I think that you’re lucky to have found one. They are a rare breed, and I only knew of two and now three with the one you found. The movement disorder neurologist that I go to is Dr Kevin Klos. He has his own practice and is not affiliated with any hospital or medical facility. I’ve been going to him for probably 12 years with my initial visit being to treat Tourette’s syndrome what I’ve had since a child. I was able to get in to see him and after I did people in my support group can’t believe that I actually got an appointment with him. I think it’s that way with all movement disorder neurologists. I’m very satisfied with him. He also does research.
Congratulations on finding a MD neurologist. I hope your appointment is not too far out.

Thanks John 🙂 I was guessing that was who you were seeing and I read good reviews about him. I checked with his office and they told me he was accepting new patients but they did not accept any type of insurance . A cash only office. Being on Social Security as my only source of income, that became a nonstarter for me 🤔😖. I will be seeing my new neurologist middle of November and maybe I will learn more about my stage and form of Parkinsonism then. God Bless and let’s keep in touch or maybe even meet for lunch sometime!

But. I take it 3x per day .

Hi Mark.! I rskr Amantadine witch I find works well for me. My Dr had also prescribed gocovri but I h a d to ask for an alternative. Ins. Problem .