I was diagnosed with RRMS on the 12th December ’17.
I’m really struggling today with trying to understand this.
My neurologist said he rarely diagnoses people my age (25) which seems odd because it seems to be the average age for diagnosis…
Most of my lesions are in my neck. Which has made for some very interesting issues over the past 8/9months. (And well many years but with no understanding that something was actually wrong).
How the heck am I supposed to accept this!
– I’m going to be part of the research with futurems, in the hopes that it’ll help others in the future as they learn how the path of progression ms will take in those with it.
Sorry I don’t know what else to do. Im just trying to learn how to accept how my life is changing constantly, my independence is going down.