Hi Everyone! Released from hospital only yesterday with the diagnosis of RRMS. MDT panel meet in 2 weeks and will be letting me know my therapy course. Getting myself fully informed of how this is going to affect mine and my families life moving forward. Having a community like this will be really h...
Hi all! I’m new here and very overwhelmed by all the support and love everyone gives each other💙💜
I was diagnosed officially last week after being “suspected” for months, after LP, symptoms and CT indicated MS but the MRI took so long to get done.
The letter I received today post MRI, stated “rapi...
I’m newly diagnosed, about 6 weeks now and my mental health is shot to pieces. I don’t think I have ever felt so depressed as a I do now. And I don’t even know why, when I was told I had MS I didn’t think I was that affected but my current behaviour would say different. I feel angry that friends don...
Hey! I was diagnosed in January of this year with R&R MS. I have recently started Vumerity and wanted to hear from more people if you are on it, the side effects you’re experiencing. I’ve noticed I feel sicky about 1-2 hours after taking my tablets lasting anywhere between 1 hour to 4 hours. I’ve al...
Hello all
I’m new to all this and really looking to connect and make some friends.
I was diagnosed with CIS about a year a go and more recently that was reviewed to a diagnosis of MS following a period of new symptoms. Mainly trigeminal neuralgia and extreme fatigue. However about a week ago I e...