mRNA – Realities

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皆さまの自身の本能、皆さまの自身の常識、そしてあなた自身の自然免疫システムを信頼してください。あなたはあなたがあなたの体に何を入れるかを決める資格がある唯一の人であり、あなたが知っていて信頼している人々からのアドバイスを受けています

私は医師でも生物学者でもないので、保健当局としての資格はありません。そしてそれがまさにポイントです。あなたはあなた自身の健康に関する究極の権威です。もちろん、信頼できる人からアドバイスを受けます。これについては、以下のｧ 16で検討します。しかし、常識的な健康上の決定は、医師や生物学者の独占的な領域ではありません。ここでは、医学雑誌、研究報告、文献レビュー記事、事例研究、プレプリント、オンラインビデオ、ハーブの参考資料から学んだことを、他の人が自分で情報の山をナビゲートできるように、情報源へのリンクとともに要約します。

医学出版物はウイルスSARS-CoV-2と病気新型コロナウィルスと呼んでいます。しかし、簡単にするために、ウイルスとそれが引き起こす病気の両方をSARS2と呼びます。これは、SARS1が改変されているためです。

1.ワクチンではありません。 mRNA薬は、SARS2ウイルスの感染を防ぎませんし、他の人への感染を防ぎません。これは、製造業者の緊急使用許可（EUA）の申請書、および例外なくこれらの薬剤のすべての試験と研究で開示されています。それらは、米国特許庁の「ワクチン」の定義を満たしていません。CDCが2021年9月にワクチンの定義を「免疫」の誘導から「免疫応答」に変更したにもかかわらず、私は以前の定義を保持し、mRNA薬を注射、接種、または注射と呼びます。

2.皆さまの自身の自然免疫システムは、コロナウイルスとすべての病原体に対する最高の保護を提供します。外来の侵入者を認識し、「オンザフライ」で生来の汎用抗体を適応させてそれらを食い尽くします。「ナチュラルキラー」（NK）細胞は、侵入する病原体に対する2番目の自然防御線を提供します。したがって、病原体に対する最も効果的な準備は、自分自身の自然免疫システムを強化することです。これは無料で簡単に行うことができます。ぐっすり眠るとDNAが修復され、抗体とNK細胞の産生が強化されます。日光、魚油、およびサプリメントは、病原体に対する免疫応答を強化し、バランスをとるビタミンDを提供します。オレガノ、タイム、タンポポ、その他のハーブの葉から作られたお茶も、自然免疫システムを刺激します。自然免疫は、堅牢でと耐久性があります。さらに、SARS2から回復した人は誰でも、SARS2に対する抗体に加えて、曝露されたときに多くを生成する細胞記憶を保持します。変異体に対する免疫は、mRNA注射によって生成された静的（進化できない）抗体の免疫よりも優れています。イスラエルでは、世界で最も高いmRNA注射率の1つであり、デルタ変異体は、注射なしでSARS2から回復した人よりも、mRNA注射を受けた人の間で13倍多く見られます。注射されたものはまた、症状を患う可能性が7倍高くなります。この研究は、「自然免疫は、BNT162b2 [ファイザー] 2回接種ワクチン誘発免疫と比較して、SARS2のデルタ変異体によって引き起こされる感染、症候性疾患、および入院に対するより長く持続するより強力な保護を与えることを示しました。」

3.NIHが資金提供する生物兵器。以前のすべての病原体とは異なり、SARS2ウイルスは、人間が設計した生物兵器であり、人間の上皮細胞とアンジオテンシン変換酵素（ACE2）受容体に感染して結合するように特別に設計されています。これらの細胞は、血管や重要な臓器の内層を形成します。通常、それらはバリアとして機能します。しかし、SARS2ウイルスは、これらの受容体にラッチするスパイクのような形のタンパク質で設計されています。この能力は、反対の初期の主張にもかかわらず、自然に進化しませんでしたノースカロライナ大学と武漢ウイルス研究所で、米国国立衛生研究所（NIH）からの資金提供を受けて、致命的な生物兵器として意図的に設計されました。これらの3つの機関はすべて、SARS2の病気の原因となるウイルスの特許を取得しましたが、自然に発生した場合は特許を取得できませんでした。 NIH、NIAID(アレルギーおよび感染症の国立研究所)、DOD(国防総省)、およびその他の米国政府の資金提供機関の高官は、この調査から生じる可能性のあるパンデミックの警告を無視しました。このNIH / WVIが設計したウイルスは、400万人以上を殺しました。

4.実際に患者を治療している医師は、何が効果的であるかについて最も信頼できる経験と証拠を持っています。アメリカの医師と外科医の協会は、ここ、ここ、そしてここで利用可能な彼らの最良の治療法の要約をまとめました。感染の初期段階では、治療は以前に他の目的で使用されていた薬剤で構成され、ACE-2細胞受容体へのウイルスの付着を阻止するという有益な副作用があります。治療の後期段階では、必要に応じて、抗凝血剤と抗炎症薬を使用します。

5.自然療法。一般的なタンポポの葉と花から作られたお茶は、SARS2がACE2細胞受容体に結合するのをブロックします。ザクロの皮の抽出物は、スパイク-ACE-2受容体の相互作用もブロックします。パイナップルに含まれるブロメラインと呼ばれる酵素は、スパイクタンパク質をブロックすることでSARS2感染を抑制し、血栓を破壊します。赤ワインはスパイクタンパク質も破壊し、抗凝血剤として作用し、血栓型心臓発作を予防することでよく知られています。レスベラトロールと呼ばれる分子がこれを行います。イチゴに一般的に見られる別の天然分子であるフィセチンは、スパイクタンパク質に強く結合するため、スパイクタンパク質の細胞への侵入をブロックします。（出典：Journal Biomolecular Structure＆Dynamics、Volume 39、No。9、page 3225、2021。) 亜鉛イオンはin vitro / ラボラトリーでSARS1を中和します。しかし、外側の細胞膜を通過して中央の細胞質に入るには、亜鉛はそれを運ぶための「イオノフォア」を必要とします。緑茶には、亜鉛イオンに結合して細胞質に運ぶ化合物が含まれています。そこに到達すると、亜鉛は（当然のことながら）レプリカーゼと呼ばれるタンパク質の形成を阻害することによってウイルス複製をブロックします。 SARS1とSARS2はどちらも、この同じタンパク質を使用して自分自身を複製します。それがなければ、どちらのウイルスもRNAのコピーを作成できず、したがって増殖できません。緑茶（EGCG、エピガロカテキンガレート）は、実際にはそれ自体でウイルス複製をブロックしますが、さまざまなウイルスタンパク質を同時に攻撃するのは良いことです。（これはin vitroでのみ、特に緑茶抽出物で研究されていますが、in vivo/体での実験が行われるまで、緑茶を飲んでも害はありません。）

6.もともとエイズワクチンを製造するための失敗した努力の一部として開発されたメッセンジャーRNA（mRNA）技術は、モノクローナル抗原特異的抗体を製造するために体を使用します。モノクローナルであるため、単一機能抗体から容易に逃れるウイルス変異体の広がりに見られるように、進化する病原体に適応することができません。抗生物質の過剰使用が細菌性病原体の耐性株を促進するのと同様に、大量接種はモノクローナル抗体を回避するウイルス変異体を促進します。ウイルス標的が進化するたびに新しい抗体をカスタム設計するよりも、製造業者がmRNA製剤を調整する方がはるかに安価であるため、mRNA技術は魅力的でした。

7.　緊急使用許可（EUA）の特異性。 EUAの手順は、もともと5　ー　6年かかるFDAの承認を回避するために開発されました。活動家や製薬会社は、新薬へのより迅速なアクセスを要求しました。これに応じて、EUAの手順は、（A）他に安全で効果的な治療法が利用できず、（B）製薬会社は危害に対する責任を免除されています。これらの条件を条件として、新薬は迅速に承認される可能性があります。倫理的には、安全で効果的な治療法が存在する場合、実験薬を提供または使用すべきではないというのが基本です。

SARS2のパンデミックは、迅速な治療法の要求をもたらし、それにより、抗体刺激mRNAの実験的大量注射に対する承認とEUAを促進しました。パニックでほとんど注目されなかったのは、他の救済策が利用できないというEUAの不測の事態でした。しかし、mRNAメーカーは、EUAを無効にする可能性があるため、その偶発性を非常に認識していました。彼らは他のすべての救済策の信用を傷つけることに着手しました。

