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Lyme Time

As the weather heats up, so does the risk of Lyme disease—and the controversy surrounding diagnosis and treatment.

Posted April 11, 2011 by Jodi O'Donnell-Ames

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The bull’s-eye rash is a telltale sign of a bite from the deer tick.
The bull’s-eye rash is a telltale sign of a bite from the deer tick.
Dr. Ken Greer/Visuals Unlimited/Corbis.

David Scharf/Science Faction/Corbis.

The bacteria that causes Lyme disease.
The bacteria that causes Lyme disease.
Visuals Unlimited/Corbis.

Medford neurologist Dr. David Lee was brought to his knees by the disease.
Medford neurologist Dr. David Lee was brought to his knees by the disease.
Photo by Michael Marmora.

Spring is upon us. That means an increase in activity for the black-legged tick—more commonly known as the deer tick. This grotesque little creature carries the bacterium (Borrelia burgdorferi) that causes Lyme disease.

Lyme disease is on the rise in New Jersey, where dense forests and vegetation provide a veritable paradise for the deer tick. In its most recent data, the Centers for Disease Control says 4,598 new cases of Lyme disease were reported in New Jersey in 2009, the second highest in the nation—and an increase from the 3,214 cases in 2008. But the CDC says the incidence of Lyme in New Jersey is actually higher, because only 10 percent of Lyme cases are reported nationwide each year—in part because many cases go undiagnosed.

Lyme has created almost as much controversy as discomfort. On the one hand is the medical establishment—doctors, scientists, government agencies—which says Lyme is a relatively mild illness that can be cured with four to six weeks of an oral antibiotic. On the other, there is a highly vocal cadre of Lyme sufferers, physicians and advocates who believe that Lyme can be life altering, with symptoms lasting for years after treatment.

The battle lines are drawn over diagnosis and treatment. A bull’s-eye-shaped rash is universally acknowledged as evidence of Lyme. But if there is no rash—or if the rash has faded with time—diagnosis gets tricky. What’s more, the typical symptoms of Lyme—fatigue, chills, fever, headache, muscle and joint aches, and swollen lymph nodes—are easy to attribute to other ailments such as flu, chronic fatigue syndrome or fibromyalgia.

“If you have the characteristic skin rash, your doctor can diagnose Lyme disease based on visual inspection,” says Dr. Gary Wormser, chief of the division of infectious diseases at New York Medical College. “If you don’t have the rash, your doctor can diagnose Lyme disease based on your history, an examination and a blood test that determines whether you have developed antibodies to the Borrelia burgdorferi bacteria.” However, he adds, “relying solely on a test can be a problem because tests can be falsely positive, or—at the very early rash stage—falsely negative.”

It doesn’t help that the deer tick in its nymphal stage—when it is most likely to bite humans—is less than one-eighth of an inch big, making it hard to see. Once on an animal or person, it can hide in hair and folds of skin. The tick can bite, fall off and leave you unaware that you’ve been infected for days or weeks. Since most patients see a general practitioner first, he or she may not be on the lookout for Lyme, especially if the patient does not develop a rash.

Such was the case with Moira Kirby, whose life changed drastically in 1998. The East Brunswick woman, then 16, began experiencing headaches, sinus congestion and exhaustion. After weeks of misery, she finally told her mother she felt ill. “We thought maybe she had the flu,” recalls Kathleen Kirby.

For years, no physician could explain Moira’s suffering. At one point, a pediatrician prescribed antibiotics for a sinus infection, but to no avail. “Moira felt like a hypochondriac,” says Kathleen. “It’s bad enough knowing that your daughter’s physically sick, but worse having her symptoms brushed off as emotional issues.”
Finally, in July 2004, Moira was diagnosed with Lyme disease. She was treated for three more years with oral antibiotics before her symptoms went away. Still, based on Moira’s case history, some doctors would say that she never had Lyme.

Further complicating matters is how the infection works. An infected tick passes Lyme to a patient through a bite. The bacterium then works its way into a patient’s bloodstream, which can take days or weeks. So if a test is administered before the bacterium has spread sufficiently to be detected, the results will be negative.

The Infectious Disease Society of America (IDSA) and the CDC have developed guidelines for testing, as well as prevention tips, lists of symptoms and recommended treatments—all available to the public on either agency’s website. Doctors are not bound to these guidelines, but adherence is common practice. IDSA and CDC protocols also serve as guides for insurance reimbursement.

