Archive for the ‘Treatment’ Category

The Three Bs – Borrelia, What, and What? Co-infections & Chronic Illness

https://www.lymedisease.org/the-three-bs-borrelia-what/

The three Bs – Borrelia, What, and What? Co-infections and chronic illness

By Nicole Bell, Galaxy Diagnostics CEO

3/10/25

While many people in the Lyme community are familiar with the three Bs – Borrelia, Bartonella, and Babesia – most people outside the community look confused when I mention these top flea and tick-borne pathogens. I understand their puzzled looks because back in 2017, I was confused too.

Even after my husband, Russ, was diagnosed with these three stealthy invaders, I focused all my research on Borrelia, the bacteria causing Lyme disease.

It ended up taking a tragic journey followed by years of studying the research to gain an appreciation for the complexities of all three pathogens – and that research is still unfolding.

In complex cases, co-infections are the rule, not the exception.

The first thing to understand when considering the three Bs, is that in complex cases, co-infections are common. In a survey of over 3,000 chronic Lyme disease patients published by LymeDisease.org, over 50% had co-infections, and 30% had two or more co-infections. Babesia and Bartonella top the co-infection list, each presenting in about 30% of chronic Lyme cases.

Source: About Lyme Disease Co-infections, LymeDisease.org

The second thing to understand about these pathogens is that calling them “Lyme co-infections” is misleading. All these pathogens – the other Bs and beyond – can be present without a Borrelia  infection (past or present).

The problem is that many doctors don’t have these invaders on their differential – and it’s easy for a pathogen to be considered rare if you never test for it. 

Rare disease? Or inadequate testing and data?

To understand the true prevalence of these pathogens, we need to dig into the details of each pathogen and how we count and test for them. For example, before 2013, Lyme incidence in the U.S. was estimated to be approximately 30,000 cases per year. Then, in 2013, the CDC looked at clinical records, laboratory reports, and public surveys and increased this estimate 10-fold.

In 2021, an analysis of insurance records increased the estimates again, and current data shows that approximately 500,000 Americans are diagnosed and treated annually. And since the standard of care test for Lyme leading to diagnosis and treatment is 40-60% accurate, even this number is likely underestimating the extent of the problem.

So, the question looms – what is the prevalence of the other two Bs? Are they destined for a similar exponential increase as we dig into the data? Emerging research points to yes.

Bartonella – The Hidden Pandemic

Bartonella is a genus of gram-negative bacteria that can infect humans and a wide range of animals. Googling the bacteria shows that it is the pathogen causing cat scratch disease or CSD, an acute form of the infection. But like Lyme, this pathogen has been associated with complex chronic conditions spanning multiple body systems, including the joints, eyes, heart, and brain.

Lyme disease has made people fearful of ticks, but Bartonella can be transmitted by a long list of biting insects – or vectors – including fleas, body lice, sand flies, and even spiders. Also, an underappreciated risk factor for bartonellosis is animal exposure, particularly exposure to cats, which are natural reservoirs of the bacteria.

In a study of veterinary workers, 44% were positive for Bartonella antibodies, and 28% had DNA of the pathogen detected directly from their blood. With approximately 66% of U.S. households owning at least one pet, the pathogen has the potential to be more widespread than generally thought.

Dr. Ed Breitschwerdt from North Carolina State University’s veterinary school has studied Bartonella since the 1990s. The advanced testing methods developed in his lab by collaborator Dr. Ricardo Maggi have uncovered key links between the pathogen and complex illnesses, such as arthritis, chronic fatigue, and fibromyalgia.

Neuropsychiatric conditions

Recently, using innovations in advanced PCR technology, the lab has made groundbreaking discoveries linking Bartonella and neuropsychiatric conditions, such as schizophrenia.

The investigation into schizophrenia started the way many discoveries in medicine do, with one case. A 14-year-old boy – who we will call Michael – suffered from sudden onset psychosis and received a formal diagnosis of schizophrenia. Michael was referred to Dr. B’s lab because he had marks on his skin, called striae, consistent with a Bartonella infection.

Dr. B and his team used their advanced test methods to confirm that Michael was infected with Bartonella. Upon treatment with the appropriate antibiotics, his symptoms evaporated.

