The COVID-19 ‘vaccine’ will increase your risk of seven major cancers
2025 Dec 11, 11:27pm 96 views 3 comments
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1
HANrongli
2025 Dec 12, 10:59am
Please support funding for Dr Sansone's legal fight in Florida. His heart function has declined to critical 15-20% and he is arguing that his congestive heart failure and its worsening is caused by COVID19 vaccine shedding. Despite his illness, he has continued to fight for humanity. Thank you for your support.
MRNA Bioweapons Prohibition Case:
Emergency Motion for Preliminary Injunction and 3.5
Hour Evidentiary
Hearing
請為Sansone博士在佛羅里達州的法律鬥爭提供資金。 他的心臟功能已經下降到15-20%的臨界，他認為他的充血性心力衰竭及其惡化是由新冠肺炎疫苗脫落造成的。 儘管他生病了，但他繼續為人類而戰。 感謝您的支援。
MRNA生物武器禁令案件：緊急動議初步禁令和3.5小時的證據聽證會
博士 約瑟夫·桑松
12月12日
Please support funding for Dr Sansone's legal fight in Florida. His heart function has declined to critical 15-20% and he is arguing that his congestive heart failure and its worsening is caused by COVID19 vaccine shedding. Despite his illness, he has continued to fight for humanity. Thank you for your support.
MRNA Bioweapons Prohibition Case:
Emergency Motion for Preliminary Injunction and 3.5
Hour Evidentiary
Hearing
請為Sansone博士在佛羅里達州的法律鬥爭提供資金。 他的心臟功能已經下降到15-20%的臨界，他認為他的充血性心力衰竭及其惡化是由新冠肺炎疫苗脫落造成的。 儘管他生病了，但他繼續為人類而戰。 感謝您的支援。
MRNA生物武器禁令案件：緊急動議初步禁令和3.5小時的證據聽證會
博士 約瑟夫·桑松
12月12日
2
HANrongli
2025 Dec 12, 3:44pm
MRNA Bioweapons Prohibition Case: Court Dismissed Again Reporter’s summary
DR. JOSEPH SANSONE
DEC 12
Reporter’s Summary:
According to the author, human beings can maintain their health only through their own knowledge and wisdom, and questioning and critical thinking are essential. … The author asserts that the COVID-19 virus and COVID vaccines, which originated in the communist CCP state, along with what the author describes as four years of election fraud in the United States, represent the darkest period in human history. The author characterizes these events as a long-planned, carefully orchestrated, multilayered strategy of communist authoritarian influence targeting people worldwide—persecuting conscience, suppressing speech, desecrating academia, trampling on the law, abusing power, and distorting truth.
/ French Free Health and Human Rights Journalist: Han Rongli
记者综述：人类维护健康只能靠自己的知识与智慧、质疑及批判性思维至关重要！…始于共产主义中共国的新冠病毒与新冠疫苗，同步于美国窃选舞弊的四年人类历史最黑暗时间，是蓄谋已久、精心策划、层层布局，对全球人类的共产威权统战手段，迫害良知、钳制言论、亵渎学术、践踏法律、腐败滥权、颠倒黑白。/ 法国自由健康人权记者：韩荣利
https://open.substack.com/pub/josephsansone/p/mrna-bioweapons-prohibition-case-dea
READ IN APP
The court dismissed my case with prejudice. This means I can’t amend my complaint and can appeal. I will evaluate over the weekend for grounds for an appeal. MRNA
生物武器禁令案：法院再次驳回
记者综述：
博士。 约瑟夫·桑索尼
12 月 12 日
在应用程序中阅读
法院有偏见地驳回了我的案件。 这意味着我无法修改我的投诉并可以上诉。 我将在周末评估上诉的理由。
MRNA Bioweapons Prohibition Case: Court Dismissed Again Reporter’s summary
DR. JOSEPH SANSONE
DEC 12
Reporter’s Summary:
According to the author, human beings can maintain their health only through their own knowledge and wisdom, and questioning and critical thinking are essential. … The author asserts that the COVID-19 virus and COVID vaccines, which originated in the communist CCP state, along with what the author describes as four years of election fraud in the United States, represent the darkest period in human history. The author characterizes these events as a long-planned, carefully orchestrated, multilayered strategy of communist authoritarian influence targeting people worldwide—persecuting conscience, suppressing speech, desecrating academia, trampling on the law, abusing power, and distorting truth.
