So having to do a mandatory reconsideration for my pip but I requested my PA4 form that has just come today and basically the reason I cant do things is because I'm overweight not because I have ms. This has really upset me because I have to get my head round this life long illness that as changed m...

Had rrms for 25 years now diagnosed with spms. Due to start mayzent/siponimod after being on Tysabri for 20 years. Anyone gone through something similar? And what’s been your experience?

This summer was supposed to be sunshine, fresh air, and making memories. Instead, I spent most of it fighting my own body, pain, inflammation, spasticity, fatigue, and one thing after another. And now, as we head into fall, I’m still not feeling 100%. I have another MRI coming up, and I’m waiting t...

I couldn't go when I was relapsing but I've started again and forgot how it cheers me up. Not only because gym does that but because I'm well enough to actually go Yayyyy :))))

My Doctor has talked about potentially moving to an infusion treatment. Is anyone willing to share any side affects they have experienced after infusion? Heard 2 weeks of flu like symptoms, head exhaustion...wondering what others have felt.

Hello everyone, I take Fingya, an immunosuppressant medication; I take one pill daily. Because of this, I really can't handle the cold—I get sick very easily. What do you do to support your immune system? Besides eating winter fruits rich in Vitamin C, I also drink turmeric mixed into hot water. I...

♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️ I am writing to you as a fellow community member from North Africa (Libya). Since I am not fully fluent in English, I often find myself having to constantly copy posts, search on Google Chrome, and switch back and forth just to translate content. It has become quite tire...

Hi everyone, how are you all doing? I was diagnosed with MS in 2024, when I was 22, and I’m 25 now. As I mentioned in the title, I’ve been feeling really lonely since my diagnosis. I know MS is considered a relatively common disease, but I don’t know anyone my age who has it. Sometimes it feels li...

Is just me? https://suno.com/s/0gLvhDcb7ZsSK4y7

Hi all, I was diagnosed 2001 RRMS tried Avonex for 3 years but could cope with the injections, no further contact with Neurologist and decided just to live life taking LDN. Now back in the system and am SPMS. I use an active manual wheelchair but can't blame the ms entirely for that - I have drop ...