Blood transfusions, Covid 19 injections and Turbo cancer

In Feb. of 2025, I wrote an article on how my husband got tainted blood during his cancer treatments. Ever since 2022, I've seen Facebook post after post about how the blood supply is safe and that the spike protein doesn't stay in the blood supply and it doesn't cause turbo cancer. I've also seen many posts on how turbo cancer is a made up term and doesn't exist. This article will disprove those theories.

First, lets look at the safety of the blood supply. As I stated in that February article, the Red Cross didn't believe me and in fact called me a liar outright. And that I didn't see what I saw and what I was saying was impossible. The blood supply isn't safe, it has never been safe. It took the Red Cross 10 years to acknowledge there was a huge risk in the 80s from the HIV/AIDS being in the blood supply. As it was, many hemophiliac patients got HIV/AIDS tainted blood and subsequently developed HIV. I spent a year doing volunteer work in the blood center in the late 80s, so I was coming in at the tail end of their acknowledging the risk. I saw short cuts being taken because they "knew the person" and other things. I won't go into specifics but as a result of what I saw, I rejected all blood products when I lost 65% of my blood supply March 28, 1990 due to postpartum hemorrhaging. It took a year to get back on my feet, but I did it......all while nursing a newborn.

When a person received a Covid injection, they are told the spike protein stays in the arm and is gone within a day or 2. Studies are now showing this to be inocrrect. It's being found in the testes, the ovaries, the heart and so on. Dr. Peter McCullough has said that the spike protein is being seen YEARS later. The manufacturers knew in 2022, that the spike protein stays in the body for 6 months.

In 2024, Japan was calling for caution on blood products from vaccinated people. All while the the American Red Cross was stating that the blood supply was safe.

In this article, based on these circumstances and the volume of evidence that has recently come to light, we call the attention of medical professionals to the various risks associated with blood transfusions using blood products derived from people who have suffered from long COVID and from genetic vaccine recipients, including those who have received mRNA vaccines, and we make proposals regarding specific tests, testing methods, and regulations to deal with these risks.

It has been reported from various countries around the world that genetic vaccines such as mRNA vaccines encoding spike proteins have also caused a wide variety of diseases in all organs and systems, including the nervous system, in addition to thrombosis and resulting cardiovascular disorders in vaccine recipients

There are two general mechanisms by which a modified gene introduced into the body by genetic vaccination and some of the antigens produced because of the expression of that gene can be transmitted throughout the body. First, LNPs encapsulating mRNA can spread through the body via the bloodstream from the injection site. It has already been shown that LNPs have a tendency to accumulate in specific organs, such as the liver, spleen, ovaries, testes, and bone marrow. The other is the release of pseudouridinated mRNA molecules and synthesized spike proteins as extracellular vesicles, or exosomes, from cells that have incorporated LNPs.

Since the beginning of the coronavirus pandemic and genetic vaccination, there has been much debate about the safety of blood products and their use in transfusions

Contrary to initial expectations, it was found that genes and proteins from genetic vaccines persist in the blood of vaccine recipients for prolonged periods of time and a variety of adverse events resulting from genetic vaccines are now being reported worldwide.

There is an undeniable risk that patients may experience some problems if they receive blood products derived from blood collected in, at least, a brief deferral period after genetic vaccination.

It should also be stressed that the issues discussed here are matters that pertain to all organ transplants, including bone marrow transplants, and not just blood products. The impact of these genetic vaccines on blood products and the actual damage caused by them are unknown at present. Therefore, in order to avoid these risks and prevent further expansion of blood contamination and complication of the situation, we strongly request that the vaccination campaign using genetic vaccines be suspended and that a harm–benefit assessment be carried out.

With 70% of the population taking the Covid jab, our blood supply has been permantely tainted. We can't trust the Red Cross or medical personnel to tell us the truth as they believe all blood is safe, no matter what. You provide the studies, and they still won't acknowledge it.

A study out of Thailand lays out more risks from receiving Covid jabbed blood-

Now, are you hearing about these dangers and safety protocols being put into place to protect vaccine receipients? No, of course not. All we hear is the blood supply is safe, no ifs, and or buts about it. There are studies that say otherwise.

