I am actually a patient at Hunter Hopkins. They are not in network for my insurance, so I have to pay out of pocket. It is not cheap but I certainly feel like it will be worth it in the long run. I sat and talked with the doctor for longer than I have ever talked with a doctor before. I think the talking (about symptoms, life, etc..) lasted just over three hours. They ran a variety of tests and I left that day with results I had not gotten from countless other (in-network) doctors.
Having said all of that I took the results to my Primary care physician only to listen to her bad mouth Hunter Hopkins practices and question their testing methods. She has requested a copy of the test results and data but I don't expect much from her at this point anyways. I have been seeing my PCP for two years for these symptoms and she keeps insisting that all of these symptoms that started at the same time are unrelated. Of course she spent the first eight months forcing me to be treated for depression despite my insisting that I was not depressed. I am in the process of changing PCPs now.......it is sad that those of us diagnosed with CFS have to see a medical community that for the most part doesn't believe CFS is a real thing. (After two years I can however see how one might become depressed when they can't get treatment or their primary doctor to believe them)
If you have any specific questions about Hunter Hopkins feel free to reach out to me.....I would be glad to provide any answers I can for you.