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With Summer’s Arrival, A Lyme Disease Refresher

In H.G. Wells’ novel (and Steven Spielberg’s movie) War of the Worlds, aliens from Mars invade earth, fully intending to destroy it. Earthlings are losing against the Martians until suddenly the latter start dying off. Scientists later discover the aliens had no immunity against earth’s bacteria and paid the price with their lives.

With the current Lyme disease situation, we’re the immune-weak aliens. We invaded and cleared forests and by doing so became the victims of microbes harmless to the animals carrying them. We’ve seen evidence of this with swine flu, bird flu, the Zika virus, the Elizabethkingia bacterium, and SARS. Climate change may also be a contributing factor.

The bacterium that causes Lyme disease, Borrelia burgdorferi, is classified as a spirochete, meaning it’s spiral-shaped, a cousin to syphilis. Borrelia live quite contentedly in forest mice, who do not get Lyme disease. Then a particular species of tick (the black-legged tick/deer tick) sucks mouse blood and hops over to feed on a deer, which generally do not get Lyme disease either. Or the tick hops onto you, out enjoying a summer day, communing with nature.

Unfortunately, unlike the mouse or the deer, you have no immunity against Borrelia.

The tick attaches its head and mouth to you by secreting a gummy substance called cementum. While gorging on your blood it injects the Borrelia spirochete into your bloodstream. If you spot a tick attached to you, remove it ASAP with pointed tweezers as shown in this animation. It may not be a deer tick–and not all deer ticks carry Borrelia— but it’s well established that the faster you remove an infected tick the less chance you have of developing Lyme.

Save your tick in a jar so you can identify its type using a resource such as this one, a guide to ticks by region.

Infection, symptoms, and treatment
If you do get infected with Borrelia, you’ll be coming down with what’s called acute Lyme disease. You’ll feel like you have a bad case of flu: fever, headaches, joint pains, muscle aches, brain fog. Much has been made of the famous bull’s eye red ring at the site of the bite, but since it does not appear in nearly 25% of people with Lyme, doctors no longer use it in deciding whether or not to start treatment with antibiotics.

The diagnosis of Lyme is a clinical one, based on symptoms and your doctor’s physical examination. Lab tests are useless at this point. The screening test for Lyme looks for antibodies your immune system creates in response to infection. You simply don’t have time to wait the weeks needed for your test to register the antibodies and convert from a negative to positive result.

As far as antibiotics go, doxycycline is quite safe. If you live in an area where Lyme disease is appearing, you’ve been bitten, and the tick is engorged with your blood and has likely been attached for awhile, virtually all doctors will recommend a course of antibiotics. A previous Health Tip told of my associate Dr. Paul Rubin’s personal experience with Lyme, acquired in the jungles around Madison, Wisconsin.

(I myself am writing this Health Tip looking out on a forest from a glass-enclosed porch. In the past 30 minutes deer, raccoon, fox, geese, and even feral chipmunks have ambled past. Occasionally, I dare to open a screened window to breathe in some fresh air. Let them have their world and me mine.)

Chronic Lyme disease debate
If you’ve retrieved a tick that’s infected you with Lyme, removed it, and received your four weeks of antibiotics, there’s an 80% chance you’ll be fully cured and your Lyme will become history. Real problems occur in two groups:

  1. The remaining 20% who are not treated successfully.
  2. Those who got infected but didn’t know it and were never diagnosed or treated in the first place.

One wouldn’t think this issue would generate vicious and truly juvenile battles among physicians, but doctors can be just as crazy as everyone else.

Common sense would tell you that a perfectly good descriptor for the people in these two groups would be chronic Lyme disease. Here’s the scene, years after infection: these patients are seeing doctors for a smorgasbord of symptoms very similar to fibromyalgia and chronic fatigue (CF). Most don’t even remember a tick bite. Like many with fibro and CF, they’ve seen several doctors and been told all their tests are normal (although usually they’re not tested for Lyme). Then, along the way, someone does finally run a Lyme test and lo! it’s positive.

You’d think that when presented with a symptomatic patient who tests positive for Lyme, the treatment course would be clear. After all, like late-stage syphilis, the spirochete can corkscrew its way into brain tissue, nerves, and heart muscle. Also like syphilis, many (but not all) of these patients respond well to antibiotics months or even years after the initial infection.

