Welcome to Phoenix Rising!
Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.
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Here is the definitive list of Seattle's naturopaths as rated by the Seattle community. These naturopaths have received great reviews from customers and are currently accepting new patients.
I always appreciate hearing good feedback, especially since I haven't seen any of these doctors. Tahoma Clinic did indeed look like it had changed.Dr. Cochran is my doctor, and he is great.
Dr. Iller is competent at Lyme, but scattered, and her patients are irritated as she doesn't follow through.
Dr. Labriola is awful - stay away from him. He doesn't believe in anything more than 100% of the DV of supplements, pushes his own line of supplements with substandard ingredients, and told several untruths in a public presentation I attended.
I've run into patients who say Tahoma Clinic is not what it once was.
Dr. Holly Christie on Bainbridge Island is excellent.
And Dietrich Klinghardt is in Woodinville. He's very expensive and I've seen no reason to go there, but patients fly in from all over the world.
I can related I have similar experience here. For years the kaiser system, rated one of the best HMO, just put me on different drugs, diagnostic, & random sleep study. When I left the system I was able to find my disease (previously cause) .Yes, I saw over a dozen doctors of different types at UW, Swedish, Polyclinic, Overlake, and Evergreen who were a complete waste of time and money. They had no ideas to help, couldn't understand my labs, didn't know what labs to order, and refused to prescribe anything or even refill an existing prescription, much less deal with my health, prescription and LTD insurance or fill out paperwork for a disabled parking pass.
I had to fly to California to find an MD who could help.
And the other patients I've been in contact with in this area don't seem to be improving with the local MDs they see.
ME/CFS and the first Dr, after reviewing all the testing kaiser made me go through (helpful data nevertheless), diagnose me with ME/CFS. My Dr. said it would be difficult for Kaiser to diagnostic me for ME/CFS since there's no treatment so they'll going to weed out all other options with treatment options first.What cause was found that Kaiser missed?
Yes, but you said you found the cause for your illness elsewhere. Who was able to do that and what tests did they run?
The Kaiser website you pointed to is generic Healthwise content, full of bad information.
The best way to get treated for ME/CFS is for doctors to run diagnostics on the immune and endocrine systems and look for infections, nutrient deficiencies, and microbiome disruption, then treat the problems they find. Having a diagnosis of ME/CFS in a vacuum is a dead end.
Fortinately, LA is one of the best places in the world for ME/CFS resources.
I'm just glad I'm not in Michigan .With 100% respect for @Learner1, I have to disagree having lived in LA for my entire illness (and entire life). My doctor, who is extraordinary and is also Learner's doctor, is in No. CA, about 7 hrs north of me. I found that most of the resources are in No CA (Stanford, OMI & OMF, Center for Complex Diseases, etc) and I found nothing in LA.
The exception is Dr. Chia, if you are strictly pursuing enterovirus testing and treatment, and he is in LA. But in general, I did not find doctors here to be helpful to my case and had several nightmare experiences w/my former PCP, neuros, pulmonologists, etc.
My Mast Cell doctor, however, is in LA and he is exceptional and I credit him with saving my life (but he is sadly no longer taking new patients). He would be worth flying across the country to see IMO. But in general, I have not found doctors in LA to be of any help (outside of my MCAS specialist like I said) vs. the resources in No. CA to be very helpful. I was curious who you were referring to in LA @Learner (of if you meant Dr. Chia)?
Everything is relative. There is no help in many places. There is some help to be had in LA, and it is more plentiful than almost anywhere else, though its not much.