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I have posted on here before about my son diagnosed with RRMS in 2014. He had lots of relapsing but no remitting. A couple of years ago it progressed to SPMS. Over the last year he got rapidly worse, couldn’t walk outside, furniture surfed around his house, regularly needed help to feed himself, fel...

Before I got diagnosed, I convinced myself they’d never find out what’s wrong with me - I’d drink to feel ‘normal’ when it was alcohol was actually making my mobility a lot worse. So on July 5th of this year i decided to go completely sober (making it 140 days 🎉)!! but sometimes I struggle knowing...

All MS patients are entitled to a disabled bus pass that gives them free bus travel Current symptoms and benefits are not considered, you just need to send a letter from your consultant that confirms your diagnosis and 2 passport pics. This do not apply to Scotland and all you need to do is cont...

Laying here with an electric heating pad and a hot water bottle. I always figured I could handle the cold growing up with lovely Canadian winters not so much anymore!!! Wondering if the cold intolerance is caused by the weather or these pesky brain lesions! Anyone else deal with a deep bone chill?

Keep waking up with what feels like cramp in my feet, and they are always freezing cold, even when I'm hot, is it normal ms stuff or should I see gp? don't like to bother them.

Is anyone a relapsing remitter and DMD free? I've been having large and itchy site reactions with Copaxone, which last for weeks. I look like a battered woman when going to the swimming pool as I have all of these purple marks on my legs where the reaction hasn't fully gone...High dose antihistami...

Just wondering if anybody else has changed mentally also, I suffer badly with anxiety now and cannot bare loud noises, traffic, shouting even laughing! I love staying indoors now and living like a queen. Total opposite from what I used to be x

Any tips or tricks? Is it just cow dairy I need to cut out?!