/ French Free Health and Human Rights Journalist: Han Rongli
记者综述：人类维护健康只能靠自己的知识与智慧、质疑及批判性思维至关重要！…始于共产主义中共国的新冠病毒与新冠疫苗，同步于美国窃选舞弊的四年人类历史最黑暗时间，是蓄谋已久、精心策划、层层布局，对全球人类的共产威权统战手段，迫害良知、钳制言论、亵渎学术、践踏法律、腐败滥权、颠倒黑白。/ 法国自由健康人权记者：韩荣利
https://open.substack.com/pub/josephsansone/p/mrna-bioweapons-prohibition-case-dea
READ IN APP
The court dismissed my case with prejudice. This means I can’t amend my complaint and can appeal. I will evaluate over the weekend for grounds for an appeal. MRNA
生物武器禁令案：法院再次驳回
记者综述：
博士。 约瑟夫·桑索尼
12 月 12 日
在应用程序中阅读
法院有偏见地驳回了我的案件。 这意味着我无法修改我的投诉并可以上诉。 我将在周末评估上诉的理由。
3
HANrongli
2025 Dec 12, 10:10pm
🚨 BREAKING: Your vaccinated friends are broadcasting pharmaceutical signals
mRNA vaccines turn human cells into biological transmitters. Spike-bearing exosomes persist for months in breath, saliva, sweat—creating "contagion" without infection.
This isn't conspiracy theory. It's peer-reviewed science that changes everything about transmission.
🚨 突发新闻：您接种疫苗的朋友正在广播药物信号
mRNA 疫苗将人体细胞转变为生物递质。 带有刺突的外泌体在呼吸、唾液、汗液中持续存在数月，从而在不感染的情况下产生“传染”。
这不是阴谋论。 这是经过同行评审的科学，它改变了传播的一切。
https://substack.com/@sayerji/note/c-187021858
Now, in Part III, we must confront the most unsettling implication of this entire framework: What happens when the “toxic exposure” is not environmental or incidental—but deliberately injected into billions of people worldwide?
The mRNA COVID-19 vaccines instruct human cells to produce a foreign protein—the SARS-CoV-2 spike protein—in quantities and for durations that were never fully characterized in pre-authorization trials. And if stressed or modified cells naturally package molecular signals into exosomes—and if those exosomes can transfer biologically active cargo to distant tissues—then what, exactly, might the cells of vaccinated individuals be broadcasting?
This question has been aggressively dismissed as “misinformation.” Yet the peer-reviewed literature tells a more complex, more biologically plausible, and far more consequential story—one that public health authorities have been remarkably unwilling to address. And in light of this biophysical framework, it is nothing short of astonishing that we were told the crisis was “a pandemic of the unvaccinated,” when the emerging evidence suggests the opposite may, in fact, be true.
The Mechanism: From mRNA Injection to Exosomal Broadcast
When mRNA vaccines were first authorized, the public was assured that the lipid nanoparticles remained at the injection site and that spike protein production was localized and transient. This narrative began unraveling almost immediately; yet those who questioned it, labeled as dangerous spreaders of misinformation, and summarily censored and/or deplatformed.
Biodistribution studies from Pfizer, obtained through Freedom of Information requests, revealed that lipid nanoparticles rapidly dispersed from the injection site to multiple organs—including liver, spleen, adrenal glands, and ovaries. Japanese regulatory documents showed LNP accumulation in ovaries at concentrations 118 times higher than initial plasma levels by 48 hours post-injection.
