Looking for
something specific?

Are you looking for a reliable source of information regarding your MS, treatments, new products on the horizon, newly diagnosed and don't know what to ask, anything to do with MS then please check out Multiple Sclerosis News Today. It is an American publication: https://multiplesclerosisnewstoday....

Needing advice on jobs for people with MS, I've worked in an office since pretty much being diagnosed but I've had some time off this year and now I don't know what to do...

I'm on a really exciting healing journey and I've done really well over the past four months, but I need to find a new counsellor/therapist to look into the potential causes of my MS. I know there are people out there that specialize in this but I don't know how to find them, anyone found someone r...

Hello. I was diagnosed with PPMS two and a half years ago.i had my annual (a year and a half) appointment with my consultant last week. He thinks I have a rotated facet joint in my lower back and that is contributing to mobility problems. He says the part concerned is not somewhere MS attacks. I'm g...

🚨New series klaxon 🚨 We've just launched 'Out of the blue' over on our Stories tab. Four MSers tell us how they got through an MS diagnosis that struck seemingly from nowhere. First up, we have Jen, a Canadian MSer who was completely taken by surprise by her diagnosis. Head to the Stories tab o...

Would getting my knee replacement help with pain that comes with trying to walk ???

I know its bad in the beginning but would like some more anecdotal experiences of colds and infections when on this long term - both good and bad experiences. Thanks

Hey MS family I'm still hospitalised with this relapse, I've had 5 days if methyl-pred IV. I'm still getting myoclonic jerks that are in my legs, hands, torso and head. Triggered my movement or intention movement. I've been prescribed Keppra and whilst they're less violent they're still pretty co...

This will be my 2nd relapse in 4 months and I didn’t expect another for a while as from as far as I know it’s on average twice a year but I had optic neuritis in July and I believe I also had one in March which caused unbelievably bad vertigo. Woke up this morning to my left leg unable to feel any t...

Hello friends I'm to use a new diet about ms I not drink milk not cheese and yogurt try make exercise and be happy not be stress enjoy life I eat everyday nuts I'm to eat corn bread I have stop a wheat bread I drink everyday quail eggs 5 eggs with stomach empty for 30 minutes not eat nothing ....I e...