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Hi, just thought I'd share my experience of my 1st half doze from earlier today in order that someone else may get some use from it. 1st half doze completed today in Glasgow. So far, so good. I got out about 330pm. I was given lots of advice by lots of people. Seems to have worked well. Few sweets, ...

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...

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...

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...

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...

Seems like a bit of a weird question but does stormy weather effect your ms? There is currently a storm hitting here (the first since I've been diagnosed with ms) and my head feels like what could only be described as stuffy/heavy? My ears have a constant feel to them as if they are about to pop

I know there is lots here about optic neuritis, but I wanted to ask if anyone has had their vision recovered but been left with discomfort ever since. I had ON a year ago and lost partial vision in the eye but it returned within 2 months. However now a year on I Continue to get intermittent but dail...

Hi All, I am new to this site and wanted to introduce myself. I was unofficially diagnosed with MS whilst living in the US but due to limited understanding and MRI facilities in the UK, not officially diagnosed until 2008. Currently medically retired and enjoying life. I have spent the lockdown peri...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

A few years ago before leaving the country I wanted to create a "breakfast club" in London for people with ms to meet up for a cup of coffee and a chat. Now that I'm back I want to continue from where I left. Covid permitting. Raise your hand if you might be interested!