UC has an MS dedicated specialty clinic in your city!
https://www.uchealth.com/en/neuroscience-instit...

The choice is yours. Some neuros accept that and others don’t. I tried copaxone and another, can’t remember it now...anyway neither of them worked and side affects were awful so I quit. I’m also a bit of a rebel, I went out of country for CCSVI treatment. I was a lucky one because it helped me and eased some symptoms. The neuros generally don’t like that, I am in Canada and I believe my care has reduced because of my choices. But I figure it’s all personal choice and I have a right to it. So good on you, research lots and make your own decisions.

My neurologist is Dr. Lawrence P. Goldstick with UC Health. He was my mom's neuro and when I was dxd with RRMS in 2001, he became my neuro. He's based in Cincinnati but I see him at St. Elizabeth in Dayton, Ohio. Neuros are just different but I like Dr. Goldstick because while he strongly encourages me to be on an MS med, he respects my decision to go DMD free and would never fire me as a patient like some of my other friends have had happen with their doctors.

Thank you Joani for you reply.

I actually want to change Dr Zabeti for another one.
No questions, he is a great ms specialist, but his bedside manners are very bad.

UC Neuroscience/Wadell Center for MS-I’ve been with Dr. Zabeti for almost 4 yrs. This group has saved my MS life. Check out the info below online, they have a list of MS Specialists.

(Phone number can only be seen by the question and answer creators)

https://www.uchealth.com/en/neuroscience-instit...

I can help answer any questions!