Bivši podpredsednik Pfizer dr. Michael Yeadon o cepivu za COVID-19: sem šokiran

Objavil/a naravno zdravje, dne 2020-11-21 ob 13:54:35

Twitter 6.9. 2020 

https://twitter.com/MichaelYeadon3/status/1302725169652412421

Odgovor na posvetovanje o cepivu: Spoštovani gospod Hancock, diplomiral sem iz biokemije in toksikologije in sem doktor znanosti na področju farmakologije. 32 let sem delal v farmacevtskih raziskavah in razvoju, večinoma v zvezi z novimi zdravili za zdravljenje pljuč in kože. Bil sem podpredsednik Pfizerja in izvršni direktor biotehnološkega podjetja, ki sem ga ustanovil (Ziarco - prevzel ga je Novartis). Sem dobro seznanjen z raziskavami in razvojem novih zdravil.

Prebral sem posvetovalni dokument. Redko kdaj sem bil tako šokiran in razburjen. Vsa cepiva proti virusu SARS-COV-2 so po definiciji nova. Nobeno kandidatno cepivo ni bilo v razvoju več kot nekaj mesecev.

Če je kakršno koli takšno cepivo odobreno za uporabo v kakršnih koli okoliščinah, ki NISO IZRECNO eksperimentalne, menim, da so prejemniki zavedeni v kriminalni meri. To je zato, ker ni prav nobenih človeških prostovoljcev za cepivo, ki bi lahko imeli več kot nekaj mesecev varnostnih informacij o preteklih odmerkih.

Moja skrb se ne poraja zato, ker imam negativna stališča o cepivih (jih nimam). Pač pa gre za samo načelo, za katerega se zdi, da so se mu politiki pripravljeni odpovedati, da novi medicinski posegi - v tem nepopolnem stanju razvoja- ne smejo biti na voljo subjektom drugače, kakor samo na izrecno eksperimentalni osnovi. To je moja skrb.

Razlog za to zaskrbljenost je, da ni znano, kakšen bo varnostni profil, šest mesecev ali leto ali dlje po odmerjanju cepiva. O tem nimate dobesedno nobenih podatkov in tudi kdo drug ne, ustvarjate pa vtis, da jih imate. Številni kandidati za cepivo uporabljajo novo tehnologijo, ki prej ni bila uporabljena za izdelavo cepiv. Zato ni nobenih dolgoročnih podatkov o varnosti, ki bi jih lahko pokazali v podporo smiselnosti uporabe teh cepiv. Ne pravim, da se bodo nesprejemljivi škodljivi učinki pojavili po daljših intervalih po dmerjanju. Ne: gre za to, da ne veste, kaj se bo zgodilo, a boste kljub temu pospešili razvoj in se ob tej priložnosti odrekli manjkajočim varnostnim informacijam.

Sem sumničav glede motivov tistih, ki predlagajo pospešeno uporabo v širši človeški populaciji. Zdaj razumemo, kdo ima še posebej povišano tveganje za obolevnost in smrtnost zaradi pridobitve tega virusa. Samo prostovoljcem iz teh skupin je treba zagotoviti podrobne informacije o tveganju in koristih, vključno z edino točko, ki sem jo navedel tukaj. Samo če je dano soglasje na podlagi informacij, se lahko uporabi katerokoli EKSPERIMENTALNO cepivo.

Ne zaupam vam. V tej krizi niste bili neposredni in ste se obnašali grozljivo. To počnete še zdaj in zavajate o nevarnosti okužbe preko majhnih otrok. Zakaj bi vam verjel v zvezi s poskusnimi cepivi? Dr. Michael Yeadon