The case inspired Dr. Breitschwerdt to consider a hypothesis – what if other patients were experiencing psychosis because of a Bartonella infection? Bartonella can cross the blood-brain barrier and infect endothelial cells, contributing to neuroinflammation.

The hypothesis had merit. His lab partnered with the University of North Carolina to test 17 schizophrenia patients. Sixty-five percent of those patients tested PCR positive for the pathogen, compared to 8% in healthy controls.

A subsequent study with Columbia University on over 100 patients found that people affected with psychosis were over three times more likely to have direct evidence of Bartonella in their blood than unaffected controls.

PANS

And schizophrenia isn’t the only neuropsychiatric condition linked to the pathogen. Pediatric patients with Bartonella infections have been reported to develop Pediatric Acute-onset Neuropsychiatric Syndrome (PANS) and symptoms like anxiety, obsessive-compulsive disorder, and cognitive dysfunction. Case studies have shown improvement in neuropsychiatric symptoms following treatment of the underlying infections.

With over 3 million Americans battling schizophrenia and 1 in 200 children in the U.S. affected by PANS, Bartonella may emerge as the great hidden pandemic.

Babesia – the tip of the iceberg

Babesia is a tick-borne parasitic infection, often touted as similar to malaria, because both parasites infect and replicate within red blood cells and can cause fever, chills, sweats, headache, muscle aches, fatigue, and hemolytic anemia.

Researching Babesia on the CDC Website shows that under 2000 cases were reported nationwide in 2020. The CDC notes that most Babesia cases in the U.S. are caused by Babesia microti, with occasional cases caused by other Babesia species.

Using the same advanced PCR technology that drove clinical discovery in Bartonella, Dr. B and his team turned their attention to Babesia. They found that what we “know” about Babesia may only be the tip of the iceberg.

In 82 individuals the lab was studying for Bartonella infection, 22 (27%) were also infected with Babesia. Furthermore, the top Babesia species identified was not Babesia microti, as expected from CDC data, but rather Babesia divergens (considered rare in the U.S.) and then Babesia odocoilei (considered rare in humans).

Before Dr. B’s work, only a handful of case reports in the U.S. have ever been reported for Babesia divergens. Their best-in-class assay turned up 12 new cases in a group that wasn’t even targeted for Babesia studies.

Dr. B’s team also recently published a paper where an entire family – all five members and one of their dogs – tested positive for a Babesia-divergens-like species. Similar new case discoveries have been made for Babesia odocoilei. His work poses the question – are the pathogens really rare, or are we just not testing for them properly?

Genus versus species – why it matters

Genus and species are terms commonly used by microbiologists, but when I first entered the world of tick-borne disease, I didn’t fully understand their significance. The “genus” is akin to a family name, grouping related individuals – think Hatfields and McCoys. The “species” is like the first name, identifying a specific individual in the family.

Translating this to Lyme disease, Borrelia is the genus or family name, and Borrelia burgdorferi is the species name identifying the particular pathogen.

So why does it matter? The current commercial test methods for all three Bs generally use serology or antibody testing. These assays measure antibodies created by the host’s immune response to the pathogen. The problem is that antibodies react to proteins on the surface of the pathogen, and these proteins can vary depending on the particular species.

In other words, the patriarch of the Hatfield family, Anderson Hatfield, looked and dressed differently than his son Cap Hatfield. Thus, sending out a warrant and a picture of Anderson is unlikely to lead to Cap’s arrest.

Antibody testing is similar, and testing for Babesia microti, may not accurately diagnose a case of Babesia odocoilei or Babesia divergens. There are over 100 known Babesia species, with 15 of those confirmed in human cases.

There are over 50 species of Bartonella, at least 20 of which have been documented to infect humans and other mammalian hosts. Dr. B’s research and testing technology is redefining what we know about these pathogens. And until these tests are launched commercially, millions have the potential to be misdiagnosed.

Direct Detection for BBB is Launching at Galaxy Diagnostics

Fortunately, Galaxy Diagnostics was founded by Dr. Breitschwerdt, Dr. Maggi, and Dr. Amanda Elam to bring these diagnostic advancements to market. This month, Galaxy is launching its digital PCR, direct detection assay for BBB.

