Dr. Kay is extremely knowledgable on optical Myasthenia Gravis. I highly recommend that anyone with this condition, go to see him. He spends alot of time with his patients so you may have to wait awhile. Well worth it.
I went to him to be evaluated for optic neuritis. He did some basic tests and told me I did not have it. I explained to him that my vision had deteriorated significantly in a couple weeks time and I was being evaluated for MS. He still said I did not have optic neuritis. I asked for an MRI of my optic nerves and he said it was not necessary. Well, guess, what?--The same week my visual evoked potential test from my neurologist came back saying that I did indeed have optic neuritis. A second neurologist diagnosed it too - by the palor in my eyes. By then it was too late for the IV steroids I had needed and now years later my vision never came back in one eye. I called him to tell him and his response was to brag about how he is the foremost neuro-opthalmologist in the county and how great he is. ... What a joke? Advice to others: RUN, DON'T WALK. Oh one other thing, his office billed me for tests they did not run. However, at least they admitted it and reversed the charge when I told them.
They gave me sufficient information to make a decision about my treatment plan. I wasn't worried about their equipment. It was safe and well taken care of. Their office was one of the quietest, most peaceful places I've ever visited. I was able to relax very easily. I will definitely recommend them to people I know. They were by far one of the best I've ever seen in their field. It was obvious that they've been exceeding their clients' expectations for many years.