現在，在第三部分，我們必須面對整個框架最令人不安的含義：當「有毒暴露」不是環境或附帶的——而是故意注射到全球數十億人身上時，會發生什麼？
mRNA COVID-19疫苗指示人類細胞產生一種外來蛋白質——SARS-CoV-2尖峰蛋白，其數量和持續時間在預授權試驗中從未完全表徵過。 如果應激或修飾的細胞自然地將分子訊號包裝到外切體中——如果這些外切體可以將生物活性貨物轉移到遠處的組織——那麼接種疫苗的個體的細胞究竟會傳播什麼？
這個問題被積極地駁回為「錯誤資訊」。 然而，同行評審的文獻講述了一個更復雜、更合理、更具有後果的故事——公共衛生當局非常不願意解決這個故事。 鑑於這一生物物理框架，令人驚訝的是，我們被告知這場危機是「未接種疫苗的流行病」，而新出現的證據表明，事實恰恰相反。
機制：從mRNA注射到外切體廣播
當mRNA疫苗首次獲得授權時，公眾確信脂質奈米顆粒仍然在注射部位，峰值蛋白的產生是區域性的和短暫的。 這個敘述幾乎立刻就開始解開了；然而，那些質疑它的人被貼上了錯誤資訊的危險傳播者的標籤，並被立即審查和/或取消平臺。
輝瑞透過資訊自由請求獲得的生物分佈研究表明，脂質奈米顆粒從注射部位迅速分散到多個器官，包括肝臟、脾臟、腎上腺和卵巢。 日本監管檔案顯示，注射後48小時內，LNP在卵巢中的濃度比初始血漿水準高出118倍。
Image description: Putative Biodistribution of mRNA after BNT162b2 and mRNA-1273 COVID-19 Vaccine Administration. COVID-19 vaccines inject lipid nanoparticles (LNPs) containing mRNA that encodes for the Spike protein. (Source)
Growing evidence shows that vaccine-derived spike protein can enter—and in some cases persist in—the bloodstream far longer than originally assumed. In a 2022 study, Ogata and colleagues detected circulating spike antigen in the plasma of Moderna mRNA-1273 recipients, confirming systemic distribution following injection.
https://academic.oup.com/cid/article/74/4/715/6279075
A Circulation study on vaccine-associated myocarditis later found measurable levels of full-length spike protein in affected adolescents and young adults, while asymptomatic vaccinated controls showed none—suggesting prolonged or dysregulated antigen presence in certain individuals.
https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.122.062679
More recently, researchers at Yale identified circulating spike protein months—and in some cases, more than 700 days—after vaccination in participants with persistent post-vaccination symptoms, indicating that antigen clearance may vary dramatically across the population.
https://news.yale.edu/2025/02/19/immune-markers-post-vaccination-syndrome-indicate-future-research-directions
But free-floating spike protein is only part of the story. The question we must now ask: Is spike protein being packaged into extracellular vesicles—and if so, what are those vesicles doing?
Spike Protein in Exosomes: The Evidence
In 2021, a landmark study published in the Journal of Immunology provided the first direct evidence that mRNA vaccination induces the release of spike-protein-bearing exosomes. Researchers found that circulating exosomes from vaccinated individuals contained spike protein on their surface—and these exosomes could be detected for at least four months after vaccination.
The implications are profound. These are not free-floating proteins passively circulating in blood. They are actively packaged into membrane-bound vesicles—the same vesicles that cells use to communicate information to distant tissues and, potentially, to other organisms.
If exosomes and related vesicles can transmit chemically induced injury patterns — as demonstrated in the Tylenol hepatotoxicity model — then the vesicles released by vaccine-stressed cells may similarly externalize their contents beyond the individual.
