‘While Secretary of Defense Lloyd Austin has stated that mandatory COVID-19 vaccination is needed to protect the health and readiness of the armed forces, Steven J. Hatfill, M.D., writing in the summer issue of the Journal of American Physicians and Surgeons, states that this policy has the potential to generate both short and long-term incapacitating side effects in our Special Operations soldiers.
Current mRNA products create only a short-term immunity to the original viral strains, he writes, and cannot reliably prevent infection with the now dominant strains. He refers to an Israeli study of 2.5 million patients, which found that fully vaccinated individuals were 6 to 13 times more likely to get infected with some SARS-CoV-2 variants than individuals who developed a natural exposure from a previous COVID-19 infection.
Citing growing evidence of vaccine-associated miscarriages, serious cardiac and neurologic conditions, and possible antibody-dependent enhancement (ADE) of infection, Dr. Hatfill writes that the Food and Drug Administration, with its antiquated surveillance system, is “incapable of monitoring vaccine safety and efficacy.”
Clinical trials were rushed and incomplete, he states. “As early as February 2021, some scientists were calling for a halt to the mass vaccination program.”
Dr. Hatfill also maintains that “early COVID-19 infection is unequivocally a treatable condition” and that “safe antiviral drug prophylaxis is also available for units and dependents.”
“Military readiness,” he concludes, “should be protected with early detection and diagnosis, plus early treatment and prophylaxis with a combination of safe repurposed drugs and immunologic support, rather than mandated use of incompletely tested novel products with potential serious adverse effects.”’https://aapsonline.org/covid-vaccine-mandate-will-not-protect-military-readiness/
‘We know that SARS-CoV-2 is a man-made “paravirus” if you will, created in Wuhan/Moderna laboratories and reinforced by mainstream media propaganda. But in the grand scheme, at least the first iteration released onto the world, so-called COVID-19 is a lightweight illness that is mostly just rebranded influenza.
The mRNA and viral vector injections, along with Remdesivir, combine for a quick two-year, $200 billion global racket for big pharma and Bill Gates. Ivermectin is a proven, powerful drug to treat and prevent so-called COVID-19, according to 108 peer-reviewed studies. The Ivermectin Merck patents are long expired. So the cheap, $1-per-dose, Nobel Prize-winning drug poses a serious threat not only to the emergency use authorizations for the lethal injections, but also to the temporary COVID-19 racket. But those simply cannot be the only reasons for the persistent, petulant, childish mainstream media anti-Ivermectin propaganda.
This blogger has seen scattered studies concluding that Ivermectin not only inhibits cancer cell growth, but also kills cancer cells. Perhaps placing nine said studies into one article can help disrupt the cancer industrial complex and wake up the snoozing masses.
1) American Journal of Cancer Research – 2018
This study by researchers at Unidad de Investigación Biomédica en Cáncer in Mexico concluded:
So far, at least 235 clinically-approved, non-cancer drugs have proven anti-tumor activity either in vitro, in vivo, or even clinically. Among these, ivermectin, an anti-parasitic compound of wide use in veterinary and human medicine, is clearly a strong candidate for repositioning, based on the fact that:
i) it is very safe, causing almost no side-effects other than those caused by the immune and inflammatory responses against the parasite in infected patients, and
ii) it has proven anti-tumor activity in pre-clinical studies. On the other hand, it is now evident that the use of very selective “unitargeted” drugs is commonly associated to early development of resistance by cancer cells, hence the use of “dirty” or “multitargeted” drugs is important to explore.
Some key findings by Chinese researchers at Bengbu Medical College include the following:
Recent studies have also found that Ivermectin (IVM) could promote the death of tumor cells by regulating the tumor micro-environment in breast cancer.
In an experiment designed to screen potential drugs for the treatment of leukemia, IVM preferentially killed leukemia cells at low concentrations without affecting normal hematopoietic cells.
In a study by Hashimoto, it found that IVM inhibited the proliferation of various ovarian cancer cell lines.
Experiments confirmed that IVM could significantly inhibit the proliferation of five renal cell carcinoma cell lines without affecting the proliferation of normal kidney cells, and its mechanism may be related to the induction of mitochondrial dysfunction.