亜鉛と一緒にマラリアに対して使用されるヒドロキシクロロキン（HCQ）、および熱帯寄生虫に対して使用されるイベルメクチン（IVM）は、症候性のSARS2感染患者の入院と死亡を減らします。HCQはACE2受容体（SARS2血管伝達の主要な手段）へのウイルスの結合をブロックし、IVMは細胞間シグナル伝達を改善して、隣接する細胞にウイルスの攻撃を警告し、炎症を引き起こすサイトカインを阻害し、ウイルス複製に必要なタンパク質の形成をブロックします。

有名な医学雑誌TheLancetは、HCQを心不整脈に関連付けることを目的とした記事を2020年4月に発表しました。数週間後、ランセットはこの主張のデータが存在しないことを発見し、調査会社と研究の著者は姿を消しました。 2020年6月、ランセットは記事を撤回しましたが、数か月後、医師と薬剤師は、安全で効果的な治療を処方または調剤するための免許と生計手段の喪失の脅威にさらされ、HCQについて話したり書いたりしたことでソーシャルメディアで検閲されました。 IVMの信用を傷つける同様の試みは、医療メディアや人気のあるメディアで定期的に見られ、FDAは依然として獣医と人間の治療を混同しています。代替治療法がないというEUAの不測の事態を考えると、mRNAメーカーは実際にはHCQとIVMを利用できないようにするために可能な限りのことをするしかありませんでした。悲劇的な皮肉なことに、これらの代替療法が成功すればするほど、mRNAメーカーは訴訟からのEUA免除を維持するために、それらをより徹底的に除去しようとしなければなりません。

mRNAメーカーにとって同様に重要なこととして、彼らは製品によって引き起こされた数万人の死と数十万人の負傷に対する責任に対するシールドとしてEUAを保持しなければなりませんでした。そうでなければ、訴訟は彼らを破産させる可能性があります。 2021年8月27日、FDAは、データをサポートすることなく、また通常の独立したレビューや公開コメントなしに、BioNTechmRNA製品に完全な承認を与えました。ただし、利用できません。ファイザー製品は、EUAステータスによっていかなる責任からも保護され、市場に残っています。

8.「95パーセントの有効性」。 EUAの申請について、ファイザーは、SARS-2疾患にかかった181人のうち、172人がプラセボを投与され、そのうち9人がファイザーのBioNTech接種を受けたことを発見しました。このことから、ファイザーは「95％の有効性」を主張しました。これはそれ以来広く引用されている数字です。ただし、この測定値に暗黙的に含まれる「有効性」の定義は、統計的に有意であったとしても、「ワクチン」に通常期待されるものには達していません。それ以来私たちが学んだように、多くの人々は症状を示さずにSARS2に感染します。 SARS2の存在に関するPCR検査には重大な欠陥があり、中止されました。また、ファイザーは、妊娠中の女性、子供、SARS-2で回復した患者、および高齢者をEUA前のテストから除外したため、これらのグループに関連するEUA前のテストデータはありません。

9. 実験薬。米国FDAは、ファイザーおよびその他のEUA申請を承認し、2023年10月に終了する予定の治験薬に関するデータを収集するための臨床試験を実施する許可を与えました。「調査」、「実験」、および「試験」という用語としてこの臨床試験の結果を事前に知ることはできないことを明確に示しています。しかし、これらの薬が安全で効果的であることを切に願うかもしれませんが、2年間の臨床試験が完了するまで、そしてその後、それらが確実であるという保証はありません。猛威を振るうパンデミックと同時に起こる極端な時間的プレッシャーでさえ、そのような実験の過程を加速することはできません。臨床試験の目的は、新しい実験薬がどれほど安全で効果的であるかを調べることです。

10. mRNA注射の利点。心臓病、肥満、糖尿病、免疫不全などの他の症状に苦しんでいる人々は、SARS2の追加の負担のリスクが最も高く、mRNA注射の恩恵を受けています。 mRNA注射は、体が弱くなった状態で許容されるよりも強力な免疫応答を開始することにより、SARS-2症状の重症度を軽減し、ウイルス複製を抑制し、多くの命を救います。

11. ワクチン接種後の死亡。 mRNA薬に対する個々の反応は大きく異なります。米国CDCのワクチン有害事象報告システム（VAERS）や他の国の同様のデータベースによると、腕の痛みなどの一時的な副作用は別として、注射されたものの99％はすぐに反応しません。しかし、接種された人の数が非常に多いことを考えると、深刻な副作用のほんのわずかな割合でさえ、数万人の死をもたらしました。統計学者は、とにかくいくつかの死亡が発生したであろうので、本当の尺度は予想されたものに加えて「過剰な死亡」であると警告します。同時に、注射後の死亡の多くが報告されていない可能性が非常に高いです。幾つか？誰も知らない。

統計的集合体の領域を離れて個々の症例に移ると、死因はしばしば脳卒中、心臓発作、血栓症、本質的には血栓であることがわかります。さらなる調査により、SARS2抗体の産生を刺激することを目的としたmRNAで生成されたスパイクタンパク質は、血管や重要な臓器の内層に付着していることが示されています。そこで、これらの小さなとげは、通常は滑らかな表面であるものを粗くします。血小板は、凝固の原因となる血球の一種であり、最も小さな流れの障害物の周りに凝集します。最初、これらの微小凝固は小さすぎて、心臓発作や脳卒中のリスクを評価するために使用されるCATスキャンで検出できません。 D-ダイマーテストと呼ばれるものがそれらを検出できます。 0.5マイクログラム/ミリリットルの血液未満のD-ダイマーレベルは正常です。

12. マイクロ凝固。 mRNA注射を受けた直後に死亡した人の剖検では、mRNAで生成されたスパイクタンパク質によるACE-2受容体を伴うすべての臓器の微小凝固と炎症が示され、写真を並べて比較するとはっきりとわかります。 mRNAの影響とは別に、動脈硬化症は、遺伝的要因、食事、コレステロール、ライフスタイル、および炎症に対する感受性に応じて、さまざまな人々でさまざまな速度で進行します。これらの属性に好意的に対処している人々は、おそらく、遺伝や食事などが詰まりを促進する人々よりもスパイクタンパク質に耐えることができます。これは、mRNA注射に対する即時反応の個人差、注射直後に死亡する人もいれば、即時反応を経験しない人もいる理由を説明している可能性があります。数年以内に予想よりも高い心血管系の問題が発生するかどうか、またいつ発生するかについては、さらに詳しく知ることができます。

13.心筋炎（心臓の肥大）は、mRNA注射の直接の結果として何千人もの若者に報告されています。正確なプロセスは不明ですが、おそらく他の場所で見られるのと同じ微小凝固が原因です。心臓では、通路が狭くなっていると心臓が働きにくくなり、心臓が大きくなります。損傷した心臓細胞は新しい細胞に置き換えられませんが、代わりに瘢痕組織で覆われます。これは通常、心臓病の前兆です。

14.再感染はありません。独自の生来の抗体によってSARS2から回復した人々は、SARS2の元のバージョンまたはバリアントに再感染することはめったにありません。この保護は、先天性抗体がモノクローナルではないために正確に発生します。これらは、新しい脅威に対抗するために適応および進化します。自然免疫の汎用抗体の代わりに特殊なmRNA生成モノクローナル抗体を使用すると、免疫系が変異体や新しい病原体に応答する能力が損なわれます。抗原特異的抗体は、SARS2への結合に関して自然免疫抗体を凌駕し、それによって自然免疫系のトレーニングを低下させます。 mRNA注射を受けた人は、突然変異や変異に反応することができません。なぜなら、彼らの免疫系は、SARS-2ウイルスの元の形態だけと戦うように設計された人工のmRNA生成防御システムによって引き継がれているからです。

