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Hello! I am wondering if any else has experience around this. Quick summary, I was diagnosed last year and only started treatment this week (the nhs lost my records 🙁so it was delayed). Before starting Kesimpta I asked about any vaccines I should get and was told nothing live, but I didn’t need any...

Well I think that this has been the shortest time frame I have ever been on ANY! type of medication. I was diagnosed in March of this year with heart palpitations due to the medication. I gave it fair shot and I just can not deal with the anxiety attacks feeling, the off beat of my heart once in aw...

I'm scheduled to establish with a neurologist in early July, however, right now my feet feel like their always waking up from being asleep. Kinda like ever so light fluttering that feels like they are moving when laying or sitting. Anyone else experience this? What helps?

Hello everyone my name is Doug, Life has been a bit of a whirlwind after being diagnosed with MS, Somedays are good others Seem more tedious, I’m usually a very positive person. I’ll never forget how quickly my diagnosis came out of no where but there were signs for me.. Getting Bell’s palsy and se...

Does normal food worsen MS symptoms? And do you experience so much water consumption?

Hi guys, still relatively new here and to MS. Was just curious how long people experience ‘flare ups’ for? I suffer with dizziness and weakness in my legs more than anything and it’s currently been 6 weeks since these flared up again 🫤

Did anyone experience neck pain that u can't even turn it? And what did u do

Anybody experience vision loss at any point because of MS? I’ve been partially blind in my left eye since last year. I experienced optic neuritis late July 24’, did 5 days in the hospital on high dose steroids. Vision went from blurry to dim to dark. The iv steroid did little affect leaving my vi...