Researchers at Henan University in China concluded:
We have demonstrated that ivermectin may regulate the expression of crucial molecules Caspase-3, Bax, Bcl-2, PARP, and Cleaved-PARP in the apoptosis pathway by increasing ROS production and inhibiting the cell cycle in the S phase to inhibit colorectal cancer cells (Figure 11). Therefore, current results indicate that ivermectin might be a new potential anticancer drug for treating human colorectal cancer and other cancers.
Researchers at the National Cancer Institute in Mexico City concluded the following:
Results from the present study demonstrated that ivermectin preferentially targeted the stem cell population in MDA–MB–231 human breast cancer cells. Ivermectin has been demonstrated to be safe, following treatment of millions of patients with onchocerciasis and other parasitic diseases, which makes it a strong candidate for further studies investigating its potential use as a repurposed drug for cancer therapy.
Researchers at three Chinese institutions concluded:
Those findings provided the potential targeted lncRNA-EIF4A3-mRNA pathways of ivermectin in ovarian cancer, and constructed the effective prognostic model, which benefits discovery of novel mechanism of ivermectin to suppress ovarian cancer cells, and the ivermectin-related molecule-panel changes benefit for its personalized drug therapy and prognostic assessment towards its predictive, preventive, and personalized medicine (PPPM) in ovarian cancers.
Chinese researchers at Henan University, concluded the following:
We demonstrated that ivermectin effectively inhibit the proliferation of esophageal squamous cell carcinoma (ESCC) cells by inducing mitochondrial dysfunction, suppressing NF-κB signaling and promoting apoptosis. Our results suggest that ivermectin may be a potential therapeutic target against ESCC.
Some key findings from researchers at Instituto Nacional de Cancerologia in Mexico City:
Ivermectin reduced both cell viability and colony formation capacity in the stem cell-enriched population as compared with the parental one. Finally, in tumor-bearing mice ivermectin successfully reduced both tumor size and weight. Our results on the anti-tumor effects of ivermectin support its clinical testing.
Some key findings by University of Geneva researchers are as follows:
Constitutive activation of canonical WNT-TCF signaling is implicated in multiple diseases, including intestine and lung cancers, but there are no WNT-TCF antagonists in clinical use. We report that Ivermectin inhibits the expression of WNT-TCF targets, mimicking dnTCF, and that its low concentration effects are rescued by direct activation by TCFVP16.
In vivo, Ivermectin selectively inhibits TCF-dependent, but not TCF-independent, xenograft growth without obvious side effects. Given that Ivermectin is a safe anti-parasitic agent used by 200 million people against river blindness, our results suggest its additional use as a therapeutic WNT-TCF pathway response blocker to treat WNT-TCF-dependent diseases including multiple cancers.
‘First time detection of the vaccine spike protein in a person who died after vaccination against Covid-19.
The suspicion that the spike protein formed in the body as a result of the “vaccination” against Covid-19 could be responsible for the pathologically observed inflammations and lesions of vessels has now been confirmed immunohistologically for the first time.
The pathologists Prof. Dr. Arne Burkhardt and Prof. Dr. Walter Lang and their team have succeeded in reliably detecting the vaccine spike protein in the vessels of a person who died 4 months after “vaccination” and who had vascular lesions and also vaccine-induced myocarditis. Detection was successful using an antibody specific for the spike protein by conventional immunohistochemistry on the tissue sections.
The described detection method can be applied to all organ and cell damage in which conspicuous pathological findings are found after “vaccination” against Covid-19. From this follows: For ethical, legal and scientific reasons, all histopathological examinations in connection with damage due to “vaccination” against Covid-19 must be accompanied with this method with immediate effect.’https://peoplesworldwar.com/pathology-of-vaccine-deaths-injuries-proof/
‘March 26, 2022 Iowans gathered in front of the Des Moines, Iowa Capitol to fight for their freedoms and oppose mandates. A food truck was present and Sweet to Eat Bakery sold various snacks such as pie and cookies. Several speakers gave speeches on the matter from Jim Carlin, Gary Lefler, Rick Stewart, Gina Spampinato, Kari Hartpence, to Trent Thevenot. After the event, a group of them drove around Des Moines in a convoy.
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