NOV 2017

Lyme patients file lawsuit against IDSA and insurers over treatment denials

From Courthouse News Service, Nov. 14, 2017:

TEXARKANA, Texas (CN) – Twenty-eight people claim in a federal antitrust lawsuit that Lyme disease victims are being forced to pay hundreds of thousands of dollars for treatment because health insurers are denying coverage with bogus guidelines established by their paid consultants, who falsely say the disease can always be cured with a month of antibiotics.

For actual lawsuit:

**Researchers have been saying borrelia persists for a long time.  That message is not believed by the CDC/NIH/IDSA.  Since this is a political war, not a scientific one, doctors and researchers clearly understand their reputations and jobs are at stake if they depart from the controlled IDSA narrative.  

Viable spirochetes have been found in red blood cells after refrigeration for as long as 6 weeks, and being frozen in 4 degrees C.  It’s also been found in fresh frozen plasma, below -18 degrees C, for 45 days and in plateletconcentrates, 20-24 degrees C, for 6 days.

And more just keeps coming out:

Suffering from migraine headaches, an irregular heartbeat, hearing problems and nerve pain, lead plaintiff Lisa Torrey says in the lawsuit filed Friday in Texarkana, Texas federal court that she visited 36 doctors, some of whom misdiagnosed her with multiple sclerosis and fibromyalgia and said her symptoms “were all in her head,” before she was properly diagnosed with Lyme disease.

**This “all in your head” stuff must end, and it’s a common thing Lyme/MSIDS patients hear over and over ad nauseum.  Obviously, if one thinks logically for just one moment, thousands and thousands of people can’t all be nuts.  Something is causing long-term symptoms after being infected with a tick bite – that responds to long-term antibiotics.  Do the math.**

People get the disease from the bites of infected ticks and many break out with a large red rash around the bite that looks like a bullseye.

**Yes and no.  Many never see a tick or a rash.  Requiring those for a diagnosis has caused untold harm to patients over the years.  Lyme/MSIDS is a clinical diagnosis.  Tests are rarely useful. There is congenital transmission and probably is a STD.**

There were more than 28,000 confirmed cases of Lyme disease in the United States in 2015, 95 percent of which came from 14 states in the Northeast and Midwest, according to the Centers for Disease Control and Prevention. The agency estimates that 300,000 people are infected with the disease each year.

Torrey – represented by lead attorney Eugene Egdorf with Shrader & Associates in Houston – lays part of the blame for her lack of health insurance coverage on the Infectious Diseases Society of America, or IDSA, a medical association whose 11,000 members research diseases and lead panel discussions about them. IDSA also develops clinical practice guidelines.

Torrey claims in her lawsuit that several major health insurers decided in the 1990s that treating Lyme disease was too expensive and bad for their bottom lines, so they paid IDSA-affiliated doctors – who were researching, not treating, Lyme disease – to establish arbitrary guidelines in 2000 that said the disease could be treated with 28 days of antibiotics.

“These doctors knew that short term antibiotics of twenty-eight days failed to treat up to 40 percent of patients with Lyme disease. This means more than 100,000 Lyme disease patients every year would be untreated if the IDSA guidelines were followed,” the lawsuit states.

Torrey sued the IDSA, Blue Cross and Blue Shield Association, Blue Cross and Blue Shied of Texas, Anthem Inc., Aetna Inc., Cigna Corp., Kaiser Permanente Inc., United HealthCare Services Inc., UnitedHealth Group and several medical doctors.
In addition to attorney Egdorf, Torrey and her co-plaintiffs are represented by Ryan Higgins with Rusty Hardin & Associates in Houston and Lance Lee in Texarkana.

Please also see:

Torrey claims that she and others suffering from chronic Lyme disease need antibiotics for several months until their symptoms go away, but that the IDSA doubled down in 2006 and once again tapped doctors on the payroll of the defendant health insurers to come up with even more restrictive guidelines for treating Lyme disease.

“The 2006 IDSA Guidelines actually ‘promote the idea that Lyme is a simple, rare illness that is easy to avoid, difficult to acquire, simple to diagnose, and easily treated and cured with 28 days of antibiotics,’” the lawsuit states. “Even though the IDSA guidelines are not rules or requirements, the insurance defendants treat them as ‘de facto’ law that must be followed by doctors and refuse to cover treatment beyond the IDSA guidelines.”

