SARS-CoV-2 vaccine protection and deaths among US veterans during 2021
Abstract
We report SARS-CoV-2 vaccine effectiveness against infection (VE-I) and death (VE-D) by vaccine type (n = 780,225) in the Veterans Health Administration, covering 2.7% of the U.S. population. From February to October 2021, VE-I declined from 87.9% to 48.1%, and the decline was greatest for the Janssen vaccine resulting in a VE-I of 13.1%. Although breakthrough infection increased risk of death, vaccination remained protective against death in persons who became infected during the Delta surge. From July to October 2021, VE-D for age 65 years was 73.0% for Janssen, 81.5% for Moderna, and 84.3% for Pfizer-BioNTech; VE-D for age ≥65 years was 52.2% for Janssen, 75.5% for Moderna, and 70.1% for Pfizer-BioNTech. Findings support continued efforts to increase vaccination, booster campaigns, and multiple, additional layers of protection against infection.
As shown in Fig. 2, risk of infection accelerated in both unvaccinated and fully vaccinated Veterans beginning in July 2021 and through September 2021, consistent with the time dependence observed in the Cox proportional hazards models. This pattern was similar across age groups, and risk of infection was highest for unvaccinated Veterans. Veterans who were fully vaccinated with the Moderna vaccine had the lowest risk of infection, followed closely by those who received the Pfizer-BioNTech vaccine, then those who received the Janssen vaccine.
Fig. 2. Kaplan-Meier curves illustrating cumulative risk of SARS-CoV-2 infection by vaccination status and age.(A) All ages. (B) Age <50 years. (C) Age 50-64 years. (D) Age ≥65 years. The survival function estimates time to infection detected by most recent RT-PCR assay.
Risk of death after SARS-CoV-2 infection was highest in unvaccinated Veterans regardless of age and comorbidity (Fig. 3). However, breakthrough infections were not benign, as shown by the higher risk of death in fully vaccinated Veterans who became infected compared to vaccinated Veterans who remained infection-free.
Fig. 3. Kaplan-Meier curves illustrating cumulative risk of death due to any cause by vaccination status and RT-PCR assay.(A) Age <65 years. (B) Age ≥65 years. (C) Charlson Comorbidity Index score <3. (D) Charlson Comorbidity Index score ≥3.
We observed similar results when examining the time period corresponding to the dominance of the Delta variant (fig. S1). Specifically, among those with a positive PCR test on or after July 1, 2021, vaccination was protective against death, although with some differences by age and vaccine type. For age <65 years, vaccine effectiveness against death (VE-D) was 81.7% (95% CI: 75.7% to 86.2%) for any vaccine; 73.0% (95% CI: 52.0% to 84.8%) for Janssen; 81.5% (95% CI: 70.7% to 88.4%) for Moderna; and 84.3% (95% CI: 76.3% to 89.7%) for Pfizer-BioNTech. For age ≥65 years, VE-D was 71.6% (95% CI: 68.6% to 74.2%) for any vaccine; 52.2% (95% CI: 37.2% to 63.6%) for Janssen; 75.5% (95% CI: 71.8% to 78.7%) for Moderna; and 70.1% (95% CI: 66.1% to 73.6%) for Pfizer-BioNTech.
They are experimental
They don’t provide immunity
They don’t prevent transmission
They have serious side effects
The CDC changed the definition
They are not what you were told they were
It’s literally the greatest psyop ever & I marvel at the number who were duped
— Ed ☯️ The Obsolete Man…a Free Thinker (@DowdEdward) November 5, 2021
Demons Among Us( part 1 )
Aliens are Demons, they are being passed off as creatures from space, the truth is they are the fallen Angels. This 2 part video explains what is happening in your world.
a The Birchall Centre, Lennard-Jones Laboratories, Keele University, Staffordshire, ST5 5BG, United Kingdom
b Life Sciences, Keele University, Staffordshire, ST5 5BG, United Kingdom
c Department of Clinical Neuropathology, Kings College Hospital, London, SE5 9RS, United Kingdom
Abstract
Autism spectrum disorder is a neurodevelopmental disorder of unknown aetiology. It is suggested to involve both genetic susceptibility and environmental factors including in the latter environmental toxins. Human exposure to the environmental toxin aluminium has been linked, if tentatively, to autism spectrum disorder. Herein we have used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminium content of brain tissue from donors with a diagnosis of autism. We have also used an aluminium-selective fluor to identify aluminium in brain tissue using fluorescence microscopy. The aluminium content of brain tissue in autism was consistently high. The mean (standard deviation) aluminium content across all 5 individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) μg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. These are some of the highest values for aluminium in human brain tissue yet recorded and one has to question why, for example, the aluminium content of the occipital lobe of a 15 year old boy would be 8.74 (11.59) μg/g dry wt.? Aluminium-selective fluorescence microscopy was used to identify aluminium in brain tissue in 10 donors. While aluminium was imaged associated with neurones it appeared to be present intracellularly in microglia-like cells and other inflammatory non-neuronal cells in the meninges, vasculature, grey and white matter. The pre-eminence of intracellular aluminium associated with non-neuronal cells was a standout observation in autism brain tissue and may offer clues as to both the origin of the brain aluminium as well as a putative role in autism spectrum disorder.
