After MS Taking so much away from me (Job, independence, being able to ride motorcycles, aspects of relationships etc) I often think about what I am grateful for. Being late onset (diagnosed at age 57) I have been lucky enough to be able to see my sons grow into men. I have not been paralysed from ...

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

Does anyone take choline supplements and does it help with your MS

Hey peeps, I've noticed that my symptoms increase/worsen when there are rapid or drastic changes in the atmospheric pressure. When the pressure starts rising rapidly or gets above 1025mb I feel awful. Start experiencing worse vertigo and headache. Does anyone else check the pressure and notices ...

I’m not sure if uncaring is the title I really want for this rant/observation but I started thinking of the years since my diagnosis (2002) my family members even my grown children I don’t think any one of them has really been curious enough to read about my symptoms the things I deal with daily and...

I'm so fatigued that I have to go back to bed!! This morning I woke up, said my morning prayers and then decided I'm going to go out before the heatwave hits hard at 12pm. I'm still here fatigued knackered like a cream cracker in the sahara🤣 I have to laugh ad I have no energy to cry!! I have an ...

I feel like the way my legs are having spasticity, making it difficult to walk will never go away. No matter how much I exercises. Will I always be fighting the spasticity or is it something I can get rid of? I take baclofen already. I'm sick of being at 6 - 6.5 on the disability scale and been ther...