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Well-documented, a "must see" for ALL Lyme sufferers and advocates!
Now you can easily click to Lyme facts that the opposition once embraced and now denies. This website is a collaborative effort of several independent Lyme disease advocates nationwide, designed to quickly provide you with links to countless research findings and reviews in scholarly journals online to support your activism efforts with facts & evidence to present to politicians, health care professionals and the media. http://lymecryme.com
The petition's purpose is to draw attention to the facts-- scientific facts and evidence that Lyme disease is difficult to diagnose and difficult if not impossible to cure. This petition is public and can be used by any Lyme advocate to demonstrate that his/her opinions are based on scientific evidence, and we do not stand alone. The petition can be signed anonymously for public viewing, and each signer has the option of leaving a comment.
Please do not minimize the potential of this petition. It does not detract from others' efforts but in fact, validates them. These various activities are synergistic and compatible, not competetive.
The health status of the entire World has been and continues to be compromised in several ways by combinations too powerful to be suppressed in the ordinary way.
In the early 70s chronic illness were not epidemic in our country unlike today with Fibromialgia, Chronic Fatigue, Lupus, MS, and ALS and many other debilitating illnesses that have been linked to Lyme Disease as you will see from papers on this web site.
This Web Site contains published papers from both camps that show treatment failure and inaccurate testing. We therefore demand, both United States Houses of Congress to investigate Lyme Disease Diagnosis, Testing,and Treatment protocols currently under the Center for Disease Control, CDC, The Infectious Disease Society of America, IDSA, the American Medical Association, AMA, and the American Academy of Neurology.
Well-documented, a "must see" for ALL Lyme sufferers and advocates!
Now you can easily click to Lyme facts that the opposition once embraced and now denies. This website is a collaborative effort of several independent Lyme disease advocates nationwide, designed to quickly provide you with links to countless research findings and reviews in scholarly journals online to support your activism efforts with facts & evidence to present to politicians, health care professionals and the media. http://lymecryme.com
The petition's purpose is to draw attention to the facts-- scientific facts and evidence that Lyme disease is difficult to diagnose and difficult if not impossible to cure. This petition is public and can be used by any Lyme advocate to demonstrate that his/her opinions are based on scientific evidence, and we do not stand alone. The petition can be signed anonymously for public viewing, and each signer has the option of leaving a comment.
Please do not minimize the potential of this petition. It does not detract from others' efforts but in fact, validates them. These various activities are synergistic and compatible, not competetive.
The health status of the entire World has been and continues to be compromised in several ways by combinations too powerful to be suppressed in the ordinary way.
In the early 70s chronic illness were not epidemic in our country unlike today with Fibromialgia, Chronic Fatigue, Lupus, MS, and ALS and many other debilitating illnesses that have been linked to Lyme Disease as you will see from papers on this web site.
This Web Site contains published papers from both camps that show treatment failure and inaccurate testing. We therefore demand, both United States Houses of Congress to investigate Lyme Disease Diagnosis, Testing, and Treatment protocols currently under the Center for Disease Control, CDC, The Infectious Disease Society of America, IDSA, the American Medical Association, AMA, and the American Academy of Neurology.
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/