EMPIRE STATE LYME DISEASE ASSOCIATION

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OPMC Reform

Signed by Gov. Paterson 2008

and

NYS Doctors are Offered Some Protection

 

Empire State Lyme Informational Brochures (free)-also, you can ask for a customized version for your group

 

Tick- Info Plus (Download 97 page Tick Management free)

 

Lyme and Tick-

Borne Disease Info

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**PREVENTION**

 

Lyme tests are not accurate-2005 John Hopkins study

 

Articles on the Persistence and Virulence of Lyme

by Miklossy, Luft, Barthold,  others

 

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Empire State Lyme en Espańol

 

Michele Moynihan's Presentation "Lyme Disease: Be Lyme Wise* is a Great Educational Presentation for School Children 

 

LYME BOOKS

and Books on 
Tick-Borne Diseases
plus

FREE: THE THIRD

GREAT PLAGUE

 

**Empire State Lyme Disease Association ~ Our Yahoo Discussion Group**

 

Children

Autism and Lyme Disease

Children

LYME & Pregnancy by John Drulle, MD

 

Misdiagnosis

Alzheimer's and Lyme Disease

 

LYME BORRELIOSIS and MULTIPLE SCLEROSIS

 

Worm Parasites, FILARIASIS Nematodes in ticks?

Nematode Spirochete Farmers

Nematode-Bacteria- Symbiosis

10 Questions For Scientists

 

Heart Disease & Lyme Disease & Lyme Carditis
 

Antibiotic

Resistance

 

ILADS TIPS TO AVOID CHRONIC LYME DISEASE

 

**US Senator Chuck Schumer, NY, on the
Board of Empire State 
Lyme Disease Association
**

 

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In Memory

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letter to the NYS Senate's Task Force on Lyme and Tick Borne Disease

Empire State Lyme Disease Association, Inc
Contact: Eva Haughie PO Box 874 Manorville, NY 11949 631-878-6657 or 631-905-8513
Website www.EmpireStateLymeDiseaseAssociation.org  email EmpireStateLyme@aol.com

In 1988 only five doctors told me that I didn’t have Lyme until I was diagnosed. From 1987 to 1989, my mother believed that she had a nervous breakdown until she was finally diagnosed. Yet, I don’t feel that there was as much denying of Lyme then as there was ignorance of Lyme.
Later on, ignorance became denial and truth became hard to find as the scientific feud between the Infectious Diseases Society of America and the International Lyme and Associated Diseases Society raged on.
Does a scientific feud explain what has happened and why so many people have been left to suffer and yes, die?
An IDSA doctor once admitted that he would lose his NIH funding if he reported too many positive Lyme disease test results. If what the IDSA doctor said is true, what would justify saying a positive test result is negative? There’s no understanding this at all.
Obviously truth is especially important to Lyme patients. Many times, we learn something new that overrides old truth, like what you were told was all in your mind is really a plethora of tick-borne infections or like your negative test result was really positive. (Which happened at the university where the doctor mentioned above worked; we know several patients who were told they had negative test results and they later found the results were definitely positive. My daughter was a victim of Lyme and also a victim of being told her test result was negative when it was truly positive.)
Truth, ethical behavior, moral values, moral code, principles should be especially foremost in science. There have been numerous articles about ethics in science going awry. Why have our researchers been blacklisted? Why would anyone want the number of reported positive blood test results kept to a falsified low number? Why has our good science been rejected, ignored, and denied?
One reason is that IDSA is in control. A few brave individuals have switched sides but think about it, if our side is correct, and if the other side knows it, then most of them are simply too cowardly to admit the truth. You could have sympathy for them, as they could face ruination, lose all credibility, be sued, and lose their practices, if they told the truth. No sympathy? Well at least it is easier to see why they have to fight us. And fight they do, for how can a multi-award winning film documentary like Under Our Skin receive anything but rave reviews? If you want to be shocked, read what the ALDF and others wrote about it. Then think again, of how much is at stake if they admit the truth.

There are 14 IDSA Lyme guideline authors. A quote from their website: “Today, IDSA is no longer a small, elite group, but a large and growing Society (of) 9,000 plus members.” (Lyme organizations’ membership is over 150,000 members)

Consider the fourteen IDSA Lyme guideline authors in proportion to their own members, these 14 only comprise 0.156 percent of the IDSA membership.

From “A Census of Actively Licensed Physicians in the United States, 2012” the number of licensed physicians in the US is 878,194. IDSA membership is 9000. If you divide 9000 by 878,194, you get 0.01025. Or, the IDSA represents only 1 percent of all US doctors! And think: the 14 guideline authors comprise a measly 0.002 percent of all US physicians! (0.002 percent can be stated as two one thousandths of a percent!)

There are between 10.000.000 - 15.000.000 (ten million to fifteen million) doctors in the world. (http://wiki.answers.com/Q/How_many_doctors_are_in_the_world) The 9000 IDSA members divided by the lower number of 10million = .0009 which means that the total IDSA membership comprises 0.09 percent of the world’s doctors. If you do the math for the 14 guideline authors, the number is negligible, that is these 14 can be considered as zero percent of the world’s physicians.
Yet these 14 dictate diagnosis and treatment of Lyme disease. These piddling 14 are dictating to the entire world’s population! NY has one of the highest numbers of reported cases. The suffering here in NY, as across the world, is terrible beyond description. And what is wrong with the CDC, etc, that they religiously follow this piddling small amount of the world’s scientists and doctors? Is the problem that Lyme is big business? Big business is usually controlled by a small number of people. That’s okay if those in control are correct and also tell the truth.
 

 

Lyme WebRing Here.

The Empire State Lyme Disease Association, Inc. is a nonprofit charitable organization incorporated in NYS and dedicated to education, prevention,  awareness and patient support for tick-borne illnesses including Lyme disease.  Our goal is education about prevention of tick bites and the importance of early diagnosis of the diseases transmitted by ticks.  We offer patient support and work for awareness of the need for health care for victims of both early and later diagnosed tick-borne diseases.Information on this site is offered to help further awareness of Lyme and associated diseases.  We hope that the information will help you to become more familiar with the subject of tick borne illnesses, but the information on this web site should not be used as a substitute for medical advice, diagnosis, or treatment. The information on this web site does not represent endorsement or an official position of Empire State Lyme Disease Association, Inc. or any of its directors, officers, advisors or members. Please consult a physician for all medical advice, including advice on testing, treatment and care of a patient who has or may have Lyme or any associated tick borne diseases Back to Top