Að gulltryggja að engin verði eftirmál

Á Íslandi hefur Samfylkingin „tekið að sér” að gulltryggja lyfjaframleiðendum og stjórnendum íslenska heilbrigðiskerfisins að ekki verði eftirmál umframdauðsfallanna, veikindanna og skaðans á æxlunarfæri beggja kynja af völdum bóluefnanna með því að tefla landlækni fram í oddvitasæti listans sem verðandi heilbrigðisráðherra. Þar með er tryggt að engin rannsókn fari fram hérlendis á skaðsemi mRNA efnanna. Rannsókn sem hægur leikur er að framkvæma með ópersónugreinanlegum hætti með samkeyrslu gagna um bólusetningar við gögn úr heilbrigðiskerfinu.

Í rannsóknargögnum Pfizer sem gerð er ítarleg grein fyrir í bókinni The Pfizer Papers kemur fram að innan þriggja mánaða frá upphafi bólusetninga í desember 2020 lá fyrir að bóluefnin komu ekki í veg fyrir smit á Covid til og frá bólusettum einstaklingi. Orðalagið sem Pfizer notar í eigin rannsóknargögnum um þessa lykilstaðreynd er “vaccine failure” and “failure of efficacy.” Að neðan er örstutt og hvergi nærri tæmandi upptalning á staðreyndum um skaðsemi mRNA bóluefnanna sem fálkaorðuþegunum hjá Embætti landlæknis mátti vera ljós þegar líða fór á fyrsta ár bólusetninganna 2021. Og enn er farið með sprautuna um ganga hjúkrunarheimilanna að fyrirmælum landlæknis. 

Pfizer hired 2,400 fulltime staffers to help process “the large increase of adverse event reports” being submitted to the company’s Worldwide Safety database.

Pfizer knew by April 2021 that the injections damaged the hearts of young people.

Pfizer knew by February 28, 2021—just ninety days after the public rollout of their COVID vaccine—that its injection was linked to a myriad of adverse events. Far from being “chills,” “fever,” “fatigue,” as the CDC and other authorities claimed were the most worrying side effects, the actual side effects were catastrophically serious.

These side effects included: death (which Pfizer does list as a “serious adverse event”). Indeed, over 1,233 deaths in first three months of the drug being publicly available.

Severe COVID-19; liver injury; neurological adverse events; facial paralysis; kidney injury; autoimmune diseases; chilblains (a localized form of vasculitis that affects the fingers and toes); multiple organ dysfunction syndrome (when more than one organ system is failing at once); the activation of dormant herpes zoster infections; skin and mucus membrane lesions; respiratory issues; damaged lung structure; respiratory failure; acute respiratory distress syndrome (a lung injury in which fluid leaks from the blood vessels into the lung tissue, causing stiffness which makes it harder to breathe and causes a reduction of oxygen and carbon dioxide exchange); and SARS (or SARS-CoV-1, which had not been seen in the world since 2004, but appears in the Pfizer documents as a side effect of the injections). 

Thousands of people with arthritis-type joint pain, one of the most common side effect, were recorded. Other thousands with muscle pain, the second most common. Then, industrial-scale blood diseases: blood clots, lung clots, leg clots; thrombotic thrombocytopenia, a clotting disease of the blood vessels; vasculitis (the destruction of blood vessels via inflammation); astronomical rates of neurological disorders—dementias, tremors, Parkinson’s, Alzheimer’s, epilepsies. Horrific skin conditions. A florid plethora of cardiac issues; myocarditis, pericarditis, tachycardia, arrhythmia, and so on. Half of the serious adverse events related to the liver, including death, took place within seventy-two hours of the shot. Half of the strokes took place within forty-eight hours of injection.

 

Að skaða æxlunarfærin var ekki óviljaverk

Í bók Naomi Wolf sem byggir á rannsóknargögnum Pfizer kemur fram hvernig áhrifum mRNA bóluefnis Pfizer virðist frá upphafi og meðvitað hafa verið ætlað að hafa skaðleg áhrif á æxlunarfæri beggja kynja. Skýrist nú hvers vegna FDA og Pfizer vildu halda gögnunum leyndum næstu 70 árin. Við lestur bókarinnar verður spurningin um vitneskju lykilstarfsmanna heilbrigðiskerfisins um skaðsemi bóluefnisins vorið 2024, bæði hjá Embætti landlæknis og hjá Lyfjastofnun, áleitnari:

„But what really emerged from the first forty-six reports, was the fact that though COVID is ostensibly a respiratory disease, the papers did not focus on lungs or mucus membranes, but rather they center, creepily and consistently, on disrupting human reproduction.

