New to MS
Hi everyone. I'm 33 years old and not so long ago I been diagnosed with RRMS. It took me a while to accept it and figured out what's happening with me. Still very new to it, trying to get as much information as possible. Thanks to everyone for sharing their stories, it's really helps.
Hi 👋 I was diagnosed this year too, by phone. It’s been really helpful having this site to look at! About to have my first meeting with my MS nurse - over the phone - and I’m weirdly nervous about it. I see you’re on Tecfidera, how are finding it?
Hi Sammy33, I have not been diagnosed (mostly due to Covid) I expect one in the next couple of months. Really scary to have a diagnosis during current climate. The MS NHS team have been supportive. I am missing community support. This site has helped me reach out to people who understand the comings and goings of MSness. Welcome 👍