Guest guest Posted August 9, 2010 Report Share Posted August 9, 2010 Hi Jeri, Yes, I will be back-channeling you soon - swamped for the next few days. I just have a couple little questions. I have decided to start a good doctor list. I have never known why we don't have one. Group: Please send me your ME/CFIDS doctor for leading edge stuff and your regular doctor that is understanding and helpful to you for non-leading edge stuff. Include contact information including phone, email and website if applicable, their specialty and what you think their strengths are. I will begin the list and provide it to anyone who requests the list. Perhaps even put it in the files section. Many thanks everyone. Marti > > Hi Marti, > > > I am shocked because she is one of the top CFIDS docs and most of the top ME/CFIDS docs charge thousands. > > That doesn't really mean anything in her case since she's a Professor of > Medicine and Psychology at the University of Miami. (Her office and > clinic are at the VA Hospital.) The fee scale is set by the University, > not Dr. Klimas. I understand she's opened a private clinic now, too. > The fees there are exorbitant and not covered by Medicare. She still > has her clinic at the VA. She only sees patients there on Thursdays, so > it's hard to get an appointment. I have no idea what the waiting time > is these days. When I first went to see her, I only had to wait three > months to get my first appointment. > > > I have never been on straight Medicare. I tried to research it last time around but wasn't clear-headed enough to make sense of my options. > > That's all I've ever been on since I was eligible for it in 1994. I > can't afford anything else, and it allows me to see any physician any > place I care to go. Where I live, most doctors are morons (I'm an > ex-medical professional and knew a lot of them), so I often have to go > out of area. I also have MCS, which is way far worse than my CFIDS > (I've treated it myself with great success since 1991), and they don't > believe in MCS around here. I have to travel nearly 100 miles one way > to see my MCS doctor. > > > Thanks for outlining this information. This is tremendously helpful and I think I will start considering switching next time around. I have friends in Florida so that would help with expenses. > > You're welcome. If you have any questions at all, email me privately. > I have unlimited long distance for the USA, so I'd be happy to call you, > if you wish. Original Medicare isn't perfect, but it's pretty damned > good insurance. And it sure beats no insurance at all! > > Jeri <teewinot13@...> > @>--->---->-------------------<----<---<@ > Dr. Pall's NO/ONOO- Theory/Treatment Discussion Group: > TenthParadigmSociety > @>----------<---------->-----------------------<----------<----------<@ > The Tenth Paradigm - Dr. Pall's Website for CFS/MCS/FM/ETC.: > http://www.thetenthparadigm.org > @>----------<---------->-----------------------<----------<----------<@ > MCS-SinglesConnection: For all singles MCSers 18 and over: > MCS-SinglesConnection > @>----------<---------->----------<----------<----------<@ > MCS-Florida - For All Chemically Sensitive Floridians > MCS-Florida > Quote Link to comment Share on other sites More sharing options...
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