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Hi everyone am new to this am 20 year old and just be diagnosed with RRMS on the 12 January 2026. I can’t get my head round how I have ms and I feel like locking myself away in a dark room because I feel like a burden to my family. Any advice

Good morning, I was diagnosed last week after experiencing my first symptoms (slurring my words and off balance) which landed me a 7 day hospital stay. I am home now and feeling more like myself. I haven’t been able to schedule a follow up with the hospital neurologist (they have no appointments av...

Hello, I’d love to hear from fellow gym bunnies and how you modify your workout and how many times a week you train? I’m 53 newly diagnosed RRMS and have lost so much of my hard earned muscle and want to get it back and drop some body fat. TIA

Any help secondary progression MS Gave up work as couldn’t cope. Going to see if I can claim from SS next week. Any advice appreciated. Thanks

I just got diagnosed with MS from visiting the ER where I live on March 24th they did two MRIs on me the first one was without contrast where they found white matter on my brain and did a second MRI with contrast where they found the lesions in my brain and cervical spine. I just got an appointment ...

I was looking for a new friend on here. I was diagnosed with rrms last week.

Hey everybody 👋 i was recently diagnosed with MS in February this year. I'm due to start Kesimpta as my medication in the next couple of weeks. I'm just curious - how was everybody diagnosed? Has anyone ever been diagnosed without a lumbar puncture? I was diagnosed based off of MRI & CT scans along...

I recently started losing vision in my left eye and it led to my MS diagnosis. My doctor wanted me on Briumvi but the lovely American Healthcare system says I have to try the cheaper option kesimpta first. Hoping it works anyways, has anyone had experience where their insurance forced them to try so...

So after 17 years yesterday I found out I have ms although it’s still classed and probable only because I’m waiting for some bloods to come back. Also because I went private I have to be referred to the neuro inflammatory team through the nhs for them to tell me what type of ms and what treatment I’...