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Hello you lovely lot. I was diagnosed with RRMS on July 24 over the phone and have my first phone appointment with my MS nurse next week. I’m not a huge fan of phone appointments - would be so much nicer to meet face to face - but covid means it’s all by phone. Anyway I want to make sure I make the ...

Does anyone have any experience applying for the Access to Work Grant? If so, I have a few questions I was wondering if anyone if the wiser on; -Do I need to have a registered business and if so for how long? -Whats the minimum I can earn per week? (it says "up to" £160/week but I don't know if the...

Hi everyone, I keep getting stomach pains, pressure down below. Sure it is uti. I keep on getting these. I must admit, I don't drink water really. Are people with ms more acceptable to uti ? Does anyone else get this ? Thanks.

Hi all, I'm a 52 year old male just diagnosed with Primary Progressive MS. It's mostly affecting my left leg so far, with foot drop, altered gait and weakness. I can no longer stand up from a squat on that leg, which is scary for a guy who's been healthy, strong and physically active his whole life....

I would like to ask can doctor(s) be sure in the beginning that I have PPMS 100 %? I was taken basic magnetic photos and likvor sample. I had lots of inflammations (lesions) in spine and brain for years according to doctor. By those I was given PPMS sentence. Can it really be true?

Hi all, I am new to this site. I am currently in limbo. I do not have a diagnosis, although the neurologist felt it probably is MS. Limbo is difficult because I do not fit in with any group. One minute I am up, and then I am down. This is uncertainty. I guess a lot of people out there have experienc...

Hope everyone is doing well! Tough time but we've made it this far. I have been furloghed sinced the end of March, my job isn't technically allowed to be open until the 1st of October. It would seem there's a high chance they won't open until next year. This would mean I will have to find a new j...

My legs have completely given up on me, they are unbelievably solid, like Stonehenge. I am currently on no medication, trying to see if this is a relapse or something. This has lasted 2-3 weeks already and seems to be gradually getting worse. Does anyone have any ideas on what I could be doing to im...

Hi Everyone - I am newly diagnosed. I go in next week for my prescription. I am curious...is this it? My memory and brain are not functioning very well...is it just always going to be like this? I don’t think working anymore will be an option for me if I am unable to improve. My physical abilities h...

I have been feeling so crappy. I am diagnosed with RRMS since 1998 at age of 28. No real problems until 2017! When I had a flare up main symptom dizzy and fatigue - severe. I recovered nearly complete, went on my first dmt copaxone. Annual mris were fine, a couple of small lesions even disappeare...