15.病原性プライミング。 SARS2から回復した人は、再感染のリスクがありません。それらの抗体が回復後数ヶ月で減少したとしても、それらは細胞記憶を保持し、さらなる曝露でそれらの抗体を再生成します。これらの先天性抗体は、SARS2の変異や変異とともに進化します。しかし、免疫システムが正常に機能しているこれらの人々が、追加の特殊目的の抗体を生成する注射を行うと、彼らは自分の免疫システムを破壊するだけでなく、自然免疫とmRNAの組み合わせである「病原性プライミング」のリスクも冒します。 -生成された抗体は、体自身の細胞を攻撃する余剰を作成します。この「サイトカインストーム」はほとんどの場合致命的です。したがって、SARS2感染から回復した人は、たとえ感染に無症状があったとしても、mRNA薬を避けるべきです。

16. 信頼。他の人間の活動では、医療よりも信頼が不可欠です。私たちの健康と人生を他の人に委ねるには、他の環境ではもうほとんど感じられないような信仰が必要です。それでも私たちは、未知の効果で、私たちが何も知らない何かを私たちの体に注入するように求められています-いいえ、多くの場合、強制されます-。私たちは、白い白衣を着ている人々に盲目的で受動的な信頼を置いて、従うべき科学があるかのように「科学に従う」ように言われています。彼らの指示は私たち自身のためであると言われていますが、彼らが私たちを知らず、私たちが彼らを知らない場合、どうすれば彼らは私たちにとって何が良いかを知ることができますか？信頼は、個人的な関係は別として、不定形で自由に動く属性として存在することはできません。信頼は、個人間の経験と相互の知識に基づいている場合にのみ授けることができます。

私たちの体に実験物質を注射するように交互に懇願し、脅迫している公衆衛生当局について、私たちは何を知っていますか？米国国立衛生研究所（NIH）と国立アレルギー感染症研究所（NIAID）が、共産主義者が管理するウーハン（中国）ウイルス学における生物兵器の機能獲得研究と開発を研究し、資金を提供したことを私たちは知っています。研究所（WVI）。そしてそこから、現在の疫病とパンデミックが発生しました。彼らの役割を隠すために、これらの人々は、SARS2の起源の正確な追跡を可能にするデータを破壊し、沈黙させ、打ち切り、場合によっては、問題の事実を報告した科学者を逮捕し、死因統計を歪めてパニックを助長しました。ますます厳しくなる恐怖のキャンペーンに従事し、実験薬を拒否する自由への異常な攻撃で最高潮に達しました。

何か問題が発生した場合、これらの役人またはその製薬会社が私たちの面倒を見てくれますか？何百万人もの人々が彼らの失望に気づいているので、答えはノーです。製薬会社は、EUAに基づいて行動する場合、いかなる責任も免除されます。責任シールドを削除する必要がある完全なFDA承認は、入手できない製品にのみ適用されます。 FDAは、2021年8月24日に撮影されたBioNTechにそのような承認を与えましたが、これは実際には入手できない製品です。同時に、ファイザーショットは、EUAの下でのみではありますが、引き続き利用可能であり、責任を免除されます。この法的な官僚的な操作のすべては、公衆衛生当局と製薬会社が彼らの製品によってなされた危害に対する責任を免れることを可能にします。これは、介護者と患者の関係に通常適用されるような信頼を刺激するものではありません。

mRNA技術の発明者であるロバート・マローン博士は、外部のレビュー委員会とパブリックコメントなしにFDAの承認プロセスはこれまでなかったと述べています。 FDAは論争はないと主張している。マローン博士は次のように述べています。物議を醸している問題の少なくとも一つは、現在必要とされている多くの多くの研究がある心毒性です。彼らがやったことは、政府や州や企業がワクチンを義務付けることを可能にする何かを妨害することです。彼ら自身の声明によると、彼らは安全性と有効性の主張を裏付けるデータを持っていません。彼らが持っている有効性の主張は明らかに時代遅れのデータに基づいています。アルファ版とベータ版に基づいています。」

Geert Vanden Bosscheは、GSK、Novartis、Solvay、およびGates Foundationでのワクチン開発の豊富な経験を持つ、獣医学博士およびPhDウイルス学者です。彼と他の人々は3月（2021年）にパンデミック時の集団予防接種キャンペーンは、ウイルスの亜種を作成し、人工的に誘導された抗体が自然免疫系を打ち負かすこと汎用抗体。これらの予防接種キャンペーンは、彼が警告した、「現在のワクチンのどれもウイルス変異体の複製/伝達を防ぐことができないので、適応免疫脱出をさらに強化する可能性が高い」。そのようなものとして、「パンデミックの真っ只中にいる人々を免疫するためにこれらのワクチンを使用するほど、より感染性の高いウイルスになります」。

そしてそれは起こった。

ファイザー-モダナショットは、これまで以上に感染性の変異体のシリーズを生成しながら、自然免疫系を劣化させることによってパンデミックを延長しています。私たちは今、「ム」までです。おそらくギリシャ語のアルファベットのアルファとオメガの間のどこかで、ゼータの変種は皆に感染するでしょう。「ゼータ」はたまたまメキシコの麻薬カルテルの名前でもあります。薬物中毒のクマを誘導するファイザー・モダナの手段は、ゼータ・カルテルの技術に似ています – 執行者として政府を参加させ、政府の役人やメディアに賄賂を送ります。その後、生活、教育、旅行、食品購入、銀行、ショッピング、エンターテイメント、社会生活を脅かすことによって、ユーザーを怖がらせます。これらの役人とテストされていない実験薬のサプライヤーは、私たちが私たちの生活を信頼するように求められている、または強制されている人々。

代わりに、皆さまの自身の本能、皆さまの自身の常識、そしてあなた自身の自然免疫システムを信頼してください。あなたはあなたがあなたの体に何を入れるかを決める資格がある唯一の人であり、あなたが知っていて信頼している人々からのアドバイスを受けています。結局、永遠に続くことができない何か…そうはなりません。十分な数の人々が実験動物のように振る舞うのをやめ、この狂った実験をオプトアウトすると、パンデミックは終わります。

~~　ミラー・ピーター (Peter Miller)、鎌倉、2021年9月14日

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作品

識見(英語)

Take Care of Yourself

You are the ultimate authority on your own health, with advice from people you know and trust.

日本語

I am neither a medical doctor nor a biologist, therefore have no qualifications as a health authority. And that is exactly the point. You are the ultimate authority on your own health. Of course you take advice from those you trust, which we will consider in §16 below. But common-sense health decisions are not the exclusive province of doctors and biologists. Here I summarize what I have learned from medical journals, research reports, literature-review articles, case studies, preprints, online videos, and herbal references, with links to sources, so that others can navigate the thicket of information for themselves.

Medical publications call the virus SARS-CoV-2 and the disease covid or covid-19. But for simplicity, I refer to both the virus and the disease it causes as SARS2, since it is a modified SARS1.

Not a Vaccine. The mRNA drugs don’t prevent infection with the SARS-2 virus and don’t prevent its onward transmission to others. This is disclosed in the manufacturers’ applications for Emergency Use Approval (EUA) and in all tests and studies of these drugs, without exception. They don’t meet the U.S. Patent Office’s definition of a ‘vaccine’. Despite CDC’s changing its definitiion of a vaccine in Sept 2021 from inducing an ‘immunity’ to nothing more than ‘an immune response’, I retain the earlier definition and refer to the mRNA drugs as injections, inoculations, or shots.

2. Your Own Innate Immune System provides the best protection against coronaviruses and all pathogens. It recognizes foreign invaders and adapts innate general-purpose antibodies ‘on the fly’ to devour them. Natural Killer (NK) cells provide a second natural line of defense against invading pathogens. Therefore the most effective preparation against any pathogen is to strengthen one’s own innate immune system. This can easily be done at no cost: A good night’s sleep repairs DNA and reinforces production of antibodies and NK cells. Sunlight, fish oil, and supplements provide Vitamin D which enhances and balances immune responses to pathogens. Teas made from leaves of oregano, thyme, dandelion, and other herbs also stimulate the innate immune system. Natural immunity is robust and durable. In addition, anyone who has recovered from SARS2 retains antibodies against it, plus cellular memory that produces more when exposed. Immunity against variants is superior to that of the static (unable to evolve) antibodies generated by mRNA injections. In Israel, with one of the highest rates of mRNA injections in the world, the Delta variant is 13 times more prevalent among those who have received mRNA injections than among those who have recovered from SARS2 without any injection. The injected are also seven times more likely to suffer symptoms. This study ‘demonstrated that natural immunity confers longer lasting and stronger protection against infection, symptomatic disease and hospitalization caused by the Delta variant of SARS2, compared to the BNT162b2 [Pfizer] two-dose vaccine-induced immunity.‘

3. An NIH-Funded Bio-Weapon. Unlike all prior pathogens, the SARS-2 virus is a human-engineered bio-weapon, specifically designed to infect and bind to human epithelial cells and angiostatin-converting enzyme (ACE2) receptors. These cells form the inner lining of blood vessels and vital organs. Normally they act as a barrier. But the SARS2 virus has been designed with a protein shaped like a spike to latch onto these receptors. This ability did not evolve naturally, despite early assertions to the contrary — it was purpose-designed as a deadly bio-weapon, at the University of North Carolina and the Wuhan Virology Institute, with funding provided by the U.S. National Institutes of Health (NIH). All three of these institutions patented the SARS2 disease-causing virus, which could not have been patented if it had arisen naturally. Top officials of NIH, NIAID, DOD, and other U.S. Government funding agencies ignored warnings of the pandemic likely to result from this research. This NIH/WVI-designed virus has killed more than four million people.

