Looking for
something specific?

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Anyone else? Experiences?

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!

What do you do when symptoms like dizziness flare up? how to fight it? And what should I do?

I want to hear everyone's little frustrations that come with life with MS. Laughter is the best medicine so I thought this would be therapeutic 😂 I'll start in the comments, add yours below! 👇

We’ve just launched Shift.ms polls! Take part in the first poll below👇 *Bonus points if you can leave a comment and let me know: are you happy with how long it took?