Revolution Television

Revolution Television



horowitz recovering

(; August 18, 2021)–World-leading vaccine critic and whistleblower, Dr. Leonard G. Horowitz, was hospitalized on August 6, 2021 for pneumonia and multiple microbial mutations prompted by the “shedding” of the Pfizer/Moderna/DARPA ‘synthetic’ antigen, according to government records filed by the doctor in the U.S. Federal Court of Middle District, Florida on August 18, 2021. The resulting pneumonia and asthma-like symptoms (leading to Acute Respiratory Distress Syndrome) brought the doctor to the emergency room of the Lee County Hospital.


Dr. Horowitz had first recovered in October, 2020 from the presumed “COVID-19” infection prompting ‘natural immunity’ to the ‘synthetic antigen’ commonly misrepresented as “COVID.” The doctor’s initial exposure, sensitization, and immune response (akin to a hyper-sensitization reaction) was like an allergic reaction to foreign protein antigens, like pollen, causing respiratory symptoms like asthma and hay fever. In this case, however, the “spike protein antigen/immunogen” was the “dual-use” (i.e., military/commercial) “gain-of-function” bioweapon wrecking havoc on the world, Dr. Horowitz informed the Court as follows:


Chief among Plaintiff’s claims of deceptive safety advertising is the now well-evidenced fact that the PFIZER/MODERNA/DARPA “NOVEL” SPIKE-PROTEIN ANTIGEN IS THE “DUAL USE” SYNTHETIC “GAIN-OF-FUNCTION” BIOWEAPON WRECKING HAVOC ON THE WORLD UNDER THE BRAND CALLED “COVID”.


Dr. Horowitz’s pneumonia and resurgence of respiratory symptoms prompting hospitalization followed his exposure by vaccinated healthcare professionals with whom he repeatedly came into contact. Prophetically predicting these kinds of antigen ‘shedding’ and spreading risks to himself and society, the doctor had been begging the Court for “Injunctive Relief” to stop the FDA’s approval of the Pfizer and Moderna “un-safe” ‘antigen-spreading’ mRNA vaccines since fling the Horowitz v. Pfizer et. al. Complaint in early 2020. (1)


Only uncompromised justice can secure the circumstances; the health, safety, and society, in which Plaintiff’s claims arise and are increasingly being justified by the growing illnesses reported—eventually leaving every human susceptible to damage and dying prematurely, proximal to the torts and crimes reported here begging adjudication on the merits.


To read a complete copy of Dr. Horowitz’s federal filing, including the irrefutable evidence for the above statements of fact, CLICK HERE, or
To listen to Part II of the John Moore interview on Dr. Horowitz’s recovery, click the player below.
Horowitz Recovering



ANALYSIS PART I: COVID-antigen poisoned people (i.e., ‘sensitized’ or ‘hyper-sensitized’ victims) suffer difficult breathing. This is most often neglected, misdiagnosed, and blamed generically on “COVID” or “ARDS” (i.e., Acute Respiratory Distress Syndreome) for financial-benefits to corporate caregivers. This is what happened to me in Lee County Hospital in early August, 2021.


Scrutinizing the pathogenesis of this illness for accurate diagnosis and effective treatments (whether preventative or remedial) begins with understanding why breathing would suddenly become so difficult for those exposed to this “novel” antigen.(2) In other words, why would “pulmonary ventilation” suddenly become labored instead of easy as usual?


According to a leading study of this ARDS illness, “diffuse alveolar damage, thromboembolism, and nonspecific shock injury in multiple organs were the main findings.” Pathologic findings from autopsies and biopsies suggest “a unifying pathogenic mechanism for COVID-19” is the ARDS “characteristic inflammatory response, cytokine release, fever, inflammation, and generalized endothelial [i.e., inner blood vessel cell lining] disturbance.


A Yale article details more as follows:

“The term ‘acute’ appears in the name of ARDS, because the condition arises from a recent injury to the lungs.  It is characterized by the accumulation of fluid in the lungs and below-normal levels of oxygen in the blood (the medical term for this is hypoxemia).

While a variety of medical conditions may lead to ARDS, at a microscopic level they all result in damage to air sacs in the lungs (called alveoli) and the tiny neighboring blood vessels (called capillaries).

