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Bettyg Posts: 26669
VIP Member
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i've NOT read this; too small for me to read, but worth passing along to each of you since mike does extensive research. it's from mike and his girlfriend, erica, who both have lyme. bettyg, iowa lyme activst ************* METALLlC BLUE Frequent Contributor (1K+ posts) Member # 6628 posted 09-03-2010 01:14 PM In respect to my paper: Post this on as many pages as you typically access, whether it be web forums, facebook, myspace, lymenet, mdjunction, lymefriends, healingwell, or any other. Get it to the media, to friends, family and doctors who both believe and disbelieve that chronic infection is real. betty note: this is 82 pages in length! copy/FILE it for future reference.  https://acrobat.com/#d=sbb-EmpQrQTgrPoezLGreg -------------------- I am not a physician, so do your own research to confirm any ideas given and then speak with a health care provider you trust. E-mail: sbauzys@comcast.net Posts: 3045 | From Western Massachusetts | Registered: Dec 2004 BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader
NOTE: I DO "NOT" USE CHAT thanks!
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NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)
http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-
Any information provided should not be used to take the place of advice from your personal physician or other professional.
Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.
43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.
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