Joseph Ladapo - Florida
https://www.floridahealth.gov/newsroom/2024/01/20240103-halt-use-covid19-mrna-vaccines.pr.html
SV40 & P53 - Dr. Rasnick interview
discuss…
I don’t know how accurate this is, but Perplexity.ai says the video discusses the following.
The video “Turbo Cancer and the Role of SV40” by Zowe Smith discusses a concerning phenomenon of aggressive, rapidly progressing cancers (“turbo cancer”) observed since COVID-19 vaccine rollouts. The video highlights the presence of SV40 (Simian Virus 40) DNA fragments as contaminants in some mRNA vaccine batches. SV40 is an experimentally established oncogenic virus that can disable tumor suppressor proteins like p53, potentially enabling rapid tumor growth. The vaccine’s spike protein is also suggested to impair immune surveillance, allowing cancers to grow unchecked, especially under conditions of nutritional deficiencies like zinc depletion, which weakens tumor suppression.
Immune checkpoint inhibitors (ICIs), a class of drugs used in cancer therapy, aim to boost the immune system’s ability to attack tumors by blocking proteins that restrain immune cells. However, in some patients, ICIs paradoxically cause hyperprogression, an accelerated tumor growth sometimes referred to as “turbo cancer.” These drugs can also trigger cytokine release syndrome (CRS), or cytokine storms — severe inflammatory reactions characterized by excessive cytokine levels causing fever, organ damage, and potentially fatal outcomes. Managing CRS often requires immune suppression with corticosteroids or cytokine-blocking agents like tocilizumab.
The tumor microenvironment plays a key role in cancer progression by producing inflammatory cytokines that promote growth and suppress effective immune attack. Chronic inflammation can foster an immunosuppressive state that shields tumors from destruction, complicating treatment responses. The interplay between immunotherapies, tumor-induced inflammation, and cytokine storms is complex and sometimes precipitates clinical deterioration rather than tumor control, as emphasized in the video’s narrative about immune dysregulation contributing to rapid cancer progression.
The video critiques mainstream medicine for insufficiently investigating possible links between vaccine components (like SV40 DNA fragments), immune impairment from spike proteins, and aggressive cancers. It stresses the importance of recognizing nutritional factors such as zinc deficiency, which may compromise tumor suppressor proteins (e.g., p53) and immune defenses, further enabling “turbo cancer” development. The overall message is a call for open scientific inquiry into the multifaceted causes of these aggressive tumors beyond prevailing medical consensus.
In summary, the video and related discussions integrate alternative perspectives on how viral contaminants in vaccines, immune checkpoint inhibitor therapies, cytokine storms, and nutritional deficiencies might interrelate to create an environment conducive to rapid tumor progression. Immune system disruption—whether by pharmaceuticals, viral elements, or nutrient imbalances—can paradoxically fuel aggressive cancers, a concept central to the “turbo cancer” phenomenon depicted by Zowe Smith and corroborated by related scientific insights on immune modulation and cancer biology.
References.
- Zowe Smith Rumble interview on vaccine adverse effects and turbo cancer
- YouTube video by Dr. John Campbell explaining SV40 contamination and cancer mechanism
- Interview with oncologist Dr. William Makis on aggressive cancer rise
- Video on genetic sequencing linking Pfizer vaccine to tumor DNAThe video featuring Zowe Smith on “Turbo Cancer and the Role of SV40” explains these main points:
- Since COVID-19 vaccines began rolling out, there have been cases of extremely rapid cancer progression, sometimes leading to death within days. This aggressive cancer has been informally called “turbo cancer.”
- SV40, a virus known experimentally to cause cancer by disabling tumor suppressor genes like p53, has been found as DNA contamination in some COVID mRNA vaccine batches.
- The SV40 DNA in vaccines might enter human cells via lipid nanoparticles, potentially interfering with cellular mechanisms that prevent tumor growth.
- The vaccine’s spike protein may impair immune system cancer surveillance, allowing tumors to grow unchecked and aggressively.
- Zinc deficiency is highlighted as a factor that weakens the body’s tumor suppression, possibly worsening outcomes.
- The speaker criticizes mainstream medicine for not adequately investigating or documenting vaccine-related cancer cases.
- The video calls for more open scientific inquiry into these aggressive cancers and their possible link to vaccine components.
The video “Turbo Cancer and the Role of SV40” argues that mainstream scientists have made critical mistakes by underestimating or dismissing SV40’s role as an extremely potent cancer stimulant, despite strong molecular evidence showing SV40’s ability to disable tumor suppressor proteins like p53 and promote rapid cancer progression in animal and cellular models. It claims that mainstream research overly relies on epidemiological studies that may miss rare but severe effects and often downplays documented detections of SV40 DNA and proteins in human tumors, including in vaccine contaminants. This dismissal, the video contends, has hindered recognition of SV40’s contribution to aggressive “turbo cancer” cases potentially linked to vaccines, calling for urgent open investigation of SV40’s oncogenic impact to better understand and prevent rapid, severe cancers. The video “Turbo Cancer and the Role of SV40” does not claim SV40 alone causes turbo cancer. Instead, it presents SV40 as a strong oncogenic factor that, when combined with other elements such as immune system impairment (possibly related to the vaccine spike protein), nutritional deficiencies like zinc depletion, and immune checkpoint inhibitor effects, contributes to the rapid, aggressive cancer dubbed “turbo cancer.”
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By the way, J J Couey might be among the most knowledgeable about vax dangers.
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Thank you for breaking that video down for me; helps until my hearing recovery. Im going to try the oxide treatment. Was your summary part 2 and 1 or just part 2?