The average person has close to 500 million alveoli in their lungs, each of which is responsible for performing two critical tasks—transporting oxygen into the blood in the capillaries and removing carbon dioxide from the blood. (All of our tissues and organs need a constant supply of oxygen-rich blood to stay healthy.)

Damage to the alveoli and neighboring capillaries reduces the ability of the lungs to send oxygen into the blood. This happens because the lung injury causes fluid to leak into the spaces between the capillaries and the alveoli. Pressure on the alveoli increases, and eventually fluid gets in there, too. This is what gives ARDS its characteristic trait—accumulation of fluid in the lungs, causing the alveoli to collapse. This leads to a series of cascading problems, each further decreasing the lungs’ capacity to move oxygen into the blood, directly impacting the body’s tissues and organs.

What’s more, ARDS also triggers an immune response. The injury causes a release of cytokines—a type of inflammatory protein—which then bring neutrophils, a type of white blood cell, to the lung. But problems arise when some of these proteins and cells leak into nearby blood vessels and, via the circulatory system, are sent throughout the body, causing inflammation in other organs. This inflammation, in combination with low levels of blood oxygen, can lead to such problems as organ failure and sometimes multiple organ failure. . . .

ARDS is a serious condition. Even with treatment, about 25% to 40% of people with ARDS do not survive.

In general, people with ARDS caused by direct lung injury have worse outcomes than those with indirect causes of lung injury. Other issues that can have a negative effect on outcome include advanced age and certain chronic medical conditions, including liver disease, cirrhosis, alcohol abuse, and long-term immunosuppression.

While the mortality rate for ARDS is significant, recent advances in treatment have significantly increased the chances of survival and recovery. Patients who survive ARDS typically require some form of physical therapy to rebuild muscle tone. Most people who survive ARDS go on to recover their normal or close to normal lung function within six months to a year. [Emphasis added.]

Others may not do as well, particularly if their illness was caused by severe lung damage or their treatment entailed long-term use of a ventilator. [Emphasis added.] Their reduced lung function may affect daily routine and activities, or it may only occur during strenuous activity, for instance, while exercising.


Pulmonary ventilation is dependent on three types of pressure: atmospheric, intra-alveolar, and interpleural.”  Rule out number one: atmospheric pressure, because this affects everyone.


Intra-alveolar and interpleural pressures should be considered important here because ‘something’ (namely the foreign protein antigen (2) is impacting normalcy and the inflow and outflow of oxygen to these cells and tissues.


“[B[reathing is also dependent upon the contraction and relaxation of muscle fibers of both the diaphragm and thorax.”


With breathing “also dependent upon the contraction and relaxation of muscle fibers of both the diaphragm and thorax,” as well as the smooth muscles in the blood vessels constricting blood flow and oxygen delivery to and through the alveoli and beyond due to cell-mediated immunity and histamine release, the normalcy versus pathology of all of these muscle fibers in the lung, the diaphragm, and thorax is important to consider in treating this asthma-like disease.


Dr. Cameron Kyle-Sidell’s Early Warning

Very early in the “COVID-19 pandemic,” New York Doctor, Cameron Kyle-Sidell, characterized the illness as “Oxygen Deprivation Syndrome” neglected by experts. Dr. Horowitz published this telling video on RevolutionTelevisionnet as shown below.


Dr. Sidell warned the medical establishment: “In treating these patients I’ve witnessed medical phenomenon that just don’t make sense in the context of treating a disease that is supposed to be a ‘viral pneumonia’. ‘Acute Respiratory Distress Syndrome’ (ARDS) is the paradigm every hospital in the country is working under. . . that is untrue. In short, I believe that we are treating the wrong disease. And I fear that this misguided treatment will lead to a tremendous amount of harm to a great number of people in a very short time. . . .”

Alternatively, Dr. Sidell considered “that some kind of viral-induced disease most resembling ‘high altitude sickness’ [is being overlooked and neglected]. These patients are slowly being deprived of oxygen. I have seen patients depending on oxygen take off their oxygen [masks] and quickly progress into a state of anxiety and emotional distress, and eventually get blue in the face. And while they look like patients absolutely on the brink of death, they do not look like patients dying of pneumonia. . . .”