For Lyme, the IDSA recommends a biochemical test called the enzyme-linked immunosorbent assay (ELISA). If the ELISA is positive, a second test, the Western blot, is performed. Both typically are covered by insurance companies. Other available Lyme tests, including a screening offered by IGeneX, a lab in Palo Alto, California—used in Moira Kirby’s ultimate diagnosis—sometimes are not covered.

Some doctors fault this regimen, saying a positive ELISA should not be the benchmark for ordering a Western blot. “The Western blot was designed to test for Lyme-specific proteins and is a better indicator of Lyme disease,” says Dr. Lincoln P. Miller, vice chief of the section of infectious disease at Saint Barnabas Medical Center and clinical associate professor of medicine at UMDNJ.

If the ELISA and Western blot are negative, a doctor can still suspect Lyme based on a patient’s health history and symptoms. If the patient lives in a Lyme area—Morris, Hunterdon, Sussex and Burlington counties are known to have the greatest concentration of deer ticks in New Jersey—and there are symptoms, a clinical diagnosis (or medical conclusion) can be made. “New Jersey is endemic for Lyme disease and other tick-borne diseases, so clinicians should always consider these infections when they are confronted with a patient who has a fever and has potentially had contact with a deer tick,” says Miller.

Dr. David Lee, a neurologist in Medford, says he had symptoms for seven months but tested negative. He used both tests; his eighth test, a Western blot, was positive. “Did I have Lyme even though the tests were negative? Absolutely! I was a textbook patient,” says Lee. A second-degree black belt, Lee says the disease brought him to his knees, literally. He resorted to crawling around.

On the other hand, a positive test can also be misleading. “Many of the patients who come to me are looking for a second opinion,” says Dr. John Salaki, an infectious-disease specialist with Atlantic Health in Morristown. “I explain to them that the antibiotic they received has ‘killed the bug’ but the blood test result is a response of their immune system to their infection. So the test may remain positive as a marker of their exposure to Lyme, even after having received appropriate treatment for this infection.”

While the Lyme debate thrives, so do ticks in warm weather. May is Lyme Disease Month, and now is a good time to learn about prevention and detection (see box, page 37). New Jersey has many kinds of ticks that carry illnesses—such as Rocky Mountain spotted fever—but Lyme is the most prevalent.

For most cases, the IDSA’s 2006 guidelines for treating Lyme recommend a single course of antibiotics lasting 10 to 28 days. A single dose of an antibiotic may also be used to treat Lyme disease preventively in certain high-risk patients who believe they have been bitten by a tick but do not have symptoms. On occasion, a second course of antibiotics might be recommended.

Unfortunately, this standard treatment regimen does not relieve the symptoms for all patients. This could mean they were misdiagnosed (and didn’t actually have Lyme), the antibiotic was ineffective or they have long-term damage that is harder to treat.

Some in the medical community believe Lyme disease can linger for years (even after treatment) with severe consequences; they refer to this condition as chronic Lyme. Crippling arthritis, dementia, breathing difficulties and impaired vision are just some of the symptoms they attribute to chronic Lyme.

Here the controversy reaches a crescendo. The IDSA does not recognize the existence of chronic Lyme. Instead, it refers to long-term symptoms as late- or post-Lyme. And the IDSA guidelines don’t support long-term antibiotic treatment. “The IDSA’s primary goal is to ensure that people with Lyme disease get the best possible care, and that the treatment IDSA recommends is safe, effective and well-supported by the medical evidence,” says John Heys, IDSA public affairs officer.

Don’t tell that to Ewing resident Brian Pauly, who attributes his long-time ailments to Lyme. His suffering began with the appearance of a rash in 1996. Without additional symptoms, he and his doctor thought nothing of it. Three years later, however, “I started having extreme exhaustion and muscle fatigue and knew that something was seriously wrong,” says Pauly. “Several Western blots came up negative and no one suspected Lyme.” Then Pauly paid $400 out-of-pocket for a Lyme screen from IGeneX, which came up positive.

By that point, Pauly says, “I was unable to work and on Medicaid, which only paid for six weeks of antibiotics, and my health has continued to deteriorate.” These days, says Pauly, a former house painter, “I am home bound most of the time.”

Representatives of several insurance providers, including Medicaid, say the insurers follow IDSA guidelines in making decisions on reimbursement, but will cover additional medically necessary treatments on a case-by-case basis.

