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Hi all , I have got diagnosed about 2 and a half months ago.. Had 2 MRI scan that showed numerous lesions on my brain and neck,I straight away started a raw vegan diet without tomato that helped me with feeling energetic and positive , I take vitamin D , B12 , folate , fishoil, magnesium Yesterda...

I'm kind of not ready to tell this part because it's not easy. Perhaps I will find a way. Thank you!

What do you compare it too, and where does it hurt.

New to this community. just looking for some guidance into what lifestyles people have with their MS symptoms. also just reaching out to hear people stories and experiences and how it might relate to my own experiences. I’ve come to the realization that I need to reach out to others that are going t...

Hi, I just wanted to make an introduction post. My names Allina, I was diagnosed with rrms at the end of September in 2022, right before I turned 18. I've been on treatment for roughly a year now, trying to slow the fast progression I was having. I'm a mother of two beautiful babies, a nursing stude...

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...