4. Doctors Who Are Actually Treating Patients successfully have the most reliable experience and evidence of what works. The Association of American Physicians and Surgeons has compiled a summary of their best treatment practices, available here, here, and here. In early stages of infection, treatment consists of drugs previously used for other purposes, which happen to have the beneficial side-effect of blocking virus adherence to ACE2 cell receptors. Later stages of treatment, if needed, use blood thinners and anti-inflammatory drugs.

5. Natural Remedies. Tea made from the leaves and flowers of common dandelion blocks SARS2 from binding to ACE2 cell receptors. Pomegranate peel extract also blocks spike-ACE2 receptor interaction. An enzyme found in pineapples, called bromelian, inhibits SARS-2 infection by blocking the spike protein, and also breaks up blood clots. Red wine also disrupts the spike protein and is well-known to act as a blood thinner, preventing clot-type heart attacks. A molecule called resveratrol does this. Fisetin, another natural molecule commonly found in strawberries, binds strongly to spike protein, thus blocking spike protein entry into cells. (Source: Journal Biomolecular Structure & Dynamics,Volume 39, No. 9, page 3225, 2021.)

Zinc ions neutralize SARS1 in vitro, in a lab dish. But in order to pass through outer cell membranes into the central cell cytoplasm, zinc requires an ionophore to carry it there. Green tea contains a compound that does that — binds to zinc ions and carries them into cell cytoplasm. Once there, zinc blocks virus replication by inhibiting formation of a protein called (not surprisingly) replicase. Both SARS-1 and SARS-2 use this same protein to replicate themselves. Without it, neither virus can make copies of their RNA, and thus cannot proliferate. Green tea (EGCG, epigallocatechin gallate) actually blocks viral replication on its own, but it’s nice to attack various viral proteins at the same time. (While this has only been studied in vitro, and specifically with green tea extract, there’s certainly no harm in drinking green tea pending in vivo human experiments.)

6. Messenger-RNA (mRNA) Technology, originally developed as part of a failed effort to produce an AIDS vaccine, uses the body to manufacture monoclonal antigen-specific antibodies. Being monoclonal, they are unable to adapt to evolving pathogens, as is seen with the spread of viral variants that readily escape single-function antibodies. Similar to the way over-use of antibiotics promotes resistant strains of bacterial pathogens, mass inoculation promotes viral variants that evade monoclonal antibodies. The mRNA technology was attractive because it is much less expensive for manufacturers to adjust mRNA formulations than to custom-design new antibodies every time a viral target evolves.

7. Peculiarities of Emergency Use Authorization (EUA). The EUA protocol was originally developed to circumvent FDA approval taking five to six years. Activists and drug companies demanded faster access to new drugs. In response, the EUA protocol provided that if (A) no other safe and effective treatments are available, and (B) drug manufacturers would incur no liability for harm, new drugs could get expedited approval. Ethically, it’s elementary that if a safe and effective remedy exists, then an experimental drug should not be offered or used.

The SARS2 pandemic brought demands for a quick remedy, and with it expedited approval and EUA for experimental mass injections of antibody-stimulating mRNA. Little noted in the panic was the EUA’s contingency on the unavailability of any other remedy. However, the mRNA makers were very much aware of that contingency, because it could nullify their EUA. They set out to discredit all other remedies.

Hydroxylchloroquine (HCQ), used against malaria, together with zinc, and Ivermectin (IVM), used against tropical parasites, reduce hospitalization and deaths among symptomatic SARS2-infected patients. HCQ blocks viral binding to ACE2 receptors (the primary means of SARS2 vascular transmission), and IVM improves inter-cellular signaling to alert neighboring cells to viral attack, inhibits inflammation-causing cytokines, and blocks formation of proteins required for viral replication.

The prestigious medical journal The Lancet published an article in April 2020 purporting to link HCQ to heart arrhythmia. Several weeks later, The Lancet discovered the data for this assertion did not exist, and the research firm and authors of the study disappeared. In June 2020 The Lancet retracted the article, though months later doctors and pharmacists were still being threatened with loss of licensure and livelihoods for prescribing or dispensing a safe and effective treatment, and being censored in social media for talking or writing about HCQ. Similar attempts to discredit IVM appear regularly in medical and popular media, and FDA still confuses veterinary and human treatments. The mRNA makers actually had no choice but to do everything possible to make HCQ and IVM unavailable, given the EUA contingency of there being no alternative treatment. With tragic irony, the more successful these alternative remedies are, the more thoroughly the mRNA makers must try to remove them, to maintain their EUA immunity from lawsuits.

Of equal importance to the mRNA makers, they had to retain their EUA as a shield against liability for the tens of thousands of deaths, and hundreds of thousands of injuries, caused by their products. Otherwise lawsuits could bankrupt them. On August 27, 2021, FDA granted full approval to the BioNTech mRNA product without supporting data, and without the usual independent review and pubic comment. It is not available, however. The Pfizer product remains on the market, shielded by its EUA status from any liability.

8. ’95 Percent Efficacy’. For its EUA application, Pfizer found that of 181 people who got SARS2 disease, 172 of them had received a placebo, nine of them Pfizer’s BioNTech inoculation. From this, Pfizer claimed ‘95 percent efficacy‘, a figure which has been widely quoted since. However, the definition of ‘efficacy’ implicit in this measure, even if it were statistically significant, falls short of what one would normally expect of a ‘vaccine’. As we have since learned, many people contract SARS2 without showing symptoms; the PCR tests for presence of SARS2 are seriously flawed and have been abandoned. Also, Pfizer excluded pregnant women, children, SAR2-recovered patients, and the elderly from its pre-EUA testing, so there are no pre-EUA test data pertaining to these groups.

9. Experimental Drugs. The U.S. FDA approved Pfizer’s and the others’ EUA applications, granting them permission to run a clinical trial to gather data on their investigational drugs, scheduled to conclude in October 2023. As the terms investigational, experimental, and trial clearly indicate, the outcome of this clinical trial cannot be known in advance. However fervently we may wish these drugs to be safe and effective, there can be no assurance that they are until completion of the two-year-long clinical trial in October 2023 and thereafter. Not even the extreme time-pressure coincident with a raging pandemic can accelerate the course of such an experiment. The purpose of a clinical trial is to find out how safe and effective a new, experimental drug may be.

10. Benefits of mRNA Injections. People suffering from other conditions such as heart disease, obesity, diabetes, and immuno-compromise, who are most at risk from the additional burden of SARS2, benefit from the mRNA injections. By causing the body to mount a more vigorous immune response than its weakened condition would otherwise permit, the mRNA injections mitigate the severity of SARS2 symptoms and stifle viral replication, saving many lives.

11. Post-Vaccine Deaths. Individual reactions to the mRNA drugs vary widely. Leaving aside transient side effects such as sore arms, 99 percent of those injected have no immediate reaction, according to the U.S. CDC’s Vaccine Adverse Event Reporting System (VAERS) and similar databases in other countries. However, given the very large number of people inoculated, even a small percentage of severe adverse effects has resulted in tens of thousands of deaths. Statisticians caution that since some deaths would have occurred anyway, the true measure is ‘excess deaths’ in addition to what would have been expected. At the same time, it is very likely that many post-injection deaths go unreported. How many? We don’t know.