The Lyme Disease Association, a national advocacy group based in New Jersey, wants the disease diagnosis to be based on symptoms, with the testing serving as an adjunct rather than as the authority. “Since the test for Lyme is not accurate, you can test negative and still have the disease, and since the science shows that Lyme bacteria can live after treatment, mainstream medicine needs to rethink its obsolete ideas about Lyme disease and Lyme patients,” says Pat Smith, a Wall Township resident and president of the LDA.

On its website (lymediseaseassociation.org), the LDA refers Lyme sufferers to a directory of what it calls Lyme-literate medical doctors—or LLMDs. Smith says there are about a dozen in New Jersey. Although this is not an officially recognized specialty, the association defines an LLMD as “knowledgeable about chronic Lyme disease and often about many other tick-borne diseases.” The group also acknowledges that there have been investigations of and sanctions against some so-called LLMDs for practicing outside of protocol in New Jersey.

Some doctors treat ongoing Lyme symptoms with intravenous antibiotics, which can require the services of a visiting nurse—yet another expense that insurance might not cover. Some patients like Pauly seek alternative treatments, such as chelation, acupuncture or vitamin or oxygen therapy, which generally are not covered by insurance, but may cost less than IV treatment and nursing care.

The IDSA is pessimistic about the long-term use of IV antibiotics for suspected Lyme. “Although some people may feel better, it doesn’t prove that the antibiotic cured or suppressed infection,” the IDSA says on its website. “Sometimes, the belief that a treatment is helping can be enough to make people feel better. This is called the placebo effect and it is a well-documented medical phenomenon.”

IDSA’s Heys adds, “Antibiotics also have anti-inflammatory effects that may help alleviate certain symptoms. Or, in some cases, patients may have another infectious disease that is responsive to antibiotics.”

However, a 2006 study at Columbia University by Dr. Brian Fallon published in the journal Neurology concludes: “Lengthier courses of antibiotics are helpful in reducing neurologic symptoms related to chronic Lyme disease.”

And the National Institutes of Health, while stating that most Lyme patients can be cured with a few weeks of oral antibiotics, acknowledges, “Patients with certain neurological or cardiac forms of illness may require intravenous treatment.”

Talk of a placebo effect rankles Pat Smith. “While enduring tremendous pain and debilitation as Lyme progresses,” she says, “patients are subject to scorn, ridicule, ignorance and paternalism from much of mainstream medicine who reserve compassion and open mindedness for those they think are ‘really sick,’ the implication being Lyme is a disease hard to catch and easy to cure, and its victims are often faking illness.”

A further aspect of the controversy is raised by patients and doctors who believe Lyme can be passed congenitally through the birth canal. “My son has congenital Lyme and it’s a serious issue,” says one New Jersey woman, who requested anonymity. In fact, she says, four of five family members battle the disease. And she says her family is not alone. “We group of mothers have proof on paper to show that our children contracted Lyme from us. Yet, does the IDSA recognize this issue? No. Are we covered by insurance companies? No.”

Wormser, the infectious diseases chief at New York Medical College and an IDSA panel member, says research will help soften the Lyme debate. “More research on what causes lingering symptoms such as fatigue is needed in Lyme disease and other infections,” he says. “Some patients are receiving unconventional treatment—specifically, long-term antibiotics for months or years—for symptoms like fatigue. But studies show that two to four weeks of antibiotic treatment clears up a Lyme infection, and longer antibiotic treatment can be harmful. If research could pinpoint the true cause of the lingering symptoms, then better treatments might be found.”

The Lyme controversy has not escaped Congress. “It is critical that we identify biases and impediments that are constraining the science on Lyme disease and open up the dialogue to honest and transparent debate,” says Representative Chris Smith, founder and co-chair of the Congressional Lyme Disease Caucus. “The scientists who have long been marginalized, treating physicians who have felt intimidated and threatened, and, most importantly, sick patients, need our help.”

Jodi O’Donnell-Ames is a freelance writer. A resident of Titusville, she underwent successful treatment for Lyme several years ago.