By the time Pfizer's vaccine rolled out to the public, the pharmaceutical giant knew that they would be killing babies and significantly harming women and men’s reproduction. The material in the documents makes it clear that damaging human’s ability to reproduce and causing spontaneous abortions of babies is “not a bug, it is a feature.”

Pfizer told vaccinated men to use two reliable forms of contraception or else to abstain from sex with childbearing-age women. In its protocol, the company defined “exposure” to the vaccine as including skin-to-skin contact, inhalation, and sexual contact. Pfizer mated vaccinated female rats and “untreated” male rats, and then examined those males, females, and their offspring for vaccine-related “toxicity.” Based on just forty-four rats (and no humans), Pfizer declared no negative outcomes for “. . . mating performance, fertility, or any ovarian or uterine parameters . . . nor on embryo-fetal or postnatal survival, growth, or development,” the implication being that its COVID vaccine was safe in pregnancy and did not harm babies. Pfizer knew that lipid nanoparticles have been known for years, to degrade sexual systems, and Amy Kelly in fact found nanoparticles, of which lipid nanoparticles are a subtype, pass through the blood-testis barrier and damage males’ Sertoli cells, Leydig cells, and germ cells. Those are the factories of masculinity, affecting the hormones that turn boys at adolescence into men, with deep voices, broad shoulders, and the ability to father children. So, we have no idea if baby boys born to vaccinated moms, will turn into adults who are recognizably male and fertile. Pfizer enumerated the menstrual damages it knew it was causing to thousands of women, and the damage ranges from women bleeding every day, to having two periods a month, to no periods at all; to women hemorrhaging and passing tissue; to menopausal and post-menopausal women beginning to bleed again. Pfizer’s scientists calmly observed and noted it all but did not tell women.

Babies suffered and died. In one section of the documents, over 80 percent of the pregnancies followed resulted in miscarriage or spontaneous abortion. In another section of the documents, two newborn babies died, and Pfizer described the cause of death as “maternal exposure” to the vaccine.

Pfizer knew that vaccine materials entered vaccinated moms’ breast milk and poisoned babies. Four women’s breast milk turned “blue-green.” Pfizer produced a chart of sick babies, made ill from breastfeeding from vaccinated moms, with symptoms ranging from fever to edema (swollen flesh) to hives to vomiting. One poor baby had convulsions and was taken to the ER, where it died of multi-organ system failure.”

 

Ivermectin gegn krabbameini

Hversu mörgum landsmönnum hefði verið hægt að forða frá alvarlegum skaða eða hversu mörgum mannslífum hefði mátt bjarga hefði notkun lyfsins Ivermectin verið leyfð á Íslandi munum við aldrei vita. Að lyfið, hverra hugmyndasmiðir þáðu Nóbelsverðlaunin í lyfjafræði fyrir árið 2015, skuli enn í október 2024 vera bannað vekur undrun þegar horft er til niðurstaðna 105 rannsókna 1.206 vísindamanna á 220.423 sjúklingum í 30 löndum sem allar sýna að meðferð með lyfinu fækkar innlögnum á bráðadeild og dregur úr dauðsföllum auk þess að flýta fyrir bata. Fyrir krabbameinssjúklinga er bannið sérstaklega skaðlegt því nýjar rannsóknir sýna öfluga virkni lyfsins gegn tilteknum tegundum illvígs krabbameins. Heilbrigði krabbameinssjúkra geldur illu heilli (collateral damage) fyrir fjárhagslega hagsmuni hluthafa bóluefnaframleiðenda. Hverfandi líkur eru á að verðandi heilbrigðisráðherra muni beita sér fyrir endurmati á eigin banni sem landlæknis á notkun lyfsins Ivermectin.