“I fear that if we are using a ‘false paradigm’ to treat a new disease; that the method that we program the ventilator—one based on the notion of ‘respiratory failure’ rather than ‘oxygen failure’ . . . is actually doing more harm than good. . . . [This] challenges long-held dogmatic beliefs within the medical community and lung specialists which will not be easy to overcome. But I really believe they must be overcome [to prevent unnecessary morbidity and mortality].”

Common Observations, Omissions, Misrepresentations, and Medical Malpractices

According to the grossly dis-informative Mayo Clinic, “Asthma is a condition in which your airways narrow and swell and may produce extra mucus. This can make breathing difficult and trigger coughing, a whistling sound (wheezing) when you breathe out and shortness of breath.”

These signs and symptoms of ‘asthmatic attack’ are virtually identical to those reported by Dr. Sidell, et. al., before COVID became an industry.

“For some people, asthma . . . can be a major problem that interferes with daily activities and may lead to a life-threatening asthma attack. . . . Asthma can’t be cured, but its symptoms can be controlled. . . .” Mayo lies. and subsequently misses and omits the entire medical menace:

“The same substances that trigger your hay fever (allergic rhinitis) symptoms, such as pollen, dust mites and pet dander, may also cause asthma signs and symptoms,” Mayo admits with bold emphasis added.

Mayo’s propaganda, here referencing James T C Li, M.D., Ph.D., an allergy specialist, falsely explains the link between allergies and asthma, thusly:

“How does an allergic reaction cause asthma symptoms?

“An allergic response occurs when immune system proteins (antibodies) mistakenly identify a harmless substance, such as tree pollen, as an invader. In an attempt to protect your body from the substance, antibodies bind to the allergen.”

Unless you have studied immunology and related molecular biology Mayo readers don’t recognize the FRAUDULENT MISREPRESENTATION in the deceptive/diversionary propaganda:

“An allergic response occurs when immune system proteins (antibodies) mistakenly identify a harmless substance, such as tree pollen, as an invader.”

That is FALSE.

More correctly, “An allergic response occurs when immune system CELLS (not “proteins” or “antibodies” as misrepresented), CORRECTLY “identify a harmless substance, such as tree pollen, as an invader” that combines with a normal piece of protein in your body. That omitted, and misrepresented FACT, is called an “ANTIGENIC COMPLEX.”

THAT OMITTED AND MISREPRESENTED FACT IS MEDICAL/LEGAL TREACHERY. It occurs most commonly by VACCINATIONS THAT INJECT THE ANTIGENS FORMING ‘ANTIGENIC COMPLEXES’ THROUGH THE PROTECTIVE SKIN BARRIER. These injections enable global genocide (or “iatrogenocide”–the mass-killing and enslaving of populations by physicians in favor of Big Pharma and the depopulation elite).


Concluding the Mayo misrepresentation, “[i]n an attempt to protect your body from the substance, antibodies bind to the allergen.”

BUT your own antibodies also bind to your own host cells and proteins when they form antigenic complexes as a result of vaccination protein antigen injections.  This pathogenesisis causes AUTO-IMMUNE REACTIONS AND DISEASES INCLUDING ASTHMA, HAY-FEVER, ALLERGIES, AND NEARLY 100 OVERLOOKED OR MISREPRESENTED ILLNESSES LIKE ‘COVID-19″.

“The chemicals released by your immune system lead to allergy signs and symptoms, such as nasal congestion, runny nose, itchy eyes or skin reactions,” Mayo concludes. “For some people, this same reaction also affects the lungs and airways, leading to asthma symptoms.”

AND NOW the same is true for the so-called “COVID disease.” This illness has been misdiagnosed and misrepresented as sourcing from “a coronavirus” when, in FACT, the diseases sources from the antigenic (spike) proteins injected into victims via vaccinations/ intoxications, and other means of exposure to the same antigens via ‘shedding,’ coughing, or other ways of spreading.

Clear-and-convincing evidence of this most reasonable and responsible thesis can be found throughout science. For instance, Saparna Pai, e. al. published,What lies beneath the airway mucosal barrier? Throwing the spotlight on antigen-presenting cell function in the lower respiratory tract.”