When we leave the territory of statistical aggregates and move to individual cases, we find that the cause of death was often stroke, heart attack, thrombosis — essentially blood clots. Further investigation shows that the mRNA-generated spike proteins — which are intended to stimulate production of SARS-2 antibodies — attach themselves to the inner linings of blood vessels and vital organs. There these tiny thorns rough-up what is normally a smooth surface. Platelets, the type of blood cell responsible for clotting, aggregate around the tiniest flow-impediment. At first, these micro-coagulations are too small to be detected by CAT-scans that are used to assess risk of heart attack and stroke. Something called a D-dimer test can detect them. D-dimer levels less than 0.5 micrograms/ milliliter of blood are normal.

Micro-Coagulations. Autopsies of those who have died soon after receiving mRNA injections show micro-coagulations and inflammation all organs with ACE-2 receptors by mRNA-generated spike protein, clearly visible in side-by-side photo comparisons. Quite apart from mRNA effects, arteriosclerosis progresses at different rates in different people, depending on hereditary factors, diet, cholesterol, lifestyle, and susceptibility to inflammation. People who are favorably disposed on these attributes can probably tolerate spike proteins better than those whose heredity, diet, etc. facilitate clogging. This may account for individual differences in immediate reaction to the mRNA injections, why some people die soon after injection, and others experience no immediate reaction. We will know more if and when higher than expected rates of cardio-vascular problems show up in several years.

13. Myocarditis — enlargement of the heart — has been reported in thousands of young people as a direct result of mRNA injections. The exact process is unknown, but is probably due to the same micro-coagulations seen elsewhere. In the heart, constricted passageways make the heart work harder, enlarging it. Heart cells when damaged are not replaced with new cells, but instead are covered with scar tissue, typically a precursor of heart disease.

14. No Re-Infection. People who have recovered from SARS-2 by means of their own innate antibodies rarely get re-infected with the original version of SARS-2 or with variants. This protection occurs precisely because innate antibodies are NOT monoclonal — they adapt and evolve to counter the new threat. Substituting a specialized mRNA-generated monoclonal antibody for innate general-purpose antibodies impairs the ability of the immune system to respond to variants and new pathogens. Antigen-specific antibodies out-compete innate antibodies for binding to SARS-2, thereby degrading training of the innate immune system. Those who have received mRNA injections are unable to respond to mutations or variants, because their immune systems have been taken over by an artificial mRNA-generated defense system, designed to combat only the original form of the SARS-2 virus and nothing else.

15. Pathogenic Priming. People who have recovered from SARS-2 have trivial risk of re-infection. Even if their antibodies are reduced in number several months after recovery, they retain cellular memory that re-generates those antibodies upon further exposure. These innate antibodies also evolve along with SARS-2 mutations and variants. If, however, these people with a healthy functioning immune system take an injection that generates additional special-purpose antibodies, they not only disrupt their own immune system, they also run the risk of ‘pathogenic priming’, the combination of innate antibodies plus mRNA-generated antibodies creating a surplus which attacks the body’s own cells. This ‘cytokine storm’ is almost always fatal. Thus anyone who has recovered from SARS2 infection, even if the infection was symptomless, should avoid any of the mRNA drugs.

16. Trust. In no other human activity is trust more essential than in medical care. To entrust our health and our life to another person requires faith such as we hardly ever feel anymore in other settings. And yet we are being asked — no, forced, in many cases — to inject something into our bodies of which we know nothing, with unknown effects. We are told to follow the science as if there were any science to be followed, with blind, passive trust in people wearing white lab coats. We are told their directives are for our own good, but how can they possibly know what is good for us if they don’t know us and we don’t know them? Trust cannot exist as some amorphous, free-floating attribute, apart from a personal relationship. Trust can only be bestowed when based on inter-personal experience and mutual knowledge.

What do we know of the public health officials who alternately beg and threaten us to inject an experimental substance into our bodies? We know that the U.S. National Institutes of Health (NIH) and the National Institute of Allergic and Infectious Diseases (NIAID) researched and funded gain-of-function research and development of a bio-weapon at the Communist-controlled Wuhan (China) Virology Institute (WVI). And from that the present plague and pandemic originated. To conceal their role, these people destroyed data that would have allowed accurate tracing of SARS2 origins, silenced, censored, and in some cases arrested scientists who reported the facts of the matter, distorted cause-of-death statistics to promote panic, and otherwise engaged in an increasingly strident campaign of fear, culminating in extraordinary attacks on freedom to refuse an experimental drug.

Will these officials or their drug suppliers take care of us if something goes wrong? As millions of people are finding out to their dismay, the answer is no. The drug companies are exempt from any liability when acting under EUA. Full FDA approval, where the liability shield must be dropped, applies only to a product that is not available. FDA granted such approval to a BioNTech shot on August 24, 2021, a product that is not actually available. At the same time, the Pfizer shot is still available, though only under EUA, exempt from liability. All of this legal-bureaucratic maneuvering lets public health officials and drug companies escape responsibility for harm done by their products. This does not inspire the sort of trust usually applicable to the relationship of caregiver and patient.

Dr Robert Malone, the inventor of mRNA technology, says there has never been an FDA approval process without an external review committee and public comment. FDA claims there is no controversy. Dr Malone says ‘There’s been a ton of controversy. Not the least of the controversial issues is the cardio-toxicity for which there are many many studies now required. What they’ve done is jam through something that will enable governments and states and companies to mandate vaccines. By their own statements, they don’t have the data to support the safety and efficacy claims. The efficacy claims that they do have are clearly based on data that is outdated. It’s based on the Alpha and Beta variants.‘

Geert Vanden Bossche is a Doctor of Veterinary Medicine and Ph D virologist with extensive experience in vaccine development with GSK, Novartis, Solvay, and the Gates Foundation. He and others warned back in March (2021) that undertaking a mass vaccination campaign during a pandemic would create viral variants, and that the artificially induced antibodies would out-compete innate immune-system general-purpose antibodies. These vaccination campaigns are, he warned, highly likely to further enhance adaptive immune escape as none of the current vaccines will prevent replication/transmission of viral variants. As such, The more we use these vaccines for immunizing people in the midst of a pandemic, the more infectious the virus will become.

And so it has done.

The Pfizer-Moderna shots are prolonging the pandemic by degrading innate immune systems, while generating a series of ever more infectious variants. We’re up to mu now. Perhaps somewhere between Alpha and Omega in the the Greek alphabet, a Zeta variant will descend on the populace. That happens also to be the name of a Mexican drug cartel. The Pfizer-Moderna method of inducing drug addiction bears an uncanny resemblance to the Zeta cartel’s technique — enlist government as enforcer, by bribing government officials and media, and terrify users into complying by threatening their livelihoods, education, travel, food purchasing, banking, shopping, entertainment, and social life. These are the people we are being asked or forced to trust with our lives.

Instead, trust your own instincts, your own common-sense, and your own innate immune system. You are the only one qualified to decide what you put into your body, with advice from people you know and trust. Eventually, something that cannot go on forever… won’t. The pandemic will end when enough people stop acting like lab-rats, and opt-out of this mad experiment.

~~ Peter Miller, September 15, 2021

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On pattern recognition and the engineering of consent

Artwork

Sayings — on Viruses

‘We need to increase public understanding of the need for medical countermeasures such as a pan-coronavirus vaccine. A key driver is the media and the economics will follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of the process.’ — Peter Daszak, Eco-Health Alliance

Transcript of testimony by Dr Christina Parks before Michigan (U.S.A.) House of Representatives, on HR 4471, a Bill to ban employers from forcing employees to take vaccinations, Aug 2021

I have a PhD in cellular and molecular biology from University of Michigan Medical School, so I’m very well-versed in the science of both these mRNA gene therapy vaccines, this kind of technology as well as what the vaccine is designed to do in the body, what it can do, what it can’t do. This is extremely complex science that has been over-simplified in the media to basically take away our freedom of choice. What I want to address today is the fact that vaccine requirements and mandates are based on the faulty assumption that the vaccines prevent transmission of the pathogen.

