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My name is SCHULZ ALICE and i am 46 years old . I was born on 19/01/1974 in Carinthia (Klagenfurt)Austria . I grew up there till the age of 20 when i started having Vision problems,Fatigue and weakness,Bladder and bowel dysfunction,Sexual dysfunction,Cognitive problems. Since i was still young i nev...

Hi all Does anyone have additional illnesses like fibromyalgia? I have a lovely combination of illnesses and other conditions. I have had fibro and cfs since 2008/9. Has anyone managed to find the happy medium between rrms and fibro?

I was diagnosed with RRMS mid May 2020 at the age of 28. All rather shocking because the only symptom I've experienced is optic neuritis. It has been said that I need to start on Tecfidera next week. I'm feeling pretty anxious about this. More so because all my neurologist seems to say is 'No-one ha...

Hi i am new to this site i am 53 and was diagnosed with RR ms when i was 19 only got told about this site recently nice to find people in the same situation and now what its like hope everyone is fine and safe at this unsure time. I am at the moment ok just sat waiting like some of you to start new ...

Hello everyone, as the title suggests I'm new here. Although, I've been lurking for some time. I got diagnosed with MS last week after a lot of barking up the wrong tree. I'm a Police Officer and in 2016 I decided to apply to transfer to firearms. The fitness test is a bit harder for this but didn't...

Hello everyone, hope you are all well.......... It looks like I am/ have been starting to relapse. For a few weeks now my legs are heavy and numb and I am waking up in the morning needing almost 30 minutes to get my legs moving before I can get out of bed. My vision is going hazy throughout the day...

Good short post and a film featuring several Shift.ms ers. https://multiple-sclerosis-research.org/2020/06/the-human-side-of-ms-and-research-a-short-film/ @longboat

gf.me/u/x7wuvv I have Ms / nmo and it is very severe with repeated attacks of optic neuritis and leg weakness At this point I am desperate to try anything Please can people donate Thank you

Hi All; I am new to the forum and i will be honest in that i have a problem speaking to my GPs due to neglect in the past which lost me my first born.. I have strong symptoms of MS and dared to mention it to 2 diferent GPs but was fobbed of,especially when i mentioned the heat intollerance; all i go...

Hi; only just joined and hope i am doing this right folks..I am undiagnosed. I have mentioned twice to GPs that i am sure i have MS but they brushed it off saying such as,MS sufferers dont have problems with heat like i do so i want s to see a private Neurologist but i still need a referral letter o...