Primary MS
I have been getting tested for a couple of years with my neurologist stating I did not have Ms. This last round of MRI’s I have a new lesion 6-7mm in the back of my head. Radiologist states from my last mri to this one I have had change and he states it is in line with primary Ms. I spoke to the nurse who stated Dr. said no more testing is needed that the next appointment we will go over treatment plan. Any suggestions on what kind of research on treatments before hand and what kind of questions to ask?
Sorry, this all sucks, but try to find to keep your mind off it.
Not sure on what to ask as i asked nothing just went with what they told me. I have ppms also and was told ocrevus if insurance would cover it as it’s expensive and insurance doesn’t like to pay for it. I’ve been on it since Aug of last year had my first 2 half doses and first full dose back in feb. Has been alright for me tho no side effects and last mri showed nothing new since starting. Was some new from my dead zone space between first mri in beginning of may last year till Aug when started treatment.