Guest guest Posted June 6, 1995 Report Share Posted June 6, 1995 PLAIN AND BLUNT INS COMPANYS HAVE TOLD MY DOC TO QUIT LOOKING FOR LYMES IN YOUR PATIENTS ...... THOUGHT YOU ALL WOULD LIKE THAT CINDY IN MICH Re: [Lyme-aid] CFS and Lyme > In a message dated 6/6/00 2:51:04 AM Central Daylight Time, LTShepler@... > writes: > > << The CFS docs seem to know virtually NOTHING about Lyme disease. >> > > Mine finally does as I think I was one of the first to be tested positive for > Lyme in her practice. Now, understand we are in Texas where obviously there > is some Lyme but not like the Northeast where it would be a standard test for > the symptoms that are there. But now I believe she makes it a standard test > for those who present themselves with CFS and does regular IV treatment. > Most are like me, they have been sick so long that a regular oral treatment > program does no good. And also, she has a lot of experience in the immune > system, treating CFS and HIV patients in her practice. I find that the > infectious disease specialists and other LLMD's may not have the experience > with the immune system. > > And, yes I believe my Lyme Disease caused my immune system to be > dysfunctional and the CFIDS I have. > > ------------------------------------------------------------------------ > Old school buds here: > 1/4057/8/_/484634/_/960317736/ > ------------------------------------------------------------------------ > > Many thanks to our founder and friend, Marta McCoy, for making what it is today. > > > Easy Reference: > Send a blank email message to: > > -Subscribeegroups - Subscribe to the list through email > -Unsubscribeegroups - Unsubscribe from the list > -Digestegroups - Switch your subscription to a digest format > -Normalegroups - Switch your subscription to normal > > Please send messages not related to Lyme disease to -Offtopicegroups > > Archives can be accessed at lyme-aid > > Please visit the chat room at chat/lyme-aid > > > Quote Link to comment Share on other sites More sharing options...
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