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Prevention Pointers

Ticks live year-round, but become more active as the weather heats up. That means the incidence of bites from deer ticks begins to increase in May. Here are some tips on how to reduce your risk:

•When hiking in wooded areas, walk in trail center, not near trees and shrubs.
•Use a repellent with DEET on skin and clothing.
•Cover up! Protect your legs with long pants and keep the pants legs tucked into your socks to make it harder for ticks to hitch a ride.
•Ticks like to be warm. Once on a body, they go to underarms, behind legs, head and neck. If possible, cover these areas.
•Check for ticks regularly. If you find a suspected tick, remove it carefully and save it for identification.
•If you develop a rash, circle it with a permanent marker and take a picture. This will help determine if the rash is growing.

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Comments

This is an excellent article-well written and timely! Thank you!

Posted by: Sara Holcombe, Titusville | Apr 21, 2011 00:51:39 AM |

Tick Bite ER Visit

On may 8th I took my son to the ER at the Princeton hospital to remove a tick from the back of his head. We went to the Morris county Lewis park in Morristown for a Mothers day picnic.I have never experienced a tick so i took him to the ER. It was stuck to his scalp. The doctor removed the tick and threw it in the garbage disposal. I asked if i need to do anything further they said NO. just clean the wound and gave me 2 satchels of Bacitracin. On returning home I reviewed various websites regarding tick bites. I immediately called back the hospital and asked to speak to the doctor who treated us. I was told he was with the patient and the nurse told me that It WAS NOT REQUIRED TO SAVE THE TICK. Should the tick have been saved ? Why did they threw it away ? when it can be checked for diseases. I am not sure what should I do to ensure that my child is not infected. I feel really bad and surprised that the doctor gave me no information stated in your article. My daughter is also complaining of stiff neck and aches and pain. I really think it should be standard practice to save the Tick and test it. Instead of waiting for our children to get sick and then seek treatment.

Posted by: NR, Belle Mead, NJ | May 18, 2011 19:18:05 PM |

Lyme Disease

I grew up in NJ and my 15 year old daughter attended a tennis camp in Princeton the summer of 2008. She became hoarse which was the first time that had ever happened and said she was tired and did not play well. On October 31, 2008 she woke up unable to walk, dizzy, 104 F fever, sore throat and crushing fatigue. That started the three year nightmare that we are still dealing with. She does not remember a tick bite ever. Finally after many months of mis-diagnoses she has tested Center for Disease Control positive for Borrelia, one of the spirochetal infections of lyme disease. In Additon, she has tested positive for Ehrlichia, Babesia duncani, Bartonella, HHV-6, HSV-1, and had bells palsy, Papillomaviruses and deveoloped a huge mosaic wart on the underside of her foot. Parvovirus B-19 has also shown IgG antibodies and finally IgM response 5 times for Brucella. I have lyme and have some of the same infections and also EBV, CMV, Toxoplasmosis, Chlamydia pneumoniae, Mycoplasma pneumoniae to name a few. A brilliant student and great tennis player has missed almost three years of the International Baccalaureate program and is trying to finish high school on line. Her immune system is overwhelmed with all these pathogens so 14 days of doxycycline DID NOTHING! She was so ill that she could not keep any doxy in her system. 14 days or 30 days or any other arbitrary amount is not going to handle the myriad of infections that a person has received from a tick, flea, biting fly, etc. There are so many that lyme is not just an infection with Borrelia.

Posted by: Dolores Claesson, Succasunna | Sep 07, 2011 18:27:34 PM |

Tests needed for lyme disease sufferers

Lymies...I would get all these tests...



Western Blot for Borrelia, also test for Borrelia hermsii, and Babesia duncani and microti and Quest can test for duncani, Bartonella henselae and quintana, Brucella, Tularemia, Coxiella burnetti or Q fever, many rickettsias ie Rocky Mountain Spotted Fever, Typhus, Ehrlichia, Anaplasma phagocytophilum, EBV, CMV, all Coxsackie viruses, and now Powassan virus and its cousin Deer Tick Virus, HSV 1 and 2, HHV 1-8 if available.



Parvovirus B -19 papillomaviruses, Toxoplasmosis, Chlamydias and Mycoplasmas and get genetic tests for hypercoagulation like Mthfr and Factor V leiden, and test all your IgG subclasses 1-4, and CD 57 and C3a and C4a and CBS mutations and HPU/KPU and mold testing since so many of us have issues with mold. ECP or eoisonophil cationic protein seems to suggest to docs that you have babesia.



Also transfer growth factor b-1 and Beta Strep. High CD 57 counts may be associated with Beta Strep. Heavy metals have a part in this and we are low in Secosteroid D or vitamin D and some are low in Potassium and others iron.