In this model, the vaccinated body becomes:
This is the broadcasting paradox — and its implications for public health, chronic illness patterns, and the interpretation of “outbreaks” in highly vaccinated
图片描述：BNT162b2 和 mRNA-1273 COVID-19 疫苗接种后 mRNA 的假定生物分布。 COVID-19 疫苗注射含有编码 Spike 蛋白 mRNA 的脂质纳米颗粒 (LNP)。 （来源）
越来越多的证据表明，疫苗衍生的刺突蛋白可以进入（并且在某些情况下持续存在）血液中的时间比最初假设的要长得多。 在 2022 年的一项研究中，Ogata 及其同事在 Moderna mRNA-1273 受体的血浆中检测到循环刺突抗原，证实了注射后的全身分布。
https://academic.oup.com/cid/article/74/4/715/6279075
一项关于疫苗相关心肌炎的循环研究后来发现，受影响的青少年和年轻人体内存在可测量的全长刺突蛋白水平，而无症状的接种疫苗的对照则没有显示出任何结果，这表明某些个体中存在长期或失调的抗原。
https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.122.062679
最近，耶鲁大学的研究人员在有持续疫苗接种后症状的参与者中发现了在接种疫苗后几个月（有时甚至超过 700 天）的循环刺突蛋白，这表明不同人群的抗原清除率可能存在巨大差异。
https://news.yale.edu/2025/02/19/immune-markers-post-vaccination-syndrome-indicate-future-research-directions
但自由漂浮的刺突蛋白只是故事的一部分。 我们现在必须问的问题是：刺突蛋白是否被包装到细胞外囊泡中——如果是，这些囊泡在做什么？
外泌体中的尖峰蛋白：证据
2021 年，《免疫学杂志》上发表的一项具有里程碑意义的研究提供了第一个直接证据，证明 mRNA 疫苗接种会诱导带有刺突蛋白的外泌体的释放。 研究人员发现，来自接种疫苗的个体的循环外泌体表面含有刺突蛋白，并且这些外泌体在疫苗接种后至少四个月内可以被检测到。
其含義是深遠的。 這些不是在血液中被動迴圈的自由漂浮蛋白。 它們被積極地包裝成膜結合的囊泡——與細胞用來向遠處組織以及可能與其他生物體傳遞資訊的囊泡相同。
如果外切體和相關囊泡可以傳遞化學誘導的損傷模式——如泰諾肝毒性模型所示——那麼疫苗應激細胞釋放的囊泡可能會類似地將其內容外化到個體之外。
在這個模型中，接種疫苗的身體變成：
這是廣播悖論——以及它對公共衛生、慢性疾病模式以及對高度疫苗接種「爆發」的解釋的影響
🚨 BREAKING: Your vaccinated friends are broadcasting pharmaceutical signals
mRNA vaccines turn human cells into biological transmitters. Spike-bearing exosomes persist for months in breath, saliva, sweat—creating "contagion" without infection.
This isn't conspiracy theory. It's peer-reviewed science that changes everything about transmission.
🚨 突发新闻：您接种疫苗的朋友正在广播药物信号
mRNA 疫苗将人体细胞转变为生物递质。 带有刺突的外泌体在呼吸、唾液、汗液中持续存在数月，从而在不感染的情况下产生“传染”。
这不是阴谋论。 这是经过同行评审的科学，它改变了传播的一切。
https://substack.com/@sayerji/note/c-187021858
Now, in Part III, we must confront the most unsettling implication of this entire framework: What happens when the “toxic exposure” is not environmental or incidental—but deliberately injected into billions of people worldwide?
The mRNA COVID-19 vaccines instruct human cells to produce a foreign protein—the SARS-CoV-2 spike protein—in quantities and for durations that were never fully characterized in pre-authorization trials. And if stressed or modified cells naturally package molecular signals into exosomes—and if those exosomes can transfer biologically active cargo to distant tissues—then what, exactly, might the cells of vaccinated individuals be broadcasting?
This question has been aggressively dismissed as “misinformation.” Yet the peer-reviewed literature tells a more complex, more biologically plausible, and far more consequential story—one that public health authorities have been remarkably unwilling to address. And in light of this biophysical framework, it is nothing short of astonishing that we were told the crisis was “a pandemic of the unvaccinated,” when the emerging evidence suggests the opposite may, in fact, be true.
