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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...

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 ...

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...

My legs have completely given up on me, they are unbelievably solid, like Stonehenge. I am currently on no medication, trying to see if this is a relapse or something. This has lasted 2-3 weeks already and seems to be gradually getting worse. Does anyone have any ideas on what I could be doing to im...

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...

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.

I’ve had RRMS for 4 years and I’ve had 2 rounds of Lemtrada. For years I’ve suffered with extreme sweating and after Lemtrada it’s gotten worse! I literally can’t leave the house as I’ve only got to move and The sweat is pouring off me. I take small electric fans everywhere with me and I have a fa...

Hey everyone, was just curious if anyone has taken MAVENCLAD and if they found that the second week (week 5) affected them more or less than the first? In terms of side effects or feeling sick, etc.

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...