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作为 "医生和科学家促进健康、自由和民主团队的一员Sucharit Bhakdi "博士教授发表了一封煽动性信件。这是一个致命的问题,会对免疫系统造成巨大损害。巴克迪 "教授认为,任何进一步使用 mRNA 疫苗的行为都会对生命和肢体造成极大的危险。他呼吁人们将命运掌握在自己手中,并将这封现已有17 种语言版本的信件传播到世界各地。他的警告科学事实、但又以人人都能理解的方式加以解释、必须传达给所有人。特别是那些盲目相信医生、媒体和政客的人,在不了解进一步接种疫苗的危险性的情况下为自己接种疫苗的人它的传播可以拯救生。这封情绪激动的信最后呼吁全世界人民站起来,立即停止所有 RNA-注射。
RNA-疫苗的新概念。
染色体是生命之书。它们的 DNA 含有重要的以蛋白质为基础的种生产配方必要时,打开书本,复制一份所需的食谱。
该拷贝是一种 MRNA,可控制蛋白质的产生。
阅读说明后,不再需要该配方,并将删除。mRNA 疫苗是染色 体配方的
短暂复制、控制特定抗原(例如SARS-CoV-2 穗状病毒蛋白)的产生。
每次注射都会产生十多亿个拷贝,即 RNA 分子。
大量生产 mRNA需要大量DNA 配方。这是如何实现的?该解决方案是
工程的基石。数以万亿计的构建指令来自细菌。
这些配方包含在06,560称为质粒的微小细菌染色体中。
细菌分裂大约需要 20 分钟。细胞数量每小时增加八倍。
这意味着,在短短几天内就能获菌得无数带有质粒的细质粒易于操作。
外来配方,即包含病毒蛋白质构建指令的基因,可以很容易地插入。
在细菌中大量繁殖后,它们被收获并用作生产mRNA 副本的模板。
然后,mRNA 分子被包装在微小的脂肪球(即所谓的脂质纳米颗粒)中。主要成分是人工生产的,可能有剧毒。在 2020 年之前,这些药物禁止用于人体。
COVID RNA 疫苗的紧急授权违反了这一规定。需要包装材料来保护 RNA 不被破坏,并使其更容易被人体细胞吸收。它们通过血液到达身体的各个器官。在那里,球体就像特洛伊木马。它们被细胞吸收并释放出货物。随后是基因产物的产生、从而引发免疫反应。免疫反应会导致特异性抗体的形成、预防未来的感染。
灾难性问题
免疫系统能识别并摧毁身体细胞产生外来蛋白质。这种情况经常发生、当我们的细胞受到病毒攻击时。我们的身体在出生时就具备了识别外来事物的能力。它能终生保护我们,因为它能有效清除受病毒感染的细胞。免疫系统的这种先天保护作用是无法抑制的。如果将含有外来蛋白质构建指令的mRNA 输入细胞,该细胞就会受到免疫系统的攻击。这是整个概念的致命问题。
每次注射的包装 mRNA数量巨大。全身会爆发无数次免疫攻击,只有在外来蛋白质的生产结束后才会停止。要花多长时间?就像疫苗制造商和监管机构所声称的那样,仅仅几天时间?