The Mechanism: From mRNA Injection to Exosomal Broadcast
When mRNA vaccines were first authorized, the public was assured that the lipid nanoparticles remained at the injection site and that spike protein production was localized and transient. This narrative began unraveling almost immediately; yet those who questioned it, labeled as dangerous spreaders of misinformation, and summarily censored and/or deplatformed.
Biodistribution studies from Pfizer, obtained through Freedom of Information requests, revealed that lipid nanoparticles rapidly dispersed from the injection site to multiple organs—including liver, spleen, adrenal glands, and ovaries. Japanese regulatory documents showed LNP accumulation in ovaries at concentrations 118 times higher than initial plasma levels by 48 hours post-injection.
現在，在第三部分，我們必須面對整個框架最令人不安的含義：當「有毒暴露」不是環境或附帶的——而是故意注射到全球數十億人身上時，會發生什麼？
mRNA COVID-19疫苗指示人類細胞產生一種外來蛋白質——SARS-CoV-2尖峰蛋白，其數量和持續時間在預授權試驗中從未完全表徵過。 如果應激或修飾的細胞自然地將分子訊號包裝到外切體中——如果這些外切體可以將生物活性貨物轉移到遠處的組織——那麼接種疫苗的個體的細胞究竟會傳播什麼？
這個問題被積極地駁回為「錯誤資訊」。 然而，同行評審的文獻講述了一個更復雜、更合理、更具有後果的故事——公共衛生當局非常不願意解決這個故事。 鑑於這一生物物理框架，令人驚訝的是，我們被告知這場危機是「未接種疫苗的流行病」，而新出現的證據表明，事實恰恰相反。
機制：從mRNA注射到外切體廣播
當mRNA疫苗首次獲得授權時，公眾確信脂質奈米顆粒仍然在注射部位，峰值蛋白的產生是區域性的和短暫的。 這個敘述幾乎立刻就開始解開了；然而，那些質疑它的人被貼上了錯誤資訊的危險傳播者的標籤，並被立即審查和/或取消平臺。
輝瑞透過資訊自由請求獲得的生物分佈研究表明，脂質奈米顆粒從注射部位迅速分散到多個器官，包括肝臟、脾臟、腎上腺和卵巢。 日本監管檔案顯示，注射後48小時內，LNP在卵巢中的濃度比初始血漿水準高出118倍。
Image description: Putative Biodistribution of mRNA after BNT162b2 and mRNA-1273 COVID-19 Vaccine Administration. COVID-19 vaccines inject lipid nanoparticles (LNPs) containing mRNA that encodes for the Spike protein. (Source)
Growing evidence shows that vaccine-derived spike protein can enter—and in some cases persist in—the bloodstream far longer than originally assumed. In a 2022 study, Ogata and colleagues detected circulating spike antigen in the plasma of Moderna mRNA-1273 recipients, confirming systemic distribution following injection.
https://academic.oup.com/cid/article/74/4/715/6279075
A Circulation study on vaccine-associated myocarditis later found measurable levels of full-length spike protein in affected adolescents and young adults, while asymptomatic vaccinated controls showed none—suggesting prolonged or dysregulated antigen presence in certain individuals.
https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.122.062679
More recently, researchers at Yale identified circulating spike protein months—and in some cases, more than 700 days—after vaccination in participants with persistent post-vaccination symptoms, indicating that antigen clearance may vary dramatically across the population.
https://news.yale.edu/2025/02/19/immune-markers-post-vaccination-syndrome-indicate-future-research-directions
But free-floating spike protein is only part of the story. The question we must now ask: Is spike protein being packaged into extracellular vesicles—and if so, what are those vesicles doing?
Spike Protein in Exosomes: The Evidence
In 2021, a landmark study published in the Journal of Immunology provided the first direct evidence that mRNA vaccination induces the release of spike-protein-bearing exosomes. Researchers found that circulating exosomes from vaccinated individuals contained spike protein on their surface—and these exosomes could be detected for at least four months after vaccination.
