Treatment options
Hello everyone I’ve posted in here once before but I’m 23M with et (I think) I was diagnosed at 20 by my neurologist and all she did was have me press my hand against her hand and said yep you have ET I did also get an ct scan and nothing popped up. She has me on a yearly appointment basis now and when I just went in there a month ago I told her I was struggling with the 10mg propranolol so she upped it to 20 mg with no difference. I’ve asked about primidone I think was the name and she came across as adamant that it wouldn’t be any better for me
I guess I’ll get to the point, do you guys think I should maybe try to find a different neuro or is a movement disorder specialist a better option? I’m not sure if they’re the same profession or not. My career needs a better option to get better treatment.
Thanks in advance for any advice or help on the matter