Worried
I have PPMS and it is progressing so quickly. I’m terrified of losing the small amount if mobility I have left. Has anyone else out there had a similar experience and any advice on how to keep on top of this. It’s overwhelming for me and my family.
Obviously not knowing your circumstances may mean the following is inappropriate. Have you spoken to your neurologist about Ocrelizumab, as it has a license for PPMS? Just a thought.
I had an MRI scan yesterday to see if I am eligible to start the treatment.