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Does anyone have advice on walking aids, I’ve got mild drop foot but unless my husband fetches me I trolley, I don’t really go out. Waiting to be contacted by ms nurse because of Covid it’s been really slow.

From MS Society With shielding set to be paused in all four nations of the UK in August, we want the UK Government to support people with MS who can’t safely go back to work. We’re campaigning with Age UK, the Trade Union Congress (TUC) and 9 other charities. Together, we’re calling for the furlou...

I have MS disanosed when I was 24 Ms doc said I had since I was 9 n I'm 45 now with my 10 yr old son

So am divorced from my ex, which is fine! But now he has taken our children, 2 boys, off me because apparently I am an unfit mother! Yes, I have m.s, yes I like an alcoholic beverage occasionally but HE has dictated to all, that disabled people shouldn't drink! Aaarrrggghhh! Court case online on tue...

Does anyone else get the terrible MS related toe pain ? Omg it is awful 😔

Hello have had MS since 1970, still walking but falling more but I was expecting that. Question I was on Aubagio 4yrs and stopped taking 1 month ago. Now experiencing more balance issues. What are the withdrawal symptoms if any?

After nearly 3 years of searching for answers to my wife's rapid cognitive decline, multiple tests and MRIs and second opinions it is clear she has a the syndrome of Dementia. Our local neurologist as well as the team at UCLA agree that the cause is MS. Images show significant brain atrophy. I ...

I'm going to be on ocrevus in a few weeks, what are the best options for treatment so far?

Hi there, I just finished my 1st cycle of Mavenclad treatment...free now for 4 weeks before the next lot No real side affects...just a little exhausted...more than the usual kind I could feel burning sensation while swallowing the medication..make sure anyone taking this medication has plenty of w...

Hi guys. First post, so here goes - I've gone from R/R to PPMS. It's a bit frightening but it's nice to talk to people who understand. I've been put on the W/L for Rituximab infusions although from what I'm reading the results aren't great for PPMS - anyone here have any experience? I'm determin...