Hi everyone! I’m Tiffany, 37, and I’m new here. I was diagnosed with MS in my 20s after experiencing optic neuritis, and I’ve been living with MS for almost 15 years. I’ve been fortunate to stay stable over the years, but I realized I’d really love to connect with others who understand this journey...

Hi All, it’s my first time here. I’ve had MS since 2001 and have been offered a DMT. I think Kesimpta may suit me best but I am terrified of possible side effects. I hate the unknown and whilst I think this medication could be beneficial, I’m just so frightened. Thanks for any advice you can share.

Hi everyone, I’m new here. I was diagnosed with RRMS in 2021 and have been on Ocrevus ever since. In many ways, MS has made me see life differently. I’ve been able to spend much more time with my kids, I volunteer when I can, and I genuinely feel like it’s made me a better person. I try to focus on...

Today my brithday

Hello everyone. Hope you all are doing well with this heat. Any diet suggestions to loose weight because I’ve gained lots of weight. Thank you:)

I had my ocrevus infusion for my PPMS last Tuesday. My sister arranged for me to go to this coffee morning event today in the village hall so I’d meet the local residents (mainly elderly i think). My question is, is it safe for me to go, because of the immunocompromised issue?

Finally, after years of nothing, I’m being offered a DMT - hooray! But I have to decide between Ocrevus and Kesimpta. I realise it’s different for everyone but I’m interested to hear people’s experiences. The good, the bad, the ugly! Thanks in advance!

I was taking off my DMT last November I'm getting ready to resume but instead of every month probably quarterly or whatever other month because my immunoglobined ig level has gone too low apparently is there anybody else out there that does less of a k e f i m p t a

My depression is so bad today. after I left and freaked out after my first relapse, I moved in with my mom and nothing has been the same. I don’t have any of my old friends. I barely even talk to my family and since I can’t work, I don’t have any income, so I can’t really do anything for myself. I’m...

Hello Everyone I have question has any one paused ocrelizumab after 2 years - or 3 years does ms stay stable and can you just stay off meds after this pause? Any experience will be great to know about