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Hi, just advice needed really I take flingolimod and have done for 12 years and I’ve been relapse free since. But I’m 37 now and I think it’s time to start a family always been on the fence because of my MS but I can’t allow this to scare me. I’ve spoken to my ms team and they have suggested I go on...

Has anyone had a relapse while on Ocrevus??

For you're first relapse was you given steroids to recover not knowing it was ms?

It’s been a while that I haven’t posted hope your all feeling well. Quick update on myself during with my MS. I am doing ok thank god and also been told since starting the Kesimpta I am stable and which is good news to hear as I have been through a difficult situation lately as me and my partner hav...

Been diagnosed 3 years and this is still something I struggle with. Recently I’ve had pain and sensitivity to my skin on my neck going to my ear and down my arms in various places. I don’t even want clothes to touch it and I have had skin sensitivity before but not in this place. It seems whenever I...

I’m so sorry for the long post but the relief I feel that I’ve found this app is unreal!! ❤️ So I’m curious if anybody can give me some advice on ways to exercise my feet and leg to help build its strength. In September I had covid which brought on a relapse resulting in optic neuritis. I was given...

Nine months ago, my life changed when I was diagnosed with MS in 2023. The journey since has been nothing short of transformative—physically, mentally, and emotionally. I’ve faced challenges I never imagined: enduring relentless relapses, the disconnection of not being able to feel my hands, feet, o...

I've been diagnosed with RRMS in 2020 and started Tysabri in 2021, everything went and is great, no relapses since but I just cannot stop thinking about Tysabri's side effects and what bad things does to my body. I wasn't sure I wanted to go with it in the first place and I'm stressed and frustrated...

Hi all! I am due to be starting Ocrevus in the next few weeks and wondered if anyone had any tips, or any feedback on how the treatment is, or any side effects they had? I have been through many treatments during my MS journey (Rebif, Tysabri and Lemtrada) but have recently had more activity on my...