Well that's the first week of Mavenclad completed, now got 4 weeks off before the 2nd dose this year. Been unable to sleep most nights, up at 3am every night, had one event one morning, totally unable to move, told my body to do different things, nothing happened, lucky my Wife was at home, at least...

I've been in hospital for 4 days now following two weeks of gradual escalation of symptoms. I ended up completely losing power in both legs, unable to walk a few meters with an aid, double vision and fatigue. An emergency MRI showed no new activity and it's still clinical stable which I'm really h...

Could you please tell me, has anyone ever been diagnosed as having ms by the neurologist the had a clear mri scan ? Or do you know of anyone else . Frustrated that ive been offered no further investigations.

Hi everyone. I hope your day is a good one today 💛. Can I ask, has anyone experienced severe left arm pain and hand pain, its been there a few days now, iv had before but this is very intense, like a sharp squeezing type pain that either burns or it feels extremely cold and is also going down the ...

Hi I've started my kesimpta injections today (about 30 minutes ago) and have been warned that I might feel a bit/a lot awful after the first one. I just wondered if anyone had any tips or advice to help with this potential feeling of rubbish-ness?! Thanks

Went to my first ophthalmology appointment and confirmed that my vision did get worse and that I have optic neuritis in both eyes. One is worse than the other. However, I’m still nervous about driving at night due to the light sensitivity. Does anyone else have this issue? How did you handle it?

Only recently (the past week) I’ve begun experiencing what feels like ‘tiny bugs’ or hair tickling me over my body. It isn’t consistent, it comes and goes. Anyone else experience this?

Hey all. I was recently at my neurologist and she asked whether I would be interested in switching from Copaxone to Ocrevus. I've been on Copaxone since diagnosis and its been working pretty fine for me. I don't really see the need to switch medications. Now I want to hear from yall, is the switch ...

Cast your mind back to that moment when you were sitting opposite your doctor and told “it’s multiple sclerosis”. Three words that are nothing short of life changing. When we speak to MSers about their diagnosis appointment, it’s clear that how those three words are delivered, and the care that im...

Booked tickets to see a band called Pop will eat itself at Southampton, 1865 club at weekend. Was really worried as I cant stand or walk very far,(i use a cane) rocked up at venue and spoke to site and they showed me to the balcony and gave me a stool to sit on and a great view. ( I did reach ...