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»Cepiva absolutno niso potrebna za končanje pandemije. Še nikoli nisem slišal, da bi se take neumnosti govorile o cepivih. Ne cepite ljudi, ki niso ogroženi zaradi bolezni. Prav tako se ne lotite načrtovanja cepljenja milijonov vitalnih in zdravih ljudi s cepivom, ki ni bilo temeljito preizkušeno na ljudeh. Prva napačna domneva SAGE (angleška inačica NIJZ) je, da je bilo „100% prebivalstva dovzetno za virus in da pred tem ni bilo že obstoječe imunosti.« Yeadon trdi, da je ta pojem "smešen, ker je SARS-CoV-2 resnično nov, koronavirusi pa ne. Ne obstaja "virus brez prednikov". Obstajajo vsaj "štirje endemični koronavirusi, ki povzročajo prehlad ... ki prosto krožijo v Veliki Britaniji in drugod." Tisti, ki so bili v preteklosti okuženi z „enim ali več od teh endemičnih koronarnih virusov, ki povzročajo prehlad, imajo dolgotrajno in močno imunost T-celic, ne samo na te viruse, ampak tudi na tesno povezane viruse. SARS-CoV-2 je en tak tesno povezan virus. " Dr. Yeadon je znova dal pod vprašaj strokovnost SAGE, saj je povedal: "Če ne pričakujemo takšne navskrižne imunosti ... to kaže pomanjkanje potrebnega razumevanja za izdelavo dovolj zanesljivega modela." Poleg tega dr. Yeadon trdi, da lahko test PCR, ki se uporablja za odkrivanje "primerov" COVID-19, pozitiven, če je nekdo okužen z enim od teh navadnih prehladnih koronavirusov, zaradi česar je ta test manj zanesljiv. Seveda je na podlagi končnih rezultatov teh testov več tisoč posameznikom ukazano, da omejijo svoje življenje in dajo v karanteno do 14 dni.

Na podlagi znanstvenih podatkov, dr. Yeadon ugotavlja, da je zaradi predhodne izpostavljenosti prehladnim koronavirusom »pomemben delež (30%) prebivalstva prišel v leto 2020, oborožen s T-celicami, ki so jih lahko branile pred SARS-CoV -2, čeprav tega virusa še nikoli niso srečali... SAGE se je naivno zmotil, če je mislil, da so vsi dovzetni za okužbo s SARS CoV-2.« Druga napačna predpostavka SAGE je, da se odstotek okužene populacije lahko določi z raziskovanjem, kolikšen del prebivalstva ima protitelesa. Zaradi te predpostavke SAGE meni, da je bilo do zdaj okuženih s SARS-CoV-2 manj kot 10% prebivalstva. Yeadon pa pojasnjuje, da je dobro znano, da ni nujno, da vsaka oseba, okužena z virusom dihal, proizvaja protitelesa. Medtem ko skoraj vsi tisti s pomembnimi simptomi, ki so bili sprejeti v bolnišnico, proizvajajo protitelesa, tisti z blažjim odzivom na virus ne proizvajajo protiteles. Kljub temu je bilo dokazano, da imajo vsi okuženi T-celice v krvi, ki se lahko odzovejo na SARS-CoV-2, in tako še vedno razvijajo imunost. Na podlagi dveh neodvisnih metod, ki prideta do istega splošnega zaključka, Yeadon dokazuje, da je dejanska stopnja okužbe od 20- 30%, zato je 7% ocena SAGE močno in nestrokovno podcenjena.

Vir:  https://www.lifesitenews.com/news/former-pfizer-vp-no-need-for-vaccines-the-pandemic-is-effectively-over

https://www.bitchute.com/video/9z1QCmjkcDiR/

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Angleško ministrstvo za zdravje (MHRA) ve, da bo nevarno cepivo za COVID-19 povzročilo veliko škodljivih stranskih učinkov, zato iščejo programsko opremo umetne inteligence, ki bi lahko spremljala vse pojave škodljivih posledic cepiva za COVID-19

https://ted.europa.eu/udl?uri=TED:NOTICE:506291-2020:TEXT:EN:HTML&tabId=1

Short description:

The MHRA urgently seeks an Artificial Intelligence (AI) software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reaction (ADRs) and ensure that no details from the ADRs’ reaction text are missed.

»MHRA nujno išče programsko orodje z umetno inteligenco (AI) za obdelavo pričakovanega velikega števila neželenih učinkov zdravil proti cepivu Covid-19 (ADR) in za zagotovitev, da ne bodo izpuščene nobene podrobnosti iz besedila reakcije neželenih učinkov zdravil.«

Glede na ogromen obseg navedenega cilja, dajanja teh kemikalij (cepiv) na stotine milijonov ljudi, ko vemo, da je pri uporabi cepiv običajno nekaj hudih zapletov, so lahko negativni rezultati znatni. Na primer, ena študija cepiv proti gripi, ki so jo dajali odraslim, starejšim od 65 let, je pokazala, da je približno 1% ljudi imel resne neželene učinke. Če je cepivo COVID-19 podobno za posameznike v isti starostni skupini (54 milijonov prebivalcev), bi to samo v tej starostni skupini znašalo 540.000 posameznikov, ki bi morda zaradi cepiva za COVID-19 potrebovali zdravstveno oskrbo v bolnišničnem sistemu, ki zagotavlja manj kot 925.000 postelj.

Children’s Health Defense pa je poročal, da so imela klinična preskušanja cepiva Moderna 20 % stopnjo "resnih poškodb" v skupini z velikimi odmerki cepiva za COVID-19.

