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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 all! I was diagnosed very recently with MS, on Feb. 26th 2020. Feb. 12th, 13th, 14th '20 I had a Methylprednisolone cure for 3 days, which didn't help me out of my relapse. Complaints are getting worse and my neurologist says DMT is not an option right now because of the corona virus. He says "I...

Hi everyone, I have rrms. I have been getting this excruciating shooting pain in the side of my head, it usually only last a few seconds. The pain is so bad, you just have to sit and wait till it passes. The pain isn't on my face. I have had it for years but it would only be a couple of times a ...

Never meet a group of people that are not updated on new discoveries and cures.I posted a message here to help but it was removed because admin claimed i broke house rules..How am i suppose to help other patients in the community when i can not direct them where to get a cure???If you are still with...

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?

come join is on Zoom at 11 am (uk time) where we don't just talk MS /Users/craigwatson/Desktop/Screenshot 2020-06-14 at 09.22.45.png

This may sound so needy 😂 but I was just wondering how people manage without having someone who actually has MS and understands how hard it is living with it. My partner is amazing but other than that there isn't any one else to talk to about it. I think sometimes I find having MS a very lonely exp...

Hi all, hope everyone is doing well. I just have a question...I've had MS for a few years now, rapidly evolving severe, I've had 2 courses of lemtrada but after 1 year of my last course I had new activity so my neurologist put me on copaxone injections. I wasn't eligible for ocrevus as my immune sys...

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...

Does anyone else get this.... I am seeing double but only in my right eye pain under and to the back of my eye. Been of phone with the ms nurse she said it doesn’t sound optic neuritis or classic symptoms of. Please I Just want to know if I’m going mad or not