Years ago, I saw a dr. Toth in Concord. I'm not sure what type of insurance he takes, but his practice does deal with CFS / ME. I saw him once or twice, but I couldn't afford to go because I have an HMO.
I live in San Jose and have tried many doctors and they have all been awful! I used to think Stanford must have so many good doctors but they are all pompous a@#holes and have zero bed side manners. Worst of all they try to feign empathy in the most comical ways. It's so clear they are just repeating their training: "Mr X, have I addressed all your concerns?" (this is how my neurologist ends our conversations) to which I want to say : NO! but I have to just walk out of their office having wasted hours waiting and scheduling the appointment. They cash in from my insurance, I get no closer to finding a treatment, or even anyone who is willing to take me seriously.
Anyhoo good luck finding a decent doctor in the bay area. I moved to the bay area from a small town in Canada and my doctor back there was SO much better than any of these fancy stanford/UCSF doctors I have seen over the years.
Was looking for CFS Docs recently though it turned out Dr. Gordon is still working. In my search, I contacted an old acquaintance who used to run a support group years ago. I think these are doctors who are experienced/sympathetic to CFS rather than specialists and I don't know anything about them, but here are the names she emailed me.
There are Shaw, now in Foster City, Patel in Redwood City, Dr. Green and Dr Harris.
I can try to find out more, but she is not in great shape.
Hi @Ejw18 . It is like a quest for the holy grail, isn't it? I have a PPO now and thought that might really help me find someone good, but so far, not so much luck. I have an adequate PCP (Hana Holistic) in Berkeley who was at least willing to diagnose me once I put all the facts in front of him. He even offered: you might want to see this great movie called 'Unrest.' I guess I should be grateful he had that much info.... Still, he is constantly suggesting that I try to increase my exercise, so I don't count on him for guidance. He Rxed LDN at my request and made a referral to a cardiologist once I told him that I strongly suspected POTS. It is definitely better than being told to go home and meditate. On the other hand, I see a wonderful doctor named Gabriella Heinsheimer (https://www.genbook.com/bookings/slot/reservation/30148774?category=20418340) .
She is retired and so cannot order or prescribe, but she has a lifetime of working in the trenches. She is an MD with TCM training as well as homeopathic and herbal backgrounds. I see her about once a month (in Richmond, she sees only a few patients a week) and I am reimbursed for a portion of what I pay out of pocket (usually an hour's visit for $125) by my insurance company. She is not an ME/CFS specialist, but she is neither ignorant nor arrogant, and has kept me going, given me hope and helped me through some of the worst times with this illness. She has a breadth of knowledge and a deep store of compassion and those have been more healing for me to date than anything I have received from any other physician. She doesn't have a website or anything--this is a small and very personal practice-- so seeing her for the first time was a shot in the dark for me, but we clicked and it was well worth it. For what it is worth to you.....