Hi everyone! So my last neurology visit, my Dr. tells me he is concerned that there may be a misdiagnosis, and or just want to be sure I am on the right track of my treatment plan so he ordered me to get this (Multiple Sclerosis Disease Activity Test) which I go in and get bloodwork done. I was hol...

Once a year I’m summoned to Neurology so a highly qualified person can check whether my central nervous system is still legally allowed on public roads. The appointment letter alone is terrifying. NEUROLOGY DEPARTMENT Nothing cheerful has ever followed those words. You never see: NEUROLOGY DEPA...

So I was diagnosed earlier this year with MS. It started off with my entire left side of my body being numb and felt like it was bruised all over weird combination I know. Since then I have already started my DMT. I took my maven clad since then I’ve had an extra MRI, which showed no new flareups, ...

I went to London last week from Seville! When I came out of the airport, I looked For an accessible cab for my scooter! They said yes, but it didn’t have any ramp, so they had to csrry me between four people to get me inside the car and they charged me £120 £. I thought then that it was a question...

Hi, does anyone know of any support groups for people with MS in the Derwentside area of the North East of England. Or, if not, is there anyone who’d be interested in meeting up as a group to a catch up from time to time.x

I was on Kesimpta for about 9 months. It wasn’t working so my doctor switched me to Mavenclad a month ago. I am not sure if the things I’m experiencing are related to the medication or just my MS. I had some issues when I stopped the Kesimpta. My body was confused not having it. But now I feel the...

I feel so annoyed I'm feeling weak because this is the month I'm suppose to get my infusion but my doctor wants me to try new medication which he won't tell me(if any 1 has any suggestions on MS medication that worked well for them plz comment the name)about my stupid AC stops working right when I n...

The past week I’ve been having sunburn , sizzling,like pain . Hurts to shower, put clothes on, even just move. I don’t have a sunburn, and this started on my arms, now it’s all over including my scalp. Gabapentin hasn’t done anything. It’s progressively getting worse. I messaged my neuro a few days ...

Hiya Warriors, I was needing some cover up work done and was curious about the pain now that I have MS. Any knowledge throw my way would be appreciated. Peace, Rhonda