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Has anyone had a positive experience with Dr. M!ke P0well of Fibr0my@algia Clinic in SAC-ramento
Thanks Minky Girl. I've heard of him & could kick myself in the butt for not having gone to him instead. I would kick myself but I dunno have NRG. I'll check w/NK17.
Irene, that's better than I expected. Thank you, I'll give it a shot.Dr. Montoya at Stanford probably takes Medicare, but takes at least six months to get an appointment.
http://chronicfatigue.stanford.edu
Thank you. I haven’t been on the forum for awhile so forgive the long overdue response.I searched here and there is nothing so I just googled him and the reviews are mixed and there is only one from 2014. Some love him, some think he gets a kickback for pushing supplements.
This one is from 2012
I'd had CFIDS for 2 years when I started treatment with Dr. Powell. Although his treatment plan seemed sound, at first, it eventually became apparent that he although he based his plan off a popular book, he was not well versed these methods, nor was he certified through the author's program of physician education. The biggest issue was that when I started to have severe negative reactions as a direct result of the supplements and meds, both he and his P.A. blamed me for "not wanting to get well." When I requested my records, I found that almost none of these negative consequences were noted, and those that were noted were belittled (e.g. mild nausea instead of abdominal pain). I'm now hypersensitive to all of the medications and supplements from this treatment and cannot use them, which is unfortunate, as about 5% have been shown to be helpful. Five years later, I have not recovered the level of function I lost on Dr. Powell's treatment program. .
I’ve been going to Stanford Clinic going on 8 years and I’ve yet to personally meet Dr. MontoyaDr. Montoya at Stanford probably takes Medicare, but takes at least six months to get an appointment.
http://chronicfatigue.stanford.edu
I’ve yet to personally meet Dr. Montoya