But tragically, and I feel my blood boiling as I write this, many of these patients–even with clear evidence of disease–are denied treatment because their doctor read somewhere that there’s no such thing as chronic Lyme disease.

Why the debate? Why withhold treatment?
Doctors who “don’t believe” chronic Lyme exists are usually the same group who deny the existence of fibromyalgia, CF, and other controversial illnesses I wrote about last week. They want evidence beyond a blood test for Lyme. When confronted with the positive Lyme test result, they’ll say “That’s not good enough. You probably had Lyme years ago. Or else it’s a false-positive.”

The conversation goes something like this:
Patient: You’ve given me a course of antibiotics appropriate for acute Lyme disease. Unfortunately, I’m still sick.
Doctor: Well, it can’t be Lyme. I’ve treated you for Lyme.
Patient: But I still feel terrible.
Doctor: You need a psychiatrist.

Or (even worse)
Patient: I’ve had fibromyalgia and chronic fatigue for years. I’ve read about chronic Lyme. Can you test me for this?
Doctor: No. There’s no such disease. You need a psychiatrist.

Or (the worst)
Patient: I’m no better. I paid for a Lyme test myself and it came out positive. Now can we start treatment?
Doctor: No. I don’t know anything about that lab. Really, please go to a psychiatrist.

Lyme Wars: majority and minority
The Lyme Wars are an embarrassing mess for the medical profession. By way of introduction, let me say we do this to ourselves far too often. We think that being loud and pushy and powerful will get our point across, especially to anyone who thinks outside the mainstream medical education system.

In the 19th century, Hungarian physician Ignaz Semmelweis discovered that a fatal infection, called childbed fever, affecting women who had just delivered babies was caused by bacteria carried into the delivery room by physicians themselves (who never washed their hands). After his ideas were summarily rejected by the medical community, Semmelweis suffered an emotional breakdown, was committed to a local asylum, and two weeks later was dead at age 47 after being beaten by guards.

Today, the physician majority encourages state boards to yank the medical licenses of the physician minority or pushes insurance companies drop the minority from their networks. BTW, The Cry and the Covenant by Morton Thompson is a superb novel about Semmelweis. No small number of teenagers became physicians after reading it.

Here’s a rough breakdown of where the physician majority stands:

Stance of the medical majority #1  Once an acute case of Lyme is treated, the story is over, the end. If any symptoms remain, whatever the cause, it’s not Lyme disease and there’s no Borrelia. In fact, to distance these symptoms from a Borrelia infection, the medical majority renamed these symptoms post-treatment Lyme disease syndrome (PTLDS) and recommend antidepressants and psychotherapy.

Stance of the medical majority #2  If you do have fibro/CF and someone does test you for Lyme and the result is positive, this test is merely showing an old, resolved infection unrelated to your current symptoms. Some majority doctors will actually prescribe a three-week antibiotic course, treating your chronic Lyme as an acute Lyme infection, which will likely be inadequate.

A vocal minority of physicians disagrees completely
A minority of doctors protest the PTLDS name change because it implies a psychiatric disorder. They believe the term chronic Lyme disease should remain in place. However, even among these Lyme-literate physicians, there’s no unanimity on a treatment protocol.

Stance of the medical minority #1  One group of Lyme-literate doctors, whose struggle with the conventional medical community was documented in the 2008 film Under Our Skin, believes that long courses of high-dose IV antibiotics are the best treatment to clear the body of Borrelia. However, many physicians, including those at WholeHealth Chicago, are uncomfortable with this potentially risky treatment, especially when more and more clinical trials show no benefit of high-dose antibiotics over placebo.

Stance of the medical minority #2  The other group of Lyme-literate physicians (we’re in this group), while fully acknowledging chronic Lyme disease, is focused not so much on Rambo-like antibiotics to clear every last spirochete, but rather on strengthening the patient’s immune system to clear the disease itself. This approach to infection was first described in the 19th century by Antoine Bechamp, a biologist and critic of Louis Pasteur. He believed the cause of infectious disease was not bacteria alone, but how an individual could ward off bacteria. He felt this “terrain of the patient” was of greater importance than the bacterium itself. A healthy terrain could fight an infection that could kill someone with an unhealthy terrain.

We’re seeing this now with the bacterium Elizabethkingia. The only deaths that have occurred are among patients with chronic illnesses or weakened immune systems.

