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Hi everyone, I am abit frustrated.. I can not find what l am looking for in any MS related sites. Do i have to have a relapse to get steroid injection in other words can i have steroids to dampen down the symptoms I have been experiencing? Thanks

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...

Hi I’m so sorry if this is inappropriate but I’m just upset and don’t have anyone I feel will understand to talk to. I have just come off a telephone consultation with my (very nice) GP. I had an MRI as I have been having symptoms that my GP agreed sound like MS for ages - even years. I’m 36yrs old....

Hi everyone! I'm just coming back to check in as I realise I've not been around for a while. I had NEDA (No Evidence of Disease Activity) on my last MRI and have been feeling fine since then *touch wood* I became friends with an amazing woman who also has MS and hosts a podcast about living with a...

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.

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...

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...

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...

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...

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 ...