US National Library of Medicine
National Institutes of Health – Oct 2012
Goldman GS, Miller NZ.
Author information
Computer Scientist, Pearblossom, CA 93553, USA. gsgoldman@roadrunner.com
Abstract
In this study, the Vaccine Adverse Event Reporting System (VAERS) database, 1990-2010, was investigated; cases that specified either hospitalization or death were identified among 38,801 reports of infants. Based on the types of vaccines reported, the actual number of vaccine doses administered, from 1 to 8, was summed for each case. Linear regression analysis of hospitalization rates as a function of (a) the number of reported vaccine doses and (b) patient age yielded a linear relationship with r(2) = 0.91 and r(2) = 0.95, respectively. The hospitalization rate increased linearly from 11.0% (107 of 969) for 2 doses to 23.5% (661 of 2817) for 8 doses and decreased linearly from 20.1% (154 of 765) for children aged <0.1 year to 10.7% (86 of 801) for children aged 0.9 year. The rate ratio (RR) of the mortality rate for 5-8 vaccine doses to 1-4 vaccine doses is 1.5 (95% confidence interval (CI), 1.4-1.7), indicating a statistically significant increase from 3.6% (95% CI, 3.2-3.9%) deaths associated with 1-4 vaccine doses to 5.5% (95% CI, 5.2-5.7%) associated with 5-8 vaccine doses. The male-to-female mortality RR was 1.4 (95% CI, 1.3-1.5). Our findings show a positive correlation between the number of vaccine doses administered and the percentage of hospitalizations and deaths. Since vaccines are given to millions of infants annually, it is imperative that health authorities have scientific data from synergistic toxicity studies on all combinations of vaccines that infants might receive. Finding ways to increase vaccine safety should be the highest priority.
The Association of American Physicians and Surgeons notes that, because of public concerns that mercury (as thimerosal) in childhood vaccines might be contributing to soaring rates of autism, this component was mostly phased out as a “precaution.” Autism rates continued to rise, prompting authorities to assert that autism is not linked to mercury in vaccines and that vaccination policies are safe and appropriate, writes Neil Z. Miller in the winter issue of the Journal of American Physicians and Surgeons.
ABSTRACT
Aluminum is a neurotoxin, yet infants and young children are repeatedly injected with aluminum adjuvants from multiple vaccines during critical periods of brain development. Numerous studies provide credible evidence that aluminum adversely affects important biological functions and may contribute to neurodegenerative and autoimmune disorders. It is impossible to predetermine which vaccinated babies will succumb to aluminum poisoning. Aluminum-free health options are needed.
PDF: http://www.jpands.org/vol21no4/miller.pdf
Study Shows Evidence of Inflammatory Cells Loaded with Aluminum Crossing the Blood-Brain Barrier and Meningeal Membranes
(November 27, 2017) Staffordshire, UK — A new study published in the Journal of Trace Elements in Medicine and Biology provides the strongest indication yet that aluminum is an etiological agent in autism spectrum disorder (ASD), according to researchers at Keele University in England.
The study used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminum content of brain tissue from five donors who had died with diagnoses of ASD. The results showed the donors to have had some of the highest values of aluminum yet measured in human brain tissue.
The mean (standard deviation) aluminum content across all five individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) mg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. Previous measurements of 60 brains from humans not diagnosed with ASD showed an average content of 1 mg/g dry wt. of brain tissue.
“One has to wonder why aluminum in the occipital lobe of a 15-year-old boy with autism would be a value that is at least 10 times higher than what might be considered acceptable for an elderly adult?” said Christopher Exley PhD, Professor in Bioinorganic Chemistry and author of the study. Another ground-breaking study by Exley and his team, published earlier in the year, identified similarly high levels of aluminum in the brains of individuals who died of familial Alzheimer’s disease.
When it comes to the most widely used adjuvant ingredient found within vaccines, aluminum, many questions have yet to be answered, particularly when it comes to where the aluminum goes after injection, an issue known as biopersistence.
One reason this question arises is because a causative role has been established in what’s known as macrophagic myofasciitis (MMF) lesion in patients who have myalgic encephalomyelitis, or brain inflammation. Myalgia, arthralgia, chronic fatigue, cognitive dysfunction, dysautonomia, and autoimmunity have been temporally linked to aluminium adjuvant-containing vaccine administration (Gherardi and Authier, 2003; Authier et al., 2003; Exley et al., 2009; Rosenblum et al., 2011; Santiago et al., 2014; Brinth et al., 2015; Palmieri et al., 2016).
