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Hello, looking for some words of wisdom, am fairly recently diagnosed (March this year) luckily symptoms have been fairly manageable so far. However Thursday morning I woke up without much sight in my right eye, trip to eye casualty later and diagnosis of optic neuritis. They’ve said it will heal it...

I’m a teacher but because of my new MS diagnosis I’m leaving at least for the next few years to figure out my health. Where I’m at now physically I don’t know if I can do an in person job. Online teaching, too, is still very taxing mentally, and I don’t feel I could be up to par for that. Are ther...

I've just resived my first prescription on medical cannabis. I'm nervous because I have had bad experiences with it in the past. I almost looking my partner last year. When my dad passed I smoked it all the time to escape (before MS diagnosis) so I pushed everyone away. I know it is going to be pos...

When I was diagnosed with MS the only option I was given for DMT was Tecfidera, my last MRI was stable but I only had an MRI on brain & neck & not spine in the last 6 months I’ve starting to have back pain & weakness & my walking has got worse, I’m just wondering why I wasn’t given any options?

Hi, I’ve been reading a few posts today as having what I call ‘one of my bad days!!’and I’ve noticed a few of you mention an annual MRI. I’ve been diagnosed 5years now and not had an mri for at least 4yrs. I have quite a few liaisons and get varied pains throughout my body as well as issues with my ...

Hey everyone (sorry long post) Looking for advice, opinion or just really something. I completed mavenclad treatment in 2023 and have been having regular monitoring - all ok. I recently had mri and results have shown a new lesion - this was obviously a kick in the butt but after meeting with my c...