from Huffington Post,  January 9, 2017

by Mary Beth Pfeiffer


Too many science journals telling him to take his research elsewhere. Too many deftly worded rejections. Too little inclination to engage in a fair fight over the facts and fiction of Lyme disease.

Dr. Lee’s experience is shared by many researchers I have interviewed, in the U.S. and Europe, in five years of writing about a disease on which scientific debate is limited and tightly controlled. Some 380,000 Americans were infected with the tick-borne spirochete in 2015, leaving 20,000, by conservative estimates, with unresolved joint pain, cognitive lapses, fatigue and other problems. Another 232,000 are estimated to be infected annually in Western Europe. Many suffer because of a poor test and delayed diagnoses, issues that have been largely dismissed in mainstream journals.

Lee decided to take on some of the biggest names in Lyme disease, after their Dec. 15 publication of an article, in Nature Reviews Disease Primers, that repeated the doctrines that have ruled Lyme disease care for nearly a generation. But his effort to rebut the article, centering on his call for better early diagnosis, was quickly squelched.

‘’Within days to weeks, [Lyme disease spirochetes] disseminate to other regions of the body or to other organs, the central nervous system, heart or joints.” — Steere article, which endorses waiting for a positive test to treat

“The point raised about requiring newer, better tests for diagnosis is undeniable, and the authors do discuss that,” Primers’ chief editor Mina Razzak wrote in a Dec. 20 email to Lee. “While I agree open dialogue and discussion is needed, this journal is not the best place for that…I am afraid we will not pursue publication of your letter.” Yes we agree there are problems, the editor was saying. Sorry, we won’t let you air them.

Lee, director of Milford Molecular Diagnostics, Milford, Connecticut, had other ideas, however. He posted his challenge on PubMed Commons, an open-access alternative that allows comment by published scientists, where it appeared below the article abstract.

Come back in a few weeks

The 850-word comment argues that Lyme infections have been allowed, even encouraged, to fester. How? Under long-established guidance, repeated in the article, that physicians wait for a positive test before treating patients without the Lyme rash. Lacking a good early test, doctors thus tell non-rash patients who have wrongly tested negative — as 50 to 80 percent of early cases do, the paper admits — to return in awhile, giving the insidious Lyme pathogen time to grow. By then, in what is called the convalescent phase, many patients feel better and do not return, only to be sickened later.

“The authors seem to advise the medical practitioners to not treat Lyme disease patients until the proliferating spirochetes in the host have elicited certain immune responses which can be confirmed by serologic tests,” wrote Lee, capturing the inexplicable logic of a flawed test. “Such practice should not be accepted or continued for obvious reasons.”

The article’s lead author was Allen Steere, who first investigated the disease when it emerged in Connecticut in the 1970s. Others included Gary Wormser, lead author of controversial Lyme treatment guidelines; Frank Strle, another guidelines author, and Paul Mead, an epidemiologist who has specialized in vector-borne diseases at the U.S. Centers for Disease Control and Prevention.

On behalf of the CDC, Mead disputed Lee’s critique.

“CDC encourages prompt treatment of early Lyme disease. The suggestion that CDC is advising medical practitioners to withhold treatment until after the organism has disseminated is [his emphasis] incorrect,” he wrote in an emailed statement. “The recommendations for serologic testing are for patients who already have signs and symptoms suggestive of disseminated infection.”

Lyme disease can be diagnosed early, the CDC website states, ‘in patients who present with [a Lyme] rash.’ It does not say anything about people with symptoms but not the rash.

But patients have symptoms before the disease has disseminated, according to the CDC itself. Its website lists three symptoms of “localized” — or not disseminated — infection: the rash, flu-like symptoms and swollen lymph nodes. However, the agency includes just one symptom to support diagnosis: “During the localized (early) stage of illness, Lyme disease may be diagnosed clinically in patients who present with [a Lyme] rash.” Not the flu, not abnormal lymph nodes.

CDC’s fine line

While the CDC’s website is carefully worded, the paper that Mead signed onto is crystal clear:

“Demonstration of borrelial infection by laboratory testing is required for reliable diagnosis of Lyme borreliosis, with the exception of erythema migrans,” the name for the reddish Lyme rash.

In one venue, namely the article on which he is a co-author, Mead is unequivocal that only tests can diagnose early non-rash infection. In the other, he and the CDC walk a fine line, approving diagnosis for those with the rash, but silent on the rest.

I asked Mead whether the CDC agreed with the article’s contention that a positive test is “required” without the rash, which, a CDC web page says, appears in 60 to 80 percent of cases. He noted that the article refers to “reliably” diagnosing, as opposed to treating, early disease, a distinction perhaps without a difference. He nonetheless left room for treatment based on symptoms.

With regard to empiric treatment of possible early Lyme disease,” he wrote,

“clinicians should consider the patient’s signs and symptoms, the many other diseases that may produce similar symptoms (including other tickborne and non-tickborne infections), and the risks and benefits of presumptive antibiotic treatment.”

Read the entire article on Huffington Post.



This 2017 deserves our attention because nothing’s changed in Lyme-land since it was written.

The “damned if you do, damned if you don’t,” is flagrant and reminiscent of the book “Catch 22.”

What’s new since then?

Mead pleads guilty to sex abuse:

Steere is behind the failed Lymerix vaccine which caused many to develop Lyme:

Wormser, the lead author of the unscientific 2006 IDSA Lyme disease treatment guidelines, is a pharmaceuticals consultant and lectures as a biowarfare expert.[12]He worked for the private Yale Corporation[13] that worked closely with the biowarfare tick lab across the Long Island Sound from Lyme, Connecticut, which also controlled the initial response to the Lyme Epidemic in the Northeast.

For an informative slide show on Wormser:

Strle has been listed as having an intellectual conflict of interest being on the Lyme guidelines panel:

Hmmmmm….. perhaps these issues have something to do with the fact that knowledge and treatment of this disease hasn’t budged in over 40 years.