“Evidence that aluminum-coated particles phagocytozed in the injected muscle and its draining lymph nodes can disseminate within phagocytes throughout the body and slowly accumulate in the brain further suggested that alum safety should be evaluated in the long term.”
US National Library of Medicine
National Institutes of Health – Jun 2015
Eidi H – 1,2, David MO – 3, Crépeaux G – 4, Henry L – 5, Joshi V – 6, Berger MH – 7, Sennour M – 8, Cadusseau J – 9,10, Gherardi RK – 11, Curmi PA – 12.
Author information
1 Institut National de la Santé et de la Recherche Médicale (INSERM) – UMR 1204, Université Evry-Val d’Essonne, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Evry, France. housam.eidi@gmail.com.
2 Inserm – U955, Université Paris Est, Faculté de Médecine, Créteil, France. housam.eidi@gmail.com.
3 Institut National de la Santé et de la Recherche Médicale (INSERM) – UMR 1204, Université Evry-Val d’Essonne, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Evry, France. MO.David@iut.univ-evry.fr.
4 Inserm – U955, Université Paris Est, Faculté de Médecine, Créteil, France. guillemette.crepeaux@gmail.com.
5 Institut National de la Santé et de la Recherche Médicale (INSERM) – UMR 1204, Université Evry-Val d’Essonne, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Evry, France. laetitia.henry@wanadoo.fr.
6 Institut National de la Santé et de la Recherche Médicale (INSERM) – UMR 1204, Université Evry-Val d’Essonne, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Evry, France. vandana.joshi@univ-evry.fr.
7 Laboratoire Pierre-Marie Fourt, Centre des Matériaux de l’Ecole des Mines de Paris and CNRS UMR 7633, Evry, France. marie-helene.berger@mines-paristech.fr.
8 Laboratoire Pierre-Marie Fourt, Centre des Matériaux de l’Ecole des Mines de Paris and CNRS UMR 7633, Evry, France. mohamed.sennour@ensmp.fr.
9 Inserm – U955, Université Paris Est, Faculté de Médecine, Créteil, France. josette.cadusseau@inserm.fr.
10 Faculté des Sciences et Technologie UPEC, Créteil, France. josette.cadusseau@inserm.fr.
11 Inserm – U955, Université Paris Est, Faculté de Médecine, Créteil, France. romain.gherardi@hmn.aphp.fr.
12 Institut National de la Santé et de la Recherche Médicale (INSERM) – UMR 1204, Université Evry-Val d’Essonne, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Evry, France. pcurmi@univ-evry.fr.
Abstract
BACKGROUND:
Aluminum oxyhydroxide (alum) is a crystalline compound widely used as an immunologic adjuvant of vaccines. Concerns linked to alum particles have emerged following recognition of their causative role in the so-called macrophagic myofasciitis (MMF) lesion in patients with myalgic encephalomyelitis, revealing an unexpectedly long-lasting biopersistence of alum within immune cells and a fundamental misconception of its biodisposition. Evidence that aluminum-coated particles phagocytozed in the injected muscle and its draining lymph nodes can disseminate within phagocytes throughout the body and slowly accumulate in the brain further suggested that alum safety should be evaluated in the long term. However, lack of specific staining makes difficult the assessment of low quantities of bona fide alum adjuvant particles in tissues.
METHODS:
We explored the feasibility of using fluorescent functionalized nanodiamonds (mfNDs) as a permanent label of alum (Alhydrogel(®)). mfNDs have a specific and perfectly photostable fluorescence based on the presence within the diamond lattice of nitrogen-vacancy centers (NV centers). As the NV center does not bleach, it allows the microspectrometric detection of mfNDs at very low levels and in the long-term. We thus developed fluorescent nanodiamonds functionalized by hyperbranched polyglycerol (mfNDs) allowing good coupling and stability of alum:mfNDs (AluDia) complexes. Specificities of AluDia complexes were comparable to the whole reference vaccine (anti-hepatitis B vaccine) in terms of particle size and zeta potential.
RESULTS:
In vivo, AluDia injection was followed by prompt phagocytosis and AluDia particles remained easily detectable by the specific signal of the fND particles in the injected muscle, draining lymph nodes, spleen, liver and brain. In vitro, mfNDs had low toxicity on THP-1 cells and AluDia showed cell toxicity similar to alum alone. Expectedly, AluDia elicited autophagy, and allowed highly specific detection of small amounts of alum in autophagosomes.
CONCLUSIONS:
The fluorescent nanodiamond technology is able to overcome the limitations of previously used organic fluorophores, thus appearing as a choice methodology for studying distribution, persistence and long-term neurotoxicity of alum adjuvants and beyond of other types of nanoparticles.
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.
Poland GA, Jacobson RM.
Author information
Department of Internal Medicine, Mayo Vaccine Research Group, Mayo Clinic and Foundation, Rochester, MN.