Many are deficient in all amino acids.



Our hormones are a mess and the whole HPA Hypothalmic pituitary axis is the problem. We can have probs with our adrenals and thryoid...we do not convert T4 to T3 and in my case I have high reverse T3 or rT3.



We are quite low in testosterone as well. Check out every hormone in your body, amino acids and vitamins and minerals. There are over 100 viruses we can get from a tick and also many parasites.



The labs that insurance covers can’t find a parasite when we can see it under the microscope. Quest at Nichols Institute in Valencia California can culture samples and might even be able to distinguish Brucella suis from melitensis or arbortus.



We also need an MRI of our brain with and without contrast. Many lymies are showing up with pituitary adenomas and pheomchromocytomas. Make sure that you do not have these. I have spent years trying to figure out what is in us and so far this is what I have seen.



Unfortunately your physician may take years to order all the necessary tests. Make sure you get tested sooner rather than later. One more thing .....you may get tested for Brucella today and 2 years from now may show up IgM positive. The immune system is overwhelmed with all these pathogens.

Posted by: Dolores Claesson, Succasunna | Sep 07, 2011 18:42:15 PM |

Pathogens in Austrian hunters...

http://www.ncbi.nlm.nih.gov/pubmed/15508783


Antibodies to these pathogens were found in Austrian hunters. What do you think they can find in lyme patients if they really look ???

Posted by: Dolores Claesson, Succasunna | Sep 07, 2011 18:47:26 PM |

Lyme Disease

Thanks for this excellent article if only the media would do more such excellent work regarding Lyme Disease then hopefully less people would unwittingly fall into this dreadful disease suffering years of chronic debilitating and painful ill health.
It is time the IDSA proved that Lyme is eradicated from patients in all cases conclusively - they can not,it is only based on their OPINIONS - on the contrary there are many published studies that show the infection persists following extensive courses of antibiotics. Plus studies in mice, dogs and monkeys that find the infection after 3 months of Antibiotics.

With two standards of care most of us who have failed the IDSA standard if we are lucky to hear about an alternative standard of care such as ILADS and lucky enough to afford private treatment find our health and lifes are restored on longer courses of antibiotics.

Interesting investigation into patent applications by IDSA colleagues for research grants for a Vaccine for Lyme will show that the same people who deny chronic lyme can be an ongoing infection actually contradict themselves in their patent applications acknowledging a chronic persistent infection that is difficult to treat with inadequate tests.

The research is all there to expose the IDSA guidelines for what they are outdated and biased and based mostly on opinion and yet they are allowed to influence guidelines not just in US but most European countries to but times are changing and patients with the help of the Internet can become better informed and work towards getting treatment that helps them.

Posted by: Joanne Drayson, Guildford UK | Apr 23, 2012 22:15:25 PM |

Neuropsychiatric Lyme

As a school counselor who works primarily in one of NJ’s rural regions, I routinely see kids who are diagnosed with bipolar disorder, ADD/ADHD, panic and anxiety attacks, major depression, etc... Many of these kids do not respond to conventional medication and/or therapeutic intervention and have histories of tick bites that have gone unconsidered in what is often multiple mental health and learning evaluations. It has been my experience that a significant amount of kids manifesting various psychiatric symptoms have been found to be infected with Lyme borrelia (as well as other coinfections, in some cases) when examined and tested by Lyme literate doctors. I have witnessed psychiatric symptoms improve and-in some cases-disappear with appropriate antibiotic treatment.

In light of New Jersey’s indisputable saturation with Lyme infected ticks, I firmly believe it is essential for the history of tick exposure/bites to be included in all mental health and learning disability evaluations, and that all NJ mental health and child study team professionals be educated in the recognition of possible neuropsychiatric Lyme.

Posted by: Nancy Baumgartner, Oxford | Apr 24, 2012 01:53:04 AM |

Seronegative Lyme until Doxy Provocation

For over 15 years I was diagnosed with ME/CFS and Fibro. Lyme tests continually came up negative and I was not a typical lyme patient. I went on a doxycycline provocation and low and behold got a positive PCR test from Igenex. I am finally seeing the illness move with antibiotics, gcmaf, high dose oral and IV vita C, B12 and folic acid among other supps. I have a long way to go but am more hopeful than ever.

Karen

Posted by: Karen R, West Caldwell | Apr 24, 2012 15:30:12 PM |