This assay has been instrumental in driving clinical discovery in Dr. B’s lab and will now be commercially available to practitioners. Top features of the assay include:

  • Genus level detection, detecting each pathogen regardless of species.
  • Ultra-sensitive, digital PCR, which increases detectability for low abundance pathogens.
  • Multiplexed detection to provide three results in a single test.

The BBB assay is a blood-based assay that detects the DNA of each pathogen. The approach has previously been used only in a research setting, but the team at Galaxy has now validated the assay for commercial use.

Bartonella and Babesia – but what about Borrelia?

The BBB assay is a blood-based approach, and it is essential to note that blood is NOT the best matrix for Lyme Borrelia, as I have discussed previously.

Galaxy recommends its urine antigen test for Lyme since the concentrations of Lyme Borrelia are so low in the blood that a blood draw is unlikely to capture the pathogen in the test tube. And no matter how sensitive the technique is, if the pathogen isn’t in the tube, there is no way to detect it.

So then, why is Borrelia included in the BBB assay? The answer goes back to the genus versus species issue. While the species associated with Lyme Borrelia often hide in tissues and don’t free-circulate in high copy numbers in blood, the species associated with Relapsing Fever Borrelia do replicate to high numbers in the blood.

As a result, combining the BBB assay with Galaxy’s Nanotrap urine antigen test for Lyme provides optimal coverage for the top flea and tick-borne infections at the genus level.

Coming Full Circle – Avoiding Cases like Russ

After my husband Russ passed, the engineer in me knew there had to be better options. I immersed myself in the research and found Dr. B’s published peer-reviewed results. I introduced myself to the Galaxy team, and as I dug in, I became even more convinced that their technology would provide the clarity I craved as a caregiver.

In June 2024, I became Galaxy’s CEO to bring these advanced testing techniques to a broader market. We crystallized our mission to provide a new standard of care for diagnosing these devastating flea and tick-borne diseases. With the commercial launch of the BBB assay, we are one step closer to that goal. I know that Russ is watching – and smiling.

Nicole Bell, CEO of Galaxy Diagnostics, is also the author of What Lurks in the Woods and The State of Lyme Disease Research

For more:

Society Reaches ‘Peak Insanity’: Trillions Invested in mRNA ‘Vaccines’ & Therapies

https://jamesroguski.substack.com/p/mrna-products-in-the-development?

mRNA Products in the Development Pipeline

Trillions of dollars are being invested in developing hundreds of mRNA “vaccines” and other mRNA-based “therapies.” Our society has reached “Peak Insanity.”

 
 

Moderna CEO Wants mRNA Factory on Every Continent

Moderna has dozens of mRNA “vaccines,” and cancer therapies, in their development pipeline:

Moderna’s dozens of mRNA ‘vaccines’ in development:
  1. mRNA-1010 (Flu) CLINICAL TRIAL NCT05606965

  2. mRNA-1011 (Flu) CLINICAL TRIAL NCT05827068

  3. mRNA-1012 (Flu) CLINICAL TRIAL NCT05827068

  4. mRNA-1018 (Pandemic Flu) CLINICAL TRIAL NCT05972174

  5. mRNA-1020 (Flu) CLINICAL TRIAL NCT05333289

  6. mRNA-1030 (Flu) CLINICAL TRIAL NCT05333289

  7. mRNA-1045 (Flu + RSV vaccine) CLINICAL TRIAL NCT05585632

  8. MRNA-1073 (COVID + FLU) CLINICAL TRIAL NCT05375838

  9. mRNA-1083 (Flu + COVID vaccine) CLINICAL TRIAL NCT06694389

  10. mRNA-1189 (EBV vaccine to prevent infectious mononucleosis) CLINICAL TRIAL NCT05164094

  11. mRNA 1195 (EBV vaccine to address EBV sequelae) CLINICAL TRIAL NCT05831111

  12. mRNA-1215 (Nipah vaccine) CLINICAL TRIAL NCT05398796

  13. mRNA-1230 (Flu + COVID + RSV vaccine) CLINICAL TRIAL NCT05585632

  14. mRNA-1273 (COVID-19 vaccine Spikevax®)