Abstract
BACKGROUND:
Measles is the most transmissible disease known to man. During the 1980s, the number of measles cases in the United States rose dramatically. Surprisingly, 20% to 40% of these cases occurred in persons who had been appropriately immunized against measles. In response, the United States adopted a two-dose universal measles immunization program. We critically examine the effect of vaccine failure in measles occurring in immunized persons.
METHODS:
We performed a computerized bibliographic literature search (National Library of Medicine) for all English-language articles dealing with measles outbreaks. We limited our search to reports of US and Canadian school-based outbreaks of measles, and we spoke with experts to get estimates of vaccine failure rates. In addition, we devised a hypothetical model of a school where measles immunization rates could be varied, vaccine failure rates could be calculated, and the percentage of measles cases occurring in immunized students could be determined.
RESULTS:
We found 18 reports of measles outbreaks in very highly immunized school populations where 71% to 99.8% of students were immunized against measles. Despite these high rates of immunization, 30% to 100% (mean, 77%) of all measles cases in these outbreaks occurred in previously immunized students. In our hypothetical school model, after more than 95% of schoolchildren are immunized against measles, the majority of measles cases occur in appropriately immunized children.
CONCLUSIONS:
The apparent paradox is that as measles immunization rates rise to high levels in a population, measles becomes a disease of immunized persons. Because of the failure rate of the vaccine and the unique transmissibility of the measles virus, the currently available measles vaccine, used in a single-dose strategy, is unlikely to completely eliminate measles. The long-term success of a two-dose strategy to eliminate measles remains to be determined.
An investigation into an outbreak in a high school in a town that was heavily hit by the virus found that about half of the cases were in teens who had received the recommended two doses of vaccine in childhood — in other words, teens whom authorities would have expected to have been protected from the measles virus.
It’s generally assumed that the measles vaccine, when given in a two-dose schedule in early childhood, should protect against measles infection about 99 per cent of the time. So the discovery that 52 of the 98 teens who caught measles were fully vaccinated came as a shock to the researchers who conducted the investigation.
“That’s the real question. How could that have happened?” said Dr. Gaston De Serres, an infectious diseases expert with Quebec’s public health agency and one of the authors of the study.
In an interview before the start of the conference, De Serres would not name the highly affected town or the high school in it.
But he suggested the discovery that as many of the cases were fully vaccinated as unvaccinated raises a serious question about whether the timing of the delivery of the first dose of measles vaccine is undermining the efficacy of the prevention program.
The vaccine can’t be given earlier, because of a phenomenon that helps babies survive infancy. Children are born without a fully developed immune system — it starts to build as babies become exposed to a variety of disease threats over their first few years.
In pregnancy and after birth, through breastfeeding, babies acquire antibodies from their mothers that tide them over until they can make their own. But that means if they are given the measles vaccine — which is made from weakened live viruses — too early, their mothers’ antibodies will kill the vaccine viruses, preventing protection from being induced.
US National Library of Medicine
National Institutes of Health – 2006
Abstract
Here we describe symptomatic transmission of the Leningrad-3 mumps vaccine virus from healthy vaccinees to previously vaccinated contacts. Throat swab and serum samples were taken from six symptomatic mumps cases and from 13 family contacts. Assessment of serum IgG and IgM anti-mumps virus antibodies and IgG avidity testing was performed using commercial test kits. Sera neutralizing antibodies were measured by plaque reduction neutralization assay using the L-3 vaccine mumps virus as the target. All six of the symptomatic mumps cases and three contact subjects tested positive for mumps by RT-PCR. The genomic sequences tested (F, SH and HN genes) of all nine of these samples were identical to the L-3 mumps vaccine strain. All 13 contacts were asymptomatic; however clear serological evidence of mumps infection was found in some of them. The likely epidemiological source of the transmitted L-3 mumps virus was children who were recently vaccinated at the schools attended by the six symptomatic mumps patients described here. The L-3 mumps vaccine virus can be shed and transmitted horizontally, even to subjects previously vaccinated with the same virus.
US National Library of Medicine
National Institutes of Health – 2014
Zhifang Wang,1 Rui Yan,1 Hanqing He,1 Qian Li,1 Guohua Chen,2 Shengxu Yang,3 and Enfu Chen1,*
Martyn Kirk, Editor
1 – Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou, Zhejiang Province, P. R. China
2 – Cixi City Center for Disease Control and Prevention, Cixi, Ningbo, P. R. China
3 – Sanmen County Center for Disease Control and Prevention, Sanmen, Taizhou, P. R. China
Abstract
Background
The reported coverage of the measles–rubella (MR) or measles–mumps–rubella (MMR) vaccine is greater than 99.0% in Zhejiang province. However, the incidence of measles, mumps, and rubella remains high. In this study, we assessed MMR seropositivity and disease distribution by age on the basis of the current vaccination program, wherein the first dose of MR is administered at 8 months and the second dose of MMR is administered at 18–24 months.
