I am Dr. Lewis Coleman, a retired anesthesiologist and Chair of Science and Education at the American Institute of Stress in Weatherford, Texas.
You may recall receiving a copy of my book 50 Years Lost in Medical Advance: The Discovery of Hans Selye’s Stress Mechanism via Elizabeth and Dennis Kucinich.1 The book details my discovery of the Mammalian Stress Mechanism (MSM), which explains the common mechanisms of most disease.
From its discovery by the renowned Dr. Selye (1907-1982), Stress Theory has always promised to revolutionize medicine and surgery and introduce a new era of health, longevity, and freedom from the eternal curse of disease and premature death. Today we know that when the MSM is tested and confirmed, it will elevate medicine from an art based on experiment to a science founded on a theory that enables physicians to direct their treatments at the actual cause of disease.
It is my hope that the confirmation of stress theory will restore productive medical and biological research which deciphers the code that describes the “genetic blueprint” and discovers the mechanism that transmits this information from chromosomal DNA to the cell surface to enable embryological development. These achievements may reveal many of the secrets of evolution, with implications that promise to revolutionize our entire approach to medicine.
I am addressing this “open letter” to you because I believe that your important role in the Trump administration will provide a unique opportunity to test and confirm this landmark theory, actions which until now have been politically impossible. Animal and human trials are essential to confirm the ability of stress theory to optimize surgical outcome, provide a set of simple, safe, economical, efficient, and universal treatments that control and cure all forms of disease, promote productive pharmaceutical development, slash health care costs, and refute prevailing falsehoods, beginning with the “novel” coronavirus mRNA “immunizations” that are a worthless and willful form of malpractice.
These favorable circumstances may not last.
The COVID contagion has inadvertently yielded evidence that clarifies chronic illness and explains the white clots found by morticians in the small peripheral arteries of healthy young people who died suddenly after their receiving mRNA injections. I have previously published a paper explaining how the COVID mRNA injections attack blood vessels and release abnormal quantities of von Willebrand Factor and Tissue Factor into circulation, causing chaotic MSM hyperactivity that mimics nearly every known form of disease2 and cripples oxygen transport and delivery.3 This causes either sudden death or chronic cellular oxygen starvation and explains the crippling fatigue, mental fog, muscle weakness, and antibiotic resistant infections that characterize the “Long COVID Syndrome” (syndrome meaning “we don’t know”).
The white clots are surrounded by abnormal blood clots and bathed in amyloid protein. Amyloid protein, together with collagen sclerosis and fibrosis, is invariably found in the afflicted tissues of all chronic illnesses, including atherosclerosis, hypertension, diabetes, and “rheumatoid” diseases, all of which are presently regarded as mysteries. This evidence has enabled me to understand that amyloid protein is a monomer that polymerizes into collagen. This understanding explains the abnormal white clots, as well as the fibrosis, sclerosis, and amyloidosis that characterize “rheumatoid” diseases, which until now have remained inexplicable, and provides a testable explanation of how chronic exposure to pesticides, herbicides, automobile exhaust, chlorinated water, air pollution, and emotional adversity undermine health and longevity, and how it can be neutralized through treatment.
I propose that this revolutionary hypothesis be initially tested using animal models treated with intravenous radioactive fibrinogen to determine whether the radioactivity becomes incorporated into amyloid and collagen in extravascular tissues. The animal model can also be treated with intravenous Tissue Factor to see if this provokes amyloidosis and collagen formation in blood vessels. Human clinical studies too numerous to summarize here can then be used to test the ability of stress theory to cure disease.
All such studies must be conducted with strict oversight that eliminates manipulation by commercial interests. I am available to assist in planning, performing, and proctoring these endeavors. I can be reached on 559-740-3520. My email is lewis_coleman@yahoo.com and my website is www.stressmechanism.com
Respectfully,
Lewis S. Coleman, MD
Figure 1. Photo of Robert Kennedy Jr. reading my book (Courtesy Elizabeth Kucinich)
Figure 2 Abnormal collagen “white clots” are found in the small peripheral arteries of healthy young victims of COVID injections. Collagen is the most common protein in the body. It binds cells into tissues, structures, and organs. It is the substance of ligaments, tendons, sclerosis, and fibrosis. Bone consists of collagen, calcium, and carbon dioxide. Opportunity to Ask Questions of Embalmer Richard Hirschman and Data Analyst Tom Haviland
Figure 3. Fibrinogen is the source of fibrillar blood proteins. It is continuously produced by the liver and released into blood circulation. It cannot escape from blood into extravascular tissues due to its large size, and it has no direct effect on blood coagulation. It consists of three fibrillar submicroscopic amino acid chains called alpha, beta, and gamma that are held together by “disulfide bonds.” Thrombin dissolves the disulfide bonds and releases these tiny protein chains into blood circulation. Thus freed, they are called “soluble fibrin.”