  15. mRNA-1273.815 (COVID-19 vaccine adolescents)

(See link for article)

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**Comment**

Similarly to ‘climate change,’ the world is clamoring for more mRNA – mostly due to greed.  There’s a lot of money to be made if you go with the flow, repeat the narrative, and only find what ‘the powers that be’ want you to find.  This has been going on in Lymeland for over 40 years and continues to this day.  It doesn’t matter how many reports of ineffectivenessfraud, corruption, danger, and bias come out against ‘climate change,’ or how many reports reveal the dangers of mRNA products. The band plays on….

This should tell you everything you need to know.

For more:

Metabolic Therapies: Reclaiming Cancer’s Achilles’ Heel Through The Ivermectin, Fenben, and Allulose Revolution

https://www.2ndsmartestguyintheworld.com/p/metabolic-therapies-reclaiming-cancers?

Metabolic Therapies: Reclaiming Cancer’s Achilles’ Heel Through The Ivermectin, Fenbendazole, and Allulose Revolution

WEEKEND FLASH SALE TARGETING CANCER’S METABOLIC CORE STARTS NOW!

The Warburg effect — Otto Warburg’s seminal observation that cancer cells preferentially ferment glucose into lactate even in oxygen-rich conditions — represents a metabolic vulnerability ripe as the perfect therapeutic target for cancer treatment.

Yet, a century after its elucidation, oncology remains tethered to genetic paradigms, sidelining metabolic strategies in favor of cytotoxic and targeted interventions that work at best on about 15% of cancers, representing an abysmal “treatment” model.

Early anecdotal findings of thousands upon thousands of patients show that administering a synergistic combination therapy of repurposed miracle drugs across a large variety of cancers is efficacious in about 80%+ of patients, representing the all-elusive until now ‘holy grail’ cancer cure.

This willful neglect of the cure in plain sight, rooted in Rockefeller Eugenics, allopathic BigPharma, and industrial influences traceable to the early 20th century, has perpetuated a cancer “care” model that prioritizes profit over lives that is designed to relieve patients of the maximum amount of money en route to torturous iatrogenic outcomes, and/or being sent home to die.

Emerging metabolic therapies, including repurposed drugs like Ivermectin (IVM) and Fenbendazole  (FBZ), alongside the rare sugar allulose, challenge this orthodoxy by directly targeting the glycolytic dependency of malignant cells. (Cancer cells are sugar dependent, whereas healthy cells use mostly oxygen to convert to energy stores.)

This highlights the Ivermectin Fenbendazole Allulose revolution sweeping the planet, with recent supply chain strains of IVM and FBZ from India with huge increases in Worldwide demand.

Hundreds of thousands of late stage cancer prognoses are being declared full remission as borders across the world are doing there level best to seize IVM and FBZ on behalf of the corrupt governmental agencies that are bought and paid for by BigPharma and their Deep State partners-in-crime.

We will now explore the mechanisms underlying these agents (IvermectinFenbendazole and Allulose) with Warburg’s insights, and their broader implications for cancer, type 2 diabetes, and obesity—conditions united by metabolic dysregulation.  (See link for article)

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For more:

Treating Bartonella: Medical Detective Pts 1-5

https://medicaldetective.substack.com/p/bartonella-the-second-great-imitator

Bartonella: The Second “Great Imitator” Underlying Many Chronic Illnesses – Part 1 of 5

Bartonella is the third “B” of the triad found in the vast majority of my chronically ill patients who suffer from chronic Lyme disease/PTLDS, along with Borrelia and Babesia.A gram-negative intracellular bacteria, it’s controversial and misunderstood and has been throwing a monkey wrench into my treatments for decades. I barely remember learning about it in medical school, except when they were teaching me about cat scratch fever in children that would cause small, localized rashes (papules) at the site of the scratch with swollen lymph nodes and fevers. It would be treated with a short course of antibiotics like azithromycin. These images show classical cat scratch disease before and after treatment when the lesions are starting to crust up.  (See link for article)

