Guest guest Posted July 28, 2003 Report Share Posted July 28, 2003 jseaton357@... wrote: > Well, hope this digests in > your head a good while as I think anyone here will have a hard time rebutting > any of my points. Notice I never say all CFS is lyme, but just to pay > attention to bacteria too. How can you rebut that, especially when you are still sick > and I am record well? Pushy about lyme? I've had CFS pushed on me all this > time. Now I want vindication and to help others. Amen. That's all well and good. And I'm glad you stated that all CFIDS is not Lyme, because that's true. There are many people like me, who have CFIDS, that contracted it due to toxic chemical exposure. I see Dr. Klimas. She doesn't push anything down my throat. In fact, there isn't much that any doctor can do for me. The doctors I do see are working to rebuild my immune system as much as possible and find others ways to give me a better quality of life. Being on SSDI, I *have* to have doctors who can tell SSA that I'm still disabled and can't work, or I lose my benefits. My bills are small because they all take Medicare. I pay only 1/4 to 1/3 of the actual bill. Yes, there are people who are misdiagnosed as having CFIDS when they really have Lyme or Lupus. I've known quite a few. There are a lot of doctors out there who don't give a damn, but there are ones who do. Don't knock them all. Teewinot @>--}-- * --{--<@ Teewinot13@... Quote Link to comment Share on other sites More sharing options...
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