Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
i am so sorry for all you are going through and all the confusion with doctors. i know how awful it is and how difficult they can make it when you are in that space before your diagnosis. i spent so much time there - even now, after my diagnosis, my neuro likes to do a lot of testing.
i don't have much technical knowledge, at least not enough together at once to share - my brain is not very clear at the moment. what i want to do right now is say hi, and share a hug with you. to let you know you are not alone.
i have thought of changing neuros, but i've done that - maybe 4 times in 15 yrs and i don't want to change again. i felt we were getting somewhere and the continuity seems important to me; i think it should be to the doctor as well.
it helps me so much to have others who understand, even if it's only that i am frustrated some times.