Methods
Cross-sectional serological surveys of MMR antibodies were conducted by collecting epidemiological data in Zhejiang province, China in 2011. In total, 1015 participants were randomly selected from two surveillance sites. Serum MMR-specific immunoglobulin G levels were tested by enzyme-linked immunosorbent assay. The geometric mean titers and seroprevalence with 95% confidence intervals (CIs) were calculated by age and gender. Proportions of different dose of vaccine by age by vaccine were also identified. Statistically significant differences between categories were assessed by the Chi-square test.
Results
Over 95% seroprevalence rates of measles were seen in all age groups except <7 months infants. Children aged 5–9 years were shown lower seropositivity rates of mumps while elder adolescences and young adults were presented lower rubella seroprevalence. Especially, rubella seropositivity was significantly lower in female adults than in male. Nine measles cases were unvaccinated or unknown vaccination history. Among them, 66.67% (6/9) patients were aged 20–29 years while 33.33% (3/9) were infants aged 8–12 months. In addition, 57.75% (648/1122) patients with mumps were children aged 5–9 years, and 50.54% (94/186) rubella cases were aged 15–39 years.
Conclusions
A timely two-dose MMR vaccination schedule is recommended, with the first dose at 8 months and the second dose at 18–24 months. An MR vaccination speed-up campaign may be necessary for elder adolescents and young adults, particularly young females.
I am injured by the flu shot
MMR vaccine injured me
My family is injured by vaccines
Hep B vaccine and Vit K made my baby sick
I Wish We Would Have KNOWN! William and Rachael tell their story of their two boys who have suffered from vaccine injury in Ireland.
Interview recorded on May 5th, 2017 in The United Kingdom
I have finally woken up to the truth about vaccines
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
Dr. Brownstein on CDC Corruption: “I am Tired of Writing About This – I See Patients Damaged by Vaccines”
CDC Whistleblower Case Three Years Later: Nothing Happening
by Dr. Brownstein’s
Holistic Medicine
I honestly cannot believe I am still writing about this. It was three years ago that a senior CDC scientist, Dr. William Thompson, claimed whistleblower protection after he issued a statement that he and his fellow colleagues altered, hid, and threw out data that showed a direct association between the MMR vaccine and autism.
CDC Whistleblower Case Three Years Later: Nothing Happening
I honestly cannot believe I am still writing about this. It was three years ago that a senior CDC scientist, Dr. William Thompson, claimed whistleblower protection after he issued a statement that he and his fellow colleagues altered, hid, and threw out data that showed a direct association between the MMR vaccine and autism. In August, 2014, I wrote in a blog post, “Now, there may be proof that the CDC not only knew about the link between the MMR vaccine and autism but they changed the data in a landmark 2004 study to hide the damning data. What did the heads of the CDC do? They altered the data and reported in 2004 (1) that there was no association between autism and the MMR vaccine. Who wrote this article? William Thompson, PhD, the whistleblower, was one of the authors of that 2004 study. He is reported to be suffering with regret and remorse over the damage that has been done to our children over the last ten years.”
The data that was altered showed a whopping 240% increase in autism cases among African American males who received the MMR vaccine before 36 months of age. Furthermore, there was a 69% increase risk in any male injected with MMR before 36 months of age. Guess which racial group has the highest incidence of autism? If you guessed African American males, you win the prize. Guess who suffers with more autism, boys or girls? If you guessed boys, you win again.
Mia, left paralyzed from the neck down after suffering a reaction to the HPV vaccine, has no feeling in her arms or legs and is unable to lift her head. Her Mother, Gini Blesky, says the symptoms of her debilitating illness all began after being given Gardasil. Parents! Please BE INFORMED now and share this crucial information with everyone you love. View this newly available docu-series right now and protect your beloved children: tinyurl.com/VaccinationEducation #Gardasil #Cervarix #RevolutionForChoice #HearThisWell #VaccineInjury #VAXXED #INFORMEDconsent
Johns Hopkins Researcher Releases Shocking Report On Flu Vaccines
In 2015, a whole new slew of flu vaccines found themselves getting approved by the Federal Drug Administration. This isn’t an uncommon practice; most flu vaccines pass inspection every year. It’s well known advice that has been passed down from doctor to patient that the flu vaccine is something that we all should get, but it has been quickly surfacing that what’s in the vaccines–especially those from 2015 and after–might actually be more damaging then simply rolling the dice on getting the flu.
The ingredient that is getting the most flack is called an adjuvant. The particular one involved is called Squalene, and it has been linked to auto-immune disease side effects. In fact, it may have been used during chemical attacks in the Gulf War. Symptoms include chronic fatigue, muscle aches, and neurologic damage.
While it may be a contested subject, it remains that we aren’t really sure what’s going into these vaccines we’re being convinced should be used. A scientist who has been working at the Johns Hopkins School of Medicine, released a report sharing his views on the subject. And they aren’t pretty.