Another study, Concerns regarding Transfusions of Blood Products Derived from Genetic Vaccine Recipients and Proposals for Specific Measures.

The volume of evidence that has recently come to light, we call the attention of medical professionals to the various risks associated with blood transfusions using blood products derived from people who have suffered from long COVID and from genetic vaccine recipients, including those who have received mRNA vaccines.

It has already been shown that LNPs have a tendency to accumulate in specific organs, such as the liver, spleen, ovaries, testes, and bone marrow

There has been considerable debate about the safety of blood products prepared from donated blood of the vaccine recipients and their use in blood transfusion

The impact of these genetic vaccines on blood products and the actual damage caused by them are unknown at present.

Currently, there are 2 pure blood suppliers.

Safe Blood

Blessed by his Blood

Now, lets look at Turbo Cancer as a result of the Covid 19 jab. Cancers in very advanced stages are being seen in younger and younger people. Stage 4 colon cancer is being seen in teenagers! The media and the medical industry are trying to gas light us into believeing this has always been the case, that this is nothing new. Those of us born in the 60s, 70s, 80s and even 90s, did you know of anyone who diagnosed with stage 4 colon cancer in high school? One of my classmates was diagnosed with leukemia shortly after graduation in 1988, unfortunately, she was gone about a year later.

These cancers are coming out of nowhere. They get a clean bill of health, then months later they are diagnosed with Stage 4 cancer.

Here are the cancers that are being seen in the late stages right now-

1. Turbo cancer – existing tumors grow exponentially quicker (plus multiple tumors in multiple organs)

2. Breast cancer

3. Recurrence (and metastasis) after complete remission prior to Covid jab(s)

4. Lung and bronchus cancer

5. Prostate cancer

6. Colon and rectum cancer

7. Stomach and esophageal cancer

Look at #3, recurrence after remission. People who have gone into remission then get the Covid jab, then get a recurrence and this time it's in the later stages. Or, if they are already fighting cancer, the cancer explodes throughout their body. This can happen with blood transfusions as well. The spike proteins can cause turbo cancer throiughout a persons body. (See my article from Feb. 2025 about what happeneed to my husband)

Over 100 studies have shown 17 ways that can cause the cancer mechanism-

1. Genome Instability-triggering mutations that initiate cancer.

2. Immune Escape-Spike protein binds and inhibits tumor suppressor genes like p53 and BRCA1, shielding cancer cells from immune destruction.

3. Impaired DNA Repair Mechanism-Spike protein interferes with essential DNA repair enzymes, increasing the risk of unchecked mutations.

4. Chronic Inflammation-Lipid nanoparticles and spike protein cause long-lasting inflammation, a well-known driver of cancer.

5. Dysregulation of the Immune System-Suppression of T cells and type I interferon weakens cancer surveillance and promotes immune evasion.

6. RNA DisruptionCodon optimization disrupts microRNA networks, destabilizing cell growth regulation and apoptosis.

7. Activation of Oncogenic Pathway-Spike protein indirectly activates MAPK and PI3K/mTOR signaling, fueling tumor growth and metastasis.

8. Tumor Microenvironment AlterationLipid nanoparticles accumulate in tumors, enhancing permeability and potentially accelerating cancer spread.

9. Awakening Dormant CancersPost-vaccination inflammation and immune disruption may trigger recurrence in patients previously in remission.

10. Alteration of Immune Surveillance-Modified mRNA blocks toll-like receptors, making tumor cells "invisible" to the immune system.

11. Frameshift Errors-Synthetic mRNA sometimes produces unintended, aberrant proteins, contributing to oncogenic risk.

12. Multiple Injections-Repeated doses exhaust the immune system and drive class switching to IgG4, promoting tolerance to tumors.

13. DNA Contamination-Residual plasmid DNA found in vaccine vials is replication-competent and could integrate into host genomes.

14. Oncogenic SV40 DNA Sequences-SV40 promoter sequences in Pfizer vials may facilitate genome insertion—this same element is used to induce tumors in lab animals.