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On December 1, 2020, the ex-Pfizer head of respiratory research Dr. Michael Yeadon and the lung specialist and former head of the public health department Dr. Wolfgang Wodarg filed an application with the EMA, the European Medicine Agency responsible for EU-wide drug approval, for the immediate suspension of all SARS CoV 2 vaccine studies, in particular the BioNtech/Pfizer study on BNT162b (EudraCT number 2020-002641-42).

Dr. Wodarg and Dr. Yeadon demand that the studies – for the protection of the life and health of the volunteers – should not be continued until a study design is available that is suitable to address the significant safety concerns expressed by an increasing number of renowned scientists against the vaccine and the study design.

On the one hand, the petitioners demand that, due to the known lack of accuracy of the PCR test in a serious study, a so-called Sanger sequencing must be used. This is the only way to make reliable statements on the effectiveness of a vaccine against Covid-19. On the basis of the many different PCR tests of highly varying quality, neither the risk of disease nor a possible vaccine benefit can be determined with the necessary certainty, which is why testing the vaccine on humans is unethical per se.

Furthermore, they demand that it must be excluded, e.g. by means of animal experiments, that risks already known from previous studies, which partly originate from the nature of the corona viruses, can be realized. The concerns are directed in particular to the following points:

  • The formation of so-called “non-neutralizing antibodies” can lead to an exaggerated immune reaction, especially when the test person is confronted with the real, “wild” virus after vaccination. This so-called antibody-dependent amplification, ADE, has long been known from experiments with corona vaccines in cats, for example. In the course of these studies all cats that initially tolerated the vaccination well died after catching the wild virus.
  • The vaccinations are expected to produce antibodies against spike proteins of SARS-CoV-2. However, spike proteins also contain syncytin-homologous proteins, which are essential for the formation of the placenta in mammals such as humans. It must be absolutely ruled out that a vaccine against SARS-CoV-2 could trigger an immune reaction against syncytin-1, as otherwise infertility of indefinite duration could result in vaccinated women.
  • The mRNA vaccines from BioNTech/Pfizer contain polyethylene glycol (PEG). 70% of people develop antibodies against this substance – this means that many people can develop allergic, potentially fatal reactions to the vaccination.
  • The much too short duration of the study does not allow a realistic estimation of the late effects. As in the narcolepsy cases after the swine flu vaccination, millions of healthy people would be exposed to an unacceptable risk if an emergency approval were to be granted and the possibility of observing the late effects of the vaccination were to follow. Nevertheless, BioNTech/Pfizer apparently submitted an application for emergency approval on December 1, 2020.

https://2020news.de/en/dr-wodarg-and-dr-yeadon-request-a-stop-of-all-corona-vaccination-studies-and-call-for-co-signing-the-petition/

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https://www.nature.com/articles/d41586-020-03219-y?error=cookies_not_supported&code=507c15a1-bd46-41a8-8019-9aabc9058b26&fbclid=IwAR3i1rv_5a4QoIwFB4bOXaU1yqaxfygv8fF3ayDKKyuGrbPQ13kdCvniTio

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https://www.unilad.co.uk/news/boris-johnson-says-anti-vaxxers-are-wrong-but-confirms-covid-vaccine-wont-be-compulsory/?source=facebook&fbclid=IwAR0S25UYYIT6QburT7yGIJ1HdHSBPxpBMlCHRlaUqwC7VVfXemFDIgGEcZU

Boris Johnson: cepivo ne bo obvezno

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Brez cepljenja ne bo potovanj:
Doroteja Novak Gosarič o cepljenju, Ministrstvo za zdravje
"Razmišljamo o aplikaciji, ki bo omogočala vsakemu, ki bo opravil cepljenje, da bo lahko dostopal preko spleta do svojih podatkov, si sam natisnil na svojem računalniku potrdilo o opravljenem cepljenju, kar bo zagotovo v veliko pomoč pri potovanju znotraj držav članic in seveda tudi izven." Doroteja Novak Gosarič, Odmevi, 26. 11. 2020
https://www.facebook.com/rtvslo.si/videos/111236930726785
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Nov 25, 2020
https://siol.net/digisvet/novice/v-sloveniji-med-najbolj-nenaklonjenimi-za-cepljenje-proti-covid-19-539052

V Sloveniji med najbolj nenaklonjenimi za cepljenje proti covid-19 - siol.net

Raziskava, ki so jo opravili za Svetovni gospodarski forum, je pokazala, da je se v povprečju 15 držav delež ljudi, ki i
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