Hello people I am a little new at this posting questions. But I thought I’d give it a go. Who better to ask than the ma community. I was diagnosed with ms after having optic neuritis About 8-9 years ago. Since then I have very few symptoms. I do suffer what I Describe as a ice cold feeling/ pai…

Social distancing is vital to stop covid-19 but it seems that no thought was given to people with reduced or limited mobility. Entrances closer to parking have been closed to limit access so I had to go to the only entrance at the other side of the building. No air cons to not spread the virus are …

Hey guys! I hope everyone is enjoying their summer as much as they can. So I always go on a binge search of any documentaries, movies or shows that deal with MS. I would love some recommendations! Only ones I have seen: – Living proof (documentary) – 100 Meters (Netflix movie) so good!

Well I’m back to see if anyone knows anything. I’ve had problems with movement disorder since 2018. – while it’s being worse the past few days alongside my spasticity. The thing that confused me is it’s like I’ve got this new tic disorder or maybe it’s just…

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 …

This heat is unbearable… Truly and utterly roasting my Cock off!