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I have RRMS and its been slowish in development. Im now on ocrevus but things are happening with my cognitive behaviour - memory, focus, clarity of thought, problem solving. This has been getting gradually worse for a few years, but i knew my job inside out, so not too much of a problem. Of course i...

Conversation at my physical therapist's office: Receptionist: Temperature is 93.7° Kind older lady: I don't think I wrote my temperature down Me to the kind older lady: Do you want me to ask for you Kind old lady: No. I don't want any ice cream. Thank you, though Me: *giggles with the kind olde...

I am a 64 yrs. old with no medical insurance. I have gradually had several unexplained physical symptoms of MS since I had a total hip almost two years ago, of course I didn’t immediately suspect MS...I have done a lot of research on every new symptom that would come along these past two years! I g...

Morning all, my name is Matt (aka R-F-J) I have recently found this site and hope that it will benefit me going forwards. I was diagnosed last year with PPMS and waiting for vaccines before I start DMTs of Ocrevus later in the year all being well. This has turned my life upside down, as am a keen ...

Hi thank you for my membership, I’m looking forward to hearing from and about you! I’m looking for advice and also keen to learn if anyone else feels like their internal thermostat is broken. I do not know what triggers it. I sweat 💦 so much that it is making me feel pretty crap. Along with the swe...

Hello! I was just wondering if there’s anyone on here that’s started the treatment Tysabri? I’m currently on Copaxone and the neurologist wants me to move over to Tysabri soon. The reason I’m asking is because I’d planned on going travelling next year and am really hoping this new treatment isn’t go...

Open bottle of wine. Smell it. Pour a glass. Taste & smell again. If you can taste and smell then you are ok, but finish bottle just to make sure.

Nicked this link from a post over on the M S Society forums......................... https://www.youtube.com/watch?v=mlQ9AFjsVK8 Just watched this documentary and I can't believe I have not seen this before. Alright it was first made approx 4 years before MS came into my life but I think it is rea...

Hello All I was diagnosed with MS back in 2003 I’ve had my ups and down I’ve never been on any forums like this before so all new to me after pushing my doctor I’ve managed to have another MRI after 17 years to see how my MS has progressed and awaiting results next week @ 39 now I am worried to be h...

Over the years a number of strange things happened physically that could not be explained. I survived them but a couple eyars ago I was told I did have MS and probably had it quite a long time. At my age, I am told there is nothing to be done, no meds so I take everyday as it comes. I paint. I plann...