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I was diagnosed in 2012/2013 , but have had symptoms for 15 years or so. I'm on Fampyra and Lyrica which seem to help. Magnesium and Lecithin very important too. I am in Germany at the moment where the treatment is amazing compared to Ireland where I am from. Anyone else out there with questions on...

What do we know about MS and menopause? How do symptoms change, Is there an increased risks of getting a relapse? How do the disability level change? Thanks ladies and sorry gents.

Hi! I am hoping to get some feedback. I am dx RRMS. Doing pretty well, on Glatopa (copaxone) about three years. Anyway, I am having serious joint pain in both hands and mainly thumbs. Maybe carpal tunnel but I have much joint pain in other areas like knees and feet. But the hands are the worst. An...

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...

Hey - anyone else feeling generally worse (more exhausted, more painful limbs, worse sleep etc.) during lockdown? All my normal day to day symptoms have kinda ramped it up over the past 12 weeks. Nothing new to make me thinks it’s new activity, just the same stuff but turned up... Love+solidarity ...

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...

I was diagnosed last year, i thought I was lucky with relatively light physical symptoms. Balance, some pain but cognitive problems are really starting again.............. Does anyone have issues of trying to make simple calculations work in your head? I find it difficult at the moment. I'm trying t...

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...

Dear All, Hope you are all safe and remaining healthy in this lock down, I have a very strait forward question. Is there a period of time for a relapse to form or strike in other words, how long does it take for a relapse to occur? Three years later after having my first relapse, I started having...

Hi, I have rrms, diagnosed in 2010, symptoms since 2007. I started copaxone in 2018, had MRI new lesions. So started tecfidera in February this year. I just wondered as i have not been on dmds for 8 years after being diagnosed. Whether the dmds would be less effective going forward, I know t...