Here is an excerpt from yournewswire.com that summarizes aspects of Peter Doshi’s report. You can find the original report at the British Medical Journal’s site. Determine for yourself if the evidence he presents is credible or not…
WATCH NOW: http://bit.ly/2wqaSvA – Watch this free 7-part miniseries featuring over 60 vaccine experts to hear both sides of the vaccine debate. Playing through August 23rd. WATCH NOW: http://bit.ly/2wqaSvA
INFERTILITY – DISEASE – DEATH … Laura Hayes, Mother of vaccine-injured children, on a mission to end the vaccine holocaust! Share this LIFE-SAVING information with your loved ones and stay informed with this groundbreaking docu-series happening now: tinyurl.com/VaccinationEducation
“Would you allow something that could cause infertility, such as nonstick chemicals and solvents, to be injected into your child? Of course not. You know that you would never want to destroy your child’s future reproductive capabilities. However, millions of mothers across America are allowing doctors to inject their children with polysorbate 80, known to adversely affect fertility. And who knows what propylene glycol (antifreeze), Triton X100 (detergent), aluminum, mercury, foreign DNA fragments, and the myriad other vaccine ingredients do to one’s future reproductive ability, especially when injected in conjunction with polysorbate 80.
We know that the HPV vaccine has caused Primary Ovarian Failure (which is premature menopause) and amenorrhea (the prolonged cessation of a female’s menstrual cycle) in girls and young women, rendering them infertile, and possibly sterile for life. We know that tetanus vaccines given to girls and women in Kenya were laced with Human Chorionic Gonadotropin (HCG), rendering them sterile. How? Administering HCG via vaccination stimulates the production of antibodies to HCG, and these antibodies then cause the woman’s body to reject embryos, effectively sterilizing her. Such an HCG-laced tetanus vaccine is in actuality a contraception vaccine.
Do you think any of these Kenyan women was told that prior to vaccination? To add to the evilness and deception, the Kenyan women were given a 5-dose tetanus program spread over a number of years, versus the 2-3 dose norm. Clearly, those vaccines were being used for induced sterility and birth control without the girls’ and women’s knowledge or consent.
Does any parent or vaccine recipient really know what is in the vaccines being injected into their child or themselves? It’s no wonder pharmaceutical companies don’t test to see whether or not their vaccine products cause infertility, they already know the answer. Instead, they simply write “not tested for impairment of fertility” on their package inserts, and our unethical government regulators let them get away with that. Interestingly, we are seeing record numbers of couples struggling with infertility issues. Coincidence?
Would you allow something that could kill your baby to be injected into your otherwise healthy child? Of course not! Mothers would lay down their lives for their children, they don’t purposefully put them in harm’s way. However, millions of mothers across America are allowing doctors to inject their children with more and more vaccines, not knowing that each and every one carries the risk of death, even more so when combined, as they most often are.
Interestingly, we are seeing record numbers of babies who are dying before their 1st birthday in the U.S., including many of “SIDS” and “SBS” (the labels that unethical doctors and unethical medical examiners use for vaccine-induced deaths instead of calling them what they are…i.e. vaccine-induced deaths). Coincidence?
Now that we have discussed what is actually in vaccines, let’s talk once more about how parental instincts have been demeaned, grossly manipulated, and obliterated, specifically, about how parents have been grievously lied to and misled, to the point where parents are now allowing things that simply do not make sense.
Imagine looking from the outside in, and seeing a tiny newborn, small infant, or trusting toddler, being held down, painfully stuck with a needle multiple times, screaming so that its face is beet red with tears, all while the child’s parents not only watch, but due to being lied to and coerced, they participate in this atrocity! What must this do to the psyche and stress hormones of a child to have this happen, time and again, while the person he trusts most is not only allowing it, but participating in it?
What would you say if you walked by the window to my house, peered in, and saw my husband and me holding down our tiny baby on the dining room table, then roughly jabbing and injecting it multiple times with toxic cocktails and true witches’ brews of ingredients…all while our baby, or child of any age, screamed bloody murder, trying to escape our grip and savagery? I imagine you would whip out your cell phone, call the police, then try to barge into our home to stop the abuse! How is what I just described any different than what goes on every minute of every day in doctors’ offices and hospitals in our country and across the world? To be very clear, it isn’t.
To state it very plainly, vaccination is child abuse in the form of medical assault and battery. With regard to adults, when vaccination is carried out against one’s will or wishes, say for school admittance, job requirements, elder care and housing, or military admission, or when carried out with one who is hesitant, or with one who is unsuccessful in resisting and refusing, it also meets the legal definition for assault and battery.
We must begin to label these vaccine atrocities for what they are: blatant and inexcusable child abuse; medical assault and battery; and when death is the result for the vaccine recipient, involuntary manslaughter. These vaccine-induced injuries, illnesses, and deaths are iatrogenic in nature, meaning they are caused by doctors and nurses. Vaccinations are crimes against humanity, and there is no time to mince words about this fact.”
