Looking for
something specific?

So I've been for some nerve conduction tests in my hands and arms because the neurologist was convinced that the numbness and pain is not MS related. I've not had the results of those tests but I've received an appointment for another MRI requested by the neurologist, 2 months after the tests and on...

I was diagnosed in 2012 after a lot of mixed things happening to my body, my pupil exploded my eardrum collapsed, live with bad tinnitus now, pain didn’t let me move for quite some time even tho I worked full time, the dizziness and numbness lack of sleep and over sleeping you all know what am talki...

I'd love to hear about anyone elses experience with these symptoms. I find it reassuring somehow? I hope others feel the same! So here's what's been going on with me, it's a pretty unpleasant experience, fair warning! I woke up after a couple of days of feeling light to medium vertigo and couldn...

Hi! My name is Erin. I was officially diagnosed with MS in August of this year. Though I had my first episode in 2007. (Optic neuritis). I requested the records from the hospital when all this started this year and while the tech who wrote the MRI report in ‘07, notes lesions and demyelination, the ...

Well, after 38 year, four consultant neurologists and three GPs, I'm cured! Yes, I don't have PPMS (or any other kind of MS for that matter). My latest consultant says that my brain is in excellent shape . . . .nothing to see. (But then there never was) My spine is clear of the lesions first seen...

Hey all - hope you’re doing well. I’ll try and make this as short as possible but I wondered if anyone has faced something similar. I have been diagnosed with FND for 5 years but I’ve started having new symptoms. While pregnant, I lost visit in my right eye 3 times (it came back each time, no inve...

I’m so sorry for the long post but the relief I feel that I’ve found this app is unreal!! ❤️ So I’m curious if anybody can give me some advice on ways to exercise my feet and leg to help build its strength. In September I had covid which brought on a relapse resulting in optic neuritis. I was given...

Does anyone else suffer with numbness especially in the feet where it feels like your feet are in blocks of ice? I'm waiting on confirmation of a diagnosis as the doctors are 95% sure it's MS but this numbness has been constant for nearly 2 weeks now. If you suffer with it have you got any tips on e...