Doctor told me when I turn 55 we can talk about stopping infussions as long as flare ups don't happen, but all this in her words is cuz of aging

Had rrms for 25 years now diagnosed with spms. Due to start mayzent/siponimod after being on Tysabri for 20 years. Anyone gone through something similar? And what’s been your experience?

Did anyone else experience issues in their relationships because of side effects. (Not being interested in intimacy). My partner has been less than supportive or understanding.

A little while ago I threw an idea out on here. What if there was something where people with MS could just talk honestly about what living with MS is actually like? Not doctors. Not neurologists. Not someone reading a leaflet explaining fatigue to people who've been fucking exhausted since Tues...

Anyone else here like to enjoy the occasional drink with dinner but need to cut or eliminate alcohol for medical reasons? My inflammation load is high and I'm dealing with a flare so I'm not even drinking my one glass of wine at dinner on Friday night now. I have tried a number of dealcholized wine ...

I am trying to decide between Kesimpta or Clabribine, does any one have any experience with any of these? Just diagnosed and have my nurse appointments next week 😏

It’s all natural, and takes some dedication and time to get used to…but I started out on the pills 20+ years ago, and now I mix in with my Metamucil every morning! Product is from a company called Mannatech, produce recommend from their long list of products is Anmbrotose!

Has anyone tried magnesium malate? What were the pros and cons? TYIA