The implications are profound. These are not free-floating proteins passively circulating in blood. They are actively packaged into membrane-bound vesicles—the same vesicles that cells use to communicate information to distant tissues and, potentially, to other organisms.
If exosomes and related vesicles can transmit chemically induced injury patterns — as demonstrated in the Tylenol hepatotoxicity model — then the vesicles released by vaccine-stressed cells may similarly externalize their contents beyond the individual.
In this model, the vaccinated body becomes:
This is the broadcasting paradox — and its implications for public health, chronic illness patterns, and the interpretation of “outbreaks” in highly vaccinated
图片描述：BNT162b2 和 mRNA-1273 COVID-19 疫苗接种后 mRNA 的假定生物分布。 COVID-19 疫苗注射含有编码 Spike 蛋白 mRNA 的脂质纳米颗粒 (LNP)。 （来源）
越来越多的证据表明，疫苗衍生的刺突蛋白可以进入（并且在某些情况下持续存在）血液中的时间比最初假设的要长得多。 在 2022 年的一项研究中，Ogata 及其同事在 Moderna mRNA-1273 受体的血浆中检测到循环刺突抗原，证实了注射后的全身分布。
https://academic.oup.com/cid/article/74/4/715/6279075
一项关于疫苗相关心肌炎的循环研究后来发现，受影响的青少年和年轻人体内存在可测量的全长刺突蛋白水平，而无症状的接种疫苗的对照则没有显示出任何结果，这表明某些个体中存在长期或失调的抗原。
https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.122.062679
最近，耶鲁大学的研究人员在有持续疫苗接种后症状的参与者中发现了在接种疫苗后几个月（有时甚至超过 700 天）的循环刺突蛋白，这表明不同人群的抗原清除率可能存在巨大差异。
https://news.yale.edu/2025/02/19/immune-markers-post-vaccination-syndrome-indicate-future-research-directions
但自由漂浮的刺突蛋白只是故事的一部分。 我们现在必须问的问题是：刺突蛋白是否被包装到细胞外囊泡中——如果是，这些囊泡在做什么？
外泌体中的尖峰蛋白：证据
2021 年，《免疫学杂志》上发表的一项具有里程碑意义的研究提供了第一个直接证据，证明 mRNA 疫苗接种会诱导带有刺突蛋白的外泌体的释放。 研究人员发现，来自接种疫苗的个体的循环外泌体表面含有刺突蛋白，并且这些外泌体在疫苗接种后至少四个月内可以被检测到。
其含義是深遠的。 這些不是在血液中被動迴圈的自由漂浮蛋白。 它們被積極地包裝成膜結合的囊泡——與細胞用來向遠處組織以及可能與其他生物體傳遞資訊的囊泡相同。
如果外切體和相關囊泡可以傳遞化學誘導的損傷模式——如泰諾肝毒性模型所示——那麼疫苗應激細胞釋放的囊泡可能會類似地將其內容外化到個體之外。
在這個模型中，接種疫苗的身體變成：
這是廣播悖論——以及它對公共衛生、慢性疾病模式以及對高度疫苗接種「爆發」的解釋的影響
癌症治療協議：對870萬人樣本規模的兩項具有里程碑意義的研究發現，新冠肺炎「疫苗」會增加你患七種主要癌症的風險
The COVID-19 ‘vaccine’ will increase your risk of seven major cancers
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世界上第二聰明的傢伙
12月11日
CANCER CURE PROTOCOL: Two Landmark Studies With 8.7 MILLION People Sample Size Found That COVID-19 “Vaccines” Increase Your Risk of SEVEN Major Cancers
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DEC 11
https://open.substack.com/pub/2ndsmartestguyintheworld/p/cancer-cure-protocol-two-landmark
As the VAIDS-induced burgeoning turbo cancer epidemic only worsens…
TIME MAGAZINE: OUR CANCER MYSTERY | WHY IT'S STRIKING US SO YOUNG
2ND SMARTEST GUY IN THE WORLD
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FEB 15
TIME MAGAZINE: OUR CANCER MYSTERY | WHY IT'S STRIKING US SO YOUNG
As this Substack has been warning for many years now, the turbo cancer epidemic is only now getting underway as a direct function of the Modified mRNA slow kill bioweapon “vaccine” platform that was foisted on humanity during the PSYOP-19 scamdemic; in other words, cancer rates will continue to explode, and the genetically modified young people will be …
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…with excess cases unrelentingly trending higher…
BOMBSHELL: Just Released American Cancer Society Annual Report On Cancer Showed 11.5% Excess Cases
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JULY 4, 2023
BOMBSHELL: Just Released American Cancer Society Annual Report On Cancer Showed 11.5% Excess Cases
This Substack has been covering the surging rise in DEATHVAX™ induced adverse events and VAIDS, with a particular emphasis on the phenomenon referred to as turbo cancer.