You immediately see the Mayo Clinic FRAUD. It is an “antigen-presenting cell” central to the function of respiration that Mayo recklessly neglects and omits from its specious science (i.e., propaganda).

To the contrary, once vaccinated or exposed to the synthetic “dual use” “gain-of-function” coronavirus spike protein antigen, then special immune cells begin to mount a defense. That defense is summarized by Pai et. al., below. Most importantly, smooth muscles surrounding the alveolar (i.e., tiny air sacs) mucosa are tightened making it more difficult to breathe. Larger blood vessels supplying the respiratory tract have smooth muscles that are similarly intoxicated by the synthetic bio-antigenic weapon. The blood vessels clamp down make breathing asthma-like.

As Pai et. al. explain, normal/natural exposures to foreign protein antigens is a part of life, and generally well-accommodated.

But the same cannot be expected, nor is being seen, with the mass production and military/commercial release if the coronavirus spike-protein antigen:

“The airways are exposed to a wide variety of inhaled antigens, and therefore, the induction of primary immunity to these antigens is tightly controlled by . . . antigen-presenting cells (APC) in the lower airways. . . This is “the mechanisms used by pathogens to modulate APC function during infectious disease,” Pai et. al., detail.

“. . . . Various subsets of [cells] and macrophages in the airways act as ‘gate keepers’ to the lung and become activated soon after pathogen entry.5, 6 Once activated, they efficiently participate in phagocytosis, killing, antigen transport and co-ordination of the innate and adaptive immune response. . . .” [Emphasis added.]

“Therefore, the discriminatory powers of the respiratory immune system are stretched to the limit as it must separate antigenic ‘noise’ from the rare pathogen signal,” in this case the “gain-of-function” spike protein antigen we now know is a synthetic bioweapon–the bioweapon sourcing COVID disease and misdiagnoses.

Concluding their scientific review considering what is actually happening to prompt asthmatic breathing problems following certain antigenic intoxications, Pai et. al, stated, the immune response to these antigens must be neutralized along with minimising collateral damage to the lung airways.

This is what is recklessly neglected in the world’s consensus-response to “COVID”. The ‘default’ T-cell response is overwhelmed and inflammatory Th2 cell-mediated immunity results. Smooth muscles contract. They clamp-down reducing small and larger airways, both restricting oxygen flow.

The wisdom of anti-histamine therapies applied to COVID is solidly evidenced by the association of immune-cell disruptions, cytokine storms, and patient deaths. This is well-summarized by Li, Zhang and Gu in FASEB Journal, thusly:

“A cytokine storm is a nonspecific inflammatory response caused by the excessive secretion of more than 150 cytokines and chemical mediators by immune or nonimmune defense cells, characterized by rapidly proliferating and highly activated T cells, macrophages, and natural killer cells.46 It is a last resort mechanism of our immune system. A cytokine storm is also a key event causing death in patients infected with coronavirus.2, 47 Thus, inhibiting overactive immune responses is very important for preventing cytokine storms.48

In this context, my federal court filing of August 18, 2021, is extremely informative and vitally-important for bringing these pathogenic and therapeutic truths to light and saving lives.


ANALYSIS PART II: It is public knowledge that Pfizer and Moderna were financed by the U.S. DoD, NIH, NIAID, to develop “novel” mRNA vaccines and related “monoclonal antibodies” to serve militarily and commercially as a so-called “defense” against the not-yet-existing/imposed/administered plague later called “COVID-19” that ’emerged’ from Wuhan China.


Every informed person knows that in order to develop a vaccine against a virus, you need the virus first. Thus, it is common sense to realize that to develop a “novel” vaccine against COVID, you first needed to mass produce the synthetic bioweapon–the so-called ‘bat coronavirus mutant’; or in this case its extremely “novel” “spike protein antigen” that accommodates transmission of the respiratory distress and disease.


This activity, scientific records document, flowed directly from HIV/AIDS virus research and related developments in commercial/military immunology during the 1980s and 1990s.


This best explains why: (1) Fauci and his inner circle criminally concealed the four AIDS virus envelop genes constructing the COVID Spike protein antigen, beginning on-or-about January 31, 2020 (as the Fauci-e-mails prove); and (2) so little medical attention is being given to the spike protein antigen as the primary source of respiratory distress and asthma-like suffering in “COVID” patients amenable to treatments other than vaccines and monoclonal antibodies profiting the ‘inner circle’ of investors/co-conspirators/plague-creators.



