Hi All,
I have just today recieved MRI results and been told I have MS.
I am beyond terrified and feel sick with worry. I have young kids and an active job as a first responder.
The thing that I am terrified of in this present moment is having PPMS rather then RRMS. My MRI results indicate I have white matter demyelination in multiple areas of my brain.
Wait times for a neurologist are months and months long here at the moment.
Can any indicate whether they a have had similar results and have RRMS rather then PPMS? Or is doesnt work that way?
I am so lost and honestly terrified.