I had HSCT for Multiple Sclerosis here in the UK. I was discharged from Hospital 11 years ago this Christmas. I have been in remission ever since, despite the MS Society UK telling me among others ‘not to do it, because the treatment was dangerous.’ Their actual words to me were ‘Don’t do it, it’s d...

I was diagnosed last year (August) after years of wondering what was wrong with me. The spasticity and restless leg symptoms are too much at times. Not to mention the weakness in my legs. Is there any advice on how to effectively manage these symptoms?

How is your body feeling as we wind down? Drop a emoji in the comments that matches your current vibe, whether it's 🛋️, 🔋, or 🌧️. No pressure to be okay.

Hi all, I was diagnosed in 2015, hit rock bottom in 2022 and couldn’t walk more than 100m. Ocrevus changed my life and I ran my first 10k yesterday. Any other MS’rs run? Looking for inspiration to do a half marathon and to spread a bit of positivity that if I can do it, anyone can! I’m not fixed bu...

What do you guys do to keep your engery up?

I was diagnose November 2025. At the age of 40. I think I’m still in shock. Sometimes i get the feeling that everything is ms but i also know it can’t be.

Hi everyone, I would really appreciate hearing from anyone in this group who has experience with Fampridine 10 mg, particularly those who have obtained it privately. I have been living with MS for approximately 12 and a half years and currently have an EDSS score of 6.5. Interestingly, although ...

My doctor had me on Wellbutrin 15mg XL for a month and he said it would help with stimulation and energy. He had me increase to 300mg XL and I’ve been having the worst headache