So 2day I saw my neurologist to talk about using new treatment for my MS but it was extremely annoying. It seemed like he didn't want 2 talk 2 me about trying anything new. FYI: I HAVE BEEN ON MY LAST TREATMENT PLAN FOR 10 YEARS. It felt like he was preoccupied wit other things and he just wanted me...

I have been taking my son to Ju-Jitsu classes since the start of the year. The class is 6 years to 99 years. Since he started the instructor has been asking me to join them on the mat. I have declined every week because of MS. Worrying if I’d be able to do the class, scared I would make a fool of my...

Looking back at your MS story, what’s one thing are you grateful for? Me: I am grateful for my family who supports me daily in the MS struggle. I’ve had MS for more than 20 years. I am also grateful to this community where I learn from my brothers and sisters on how to best deal with this monster (...

I am JC+ after ten years on Tysabri and terrified of getting PML. I’m so stressed with this and a bunch of other things in life happening that I’ve got a flare-up after ten years of smooth sailing. Anyone else JC+? How do you stay calm about the potential of PML? Thank you!

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

I struggle with both short and long term memory loss. I was diagnosed with MS when I was 38 years old and will be turn 50 this year. My memory is getting worse as the years go on. Do you have any tips or tricks to improve memory? Thanks for listening.

Hello my names Abbie, I’ve recently been diagnosed with RRMS. I’ve been tasked with choosing my own DMT but it feels abit overwhelming. Would love to hear some In person advice and experience.

I hope everyone is coping with the heat blast right now. I somewhat coped ok yesterday i did colouring pretty much all day. Ive had more spasms and painful jolts than usual. I tried to have my socks off but that was a no. Does anyone else get twitchy, sensitive, jolty feet? Having socks on helps a b...