终极灾难
2022 年,一个令人震惊的发现与这一论断不符。
甚至在注射数周后,接种疫苗的患者体内仍能检测到借助RNA 指令产生的尖峰蛋白。而这些残羹剩饭与严重的多器官炎症有关,往往是致命的疾病。是什么原因导致蛋白质的 mRNA 生成计划持续时间如此之短,又是什么原因导致炎症持续时间如此之长?一个可能的、极其可怕的新的研究成果提供了答案由 McKernan 及其同事完成。
mRNA 生成后,质粒 DNA 模板会被移除,然后再开始包装过程。
否则,质粒也会进入脂肪球。McKernan 报告说,去除质粒 DNA这一关键步骤没有认真执行。
发现大量质粒 DNA以包装形式存在。与 mRNA 一样,这种包装可确保成功地将其送入人体细胞。不同之处在于,DNA 比 mRNA稳定得多,可以作为长期生产的配方。细胞摄取功能性外源染色体表示不少于一个基因改造。可以假设,人们这些包装的细菌质粒注射了疫苗,遭受这种命运。任何外来基因的表达都会引发对产生细胞的免疫攻击。外来蛋白质的持续产生意味着细胞的死亡。这将发生在整个身体。由于血管受伤,血液中形成血凝块组织就会因缺氧而死亡。心脏是一个无法替代死亡细胞的器官。谁没听说过世界发生的神秘心脏性猝死事件?它们只是冰山一角。引发的心脏病已被提上日程,年轻人和老年人都一样。第二个无法更换死亡细胞的器官是大脑。根据疫苗损伤的部位不同,神经和心理也会发生变化。针对患者自身身体的疾病,即自身免疫性疾病,很少单独发生但由于 mRNA 感染,现在可以更频繁地在不同器官同时发病。一名 14 岁的儿童死于前所未有的多器官炎症他的悲惨遭遇说明了这种损害的非同寻常的巧合。
此外,接种疫苗还会对生育和繁殖产生巨大的负面影响。疫苗会积聚在生殖器官中,直接影响生育能力。胎盘细胞吸收血液中循环的 RNA 和DNA 可导致死胎。胎盘受损也会使外来基因进入胎儿的血液循环。接种疫苗后,脐带血中的干细胞减少并受损,有充分理由相信外来基因会进入子宫中的胎儿体内。此外,在母乳中也检测到了疫苗的包装。新生儿出生后最初几周的肠道渗透性很高,人们担心母乳喂养可能会使疫苗直接传给新生儿。这将导致新生儿细胞中的自杀机制被激活。
在实验室中,可以将偷运来的外来DNA 植入生命之书。这种情况发生在接种过疫苗的人身上,可能会产生无穷无尽的后果。控制细胞分裂和发育的精密网络一旦遭到破坏,就可能导致癌症。精子和受精卵中的突变可能会使改变的特征遗传下去导致出现偏离人类进化路径的生物。
结论 可以预见免疫系统对产生病毒蛋的细胞的攻击将导致对组织和血管的广泛而持久的损害。之所以会发生这种攻击,是因为病毒信使对人体来说是外来的。由于每种新的 mRNA疫苗都会控制一种外来蛋白质的生产,因此可以预见,类似规模的破坏将会一再发生。每接种一次强化疫苗,这些噩梦般的场景就会恶化一次。此外,还必须预料到,疫苗批次受到质粒DNA 污染的情况将不会是例外,而是常规,因为还没有一种具有成本效益的方法,能够可靠地将大规模生产的 RNA 与质粒分离。因此,在接种质粒 DNA时,细胞不可避免地会受到长期的自身免疫攻击。
将外来蓝图引入我们的身体,每个人的生命之书都可能被无可挽回地改变。如果人类染色体的组装指令被插入,无数的细胞功能就会被永久性破坏。恶性疾病可能会发生,预期寿命可能会急剧下降。无尽的疾病和痛苦可能成为受影响者的命运。,360一个恐怖的场景正在出现,它可能会影响到无数我们所爱的、我们心目中的人。我们有责任防止这种情况发生。
全世界每个人都必须站起来,立即停止所有 RNA 注射。
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(1) Bansal S. et al. (2021) Cutting Edge: Circulating Exosomes with COVID Spike Protein
Are Induced by BNT162b2 (Pfizer-BioNTech) Vaccination prior to Development of
Antibodies: A Novel Mechanism for Immune Activation by mRNA Vaccines. J Immunol
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(2) Mörz M. (2022) A Case Report: Multifocal Necrotizing Encephalitis and Myocarditis
after BNT162b2 mRNA Vaccination against COVID-19. Vaccines 10:1651.
(3) https://doctors4covidethics.org/on-covid-vaccines-why-they-cannot-work-andirrefutable-
evidence-of-their-causative-role-in-deaths-after-vaccination/
(4) McKernan K. (2023) Sequencing of bivalent Moderna and Pfizer mRNA vaccines
reveals nanogram to microgram quantities of expression vector dsDNA per dose.
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Immunity in Newborn Mammals. Front Immunol. 11:1153.