ANALYSIS PART III:  In asthma, much like we see in patients poisoned by the Pfizer/Moderna/DARPA synthetic spike protein antigenic bioweapon, histamines and antihistamines play important role in these illnesses and recoveries. The scientific/medical consensus currently claims most of those who suffer from severe allergies and asthma from hypersensitivity reactions to foreign-protein antigens “benefit considerably from antihistamines.”


A scientific literature review of this subject of histamine and anti-histamine biochemistry and molecular biology is published online. This includes a review article by Qu, Fuhler and Pan, titled “Could Histamine H1 Receptor Antagonists Be Used for Treating COVID-19?” The answer is most certainly, yes.


Yes, because the cell-mediated immunity against the synthetic antigenic bioweapon prompts histamine releases that clamp-down on the muscles that enable free-breathing.


That is why Qu et. al., in effect, recommended anti-histamines for “treating COVID-19.”



In conclusion, neutralizing the bioweaponized antigen must be the primary objective in defending against the COVID imposition and its damaging and deadly impacts.


Sedating this synthetic antigenic overstimulation of cell-mediated immunity in the human body, and normalizing its histamine/antihistamine functions is a key to survival.


This advisement, of course, supplements many previous articles in which i explained the urgency of “anti-oxidant therapies,’ neutralizing positively-charged synthetic spike-protein antigens as best you can using Vitamins C, D, E, Zinc, the anti-stress B vitamins, OxySilver w/528Hz that has proven to be a strong anti-oxidant, chlorophyll; and by reducing acidifying life-style risks.
An excellent science paper reviewing several “bitter” (i.e., negatively-charged alkalizing and anti-oxidant) natural medicines encouraging doctors and patients to relieve COVID’s respiratory distress using these alternatives is published HERE.

Vitamin C acts as a powerful natural antihistamine.

“According to a 2018 study on vitamin C in the treatment of allergies, oxidative stress plays a key role in allergic diseases. . . . Another study from 2000 suggested taking 2 grams (g) of vitamin C daily to act as an antihistamine. . . . As vitamin C is a powerful antioxidant and anti-inflammatory, it may act as a treatment for allergies.” Now add the asthmatic symptoms associated with smooth muscle contractions from spike-protein antigen-prompted histamine releases. These too may be naturally remedied by vitamin C.

Quercetin is another natural antioxidant found in foods and over-the-counter nutritional supplements. This flavonoid may help relieve some of the symptoms of histamine release and airway inflammation.

FIsh oils rich in omega-3 fatty acids may also help reduce lung inflammation and relieve asthma-like symptoms.

According to many open sources, other natural herbs that may help treat asthma include:

  • ginkgo, shown to reduce inflammation
  • mullein
  • boswellia (Indian frankincense)
  • dried ivy
  • butterbur
  • black seed
  • choline
  • French maritime pine bark extract

Coffee and tea may also be useful for treating asthmatic symptoms. Unfortunately, these consumables tend to be acidifying. That is the opposite to what you want to accomplish to neutralize the positive-charge on the spike-protein antigen.

One interesting study indicated that menthol may be added to inhalants to “decrease intracellular free Ca*+ concentration through an inhibition of voltage-dependent Ca*’ channels, thereby producing hyperpolarization of various types of cells.” Decreasing free Ca+ ions in the patient’s respiratory tract, thereby increasing negatively-charged alkalizing anions, may theoretically help neutralize the positively-charged COVID antigen delivery mechanism causing the asthmatic symptoms by way of the intoxicated T-cells prompting histamine releases.

Remember always, good alkalizing-hydration goes hand-in-hand with good oxygenation to defeat the bioweapon and respiratory distress.

Finally, psychological stress can be a killer, especially compounding damage from spike-protein antigen intoxication inflammatory reactions. Psychological stress and emotional distress precipitates cytokine releases. An analysis of 34 studies found increases in circulating IL-6, IL1B, IL-10, interferon and more in response to mental and emotional distress. Please keep this in mind when watching television and following the “news.”





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