Just feeling really defeated. Bad drop foot from recent relapse, and I almost feel as if my walking is getting a lot worse. Going to PT and trying to soldier on. Now most days my legs and feet feel like sandbags I’m pushing along. Numb cold, and sometimes lots of buzzing. Had oral steroids for four ...

MS Society UK - Trustworthy ? • MS Society UK - Trustworthy ? • My First hand experience of the MS Society The MS Society UK gave me purposeful misleading information about HSCT. On enquiring about the treatment, they said, 'Don't do it; it's dangerous. You might die!" Many neurologists were not sup...

Hello, I will be starting Ocrevus next week. I was previously on Tysabri but tested positive for JCV. I’m pretty nervous now. My neurologist said this is safer, but I know there is still a possibility for PML. Anyone have a similar experience?

I’m wondering how everyone deals with fatigue, I’ve tried magnesium and ignoring it for the last 8 years 😅 I’m not sure what to do. My sister said I should try to change my diet but even with that I’m not sure where to start !! Any recommendations would be greatly appreciated :)

Has anyone experienced severe nerve pain that can cut through a med like gabepentin?

Has anyone considered or actually gotten a second opinion after MS diagnosis? I was diagnosed from an MRI alone & after reading about Christina’s misdiagnosis I can’t shake the feeling that it could be something else. From what I’m reading online she had an MRI & spinal tap & was still somehow misdi...

I was put a tecfidera at first and I was great then second yr started feeling not good but didn’t know or couldn’t tell you why turns out it was affecting my liver and I was one step away from hospital took off straight away next day started feeling better now on the jag 3 times a week