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I was diagnosed about 9 months ago. I recently started coming to terms with my diagnosis, though most times i try to ignore it, it somehow stick its head in my business.

Hello, Today I received my first appointment with the neurologist in finding out what has been going on for me recently. I had no expectation of when I would receive this, and fully expected to be waiting a while before I would hear anything. However, now that I know the date, I feel incredibly an...

Hi all, I’m in need of a bit of a rant and to hear any tips/advice you might have. I’ve only been diagnosed for 6 months and recently as I have told more of the people close to me about my experiences and symptoms I’m getting A LOT of people saying ‘oh yeah, I get that too’ and I’m finding it extr...

Anyone else have balance issues in the heat or walking too much as their primary symptom from MS? What is some advice to help with this?

Hello my fellow MSers, I thought it would be useful to do a MS patient pack. You know my experience has been the NHS leaving me to die and then bully me. No one bullies me & Londrina! So check this out- Listen you are disabled, you have MS and depression lives with us please deny it BUT you are ...

My first infusion is this Friday!

MS did not make you strong. The fact that you decided not to commit suicide with the highest suicide rate & depresion out of all disabilities and chronic illnesses shows you are strong. But it's not even about strength, make life count if you did not already before being diagnosed. Don't justify pai...

Hello! My first post 😁 Ive had MS officially 3 years, and unofficially 5 years. Because of this, I have had lots of weird symptoms. And I think its important to always see the silver lining regardless of how small. So with that said! Have you ever had a symptom where maybe in the moment was frust...