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…the depopulation program proceeds exactly according to plan…
3 Decades Wiped from Life Expectancy of Covid-Vaxxed
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·
APR 15
3 Decades Wiped from Life Expectancy of Covid-Vaxxed
As the Modified mRNA slow kill bioweapon “vaccines” continue to wreak havoc on their genetically modified spike protein-producing subjects, the life expectancy trends are proving to be increasingly grim…
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…and now we have even more grim cancer data to parse; to wit:
Two landmark studies, encompassing 8.7 MILLION people, found that COVID-19 “vaccines” increase your risk of SEVEN major cancers:
Breast: +54%
Bladder: +62%
Lung: +53%
Prostate: +69%
Thyroid: +35%
Gastric: +34%
Colorectal: +35%
All explained by mRNA’s 17 oncogenic mechanisms.
Dr. John Campbell: According to a recent Italian study, people who received at least one dose of Covid injection are 34% more likely to get colorectal cancer, 54% more likely to get breast cancer, and 62% more likely to get bladder cancer than the unvaccinated.
Source
To longtime readers of this Substack all of this is completely unsurprising, but even as this cancer emergency intensifies far too many remain clueless or in total denial as to what has been perpetrated; namely: bioterror democide.
Luckily, readers of this Substack have known that there exists a ‘holy grail’ cancer cure in plain sight that not only can treat the “vaccinated,” but also those that have been shed upon as well as those that have developed this disease from other environmental factors, while also healing asthma, prion-based diseases like Alzheimer’s, mood disorders, Parkinson’s, Lyme Disease, Lupus, skin conditions, and various other “incurable” ailments:
Newest & Most Improved Joe Tippens Protocol
Tocotrienol and Tocopherol forms (all 8) of Vitamin E (400-800mg per day, 7 days a week). A product called Gamma E by Life Extension or Perfect E are both great.
Bio-Available Curcumin (600mg per day, 2 pills per day 7 days a week). A product called Theracurmin HP by Integrative Therapeutics is bioavailable.
Vitamin D (62.5 mcg [2500 IU] seven days a week).
CBD oil (1-2 droppers full [equal to 167 to 334 mg per day] under the tongue, 7 days a week) CBD-X: The most potent full spectrum organic CBD oil, with 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG per serving.
Fenbendazole (300mg, 7 days a week) or in the case of severe turbo cancers up to 1 gram — for prophylaxis one 150mg tablet once or twice per week
Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day — for prophylaxis one 12mg tablet once or twice per week
Hydroxychloroquine (10mg/kg/day 7 days a week) - for prophylaxis one 200mg tablet once or twice per week
Doxycycline (100mg, 7 days a week for 30-60 days)
VIR-X immune support which also greatly increases the bioavailability of both Fenbendazole and Hydroxychloroquine (2 capsules per day) — for prophylaxis 2 capsules per day
Removing sugars and carbohydrates (cancer food) from your diet and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like FLAV-X
This is the latest and most cutting edge revision to the Joe Tippens protocol which greatly increases synergistic healing by incorporating Doxycycline and Hydroxychloroquine:
DOXYCYCLINE and CANCER: At Least 12 Anti-Cancer Mechanisms of Action
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DEC 4
DOXYCYCLINE and CANCER: At Least 12 Anti-Cancer Mechanisms of Action
Why was Doxycycline Use Suppressed World-Wide Starting in 2020?
