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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...

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

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 ...

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...

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...