This is a MUST SEE docu-series – totally free! tinyurl.com/VaccinationEducation #RevolutionForChoice #VaccineInjury #TheTruthAboutVaccines #VAXXED #Infertility
STUDY: Reality Trumping Establishment Vaccine “Facts”
The past week has offered glimpses of hope for the growing number of people who know they are being lied to by the mainstream medical establishment about vaccine safety. More people are now aware that the kind of rigorous testing required for drugs to be put on the market does not apply to vaccines, or that vaccines like the HPV shot were not properly tested against a saline placebo before approval by the US Food and Drug Administration (FDA).
Yet, the medical establishment continues to omit these facts and instead focuses on why vaccine hesitancy is on the rise. Studies are being done in an attempt to understand vaccine hesitancy and come up with solutions to the “problem” of poor vaccine uptake. In 2014, the Boston Globe ran the headline Doctors Still Hesitant to Urge HPV Vaccine for Teenagers, highlighting a survey from the US Centers for Disease Control and Prevention (CDC), in which the agency stated that the inoculation rate is ‘unacceptably low.’ In 2015, NPR ran the story titled Doctors, Not Parents, Are the Biggest Obstacle to the HPV Vaccine in response to a study published in the journal Cancer Epidemiology, Biomarkers & Prevention, which found that more than a quarter of pediatricians and family doctors do not strongly endorse the HPV vaccine.
A new study in the journal PLOS One titled Misinformation Lingers in Memory: Failure of Three Pro-vaccination Strategies is an eye-opener at how clueless the medical establishment appears to be as to why its vaccine propaganda is being rejected. In this study, the researchers compared three strategies in vaccine promotion: a) contrasting myths vs. “facts,” b) employing “fact” and icon boxes, and c) showing images of non-vaccinated sick children. It should be noted that when the study’s authors refer to “facts,” they are using the term to mean vaccine propaganda. Beliefs in the autism-vaccine link and in vaccines side effects, along with intention to vaccinate a future child, were evaluated both immediately after the “correction intervention” and after a 7-day delay to reveal possible backfire effects. The study concluded the following:
“Results show that existing strategies to correct vaccine misinformation are ineffective and often backfire, resulting in the unintended opposite effect…”
Study – The Introduction of Diphtheria-Tetanus-Pertussis and Oral Polio Vaccine Among Young Infants in an Urban African Community: A Natural Experiment
Highlights
•When DTP and OPV were introduced in Guinea-Bissau in 1981, allocation by birthday resulted in a natural experiment of being vaccinated early or late.
•Between 3 and 5 months of age, children who received DTP and OPV early had 5-fold higher mortality than still unvaccinated children.
•In the only two studies of the introduction of DTP and OPV, co-administration of OPV with DTP may have reduced the negative effects of DTP.
Few studies have examined what happened to child survival when DTP and OPV were introduced in low-income countries. These vaccines were introduced in 1981 in an urban community in Guinea-Bissau from 3 months of age in connection with 3-monthly weighing sessions. Children were therefore allocated by birthday to receive vaccines early or late between 3 and 5 months of age. In this natural experiment vaccinated children had 5-fold higher mortality than not-yet-DTP-vaccinated children. DTP-only vaccinations were associated with higher mortality than DTP + OPV vaccinations. Hence, DTP may be associated with a negative effect on child survival.
Results
Among 3–5-month-old children, having received DTP (±OPV) was associated with a mortality hazard ratio (HR) of 5.00 (95% CI 1.53–16.3) compared with not-yet-DTP-vaccinated children. Differences in background factors did not explain the effect. The negative effect was particularly strong for children who had received DTP-only and no OPV (HR = 10.0 (2.61–38.6)). All-cause infant mortality after 3 months of age increased after the introduction of these vaccines (HR = 2.12 (1.07–4.19)).
Conclusion
DTP was associated with increased mortality; OPV may modify the effect of DTP.
Dr. Buchwald testimony before the Quebec College of Physicians Medical Board: Dr. Gerhard Buchwald takes the stand
A physician from Germany, Dr. Buchwald testifies through an interpreter. Dr. Lanctot tables his credentials as well as a copy of his book entitled “Vaccination: Business Based on Fear”. He is recognized as an expert on vaccination by the Committee.
Dr. Buchwald testifies that his experience includes being a medical counselor to an association of parents whose children have been injured or killed by vaccinations. He adds that he is aware of a thousand vaccination related injury cases and has had personal contact with 350 cases. In 150 of these cases, he wrote the medical opinion and acted as an advisor during the legal proceedings.
Dr Lanctot (L).: If you take this stand in your country, have you been reprimanded by the medical authorities?
