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I was diagnosed in April last year and I have had my first treatment of mavenclad but for the past three months I’ve been in a flare up and still struggling. I feel like a burden to everyone who’s looking after me I do work part time as a TA for special needs children and I love the job. I’m just so...

Them: I know some one with MS and they are not too bad. You: That's Excellent we should nominate them for ‘Person with MS Who’s Not Too Bad Award.’"

So I’ve been on Tecfidera and tolerating it very well but I found out today my first MRI on it showed new lesions meaning a change in DMT. The choices I’ve been recommended are Mavenclad or Tysabri. I understand Tysabri is more effective but I’m 24 years old and I don’t want to be in a hospital ever...

I’ve had MS for 3 years that I know of. I can no longer walk at all. Any suggestions for me? I’m 72 years old Douglas

Hi, im new to the site,I have rrms was diagnosed 2 years ago but it looks like I have had ms for around 10 year prior. Last year was a bad year for me but im back to being a functioning adult

Hi all. When i noticed the first symptoms (in hindsight, it was my foot dragging a bit doing warmup laps ) it all seemed a very slow descent over about 3 years. The last year however seems a very quick descent from a bit wobbly on the foot to struggling to walk more than 100 metres. Is this normal ...

Good morning all I had my freak out post yesterday. Today I’m a little more composed lol. I have an appointment in the 28th to discuss meds. I’m uk based. Midlands area. I know meds are different for everyone. I don’t even know what type of ms I have yet. I’m hoping relapsing and looking back I ...

Hi, I hate the way my body has decided to betray me. It started with MS 15 years ago. Not a big deal in a way before it was official I had pretty much figured it out. I am an NP. In March of 2021 while at work in an ER. I told a coworker I thought I was have a heart attack we got me into a room an...