Investigating connections between Lyme disease and dementia
Thomas Grier, Lyme disease researcher
By Thomas Grier

Recently, the National Institute on Aging, as part of the National Institutes of Health (NIH), approved the acceptance of research to study the role of microbes in causing dementia.

This announcement came right on the heels of a recent UK study detecting bacteria in the brains of Alzheimer’s patients.

This announcement was also the first step in allowing the NIH and Centers for Disease Control (CDC) to grant research money to study the role of diseases like Lyme disease and tick-borne relapsing fever in facilitating the process and progression of various dementias, including Lewy body dementia and Alzheimer’s dementia.

Recommending specific efforts to look for Lyme bacteria in Alzheimer’s brains was a very important first step.

Lyme and Alzheimer’s
As hard as it is to believe, for all the money that has been spent on Alzheimer’s dementia, not one taxpayer dollar has been spent on a multi-center human-brain study to investigate the role that Borrelia and other bacteria play in the process of Alzheimer’s disease progression.

This is despite decades of independent scientists requesting brain autopsies to detect Borrelia burgdorferi (Lyme disease) and other Borrelia species.

Independent researchers such as Dr. Alan MacDonald (retired pathologist), Dr. Judith Miklossy (neuropathologist), Dr. Paul Duray (deceased pathologist), and myself, have spent our own time and money for 20-plus years to do brain autopsies and to stain for pathogens.

We also have spent time and effort to study spinal fluids of patients with multiple sclerosis.

Our work is posted on the F1000 Research website, and also on many Lyme disease forums and Lyme disease websites. You will also find our lectures on YouTube. There are many Facebook pages posting our pathology photos. I spoke three times on Coast to Coast radio about the irrational controversies about Lyme disease that stem from a serology-based perspective rather than a pathology-based perspective.

Since this topic is controversial and there are contrary opinions among major medical institutions, Lyme pathology research has become political. Publication in American medical journals is nearly impossible. (Here is a link to our early work.)

All of us involved in this kind of research are confident that after 25-plus years of plodding along without funding, our work and our findings will finally be corroborated. Finding Lyme disease in the brains of Alzheimer’s patients is and always has been low-hanging fruit just waiting to be picked.

New lab techniques can help
The advantage we have in 2019 is that DNA FISH (fluorescence in situ hybridization) stains that we now use are 99.99% specific and give us fluorescent images of the spiral bacteria in the thin sections of Alzheimer’s patients’ brains. In other words, we both see and identify the pathogen in the brain sections simultaneously with 99.99% accuracy.

Our work disagrees with the serology-based perspective of neurologic Lyme disease. But we feel pathology is a better gold standard in medicine. Unfortunately, there are many financial conflicts of interest associated with commercial Lyme disease tests and the scientists and doctors promoting them.

I believe Lyme disease research that is entirely based on Lyme disease blood tests using 40-year-old technology simply cannot detect Lyme disease or Borrelia miyamotoi relapsing fever in living patients.

These infections are behind the blood brain barrier and inside human neurons. Borrelia biofilms are commonly and routinely seen as embedded aggregates inside amyloid plaques that are seen in Alzheimer’s brains that we have studied. (We studied 112 brains from the bank at Harvard University.)

In my opinion, the public must embrace and support this kind of medical study. Using state-of-the-art tools like confocal laser microscopes, force-atomic microscopes, and FISH stains, we can get better answers that just five years ago were beyond our grasp. This work needs to be done and needs to be well-funded.

Our small group of pathologists have already done the work. What we need and what we are asking for is corroboration by major medical authorities. We have begged for CDC funding to support a multi-center brain-autopsy study for 25 years.

Thomas Grier of Duluth, a Lyme disease researcher, studied at the University of Minnesota Duluth Medical School. A chronic Lyme disease patient, he has run the Duluth/Superior Lyme Disease Support Group since 1994.

Thomas Grier lecture
What: Public talk, with questions, on multi-center brain-autopsy study with Lyme disease researcher Thomas Grier

When: 6 p.m. Thursday, April 11

Where: Superior Public Library, 1530 Tower Ave, Superior, Wisconsin

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TOUCHED BY LYME: Baseball’s Tom Seaver diagnosed with dementia
Lyme Disease: A Bioethical Morass
TOUCHED BY LYME: Keeping records for those who have died
Tags : Lyme disease and dementia, Thomas Grier

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Dear RM Agents and Readers,

They need to be checking everyone for Spirochetes in their brain once they pass and figure out how to know before they do.

Many Blessings,
CrystalRiver