In blood, the factor VIII enzyme adds “cross-links” of fibronectin, vitronectin, plasminogen, and gelsolin to soluble fibrin to form strands of “insoluble fibrin” that exaggerate microvascular flow resistance to regulate blood flow and organ function, inhibit blood turbulence, and bind blood cells together to form viscoelastic clots that regulate tissue repair.
The alpha, beta, and gamma subunits of soluble fibrin do not affect blood coagulability. They are so small that they can escape from blood into extravascular tissues, where enzyme factors VII and X convert them into collagen that enables tissue repair.
Soluble fibrin explains several disease manifestations when it is produced in excess. In eclampsia and other critical illnesses, it causes tissue edema that disrupts organs and damages tissues; it invades and bursts the liver;4 it forms “hyaline” casts in kidney glomeruli that disrupt renal function; it appears in urine as “albuminuria;” it collects in the lungs and disrupts gas exchange; and it promotes harmful amyloidosis, sclerosis, and fibrosis.
Figure 4. Image of a viscoelastic blood clot showing how strands of insoluble fibrin bind blood cells into a viscoelastic clot. In organ tissues, which are rich in autonomic innervation, sympathetic nervous activity releases von Willebrand Factor into blood, which activates factor VIII that adds “cross links” of fibronectin, vitronectin, plasminogen, and gelsolin to fibrillar soluble fibrin to produce monomers of insoluble fibrin. The monomers polymerize into strands of insoluble fibrin that can be visualized with a microscope. https://www.nih.gov/news-events/nih-research-matters/microgel-particles-boost-blood-clotting
Figure 5 This diagram illustrates how collagen consists of the alpha, beta, and gamma strands of soluble fibrin without cross-links. Collagen is much stronger than insoluble fibrin because it lacks cross links. https://commons.wikimedia.org/wiki/File:Collagentriplehelix.png
Thank you, Kevin and Dave, for this interesting interview.
When the book first came out, I read NOBODY DIED AT SANDY HOOK, and found it quite interesting and informative, even though it probably left me with more questions than answers.
Over the years I have read a few articles at the Infowars site, but have not followed Alex Jones very much. I seem to remember something about Alex using a bullhorn in a group of people, and that brings to mind something I heard on the radio on 11 September 2001: as the people in the second tower were evacuating from the upper floors after the first tower was apparently hit by an airplane, one man who was interviewed said that on the 43rd or 44th floor (wherever they had to change elevators to continue down), there was a man with a bullhorn telling them "Everything is all right. Return back to work." The man interviewed on the radio then asked "Who was that guy? And why was he doing that?" or words to that effect. I have never heard an answer to these questions over the past 23 years.
An Open Letter to Robert Kennedy, Jr.
Dear Mr. Kennedy,
I am Dr. Lewis Coleman, a retired anesthesiologist and Chair of Science and Education at the American Institute of Stress in Weatherford, Texas.
You may recall receiving a copy of my book 50 Years Lost in Medical Advance: The Discovery of Hans Selye’s Stress Mechanism via Elizabeth and Dennis Kucinich.1 The book details my discovery of the Mammalian Stress Mechanism (MSM), which explains the common mechanisms of most disease.
From its discovery by the renowned Dr. Selye (1907-1982), Stress Theory has always promised to revolutionize medicine and surgery and introduce a new era of health, longevity, and freedom from the eternal curse of disease and premature death. Today we know that when the MSM is tested and confirmed, it will elevate medicine from an art based on experiment to a science founded on a theory that enables physicians to direct their treatments at the actual cause of disease.
It is my hope that the confirmation of stress theory will restore productive medical and biological research which deciphers the code that describes the “genetic blueprint” and discovers the mechanism that transmits this information from chromosomal DNA to the cell surface to enable embryological development. These achievements may reveal many of the secrets of evolution, with implications that promise to revolutionize our entire approach to medicine.
