for you, but I wanted to share that information with you. Since this isn't your first experience with trying a new medication, I hope the list of potential side effects doesn't out you on edge (although, with you past experiences, I don't blame you if the list DOES put you on edge.) Here's some basic information about Aubagio that you have probably already learned (including side effects) -- https://multiplesclerosis.net/treatment/aubagio/. I do hope you get some insight from other members and I know that one thing people like about this medication is NO INJECTION! So, there's one thing in the 'pro' column! I hope your start with Aubagio has been smooth and side effect free thus far! Please keep us posted! Best, Erin, MultipleSclerosis.net Team Member.