22.12.2023 | www.kla.tv/27742
作为 "医生和科学家促进健康、自由和民主团队的一员Sucharit Bhakdi "博士教授发表了一封煽动性信件。这是一个致命的问题,会对免疫系统造成巨大损害。巴克迪 "教授认为,任何进一步使用 mRNA 疫苗的行为都会对生命和肢体造成极大的危险。他呼吁人们将命运掌握在自己手中,并将这封现已有17 种语言版本的信件传播到世界各地。他的警告科学事实、但又以人人都能理解的方式加以解释、必须传达给所有人。特别是那些盲目相信医生、媒体和政客的人,在不了解进一步接种疫苗的危险性的情况下为自己接种疫苗的人它的传播可以拯救生。这封情绪激动的信最后呼吁全世界人民站起来,立即停止所有 RNA-注射。 RNA-疫苗的新概念。 染色体是生命之书。它们的 DNA 含有重要的以蛋白质为基础的种生产配方必要时,打开书本,复制一份所需的食谱。 该拷贝是一种 MRNA,可控制蛋白质的产生。 阅读说明后,不再需要该配方,并将删除。mRNA 疫苗是染色 体配方的 短暂复制、控制特定抗原(例如SARS-CoV-2 穗状病毒蛋白)的产生。 每次注射都会产生十多亿个拷贝,即 RNA 分子。 大量生产 mRNA需要大量DNA 配方。这是如何实现的?该解决方案是 工程的基石。数以万亿计的构建指令来自细菌。 这些配方包含在06,560称为质粒的微小细菌染色体中。 细菌分裂大约需要 20 分钟。细胞数量每小时增加八倍。 这意味着,在短短几天内就能获菌得无数带有质粒的细质粒易于操作。 外来配方,即包含病毒蛋白质构建指令的基因,可以很容易地插入。 在细菌中大量繁殖后,它们被收获并用作生产mRNA 副本的模板。 然后,mRNA 分子被包装在微小的脂肪球(即所谓的脂质纳米颗粒)中。主要成分是人工生产的,可能有剧毒。在 2020 年之前,这些药物禁止用于人体。 COVID RNA 疫苗的紧急授权违反了这一规定。需要包装材料来保护 RNA 不被破坏,并使其更容易被人体细胞吸收。它们通过血液到达身体的各个器官。在那里,球体就像特洛伊木马。它们被细胞吸收并释放出货物。随后是基因产物的产生、从而引发免疫反应。免疫反应会导致特异性抗体的形成、预防未来的感染。 灾难性问题 免疫系统能识别并摧毁身体细胞产生外来蛋白质。这种情况经常发生、当我们的细胞受到病毒攻击时。我们的身体在出生时就具备了识别外来事物的能力。它能终生保护我们,因为它能有效清除受病毒感染的细胞。免疫系统的这种先天保护作用是无法抑制的。如果将含有外来蛋白质构建指令的mRNA 输入细胞,该细胞就会受到免疫系统的攻击。这是整个概念的致命问题。 每次注射的包装 mRNA数量巨大。全身会爆发无数次免疫攻击,只有在外来蛋白质的生产结束后才会停止。要花多长时间?就像疫苗制造商和监管机构所声称的那样,仅仅几天时间? 终极灾难 2022 年,一个令人震惊的发现与这一论断不符。 甚至在注射数周后,接种疫苗的患者体内仍能检测到借助RNA 指令产生的尖峰蛋白。而这些残羹剩饭与严重的多器官炎症有关,往往是致命的疾病。是什么原因导致蛋白质的 mRNA 生成计划持续时间如此之短,又是什么原因导致炎症持续时间如此之长?一个可能的、极其可怕的新的研究成果提供了答案由 McKernan 及其同事完成。 mRNA 生成后,质粒 DNA 模板会被移除,然后再开始包装过程。 否则,质粒也会进入脂肪球。McKernan 报告说,去除质粒 DNA这一关键步骤没有认真执行。 发现大量质粒 DNA以包装形式存在。与 mRNA 一样,这种包装可确保成功地将其送入人体细胞。不同之处在于,DNA 比 mRNA稳定得多,可以作为长期生产的配方。细胞摄取功能性外源染色体表示不少于一个基因改造。可以假设,人们这些包装的细菌质粒注射了疫苗,遭受这种命运。任何外来基因的表达都会引发对产生细胞的免疫攻击。外来蛋白质的持续产生意味着细胞的死亡。这将发生在整个身体。由于血管受伤,血液中形成血凝块组织就会因缺氧而死亡。心脏是一个无法替代死亡细胞的器官。谁没听说过世界发生的神秘心脏性猝死事件?它们只是冰山一角。引发的心脏病已被提上日程,年轻人和老年人都一样。第二个无法更换死亡细胞的器官是大脑。根据疫苗损伤的部位不同,神经和心理也会发生变化。针对患者自身身体的疾病,即自身免疫性疾病,很少单独发生但由于 mRNA 感染,现在可以更频繁地在不同器官同时发病。一名 14 岁的儿童死于前所未有的多器官炎症他的悲惨遭遇说明了这种损害的非同寻常的巧合。 此外,接种疫苗还会对生育和繁殖产生巨大的负面影响。疫苗会积聚在生殖器官中,直接影响生育能力。胎盘细胞吸收血液中循环的 RNA 和DNA 可导致死胎。胎盘受损也会使外来基因进入胎儿的血液循环。接种疫苗后,脐带血中的干细胞减少并受损,有充分理由相信外来基因会进入子宫中的胎儿体内。