I am addressing this “open letter” to you because I believe that your important role in the Trump administration will provide a unique opportunity to test and confirm this landmark theory, actions which until now have been politically impossible. Animal and human trials are essential to confirm the ability of stress theory to optimize surgical outcome, provide a set of simple, safe, economical, efficient, and universal treatments that control and cure all forms of disease, promote productive pharmaceutical development, slash health care costs, and refute prevailing falsehoods, beginning with the “novel” coronavirus mRNA “immunizations” that are a worthless and willful form of malpractice.
These favorable circumstances may not last.
The COVID contagion has inadvertently yielded evidence that clarifies chronic illness and explains the white clots found by morticians in the small peripheral arteries of healthy young people who died suddenly after their receiving mRNA injections. I have previously published a paper explaining how the COVID mRNA injections attack blood vessels and release abnormal quantities of von Willebrand Factor and Tissue Factor into circulation, causing chaotic MSM hyperactivity that mimics nearly every known form of disease2 and cripples oxygen transport and delivery.3 This causes either sudden death or chronic cellular oxygen starvation and explains the crippling fatigue, mental fog, muscle weakness, and antibiotic resistant infections that characterize the “Long COVID Syndrome” (syndrome meaning “we don’t know”).
The white clots are surrounded by abnormal blood clots and bathed in amyloid protein. Amyloid protein, together with collagen sclerosis and fibrosis, is invariably found in the afflicted tissues of all chronic illnesses, including atherosclerosis, hypertension, diabetes, and “rheumatoid” diseases, all of which are presently regarded as mysteries. This evidence has enabled me to understand that amyloid protein is a monomer that polymerizes into collagen. This understanding explains the abnormal white clots, as well as the fibrosis, sclerosis, and amyloidosis that characterize “rheumatoid” diseases, which until now have remained inexplicable, and provides a testable explanation of how chronic exposure to pesticides, herbicides, automobile exhaust, chlorinated water, air pollution, and emotional adversity undermine health and longevity, and how it can be neutralized through treatment.
I propose that this revolutionary hypothesis be initially tested using animal models treated with intravenous radioactive fibrinogen to determine whether the radioactivity becomes incorporated into amyloid and collagen in extravascular tissues. The animal model can also be treated with intravenous Tissue Factor to see if this provokes amyloidosis and collagen formation in blood vessels. Human clinical studies too numerous to summarize here can then be used to test the ability of stress theory to cure disease.
All such studies must be conducted with strict oversight that eliminates manipulation by commercial interests. I am available to assist in planning, performing, and proctoring these endeavors. I can be reached on 559-740-3520. My email is lewis_coleman@yahoo.com and my website is www.stressmechanism.com
Respectfully,
Lewis S. Coleman, MD
Figure 1. Photo of Robert Kennedy Jr. reading my book (Courtesy Elizabeth Kucinich)
Figure 2 Abnormal collagen “white clots” are found in the small peripheral arteries of healthy young victims of COVID injections. Collagen is the most common protein in the body. It binds cells into tissues, structures, and organs. It is the substance of ligaments, tendons, sclerosis, and fibrosis. Bone consists of collagen, calcium, and carbon dioxide. Opportunity to Ask Questions of Embalmer Richard Hirschman and Data Analyst Tom Haviland
laurakasner.substack.com Nov 04, 2024
Figure 3. Fibrinogen is the source of fibrillar blood proteins. It is continuously produced by the liver and released into blood circulation. It cannot escape from blood into extravascular tissues due to its large size, and it has no direct effect on blood coagulation. It consists of three fibrillar submicroscopic amino acid chains called alpha, beta, and gamma that are held together by “disulfide bonds.” Thrombin dissolves the disulfide bonds and releases these tiny protein chains into blood circulation. Thus freed, they are called “soluble fibrin.”
In blood, the factor VIII enzyme adds “cross-links” of fibronectin, vitronectin, plasminogen, and gelsolin to soluble fibrin to form strands of “insoluble fibrin” that exaggerate microvascular flow resistance to regulate blood flow and organ function, inhibit blood turbulence, and bind blood cells together to form viscoelastic clots that regulate tissue repair.
The alpha, beta, and gamma subunits of soluble fibrin do not affect blood coagulability. They are so small that they can escape from blood into extravascular tissues, where enzyme factors VII and X convert them into collagen that enables tissue repair.
