Do I Have Babesia? – A Co-infection of Lyme Disease

Do I Have Babesia? – A Co-infection of Lyme Disease

A Common Emerging Stealth Infection by Dr. James Schaller

Below are examples of signs, symptoms and indirect ways to help increase the diagnosis of Babesia. An examination of public genetic databases shows well over thirty-five species exist, many of which have variants.

Please note that an unknown percentage of people infected have no symptoms, at least for many years.

This checklist is not meant to be used as a definitive tool to diagnose Babesia. I would suggest no definitive 100% or even 98% sensitive tool exists.

My goal is merely to decrease illness resulting from false negative patients, i.e., people who are positive but do not show up positive on a basic direct test.

Indeed, it is not uncommon for a patient with Babesia to present with a negative test result over ten times, regardless of the lab, and then to show up positive on DNA testing when exposed to two or three protozoa treatments for three days, or to have positive antibody testing six weeks after a similar provocation trial.

I do not oppose or endorse such approaches, but feel it necessary to mention that this has happened with “malaria” prevention treatment. Additionally, there have been instances in which the use of herbs, such as artesunate, for cancer prevention, has resulted in an unintended outcome: the conversion of a Babesia titer from negative to positive.

The path to expertise with Babesia is not simply to read a summary article or guidebook (of which I have authored four on the topic of Babesia). Nor is expertise acquired by viewing the sickest 1% of patients as the “norm” in Babesia diagnosis.

If someone seeks expert knowledge of the infection, it begins by reading the entire world Pub Med literature over a few years, then utilizing that knowledge by focusing on treating this infection for over five years.

In summary, how can any certain Babesia position exist, when new species that infect humans are routinely emerging, and for which there is not even a direct test—regardless of sensitivity?


You react to any derivative of Artemisia (Sweet Wormwood). *Note: the reaction does not need to last more than a day and any immediate the use of DEET or without very high personality regression right after use.

You have two tick or flea infections with two positive tick or flea borne viruses, bacteria or protozoa. The presence of other infections such as tick borne viruses or bacteria raises suspicion of a Babesia infection.

Your clinician understands the use of indirect testing and feels your lab pattern is suggestive of the presence of Babesia. This involves more than an ECP spike.

Since direct testing for Babesia by any lab misses many human species and is of variable reliability, and the common presence of Bartonella suppresses some antibody tests, a positive or “indeterminate” is likely a positive. Have you had an “indeterminate” or “borderline” Babesia result?

You have neighbors living near you with a tick or flea infection diagnosis.

Your pet(s) or family animals of any type, e.g., horses, have had outdoor exposures to areas such as brush, wild grasses, wild streams or woods. If the pets were animals such as dogs, which can be given anti-tick and flea treatments, were these animals always on schedule while a 2-3 minute exam of large white blood cells may be fully sufficient to identify cancers and other diseases, a search for over eighty Babesia red blood cell presentations under 1000x, as found in my Hematology Forms of Babesia Book, requires at least thirty minutes, which requires private contracting with a microbiologist or pathologist or a favor from a lab director. Please appreciate that stains help define whether a substance is what it appears to be.

Babesia is an emerging infection. Any certainty claims or criticism about Babesia positions without reading at least parts of 1,500 articles is a premature certainty. Again, new Babesia species are emerging every one to four months. Indeed, even a new protozoan has been found that looks like Babesia under a high powered microscope. But when it is genetically sequenced it is not Babesia or immature malaria, which can look similar. It is a new infection.

Therefore, since this is a new emerging illness, this scale is meant to merely increase awareness of Babesia, an infection that can kill patients of any age. Writings in the past fifteen years have either seen Babesia as a mere “co-infection” or a footnote of a spirochete infection [Lyme]. Anything that can hide for a couple of decades, and then possibly kill you with a clot or by other means, is not a casual infection.

Babesia cure claims should be made with the use of indirect testing birthed from extracts of superior journals read over five years. Currently, these many indirect well-established lab test patterns are not used or understood by immensely busy and smart clinicians working full-time. While this is fully understandable, I hope it may change in the coming decade.

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