The sun and therefore the heat is out here in the UK. I have never been able to stand the heat but since being diagnosed I’ve noticed that it makes my symptoms worse. This will be my first summer after diagnosis and I wondered if anyone could share some tips on how you manage MS and the heat?…

Looking for advice, I was diagnosed with MS in 2012 in high school. I have been managing well and have been taking the Copaxone for years and have been great with it. I had a period of time I was not taking anything because of insurance problems. I love the sport of volleyball have been playing it …

Hi everyone, hope you are all managing today! I have been getting symptoms since december: vertigo with nausea, bladder/bowel incontinence, the hug feeling in my torso, muscle spasms on my right side, cold spots on my face, tingling that has turned into numbness on my feet, left leg and torso, and …

Hi all, I was diagnosed with rrms 16 years ago. My family and I have had an horrendous 18 month…the stress has been unbelievable! My husband and I also lost our beloved dog (our baby😊😢) in November. I am on my 3rd relapse in 7 months (the most I have had in such a short amount of time)…

I have had a tough few months after my lemtrada round 1, caught a cold in January which became a chest infection so was off work for 4 weeks. I then went back and had been fighting work to allow me to drop my Saturday shift as I am really struggling with it. Occupational health that in the long ter…

I’m on holiday in the Tropics, for the first time in 3 years, and in the past I’ve coped pretty well although I do have heat sensitivity . I’ve lived in this kind of region as well in a couple of places. But for the first time ever (and believe me I do not sun bathe – I go to the beach…