Past two weeks or so my feet feel like they are burning. It gets so much worse when I’m back home after working for 10 hours. This is a new symptom for me and I’ve recently switched to Briumvi from Ocrevus. I was on ocrevus since 2019 and I was very stable, some flaring of old symptoms but never a...

Today my brithday

'MS Hug' be renamed 'MS agonising pain not unlike being crushed to death by an invisible titanaboa'. That is all

Hey! So i was diagnosed this past December and have been trying to not only create a support group in my area but look for support anywhere I can get it. I’ve signed up for forums and reddits. Fb groups and even made an ig dedicated. i’m hoping to meet others who are going through similar situations...

Hello all, I’m very newly diagnosed like last month, I was originally diagnosed with CIS after being admitted to hospital last September on the stroke pathway - it turns out I had inflammation on my spinal cord and brain stem giving me strange symptoms. I’m currently waiting for KESIMPTA to start a...

My Body Has Built a New Fingernail Without Consulting Neurology A few weeks ago, I slammed my hand in the car door. Nail turned black. Then fell off. Absolutely horrific scenes. Looked like my finger had been repossessed. But then something incredible happened... IT GREW BACK. Now here's the ...

Looking for encouragement can’t. Catch a break for anything in the world I can’t talk to nobody without getting a blank stare….. I don’t know if I make sense when I’m talking about anything!!!!! Does anyone have this problem

Hi, I just had my last confirmation to MS with my LP last week! I am scheduled to do my first infusion in mid August and wanted to see how everyone feels about the required shots! Pneumonia and Shingles shots! I might do the pneumonia even though my hubby thinks I should not do it! I am lost in this...

Hi. I've not been diagnosed yet. I had an MRI about 10 days ago. I was wondering if anyone knows how much longer it's likely to be until I get the results. I'm based in Derby, UK. Thanks.

Hey, my MS team have referred me to start Sativex as nothing else has helped ease the spasms or muscle pain. Have you been on this? What’s your thoughts, did it help, did you have any side effects? It’s a new one for me so it would be great to hear your experiences. Thanks so much, Diagnosed 202...