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HYDROXYCHLOROQUINE Has Potent ANTI-CANCER Mechanisms
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·
NOV 17
HYDROXYCHLOROQUINE Has Potent ANTI-CANCER Mechanisms
This Substack recently published an article on the many health benefits of Hydroxychloroquine…
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由于竞争诱导的蓬勃发展的荨麻植物癌疫情只恶化......时间杂志：我们的癌症神秘| 为什么它在世界上如此年轻的第二个聪明的家伙才能袭击我们，·2月15日杂志：我们的癌症神秘| 为什么这么年轻时，这么年轻，因为这种家喻已经警告了多年，涡轮癌疫情才现在正在作为改性mRNA缓慢杀死BioWeapon“疫苗”平台的直接功能，这是在Psyop-19期间为人类而导致的 换句话说，癌症率将继续爆炸，遗传修改的年轻人将成为......阅读完整故事......具有多余的案例，无情的趋势更高...... BOMBSHELL：刚刚发布的美国癌症协会的癌症年度报告显示为11.5％的过度案例第2款 阅读完整故事......缺课计划完全按计划进行...... 3数十年从世界上的Covid-Vaxxed第二届智能家伙拍摄的预期寿命·4月15日三十年，从Covid-Vaxxed的预期寿命擦拭，因为修改了先生 目的：两个地标研究，包括870万人，发现Covid-19“疫苗”增加了七种主要癌症的风险：乳腺：+ 54％膀胱：+ 62％肺：+ 53％前列腺：+ 69％甲肾上腺：+ 69％ John Campbell博士：根据最近的意大利研究，收到至少一种剂量的Covid注射的人可能会使结直肠癌的可能性更高，54％可能得到乳腺癌，并且比未接种的癌症更容易获得膀胱癌。 这一切都是长期读者的来源，所有这一切都是完全不成熟的，但即使这种癌症紧急情况加剧了太多仍然无能为力或完全否认对犯罪的东西; 即：生物错误划分。 幸运的是，这种家喻户口的读者已知在平原的景区中存在“神圣的Grail”治疗方法，这不仅可以治疗“疫苗接种”，而且还有那些已经摆脱的“疫苗”以及那些从其他环境因素开发这种疾病的人，同时也是治愈哮喘 寿命延伸或完美e称为伽马e的产品都很棒。 生物可用的姜黄素（每天600毫克，每周7天每天2丸）。 通过综合治疗剂称为Theracurmin HP的产品是生物可利用的。 维生素D（每周七天，62.5 MCG [2500 IU]）。 CBD油（1-2个滴注器全[等于每天167至334毫克]，每周7天）CBD-X：最有效的全谱有机CBD油，具有5,000毫克的活性大麻素和大麻 Fenbendazole（每周300mg，7天）或在严重涡轮增压癌的情况下，高达1克 - 预防一个150mg片剂每周一次或两次伊维菌素（每周24mg，7天）或在严重的情况下 阅读全文羟基氯喹有有效的抗癌机制第二次智能人士在世界上·11月17日羟氯喹有效率的抗癌机制这家垃圾最近发表了一篇关于羟氯喹的众多健康益处的文章..... 请使用代码Cure20在最新产品的羟妥核上获得20％的折扣，以及您一直在购买多年的所有令人惊叹的产品，现在就像诺贝尔奖获奖的奇迹化合物伊维霉素一样，不那么奇迹 周末闪光销售结束于12月14日（东部时间午夜），2025.向购物车添加产品时，请转到浏览器页面右上角的购物车图标，然后单击它，然后选择您将重定向到您可以重定向的查看购物车选项 只有Resolvx Health网站只提供此家具促进的所有正宗产品。