Just a question that's been on my mind 🤔 How do those of you with MS who live in hot countries manage your day to day life? Does the heat make your symptoms worse or have you found ways to adapt? Love to hear your experiences, routines and any tips that help you cope.

My husband has MS and is really struggling with the heat. Says he feels like he’s going to be sick and can’t feel his hands properly. Does anyone else experience these symptoms? And does anyone have any advice for dealing with the heat?

Just curious, how old are y'all when you were first diagnosed???

Hey i think i have ms i been getting theses symptoms for a long time they come and go blurry vison eye pain qas the first symptom i hsd numbness in my hands pain in my legs when i walk.sometimes also hand snd legs feel very weak sometimes also fatigue wow to eve. Get put of bed is effort or do anyt...

Does anyone suffer from a high heart rate while in enclosed areas with heat and no ventilation? My heart rate usually goes up could reach up to 130/140 on my watch I feel nauseous and as if I will faint Is that only me or a common MS thing?

Hi, everyone. I hope you are doing well. Has anyone tried Clemastine/tavigyl for remyelination? What were the outcomes and for how long

I been apart of a couple MS pages and events and I can’t seem to know anyone around near by… sometimes it’s just annoying when others don’t understand what you feel or go through .. I’m just blah 😑

im sitting with two fans and a ac unit lolol im still hot. lolol i used to love this weather. i have a ice blanket in the freezer lololol

Hi all! After 6 years, I’ve finally found a consultant who will prescribe Fampridine for me! I live Liverpool, UK where it is not available on the nhs so I’m paying privately! Don’t get me started on the postcode lottery of this!!!! Anyway, thankfully, other than the initial consultation fee I am ge...