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Hello all, My names Ryan. First post here. Hope you are all enjoying life as much as possible! I was diagnosed with Relapsing-Remitting this November. At the same time as this I had just started a new job, and moved house, so plenty of stress that has increased symptoms a bit. Now I know I have...

I was diagnosed over the summer of this year and I let the people closest to me know a few weeks later. My family have been a great support practically and my friends treat me the same way as always. But I’m struggling that no one is asking how I am or how I’m getting on with my MS since my diagnos...

So this is my first post….after a sit down with my consultant who said MS was probable and is arranging more MRIs to compare to my last one…..(we have had honest conversations that if it’s MS; which is likely given my symptoms, what that means and I was ok)but I received a letter yesterday confirmin...

Hi all! I just wanted to post to introduce myself! I am currently in the process of figuring out if I have MS. I also wear many hats! I am a wife, mum of an almost 3 yr old, and an occupational therapist! I would love to get insight and recommendations on managing care for a very active little one ...

Hi everyone, I have been suffering with nerve problems for years started with shooting pains in my legs then numbness on one side of face mainly my nose. I then 2 years ago started getting bad headaches and neck ache, mri showed two discs out pushing on my spinal cord. I was going to have surgery as...

Hey all. I have been diagnosed since Dec of 2019. Currently going through a flare up. I'm on aubagio. Switching to mavinclad soon. Any feedback on mavinclad? I have had a hard time physically lately and it's affecting me mentally as well. I don't feel like the strong man I have been. Any advice ...

Hi everyone! My first post on here! I found this website through a random ad or post etc. A little about me.. erm I’m from Nottingham. I was diagnosed with MS in 2004, aged 15. I had a lot of “oh so young!” “You sure it’s ms?” “You’d outgrow it!” “Are you gonna die in your 40s?!” Etc Being young I...

I was first diagnosed with CIS back in June 2021. I had developed optical neuritis in my left eye after receiving my first covid vaccine. Since then no new symptoms had developed and it seemed like that this would just be my life moving forward, until my last MRI. Two new lessons had showed up in my...

I am soo ready to lose all the excess baggage that 2022 and back that these years of not knowing what was wrong with me left me with! Instead of gaining things this year. I’m so ready to lose the bad! Anyone else?

I am soo ready to lose all the excess baggage that 2022 and back that these years of not knowing what was wrong with me left me with! Instead of gaining things this year. I’m so ready to lose the bad! Anyone else?