B.: I wrote a paper entitled, “Vaccinations: A Crime Against our Children”. I received written reprimands from the College of Physicians… In Germany, we have a law called “Kronegesetz” in the Civil Code, which stipulates that everyone has the right to freely voice his or her opinion. When I was fed up with this nonsense with the College, I drew their attention to the fact that their responses were actually a breach of those sections of the law. German judges, who deal with these issues, are very touchy on this issue… It is impossible to suppress the free speech of a physician in a free country which is why the College knew that it would lose. They also knew that the press would really have a field day. Since then I’ve heard nothing more…
L.: You mentioned earlier that the first criterion in medicine is to do no harm… And you referred to these ethics in
He continues with a brief history of his experiences in general and describes how he got interested in the whole question of immunization. He recalls that after graduating from medical school, he was a supporter of vaccination policies, as was everyone else he knew. Then he relates to the Committee the story of the eldest of his three children, born in 1957, who at eighteen months received a smallpox vaccination and who, eight days later was no longer able to stand up in his crib. Until then, his son’s development had been absolutely normal:
“He fell sick with a post-vaccination encephalitis, and ever since, I have a completely destroyed human being at home.”
It was at that time that someone approached him to become a member of a protective association in Germany. It was through this group that he got to know other vaccination damage cases.
Study – Human papillomavirus vaccination and risk of autoimmune diseases: A large cohort study of over 2million young girls in France.
RESULTS:
Among 2,252,716 girls, 37% received HPV vaccine and 4,096 AID occurred during a mean follow-up time of 33months. The incidence of AID was not increased after exposure to HPV vaccination, except for Guillain-Barré syndrome (GBS) (incidence rate of 1.4 among exposed [20 cases] versus 0.4 per 100,000 PY among unexposed [23 cases]; adjusted HR: 3.78 [1.79-7.98]). This association persisted across numerous sensitivity analyses and was particularly marked in the first months following vaccination. Under the hypothesis of a causal relationship, this would result in 1-2 GBS cases attributable to HPV vaccine per 100,000 girls vaccinated.
CONCLUSIONS:
Our study provides reassuring results regarding the risk of AID after HPV vaccination, but an apparently increased risk of GBS was detected. Further studies are warranted to confirm this finding.
Study – Detection of contaminants in cell cultures, sera and trypsin.
Abstract
The aim of this study was standardization and application of polymerase chain reaction (PCR) for the detection of contaminants in cell cultures, sera and trypsin. Five PCR protocols were standardized to assess the presence of genetic material from mycoplasma, porcine circovirus 1 (PCV1), bovine leukemia virus (BLV) or bovine viral diarrhea virus (BVDV) in cell culture samples. PCR reactions for the genes GAPDH and beta-actin were used to evaluate the efficiency of nucleic acid extraction. The PCR protocols were applied to 88 cell culture samples from eight laboratories. The tests were also used to assess potential contamination in 10 trypsin samples and 13 fetal calf serum samples from different lots from five of the laboratories. The results showed the occurrence of the following as DNA cell culture contaminants: 34.1% for mycoplasma, 35.2% for PCV1, 23.9% for BVDV RNA and 2.3% for BLV. In fetal calf sera and trypsin samples BVDV RNA and PCV1 DNA was detected. The results demonstrated that cell culture, sera and trypsin used by different laboratories show a high rate of contaminants. The results highlight the need for monitoring cell cultures and controlling for biological contaminants in laboratories and cell banks working with these materials.
Alfred Lambremont Webre – EXPERT PANEL Forced Adult vaccinations are component of extermination program Refuse all vaccines
Vaccines-The True Weapons Of Mass Destruction
Dr.Rebecca Carley.
ADVERSE REACTIONS to immunizations are more common than many people realize.
Please visit her website: http://www.drcarley.com/
Biopersistence in the Brain of Aluminum Nanoparticles from Vaccines
Posted by Merinda Teller, Ph.D, MPH on Aug 14, 2017
In the 1990s, French clinicians and researchers began noticing and reporting on a mysterious inflammatory muscle disorder with a distinctive pathological pattern that later earned the name “macrophagic myofasciitis” or MMF.1 Myofasciitis refers to inflammation of muscles and their connective tissue (fascia).
Initially, the cause and features of MMF were unknown. Subsequent research by French investigators elucidated that the deltoid muscle lesions characteristic of MMF were secondary to intramuscular injection with vaccines containing aluminum hydroxide adjuvants.2 The lesions revealed both an ongoing local immune reaction along with long-term persistence of aluminum hydroxide at the injection site.2
An ongoing series of admirably methodical studies also have confirmed a number of other post-vaccination clinical symptoms associated with MMF.3 These disabling health problems include not just muscle pain but joint pain, chronic fatigue, autonomic nervous system dysfunction, autoimmunity, and cognitive dysfunction.4 The cognitive deficiencies experienced by MMF patients mirror the cognitive impairments that have been observed to result from chronic exposure to aluminum particles.5 Together, all of these dysfunctions are “paradigmatic” of an emerging aluminum-adjuvant-related syndrome that has come to be known as ASIA (autoimmune/inflammatory syndrome induced by adjuvants).
the news network 