此外,在母乳中也检测到了疫苗的包装。新生儿出生后最初几周的肠道渗透性很高,人们担心母乳喂养可能会使疫苗直接传给新生儿。这将导致新生儿细胞中的自杀机制被激活。 在实验室中,可以将偷运来的外来DNA 植入生命之书。这种情况发生在接种过疫苗的人身上,可能会产生无穷无尽的后果。控制细胞分裂和发育的精密网络一旦遭到破坏,就可能导致癌症。精子和受精卵中的突变可能会使改变的特征遗传下去导致出现偏离人类进化路径的生物。 结论 可以预见免疫系统对产生病毒蛋的细胞的攻击将导致对组织和血管的广泛而持久的损害。之所以会发生这种攻击,是因为病毒信使对人体来说是外来的。由于每种新的 mRNA疫苗都会控制一种外来蛋白质的生产,因此可以预见,类似规模的破坏将会一再发生。每接种一次强化疫苗,这些噩梦般的场景就会恶化一次。此外,还必须预料到,疫苗批次受到质粒DNA 污染的情况将不会是例外,而是常规,因为还没有一种具有成本效益的方法,能够可靠地将大规模生产的 RNA 与质粒分离。因此,在接种质粒 DNA时,细胞不可避免地会受到长期的自身免疫攻击。 将外来蓝图引入我们的身体,每个人的生命之书都可能被无可挽回地改变。如果人类染色体的组装指令被插入,无数的细胞功能就会被永久性破坏。恶性疾病可能会发生,预期寿命可能会急剧下降。无尽的疾病和痛苦可能成为受影响者的命运。,360一个恐怖的场景正在出现,它可能会影响到无数我们所爱的、我们心目中的人。我们有责任防止这种情况发生。 全世界每个人都必须站起来,立即停止所有 RNA 注射。 参考文献: (1) Bansal S. et al. (2021) Cutting Edge: Circulating Exosomes with COVID Spike Protein Are Induced by BNT162b2 (Pfizer-BioNTech) Vaccination prior to Development of Antibodies: A Novel Mechanism for Immune Activation by mRNA Vaccines. J Immunol 207:2405–2410. (2) Mörz M. (2022) A Case Report: Multifocal Necrotizing Encephalitis and Myocarditis after BNT162b2 mRNA Vaccination against COVID-19. Vaccines 10:1651. (3) https://doctors4covidethics.org/on-covid-vaccines-why-they-cannot-work-andirrefutable- evidence-of-their-causative-role-in-deaths-after-vaccination/ (4) McKernan K. (2023) Sequencing of bivalent Moderna and Pfizer mRNA vaccines reveals nanogram to microgram quantities of expression vector dsDNA per dose. https://osf.io/b9t7m/ (5) Nushida H. et al. (2023) A case of fatal multi-organ inflammation following COVID-19 vaccination. Leg Med 63: 102244. (6) Estep B.K. et al. (2023) Skewed fate and hematopoiesis of CD34+ HSPCs in umbilical cord blood amid the COVID-19 pandemic. iScience 25: 105544. (7) Hanna N. et al. (2022) Detection of Messenger RNA COVID-19 Vaccines in Human Breast Milk. JAMA Pediatr. 176:1268–1270. (8) Weström B. et al. (2020) The Immature Gut Barrier and Its Importance in Establishing Immunity in Newborn Mammals. Front Immunol. 11:1153.
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