Does the vaccine for flu prevent transmission? No. Do the vaccines for covid prevent transmission? No. In fact they were never designed to do that. So you’re asking what about this 95% effectiveness? If you look at those clinical trials, they do not say that they prevent transmission, they expressly say that they’re measuring whether they attenuate symptoms. So they’re 95% effective based on their clinical trials at attenuating symptoms for the first variant, which is essentially gone in our population right now. The predominant variant is Delta, and CDC Director Wollensky basically said that these vaccines have no ability to prevent infection by and transmission of the Delta variant. So our policy needs not to be built on the hope of what we think, something we wanted to do, but what the data actually tell us. So does the vaccine prevent the virus from infecting and replicating in the nose and nasopharynx? No. They’ve only been shown to prevent that replication in the lungs. The mucosa is very different in the lungs and in the blood.

Studies have shown that the vaccinated, especially with the Delta variant, and the unvaccinated have similar amounts of virus in their nose and throat. In Barnstable Massachusetts the CDC tracking an outbreak of 469 cases of covid found that 74 per cent occurred in the fully vaccinated, and four out of five of those hospitalized were vaccinated. The health agencies and CDC know better and are misleading the public. What about the flu vaccine? While they have shown that basically there’s no statistical difference if you’re vaccinated and unvaccinated whether you get the flu or not. But it’s even worse because although that first year it is somewhat effective, it’s about 65% effective at preventing symptoms in you. After that it actually has negative effects.

It’s very important to see that vaccines are made to a specific variant, and when that variant mutates, the vaccine no longer recognizes it, and so it’s like you’re seeing a completely new virus. And because that’s so, you actually get more severe symptoms when you’re vaccinated against one variant, and then it mutates and then your body sees the other variants. So there’s a potential, and the science shows, that in fact with the flu if you get vaccinated in multiple years, you are more likely to get severe disease you are more likely have more viral replication and you are more likely to be hospitalized — both in adults and in children. We are seeing the same thing with covid. So we are mandating that people get a vaccine that could actually make them more sick when they’re exposed to the virus, This week a paper came out, what it showed is that with this Delta variant, when you’re vaccinated your body makes antibodies that are supposed to neutralize the virus. But they were supposed to neutralize the old variant. When they see this new variant, antibodies are taking the virus and helping it in.

We need our policy to reflect the science and we also need it to reflect our rights. As a PhD who knows the science I’m in the category of the most vaccine-hesitant group. PhDs are the most vaccine-hesitant, followed by people who have less than a high school degree, because they know what they don’t know and they don’t trust their government. The other group that is very vaccine-hesitant is African-Americans. Seventy percent of African Americans have not taken this vaccine why because they don’t trust their government. Do they have reason not to trust our government? Well, between the years of 1930 and 1970 the CDC conducted the Tuskegee experiment where they took untreated males with syphilis and they refuse to treat them even after antibiotics became available. They did not tell them that they had syphilis, they told those people that they were there to secure their health. You say well that was in the past, but I don’t think 1970 was that long ago. As an African-American and a PhD I want to ask each of you are we going to exclude 70% of African-American people from the workforce and from education? My ancestors did not work this hard I come up at from a family that worked very hard and I’m very aware that my privileges are dependent on the work of my grandmother and my great-grandmother and I have great respect for these people that put me where I am. And yet you’re telling me that my son will not be able to be educated if, based on the history of African Americans in this country, he doesn’t want to be vaccinated. So I will leave you with that question: Who are we going to exclude from the workforce? Are we going to continue with discrimination and segregation in the United States of America? Thank you. [Video]

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Transcript of remarks by Dr David Martin, July 2021

Dr David Martin

Our firm has been the world’s largest underwriter of intangible assets used in finance in 168 countries, so in the majority of the countries around the world. Our underwriting systems include the entire corpus of all patents, patent applications, federal grants procurement records, e-government records, etc. We have the ability to not only track what is happening and who is involved in what’s happening but we monitor a series of thematic interests for a variety of organizations and individuals as well as for our own commercial use, because as you probably know we maintain three Global Equity indices which are the the top performing large-cap and mid-cap equity indices worldwide. So our business is to monitor the innovation that’s happening around the world and specifically to monitor the economics of that innovation, the degree to which financial interests are being served, corporate interests are being dislocated etc. So our business is the business of innovation and its finance.

As you know we have reviewed the over 4,000 patents that have been issued around SARS Coronavirus and we have done a very comprehensive review of the financing of all of the manipulations of coronavirus which gave rise to SARS as a subclade of the beta coronavirus family. We took the reported gene sequence which was reportedly indicated as such by the ICTV (the International Committee on Taxonomy of Viruses) of the World Health Organization. We took the actual genetic sequences that were reportedly novel and reviewed those against the patent records that were available as of the spring of 2020. And what we found are over 120 patented pieces of evidence to suggest that the declaration of a novel coronavirus was actually entirely a fallacy. There was no novel coronavirus. There are countless very subtle modifications of coronavirus sequences that have been uploaded but there was no single identified novel coronavirus at all. As a matter of fact, we found records in the patent records of sequences attributed to novelty going to patents that were sought as early as 1999. So not only was this not a novel anything, it’s actually not been novel for over two decades.

Up until 1999 the topic of coronavirus was uniquely applied to veterinary sciences. The first vaccine ever patented for coronavirus was actually sought by Pfizer. The application for the first vaccine for Coronavirus which was specifically a Spike protein — so the exact same thing that allegedly we have rushed into invention — the first application was filed January 28th 2000 — 21 years ago. So the idea that we mysteriously stumbled on the way to intervene on vaccines is not only ludicrous, it is incredulous because Timothy Miller, Sharon Klepfer, Albert Paul Reed, and Elaine Jones on January 28th 2000 filed what ultimately was issued as U.S. patent 637-2224, which was the spike protein virus vaccine for the canine coronavirus, which is actually one of the multiple forms of coronavirus. But as I said the early work up until 1999 was largely focused in the area of vaccines for animals. The two animals receiving the most attention were probably Ralph Baric’s work on rabbits, and the rabbit cardiomyopathy that was associated with significant problems among rabbit breeders; and then canine coronavirus in Pfizer’s work to identify how to develop a spike protein. [These] target candidates give rise to the obvious evidence that says that neither the coronavirus concept of vaccine nor the principle of the coronavirus itself as a pathogen of interest with respect to the spike protein’s behavior is anything novel at all. As matter fact it’s 22 years old on based on patent files.

What’s more problematic and what is actually the most egregious problem is that Anthony Fauci and NIAID found the malleability of coronavirus to be a potential candidate for HIV vaccines, and so this is actually not a natural progression of a zoonotic modification of coronavirus. As a matter of fact, very specifically in 1999 Anthony Fauci funded research at the University of North Carolina Chapel Hill specifically to create — this comes directly from a patent application filed on April 19th, 2002 — you heard the date correctly, 2002 — where NIAID built an infectious replication-defective coronavirus specifically targeted for human lung epithelium. In other words we [U.S. NIAID] made SARS and we patented it on April 19th, 2002 before there was ever any alleged outbreak in Asia. Which [outbreak] as you know followed that by several months, that patent issued as US patent 727-9327. That patent clearly lays out in very specific gene sequencing the fact that we knew that the ACE-2 receptor, the ACE-2 binding domain for the s-1 spike protein and other elements of what we have come to know as this scourge pathogen, was not only engineered but could be synthetically modified in the laboratory using nothing more than gene sequencing technologies, taking computer code and turning it into a pathogen or an intermediate of the pathogen. And that technology was funded exclusively in the early days as a means by which we could actually harness coronavirus as a vector to distribute HIV vaccine.

My organization was asked to monitor biological and chemical weapons treaty violations in the very early days of 2000. You’ll remember the anthrax events in September of 2001. And we were part of an investigation that gave rise to the Congressional inquiry into not only the anthrax origins but also into what was unusual behavior around Bayer’s ciprofloxacin drug, which was a drug used as a potential treatment for Anthrax poisoning. And throughout the fall of 2001 we began monitoring an enormous number of bacterial and viral pathogens that were being patented through NIH, NIAID, and the US Armed Services Infectious Disease Program, and a number of other agencies internationally that collaborated with them. And our concern was that coronavirus was being seen as not only a potential manipulable agent for potential uses as a vaccine vector, but it was also very clearly being considered as a biological weapon candidate. So our first public reporting on this took place, prior to the SARS outbreak in the latter part of 2001. So you can imagine how disappointed I am to be sitting here twenty years later having 20 years earlier pointed out that there was a problem looming on the horizon with respect to coronavirus. But after the alleged outbreak — and I will always say alleged outbreak — because I think it’s important for us to understand that coronavirus as a circulating pathogen inside of the viral model that we have is actually not new to the human condition and is not new to the last two decades. It’s actually been part of the sequence of proteins that that circulates for quite a long time.

