I have SPMS and I'm thinking of of starting Mayzent. I'm a little nervous of taking a new medication that hasn't been on the market long, with just results from their trial. Cost is another thing. Is there assistance for the high cost? So, any insight would be appreciated.
Looking forward to starting Mayzent next week. I keep you updated on my progress
Hi Trish, I just started seeing a new neurologist. My old one did not mention anything about a med for SPMS. So, I'm not on any kind of medication for MS. Two weeks ago, when I saw the new guy he told me about Mayzent and that it was just aproved earlier this year. Being new I had concerns about it.
Hi Cheryl. How long have you been on Aubagio? Does seen to help with SPMS? My legs are getting weaker each year. I use a walker. Bad as it is, I don't want to get worse.
Thanks Trish and Cheryl for your thoughts. Wishing the best to the both of you.
Good Morning you said your seeing a Neurologist but is he a MS Specialist? There is a difference between the 2. My Dr. keeps up on all the new medications, all the research coming out. Something to thing about . Have a good day.
I also have SPMS and my Dr didn’t feel comfortable putting me on the 2 new drugs bc they have yet to prove anything yet but I am taking Aubagio for now.
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