According to the lawsuit, the 2006 guidelines reference an article by Dr. Leonard Sigal, a defendant in the lawsuit, in which he claims “’Chronic Lyme disease’ is a common clinical diagnosis in some geographic areas and is based on thinking that is at odds with scientifically validated findings.”

Torrey says the insurers began working with Sigal to deny Lyme disease coverage in the 1990s.

Sigal testified in a 1996 deposition that the defendant insurers paid him $560 an hour to review Lyme disease files for them and that he almost always denied coverage, according to the complaint.

**Please see this article for more on Sigal’s shenanigans**

Torrey claims doctors who criticized the guidelines as too restrictive put their medical licenses at risk as they were targeted by the insurers.

“As a result of their speaking out, from 1997 to 2000, more than 50 physicians in New York, New Jersey, Connecticut, Michigan, Oregon, Rhode Island and Texas were investigated, disciplined or had had their licenses removed. Many of these doctors were reported to their medical boards by the insurance defendants,” the complaint states.

The insurers also allegedly reported doctors who were treating chronic Lyme disease to state medical boards, leading many doctors to refuse to treat Lyme disease patients.

**This is happening in every state in the U.S. and numerous docs in Wisconsin causing untold stress and anxiety, $50K and more in legal fees, and patients being turned away and having to stop treatment.  When a Lyme doc suffers, we all suffer.**

The results of the treatment guidelines and doctor bullying have been disastrous for Torrey and her co-plaintiffs, she says.

They’ve been forced to travel long distances to find doctors willing to treat them, if they are healthy enough to travel, and pay thousands of dollars out of their pockets because doctors do not want to submit their claims to insurers, the complaint states.

Torrey says she suffers every day from the disease that can kill its victims.

Other plaintiffs are suing for the estates of Al Barnes, who developed paralysis before dying from untreated Lyme disease, and David Kocurek, who was an aerospace engineer and worked for NASA. Kocurek suffered from symptoms akin to the trembling and jerky movements caused by Parkinson’s disease.

“He visited more than 25 doctors and was told he did not have Lyme disease. He even tested negative for Lyme disease based on the IDSA testing guidelines,” the lawsuit states. “He was only diagnosed with Lyme disease after he researched the issue himself and convinced his doctor to test him again.”

**If I had a nickel for everyone who tells me, “I tested negative, I don’t have Lyme disease,” I’d be a millionaire.  Please know the current two-tiered CDC testing misses over half of the cases and no regular doctors are even considering the coinfections that typically come along with Lyme and are just as dangerous**

Kocurek paid for his treatments and died from the disease in April 2016.

Torrey and her co-plaintiffs seek treble damages for RICO Act and Sherman Act antitrust violations.

To back their RICO claims, they say the insurers formed an enterprise rife with mail fraud and wire fraud with the IDSA and its panelists, by mailing fees over state lines to the panelists to pay for their allegedly fraudulent Lyme disease treatment guidelines.

IDSA spokeswoman Jennifer Morales declined to comment on the lawsuit, but defended its Lyme disease guidelines in a statement Tuesday.

“While anecdotal evidence may be relevant at times, it cannot be the basis for guiding patient care. The published guideline, ‘The Clinical Assessment, Treatment and Prevention of Lyme Disease, Human Granulocytic Anaplasmosis, and Babesiosis,’ reflects the best information science provided to the broad range of physicians who might treat a patient with symptoms of Lyme disease,” she said.

**Funny comment considering the CDC recently wrote an article clearly designed to dissuade doctors from using IV antibiotics on Lyme patients based on anecdotal evidence of 5 patients:**

Cigna and Anthem said they don’t talk about pending litigation. The other insurers did not immediately respond Tuesday to emailed requests for comment.

The defendant medical doctors are Gary P. Wormser, Raymond J. Dattwyler, Eugene Shapiro, John J. Halperin, Robert B. Nadelman, Leonard Sigal and Allen Steere.



This is the inevitable outcome of ignoring and mistreating people for decades.  This is not the only lawsuit brewing and I predict much more to come.  People in Lyme-land are frustrated, suffering, and fed up.  An unprecedented anti-trust law suit of $57 million is being prepared against the CDC. They are accused of deliberately suppressing the use of an accurate DNA direct diagnostics for Lyme disease.  Human rights violation has been reported to the U.N. regarding the treatment of Lyme patients.




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