But the alleged outbreak [of SARS-1] that took place in China in 2002 going into 2003 gave rise to a very problematic April 2003 filing by the United States Center for Disease Control and Prevention. And this topic is of critical importance to get the nuance very precise, because in addition to filing the entire gene sequence on what became SARS coronavirus, which is actually a violation of 35 U.S. Code Section 101 — you cannot patent a naturally occurring substance. The 35 U.S. Code Section 101 violation, what is patent number 7220852, now that patent also had a series of derivative patents associated with it. These patent applications were broken apart because they were of multiple patentable subject matter. These include U.S. Patent 465-9270-3p which is actually a very interesting designation, U.S. Patent 7776521. These patents not only covered the gene sequence of SARS coronavirus but also covered the means of detecting it using RT-PCR. Now the reason why that’s a problem is, if you actually both own the patent on the gene itself and you own the patent on its detection, you have a cutting-edge advantage to being able to control 100% of the provenance of not only the virus itself but also its detection — meaning you have entire scientific and message control. And this patent sought by the CDC was allegedly justified by their public relations team as being sought so that everyone would be free to be able to research coronavirus. The only problem with that statement is it’s a lie. And the reason why it’s a lie is because the Patent Office not once but twice rejected the patent on the gene sequence as unpatentable because the sequence was already in the public domain. In other words prior to CDC’s filing for a patent the Patent Office found 99.9% identity with the already existing coronavirus recorded in the public domain.

And over the rejection of the Patent Examiner and after having to pay an appeal fine in 2006 and 2007, the CDC over[came] the Patent Office’s rejection of their patent, and ultimately in 2007 got the patent on SARS Coronavirus. So every public statement that CDC has made that said that this was in the public interest is falsifiable by their own paid bribe to the Patent Office. And to make matters worse, they paid an additional fee to keep their application private. Last time I checked, if you’re trying to make information available for the public to research, you would not pay a fee to keep the information private. I wish I could have made up anything I just said, but all of that is available in the public patent archive record which any member of the public can review. The United States Patent Office has not only the evidence but the actual documents which I have in my possession now.

This is critically important because fact-checkers have repeatedly stated that the novel coronavirus designated as SARS-CoV-2 is in fact distinct from the CDC patent. And here is both the genetic and the patent problem. If you look at the gene sequence that is filed by CDC in 2003, again in 2005, and then again in 2006, what you find is identity in somewhere between 89 to 99% of the sequence overlaps that have been identified in what’s called the novel subclade of SARS-CoV-2. What we know is that the core designation of SARS coronavirus which is actually the clade of the beta coronavirus family, and the subclade that has been called SARS-CoV 2, have to overlap from a taxonomy point of view. You cannot have SARS designation on a thing without it first being SARS. So the disingenuous fact-checking that has been done, saying that somehow or another CDC has nothing to do with this particular patent or this particular pathogen, is beyond both the literal credibility of the published sequences, and it’s also beyond credulity when it comes to the ICTV taxonomy, because it very clearly states that this is in fact a subclade of the clade called SARS coronavirus.

Now what’s important is on the 28th of April — and listen to the date very carefully because this date is problematic — 3 days after CDC filed the patent on the SARS coronavirus in 2003, 3 days later Sequoia Pharmaceuticals — a company that was set up in Maryland — Sequoia Pharmaceuticals on the 28th of April 2003 filed a patent on antiviral agents of treatment and control of infections by coronavirus. CDC filed three days earlier and then the treatment was available 3 days later. Just hold that thought for a second. Sequoia Pharmaceuticals and ultimately [Ablig] Pharmaceuticals became rolled into the proprietary Holdings of Pfizer, [Crysel], and Johnson & Johnson, So ask yourself a simple question: How would one have a patent on a treatment for a thing that had been invented three days earlier? The patent in question, the April 28th 2003 patent 715-1163, issued to Sequoia Pharmaceuticals has another problem. The problem is it was issued and published before the CDC patent on coronavirus was actually allowed. So the degree to which the information could have been known by any means other than insider information between those parties is zero. It is not physically possible for you to patent a thing that treats a thing that had not been published. Because CDC had paid to keep it secret. This, my friends, is the definition of criminal conspiracy, racketeering, and collusion. This is not a theory, this is evidence. You cannot have information in the future inform a treatment for a thing that did not exist. It is a RICO case and the RICO pattern which was established in April of 2003 for the first coronavirus was played out to exactly the same schedule when we see SARS-CoV show up, when we have Moderna getting the spike protein sequence by phone from the Vaccine Research Center at NIAID prior to the definition of the novel subclade. How do you treat a thing before you actually have the thing?

Before you actually have the thing on the 5th of June 2008 — which is an important date because it is actually around the time when DARPA, the Defense Advanced Research Program in the United States, actively took an interest in coronavirus as a biological weapon — June 5th 2008 [Ablig], which as you know is now part of Sanofi, filed the series of patents that specifically targeted what we’ve been told is the novel feature of the SARS-CoV-2 virus, and you heard what I just said, this is the 5th of June 2008 they found the specific sequence they targeted, what was called the poly-basic cleavage site for SARS-CoV the novel spike protein in the ACE-2 receptor binding domain which is allegedly novel, to SARS-CoV-2, and all of that was patented on the 5th of June 2008. And those patents in sequence were issued between November 24th of 2015 which was U.S. Patent 919-3780, so that one came out after the gain-of-function moratorium. That one came after the MERS outbreak in the Middle East but what you find is that then in 2016, 2017, 2019 a series of patents all covering not only the RNA strands but also the subcomponents of the gene strands were all issued to [Ablig] and Sanofi and then we have Rubius Therapeutics, we have Children’s Medical Corporation, we have countless others that include Ludwig-Maximilians-University, Protein Science Corporation, Dana-Farber Cancer Institute, University of Iowa, University of Hong Kong, Chinese National Human Genome Center in Shanghai, all identifying in patent filings that ranged from 2008 until 2017 every attribute that was allegedly uniquely published by the single reference publication. The novel coronavirus reveals quote ‘natural insertions at the S1, S2 cleavage site of the spike protein and possible recombinant origin of the SARS-CoV-2 virus, the paper that has routinely been used to identify the novel virus.

Unfortunately if you actually take what they report to be novel, you find 73 patents issued between 2008 and 2019 which have the elements that were allegedly novel in SARS-CoV-2 specifically as it relates to the poly-basic cleavage site ACE-2 receptor binding domain, and the spike protein, so the clinically novel components of the clinically unique, clinically contagious virus [were already in those 73 patents]. There was no outbreak of SARS because we had engineered all of the elements of that, and by 2016 the paper that was funded during the gain-of-function moratorium that said that the SARS coronavirus was poised for human emergence — written by none other than Ralph Baric — was not only poised for human emergence, but it was patented for commercial exploitation. A statement made in 2015 by [Eco-Health Alliance Director] Peter Daszak reported in the National Academies of Science Press publication February 12th 2016, and I’m quoting ‘We need to increase public understanding of the need for medical countermeasures such as a pan-coronavirus vaccine. A key driver is the media and the economics will follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of the process‘ end quote. Let me repeat the quote: ‘We need to increase public understanding of the need for medical countermeasures such as a pan-coronavirus vaccine. A key driver is the media and the economics will follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of the process‘ end quote.

