Haven't taken nothing but my vitamin D and my otherTrospium. I rather not take the chemo if I don't have to.

Does anyone take anything for Nystagmus? Is there anything you find works?

Would you share your vitimins, dose and brands please?

This is so new to me. I was diagnosed in April 2026 after having optic neuritis. It was very scary and I thought the headache prior was just due to stressors of life. I am scheduled to start Ocrevus in the summer. I’m trying to keep a positive attitude, I exercise five days a week and walked 1-3 mil...

Wondering how long before people see improvement after there steroids? I am nearly two week after my 5 day treatment and not really seeing much of an improvement. This normal? 😩

Hi everybody! I’m Lileas and I was diagnosed with RRMS last Nov. after a few trial and errors I’m finally settled into Kesimpta and did my first does this month. Just wanted to say hey :)

What is cause of my toes curling on affected side. The curling is starting to affect my walking and at times painful. Curling isn’t constant maybe with a flare?🤷🏽‍♀️

​Had my 1st neuro-physio appointment last week to help with my MS foot drop. I was told off for wearing sliders and Crocs (I neglected to ask, 'What should I wear then?'). I think I’m going to listen to her advice now... I tripped this morning while wearing my Crocs. FFS! What do you guys wear?