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https://medicaldetective.substack.com/p/bartonella-establishing-the-diagnosis

Bartonella: Establishing the Diagnosis, and the Role of Multiple Bartonella Species and MSIDS Factors in Chronic Illness – Part 2 of 5

 
In Bartonella Parts 1, 2, and 3, you learned the basics of Bartonella testing, symptoms, and treatment options, with a detailed discussion of laboratory work needed before starting the protocol, and how/why the medication and support supplements are being used to increase the tolerability and safety of DDDCT and HDDCT. Please review this information with your doctor before proceeding with the antibiotic protocol listed below.  (See link for article)
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https://medicaldetective.substack.com/p/treating-bartonella-2-week-pulses

Treating Bartonella: 2-Week Pulses of Antibiotics for Chronic Bartonellosis – Part 5 of 5

 
Bravo! You’ve made it to Part 5, the final Medical Detective Substack on diagnosing and treating chronic Bartonella infections. As you read in the previous 4 Substacks, Bartonella is often found in my chronic Lyme patients, at least 80% of the time, right behind active Babesia infections–watch for unexplained fevers, day/night sweats, chills, flushing, “air hunger,” and an unexplained cough if you have ongoing Babesia. (See link for article)
 
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For more:
 

Metagenomics Reveal Bartonella in the Shadow of Long COVID

UPDATE:

http://

Full Measure with Sharyl Attkisson

March 3, 2025

Harvard trained pathologist, Dr. Cole, was among the first to note mysterious blood clots in deceased people who’d been ‘vaccinated’ with the COVID gene therapy.

American virologist Dr. Robert R. Redfield, who served as the director of the CDC during the ‘pandemic,’ has admitted that reports of ‘so-called Long Covid’ are actually a cover-up for global surges of “mRNA vaccine injury.”

https://pubmed.ncbi.nlm.nih.gov/38472519/#:

Unmasking Bartonella henselae infection in the shadows of long COVID thanks to clinical metagenomics

Abstract

The diagnosis of long COVID often relies on symptoms post-COVID-19, occasionally lacking biological evidence. This case study illustrates how investigating long COVID uncovered an underlying bartonellosis through clinical metagenomics. Following mild COVID-19, a 26-year-old woman experienced persistent symptoms during 5 months, including axillary adenopathy. Pathological examination, 16 S rRNA PCR, and clinical metagenomic analysis were done on an adenopathy biopsy. The latter revealed Bartonella henselae DNA and RNA. Treatment with clarithromycin improved symptoms. This case underscores the relevance of clinical metagenomics in diagnosing hidden infections. Post-COVID symptoms warrant thorough investigation, and bartonellosis should be considered in polyadenopathy cases, regardless of a recent history of cat or flea exposures.

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**Comment**

Axillary adenopathy, or swollen lymph nodes under the armpit, are common with Bartonella – but also with other things as well.  It’s the body’s response for a foreign invader.  

For those that read information on this website know – ‘long COVID’ has been linked to the COVID gene therapy injection, as well as mask wearing, but mainstream media and research are not even considering them. Another little factoid is the fact is that another recent study admonishes against using the term Long COVID as the symptoms are no worse than those after the flu. In fact, PCR testing can’t distinguish between COVID and the flu. So, what in fact is causing lingering symptoms in some people and how severe are they actually?  

Sadly, this abstract doesn’t inform us as to the ‘vaccination’ and mask status of the patient.  A review of masks show contaminants that are carcinogenic and infectious as well the fact masks make people sick.

ALL research from here on out needs to identify the patient’s ‘vaccination’ status, how many injections they’ve received, as well as if they are mask wearers.

Hopefully, people are becoming aware that ‘vaccines’ serve as triggers to upset the immune system, which can allow hidden infections to suddenly give noticeable symptoms.

Another important point is the choice of clarithromycin for Bartonella treatment.  While this is partly a good choice, any experienced Lyme literate doctor would know to pair this with rifampin.  Antibiotic resistance can and does happen so treatment should do all to avoid this possibility, and using at least two antibiotics simultaneously is one such method, and unfortunately, even then, relapses often occur.