Here at WHC we treat chronic Lyme using a variety of approaches depending on the individual patient’s needs. Often, a combination of antibiotics is used while strengthening the patient with good nutrition, detoxification, herbal/homeopathic remedies, and stress reduction techniques. Casey Kelley, MD, focuses her practice to chronic Lyme patients, but if you have chronic Lyme you can start by seeing me.

Here’s a Lyme summary

  • You’re out in the woods and get bitten by a tick. Remove it ASAP, see if it’s a deer tick, and if it is get treatment.
  • You come down with an acute flu-like illness in spring, summer, or fall, it’s not flu season, you live in a Lyme-rich area, and you remember being in the woods but don’t remember a tick bite. Get treatment.
  • You don’t remember either of the situations above (no woods, no bite, no Lyme), but you’re chronically exhausted, achy, brain foggy, and progressively non-functional.Get tested for Lyme.
  • If you test positive for Lyme, find a Lyme-literate physician in your area. If you test negative, chronic Lyme is unlikely.

Be patient, and know that you will very likely eventually get better.

Be well,
David Edelberg, MD

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7 comments on “With Summer’s Arrival, A Lyme Disease Refresher
  1. Ken Peh says:

    Deer ticks seem to be most discussed as a disease carrier with very little information a available for other tick species. Northern Michigan has seen a tick explosion in recent years. For my area, it seems to be the Dog Tick that is most prevalent. I’m concerned that unexplained aches or pains may be related to a bite from one of these or other similar ticks. Unfortunately, I’m unable to find much information or discussion about possible complications or infections from bites from these other local varieties.

    Does anyone know of possible viruses that may be carried by these ticks that could cause problems in humans?

  2. Denise Keefe says:

    Hi Ken, I wish I could locate the documentation for the things I have read on this but I cannot. I have read that the probability of Lyme and like infections being passed in several different ways exists. Mosquitos, other tick, fleas, even the possibility of sexual intercourse with someone who is infected exists. They have found the exact same species in both people who have been married for a long time. (There are dozens of different species which can wreak havoc on humans). Lyme has been so understudied and many are in denial that chronic Borrelia (sp?) (Lyme is a term that is used to cover many different species and is used inaccurately because each disease can affect the person differently). You should definitely be checked for Lyme. I suffered for years with different health issues, depression, fatigue, brain fog, nerve pain, joint pain and the last five years difficulty walking and am no longer able to work. I was just tested in March at the insistence of my caring chiropractor and tested positive. All this damage to my body because no one took it seriously. If you do get tested, do it through the Igenix Lab in Calif. You can order the test yourself but need to get it signed off by your health care provider. I had my chiro sign off on it. I am sorry if this is too much information. I just want people to get the right treatment and all the denial to stop. Good luck to you!

  3. Jenny says:

    What protocol do you base your treatment of chronic lyme off of? Horowitz? Buehner? How extensive is Dr. Kelley’s experience in treating chronic lyme and what is her success rate? Does she treat co-infections as much? Thank you so much!:)

  4. Sarah says:

    I was treated with doxycycline after an insect bite and bulls eye rash in 2014 with 1 month of doxycycline. I gradually developed other symptoms of chronic lyme. I had the Igenx test and it came out indeterminate. My alternative doctor did not know what to make of that. Then in March, my doctor heard about a long term lyme culture from Advanced Labs. After 16 weeks the culture grew Borrelia (lyme). I’m now being treated again. If your testing comes out negative or indeterminate, I would advise the lyme culture or the new ispot test that is offered by Pharmasean labs.

  5. Dr. Kelley says:

    Jenny –
    My practice is mostly Lyme patients. I take a Functional Medicine (functionalmedicine.org) approach to chronic Lyme (and co-infections) and approach each patient with a unique plan. I will use antibiotics, herbs, homeopathy – whatever the patient needs. We have a great team here at WholeHealth Chicago with Nutritionist/Herbalist/Acupuncturist Seanna Tully and Homeopath Sujatha – to name just two – who help create a well rounded team-approach to treatment.

  6. Denise Keefe says:

    Dr. Kelley, I will be seeing you in August. I am currently doing a herbal protocol using Buhner. Is that something that you can work with?

    I am seeing some progress with it.

  7. Dr. Kelley says:


    Absolutely! Stephen Buhner is brilliant! Very happy to work with that.

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