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I have read that rrms always eventually becomes spms. Is this so? I have a neuro who says that usually by my age (53 and diagnosed at 29), ms has established the pattern it is going to be. One sounds promising and one not so much. What would clue me in that it’s becoming spms? I have more difficu...

Hi, It’s currently just gone 1am here in the UK after the hottest day this year and I am wrapped up in my duvet and I cannot stop shivering. I’m aware this is a common side effect when using Brabio/Copaxone but was wondering if anyone else has experienced similar and how long does it generally last...

Hi I have RRMS, diagnosed September last year and been on Tec since May this year. Anyway to cut long story short started weight training again after a period of not doing anything, the issue I have is after lifting weights I have had NO arm/muscle ache at all the day after, it is like I have not ...

I literally have no idea how to edit a post on here. Do you guys know how to access this or are you unable to do so here? I can’t stand spelling mistakes and my careless poor grammar at times. All the best! Regards, Jay.

Hey all, Hope everyone is well. Been not doing to bad here the last little while. Excluding today. But the last I don’t know 5 weeks or so now been feeling pretty good. Been getting stuff done outside that hasn’t been able to get done in the last 3 years. So was a lot of work. Also had to move ...

Can you imagine Jesus turning up at a nightclub? ‘I don't care who your dad is pal, you're not getting in with sandals on’."

Hi everyone, especially those with PPMS, I watched a video of Prof G via ms society & im sure one of his slides said progressive ms patients should shield. Is that correct? Colette

Good morning folks, hope everyone is keeping well. I have just come across a support group for carers and thought that there may be some here who could benefit from the group. Copy and paste time 😊 https://www.mobiliseonline.co.uk/our-story About Us There are more than 7 million people in the ...

Hi everyone. Apologies that my question is not MS related but as Psoriasis is also an autoimmune condition I'm hoping someone will have some advice. For the least 5 years, my friend has been struggling to get treatment or even get an appointment at the local NHS Trust because her "condition is not ...

Need to get something off my chest....... so fed up, diagnosed 24th March 2020. Still no communication, phone calls or anything else from any health care professional. I keep reading about asking your ms nurse for advice - think I’m losing it cos I’m still waiting.