Soluble fibrin explains several disease manifestations when it is produced in excess. In eclampsia and other critical illnesses, it causes tissue edema that disrupts organs and damages tissues; it invades and bursts the liver;4 it forms “hyaline” casts in kidney glomeruli that disrupt renal function; it appears in urine as “albuminuria;” it collects in the lungs and disrupts gas exchange; and it promotes harmful amyloidosis, sclerosis, and fibrosis.
https://www.researchgate.net/profile/Giovanni_Settanni/info Courtesy of Dr. Giovanni Setta
Figure 4. Image of a viscoelastic blood clot showing how strands of insoluble fibrin bind blood cells into a viscoelastic clot. In organ tissues, which are rich in autonomic innervation, sympathetic nervous activity releases von Willebrand Factor into blood, which activates factor VIII that adds “cross links” of fibronectin, vitronectin, plasminogen, and gelsolin to fibrillar soluble fibrin to produce monomers of insoluble fibrin. The monomers polymerize into strands of insoluble fibrin that can be visualized with a microscope. https://www.nih.gov/news-events/nih-research-matters/microgel-particles-boost-blood-clotting
Figure 5 This diagram illustrates how collagen consists of the alpha, beta, and gamma strands of soluble fibrin without cross-links. Collagen is much stronger than insoluble fibrin because it lacks cross links. https://commons.wikimedia.org/wiki/File:Collagentriplehelix.png
1 Coleman, L. S. 50 Years Lost in Medical Advance: The Discovery of Hans Selye’s Stress Mechanism. (The American Institute of Stress Press, 2021) https://www.amazon.com/Years-Lost-Medical-Advance-discovery/dp/0578822601/ref=sr_1_1?crid=3KZQIZDY7TNSO&keywords=lewis+coleman+hans+selye&qid=1638729267&sprefix=Lewis+Coleman%2Caps%2C448&sr=8-1.
2 Coleman, L. S. The Mammalian Stress Mechanism Explains COVID, Long COVID, and Sudden Death. Science Set Journal of Cardiology Research (2023). https://www.mkscienceset.com/articles_file/937-_article1692189623.pdf
3 Coleman, L. S. Oxygen Transport and Delivery, https://www.youtube.com/watch?v=efi9v86isSw&t=117s.
4 Rath, W., Faridi, A. & Dudenhausen, J. W. HELLP syndrome. J Perinat Med 28, 249-260 (2000). http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=11031696
Having David Ray Griffin and Alex Jones in the same sentence is a bit discombobulating.
But, I recognize the common theme.
For me, George Carlin’s work/words tied it all together, when he referenced the American Japanese.
Haven’t “the amendments” always been somewhat of a farce???
If you can legislate free expression, can’t you conversely legalize repression???
Isn’t speech just part of what it means to be living???
It seems like it’s getting like when a dog is “put down” when it just won’t stop barking.
Just expressing itself, cause its got something to say.
Some stupid people just can’t comprehend the language.
Like with those American Japanese???
Or Russians???
Or Iraqis???
Or Houthis???
Or Falastines???
I guess we’re all just animals to be put down, if we make the wrong sounds.
Scary shit, gentlemen.
Gonna/gotta go downtown, and make some noise, before the speech police come around.
How about???
PERMANENT CEASEFIRE NOW
The Truth will not make you free. The Bill of Rights appears to have been abolished.
The Zios have even gotten to RT, publishing articles about how the racist Dutch are tormenting the “innocent “ Maccabi footballers
By the time of the Holocaust,
whether real or imaginary,
most of the sixty six million
Christians exterminated by
the Soviet Judo-communists
were already dispatched in
ways most cruel imaginable.
What a great, great conversation. Please have Mr. Gahary back soon and often!
Thank you, Kevin and Dave, for this interesting interview.
When the book first came out, I read NOBODY DIED AT SANDY HOOK, and found it quite interesting and informative, even though it probably left me with more questions than answers.
Over the years I have read a few articles at the Infowars site, but have not followed Alex Jones very much. I seem to remember something about Alex using a bullhorn in a group of people, and that brings to mind something I heard on the radio on 11 September 2001: as the people in the second tower were evacuating from the upper floors after the first tower was apparently hit by an airplane, one man who was interviewed said that on the 43rd or 44th floor (wherever they had to change elevators to continue down), there was a man with a bullhorn telling them "Everything is all right. Return back to work." The man interviewed on the radio then asked "Who was that guy? And why was he doing that?" or words to that effect. I have never heard an answer to these questions over the past 23 years.
That is a very interesting point. Pray for Putin.