RRMS diagnosis

Hi everyone, my name is Emma. After having symptoms of what I now know to be MS since Nov 2019, last week I was diagnosed with RRMS.

I met my MS nurse today, and I’m now waiting to hear (hopefully next week) which DMT I will be offered.

Hi Emma, hope you are OK. If and when you have symptoms it is worth noting what & when so that when you chat to medical professionals you will have memory joggers or useful details.
Good luck

Hope you are doing well. At least now you have a plan, and I promise you, MS is not a death sentence. There are DMTs to help you. MS does not define you.