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Hi there, how am a newbie to the forum so hello all... I am looking for some advice to help me support a family member with MS who is quite isolated.I was wondering if anyone could advise on any technologies available to ensure my aunt feels more included and connected to friends and family. Her mo...

Hello MSers, I haven't posted in a while but I wanted to talk about COVID19. Is anyone else worried about not receiving their treatment? I'm on ocrevus and doctors have stopped my treatment as it can suppress my immune system, however, they have also confirmed that the ocrevus inside my body will ...

Hello, shiftoids, Our Coven of Covid Companionship has ceased to operate covertly, because that was too much alliteration. We're having a public, and, if all goes well, weekly Sunday night Convocation of the Covid Coven of Companionship. 6pm UK time (BST), that's 5 UTC, it should be sunday aftern...

Hi all, I’m new to the site, just thought I’d say hello. Bit a about me, I’m a Brit living down under, I have a 10 year old child.....opps I meant 11 (do birthday during covid lock down even count!?! 😂) I love playing hockey and drinking coffee looking out over the sea 🌊 Rx

Hello Lovely People.... I have RRMS, late diagnosis at 55, after 20 years of misdiagnosis. I’m on Tecfidera. I am experiencing more and disabling issues. I have to use walking sticks and by the end of the day, a mobility scooter. I have extreme pain in both feet, some evening spasms and string elect...

<p>I was diagnosed many years ago and the last 15 years have been really difficult. I continue and I do my share of complaining. But it does help having a place to go with questions. Thank you fellow warriors for your struggles are felt. Stay inside and keep hydrated.</p>

Hi I just wanted to say hello 👋

Hi I just wanted to say hello 👋

Hi I just wanted to say hello 👋

Hi I just wanted to say hello 👋