There wasn’t a lab leak. This was an intentional by weaponization of spike proteins to inject into people to get them addicted to a pan-coronavirus vaccine. This has nothing to do with a pathogen that was released, and every study that has ever been launched to try to verify a lab leak is a red herring. And there’s really nothing that is new in this, zero. These patents on everything clinically novel, 73, [were] all issued before 2019. To prove that this was actually not a release of anything, because patent 727-9327, the patent on the recombinant nature of that lung targeting coronavirus, was transferred mysteriously from the University of North Carolina Chapel Hill to the National Institutes of Health in 2018. Now here’s the problem with that under the Bayh-Dole Act, the U.S. Government already has what’s called a march-in right provision. That means if the U.S. Government has paid for research they are entitled to benefit from that research at their demand or at their whim. So explain why in 2017 and 2018 suddenly the National Institutes of Health have to take ownership of the patent that they already had rights to, held by the University of North Carolina Chapel Hill. And how did they need to file a Certificate of Correction to make sure that it was legally enforceable because there was a typographical error in the grant reference in the first filing so they needed to make sure that not only did they get it right but they needed to make sure every typographical error contained in the patent was corrected on the single patent to develop the Vaccine Research Institute’s mandate which was shared between the University of North Carolina Chapel Hill in November of 2019 and Moderna in November of 2019, when UNC Chapel Hill and NIAID and Moderna began the sequencing of a spike protein vaccine a month before an outbreak ever happened, you have all the evidence.

The script for this was written first January 6th 2004, in Bioterrorism, Emerging Infectious Diseases, Antimicrobial Therapeutics, and Immune Modulators. Moderna introduced the notion of what they called The New Normal which became the branded campaign that was adopted by the World Health Organization, the Global Preparedness Monitoring Board which was the Board upon which the Chinese Director of Center for Disease Control, Elias of the Gates Foundation, and Anthony Fauci sat together on that Board of Directors. But the the first introduction of The New Normal Campaign, which was about getting people to accept a universal pan-influenza pan-coronavirus vaccine, was actually adopted January 6th 2004 so it’s it’s been around quite quite a long time.

Moderna knew that it was going to be placed in the front of the line with respect to the development of a vaccine in March of 2019, and this is a very important date because in March of 2019, for reasons that are not transparent, they suddenly amended a series of rejected patent filings, which is a very bizarre behavior, but they amended a number of patent filings specifically to make reference to a deliberate or accidental release of coronavirus. So in March 2019 [with] the amended failed patent applications, [they] begin the process of a coronavirus vaccine development. And they began dealing with a very significant problem that they had which was they relied on technology that they did not own. Two Canadian companies Arbutus Pharmaceuticals and Acuitas Pharmaceuticals actually own the patent on the lipid nanoparticle envelope that’s required to deliver the injection of the mRNA fragment. And those patents have been issued both in Canada and in the U.S. and then around the world. Moderna knew that they did not own the rights and began trying to negotiate with Arbutus and Acuitas to make the lipid nanoparticle patented technology available to be put into a vaccine. And we know, before that in November they entered into a research and cooperative research and development agreement with UNC Chapel Hill with respect to getting the spike protein to put inside of the lipid nanoparticle so that they actually had a candidate vaccine before we had a pathogen allegedly that was running around. What makes that story most problematic beyond the self-evident nature of it is that we know that from 2016 until 2019 at every one of the NIAID advisory Council Board meetings, Anthony Fauci lamented the fact that he could not find a way to get people to accept the universal influenza vaccine, which was his favorite target — he was trying to get the population to engage in this process.

And what becomes very evident with Peter Daszak (Eco-Health Alliance), UNC Chapel Hill and others and then most specifically by March of 2019 in the amended patent filings by Moderna, we see that there is an epiphany that says what if there was an accidental or an intentional release of respiratory pathogen. And what makes that particular phrase problematic is it is exactly recited in the book A World At Risk which is the scenario that was put together by the World Health Organization in September of 2019. So months before there’s an alleged pathogen, [this book from WHO] says that we need to have a coordinated global experience of a respiratory pathogen release which by September 2020 must put in place a universal capacity for public relations management, crowd control, and the acceptance of a universal vaccine mandate. That was September of 2019 and the language of an intentional release of a respiratory pathogen was written into the scenario that quote ‘must be completed by September 2020‘.

The ACE-2 receptor was already described in the patents before 2019. Specifically the ACE-2 receptor targeting mechanism for SARS coronavirus is in publications going back to 2008, in the weaponization conferences that took place in Slovenia in Europe, all across Europe, and all across the DARPA infrastructure. We’ve known about that since 2013 and its isolation and amplification, add to this 70 amendments that merge the two. The failed [Moderna] patent applications were essentially revitalized in March of 2019, to include the ‘deliberate release of a respiratory pathogen‘ language. Their [patenting] process is similar to other pharmaceutical companies where they ever-green applications and continually modify applications to enjoy the earliest priority dates available. But that’s why you have to go back and look at the amendment of the application records to find out when the actual amendment language is put in place. Any assertion that this pathogen is somehow unique or novel falls apart on the actual gene sequences which are published in the patent record and then more egregiously falls apart in the fact that we have Peter Daszak himself stating that we have to create public hype to get the public to accept the medical countermeasure of a pan-coronavirus vaccine. And what makes that most ludicrous is the fact that as we know World Health Organization had declared coronavirus kind of a dead letter — they said that that we had eradicated coronavirus as a concern. So why having eradicated it in 2007 and 2008, why did we start spending billions of dollars globally on a vaccine for a thing that had been eradicated by declaration in 2008? That falls into the zone of incredulity, to say the least.

The entirety of the evidence then is that this is a tool — the coronavirus and the vaccines, this is a tool and the interest of DARPA in creating a biological weapon out of this. This is a tool for everything else that latches onto this, including population control. This was seen as a highly malleable bio-weapon. There is no question that by 2005 it was unquestionably a weapon of choice. Unfortunately very well-meaning people get trapped into conversations about whether we’re having a vaccine for a virus. The fact of the matter is we’re not. We are injecting a spike protein mRNA secret mRNA sequence which is a computer simulation; it’s not derived from nature, it’s a computer simulation of a sequence which has been known and patented for years. And what we know is that that sequence is reported across phone conversations that took place between Moderna and the [NIH] Vaccine Research Center. The story that this is somehow prophylactic or preventative flies in the face of 100% of the evidence because the evidence makes it abundantly clear that there has been no effort by any pharmaceutical company to combat the virus. This is about getting people injected with the known-to-be-harmful spike protein. So the cover story is that if you get an expression of a spike protein you’re going to have some sort of general symptomatic relief but the fact of the matter is there has never been an intent to vaccinate a population as defined by the vaccination universe [namely, to prevent infection].

When Anthony Fauci tried desperately to get some of his quote ‘synthetic RNA vaccines’ [for HIV] published he had his own patents rejected by the Patent Office, and I want to read what the patent office told him when NIAID’s own Anthony Fauci thought that he could get an mRNA-like vaccine patented as a vaccine. And here’s the quote: ‘These arguments are persuasive to the extent that an antigenic peptide stimulates an immune response that may produce antibodies that bind to a specific peptide or protein, but it is not persuasive in regards to a vaccine.‘ This is the Patent Office. The immune response produced by a vaccine must be more than merely some immune response, it must also be protective as noted in the Patent Office action. ‘The art recognizes the term vaccine to be a compound which prevents infection. Applicant has not demonstrated that the instantly claimed vaccine meets even the lower standards set forth in the specification let alone the standard definition for being operative. In regards therefore claims five, seven, and nine are not operative.‘ As the anti-HIV vaccine which is what he was working on is not patentable utility. So Anthony Fauci himself was told by the Patent Office themselves that what he was proposing as a vaccine does not meet the patentable standard, the legal standard, or the clinical standard.

This is the problem going back to the very beginning of what’s alleged to be a pandemic. We do not have any evidence that the gene sequence alteration had any clinical significance whatsoever, There has not been a single paper published by anyone that is actually established that anything novel since November of 2019 has clinical distinction from anything that predates November of 2019. The problem with the 73 patents that I described is that those 73 patents all contain what was reported to be novel in December and January of 2019 and 2020 respectively, so the problem is that even if we were to accept that there are idiopathic pneumonias, even if we were to accept that there are some sets of pathogen induced symptoms, we do not have a single piece of published evidence that tells us that anything about the subclade SARS-CoV-2 has clinical distinction from anything that was known and published prior to November 2019 in 73 patents dating to 2008.

Influenza did not leave the human population. Influenza was a failed decade-long pan-influenza vaccine mandate that was desperately desperately desperately promoted by governments around the world. They failed and they decided if influenza doesn’t deliver on the public promise of getting everybody to get an injection, let’s change the pathogen.

Dr David Martin’s remarks are transcribed from here.