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Years ago I needed to change my life completely. Why? That was not my choice but my health conditions. I was diagnosed with MS and it felt heavy to carry with me. I was afraid to dream about the future or even live a day with love, care, and understanding to myself. I felt guilty when I wanted to ...

I literally have no idea how to edit a post on here. Do you guys know how to access this or are you unable to do so here? I can’t stand spelling mistakes and my careless poor grammar at times. All the best! Regards, Jay.

Well I'm back to see if anyone knows anything. I've had problems with movement disorder since 2018. - while it's being worse the past few days alongside my spasticity. The thing that confused me is it's like I've got this new tic disorder or maybe it's just worse i dont know. Basically in the pas...

Hey pals, here is a video of me talking about my MS pain, and they have animated me!!! Please watch and share as you feel appropriate :) Happy Festive Times xxx https://youtu.be/DD6DCgB1SsY

So I’ve had my appointment with my Neurologist over the phone I’m going to start Beta interferon injections to start. I have a appointment for blood tests and to be shown how to inject myself . Hopefully things will move forward Well. It’s been a really hard few months as my brother was taken into ...

Hi! I<code>m not usually the one to write and ask, but there come moments like this when it</code>s just a natural action. So to the point...I understand your questions, life challenges, your ups, and down days. I`m an MS mom and have the disease for 17 years now. So the first time I met MS as a dia...

Hi all hope all well. I was just wondering if anyone knows anything about back support btace/vest to help, with back pain and posture 👍

I signed a contract for conducting clinical trials of the drug. My relatives did not approve of my decision and each time they scared me with scary stories and the fact that I would be an experimental mouse🤷. In Ukraine, MS treatment is very expensive, and I think that for me this is a chance to ge...

Hello to everyone, I have just joined you. I was initially diagnosed in 2009 with ADEM &amp; thought it was benign MS. I have had ongoing symptoms over recent years which led to a recent MRI showing multiple lesions. The Consultant has diagnosed MS and referred me to Queens Square in London. I ...