15. Deregulation of the Renin-Angiotensin System (RAS)-Spike-induced AT1R activation fosters oxidative stress and uncontrolled cell proliferation.

16. Destruction of the Microbiota-The injections deplete bifidobacteria, weakening immune balance and impairing anti-cancer responses.

17. Increased Resistance to Treatments-Spike exposure prolongs cancer cell survival during chemotherapy, possibly driving treatment resistance.

Another study shows 300 peer reviews studes that shows Covid 19 cancer studies across 27 countries.

Across all 66 case reports/case series (333 cancer cases), cancers were distributed as follows:

Lymphoma: ~38%

Carcinoma: ~16%

Other tumors: ~16%

Melanoma: ~9%

Sarcoma: ~9%

Glioma/Glioblastoma: ~7%

Leukemia: ~6%

Among COVID-19 vaccination–associated cases, lymphoid malignancies were even more prominent:

Lymphoma: ~43%

Carcinoma: ~16%

Sarcoma: ~11%

Other tumors: ~16%

Melanoma: ~5%

Glioma/Glioblastoma: ~4%

Leukemia: ~5%

SARS-CoV-2 infection–only cases were rare and showed a limited tumor spectrum:

Carcinoma: ~40%

Glioma/Glioblastoma: ~40%

Melanoma: ~20%

Cases involving both SARS-CoV-2 infection and COVID-19 vaccination showed a broader distribution:

Melanoma: ~29%

Other tumors: ~29%

Lymphoma: ~14%

Leukemia: ~14%

Glioma/Glioblastoma: ~14%

Across the 333 cancer cases:

~50% of cases occurred within 2–4 weeks of vaccination

Some appeared within 7–14 days

Others emerged over 2–6 months or longer

Several underlying studies reported mean onset intervals of ~8–9 weeks

I know what you are thinking, there are just small numbers of people who have gotten cancer after getting the shot. That isn't true. There are MILLIONS of people who have gotten cancer after getting the Covid jab.

South Korea (≈8.4 million individuals):

A nationwide cohort analysis identified statistically significant associations between COVID-19 vaccination and multiple cancer types, including thyroid, colorectal, lung, breast, and prostate cancers. Associations varied by vaccine platform, cumulative dose, age, and sex, indicating heterogeneity rather than a uniform background effect.

Italy (≈300,000 individuals):

A population-based study found higher cancer hospitalization rates among vaccinated individuals, with the strongest signals observed at shorter latency intervals following vaccination.

U.S. military (≈1.3 million service members):

Longitudinal surveillance data documented a post-2021 increase in T/NK-cell lymphomas coinciding with the transition from the pre-pandemic period to near-universal COVID-19 vaccination in this highly structured population.

Here is the link to the full study for the data above- COVID vaccination and post-infection cancer signals: Evaluating patterns and potential biological mechanisms

Another study COVID-19 mRNA-Induced “Turbo Cancers”-

Turbo cancer isn't a formally recognized oncologic classification, but the term has gained traction among clinicians describing a pattern of unusually aggressive, rapidly progressing cancers—particularly among younger individuals and those previously in remission.

Dr William Makis is a Immunologist, Oncologist, Nuclear Medicine Specialist, this is what he says about turbo cancer-

A newly apparent phenomenom where people are presenting suddenly and late with rapid tumours, already often advanced with metastasis (spread to distant sites). The tumours don't respond as normal to treatments, and patients often die in weeks or months from diagnosis. They are generally younger than usual, too. After a hundred years and trillions of dollars on the so-called ‘war on cancer’, still the most important predicitve factor for survival is early diagnosis, so these rapidly developing cancers are disastrous, and their scale is unprecedented.

The Covid jab contains SV40. This was used in the polio vaccine between 1955 and 1963. Many people developed cancer as a result of monkey kidney cells being put into the vaccine. And now it's being used again in the Covid jab.

Dr Peter McCullough talks about turbo cancer in this video.

Not one of us regrets NOT taking the vaccine. I hope the info provided in this article provides the info that proves once and for all the blood transfusions aren't safe and turbo cancer real.

Stay strong.