Category Archives: Pregnancy and birth

DTaP vaccine for Pregnant Women Adverse Events and AUTISM

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Prenatal Tetanus, Diphtheria,Acellular Pertussis Vaccination and Autism Spectrum Disorder

      Adverse Events:

increased risk of lower birthweight
increased risk of preterm birth
hard selection against males
increased risk of gestational diabetes
increased risk of gestational hypertension
earlier need for prenatal care

Read Study

VLA COMMENT: First it was the flu shot despite Dr. Gary Goldman’s study that there was an increase of fetal death reports by 4,250%.  CDC recommends pregnant women get the whooping cough vaccine between 27 and 36 weeks of each pregnancy, preferably during the earlier part of this time period. The American College of Obstetricians and Gynecologists and the American College of Nurse-Midwives support this recommendation.

Invitro vaccine recomendations:

Some doctors may hesitate to immunize pregnant women, but the committee assures us this is due to the possibility for congenital anomalies or spontaneous abortions being falsely attributed to the vaccination. There are very few vaccinations contraindicated during pregnancy , and in some cases the benefits of the vaccination outweigh the risks. This is especially true in instances of military service or travel to countries where a disease is highly prevalent, occupations that present risks for exposure to a disease, and those who are immuno-compromised or chronically ill. (read more..)

Italy’s final vote: No mandatory vaccines

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League leader Matteo Salvini called required vaccines “useless” and said they were “in many cases dangerous, if not harmful”.

Now, they won’t be required.

By a vote of 148 to 110 in the upper house of parliament, Italy has squashed mandatory vaccine laws and aims to be “more inclusive. READ MORE…

READ DETAILS….

NOTE:  The Democratic party passed the original mandatory vaccine law in June of 2017, but now, a year later and in the midst of a revolution in Italy, parents will no longer have to comply. The Democrats originally used a measles outbreak as the fuel for the law’s passage.

VLA Comment:  Check out the summary of Italian commission report…

Aluminum Adjuvants in Vaccines: Testing a substitute adjuvant with new HepB shot

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In February 2018, the FDA and CDC approved the recommendation for a new hepatitis B vaccine, Heplisav-B targeting adults over the age of 18. The U.S. Food and Drug Administration (FDA) had twice rejected the application for licensure for Heplisav-B in the past four years because of safety signals. Heplisav-B differs from other licensed hepatitis B vaccines in that it contains a new synthetic adjuvant known as cytosine phosphoguanine 1018 (CpG 1018) composed of short synthetic DNA molecules. In 2016, the FDA rejected an application for licensure for the Heplisav-B vaccine, because the agency was concerned about an increased rate of heart attacks and deaths in people who had been given the vaccine. During the trial, approximately 14 subjects had heart attacks. In July 2017, the FDA committee convened to re-evaluate the scientific evidence and make a decision on whether Heplisav B should or should not be approved for use in the U.S. This committee had only one cardiologist on the team, Milton Packer, MD, who is a distinguished scholar in cardiovascular science at the Baylor University Medical Center in Dallas, Texas. According to Dr. Packer, it was possible that the Heplisav B vaccine’s novel adjuvant was related to the higher number of heart attacks in study participants who received the experimental vaccine. He stated: “To know if the 7 -1 heart attack imbalance represented a real risk, we’d need comparative data in 50,000 people.” However, the only way to conduct such a large trial would be to approve the vaccine and see what happens in the public. With Dr. Packer abstaining in his vote to recommend the vaccine, the FDA committee approved it anyway. Dr. Packer stated: “Why did I abstain? Based on the available data, it was impossible for anyone to know if the increase in heart attack risk was real. There is a simple rule in life: if you don’t know, you should say you don’t know.” The vaccine is now available to the public, and all those who receive it are basically guinea pigs to find out if heart attacks will result from the experimental vaccine, and if it will continue to have FDA approval.

Read more…

[Impact of different adjuvants on immunogenicity of the HBV particle vaccine containing the S + preS1 fusion antigen in Balb/C mice].

Study on combining Aluminum with 1018   (CPG1018 as above)

Study: Cytochrome P450 1A1 and 1B1 promoter CpG island methylation regulates rat liver injury induced by isoniazid

HPV (Gardasil) Cochrane BOGUS STUDY details

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What happened to Cochrane?

Cochrane, a non-profit organization whose research helps individuals make informed health decisions, published a review in May 2018 claiming that the HPV vaccine helps prevent cancer and precancerous changes in the cervix with no serious side effects. The review aimed to increase public confidence in the HPV vaccine – both its efficacy in cancer prevention and its long-term safety. This publication has the potential to affect the opinions of many people regarding the HPV vaccine, possibly reassuring some parents and convincing them to choose it
for their children. READ ARTICLE

VLA Comment: The article is interesting to read however, the link to the BMJ review of the HPV Cochrane study shows the poor and fallacious design of the study whose conclusion is that the HPV vaccine is safe.  The Cochrane HPV vaccine review was incomplete and ignored important evidence of bias

Pfizer Vice President blows the whistle on ‘deadly’ vaccines.

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Pfizer Vice President Dr. Peter Rost blows the whistle on ‘deadly’ vaccines.

The former vice president of the world’s largest pharmaceutical company has blown the whistle to expose the true dangers of mandatory vaccinations. Dr. Peter Rost lifted the lid on vaccines and revealed that the Gardasil inoculation, in particular, is in fact, “deadly”. In a shocking exposé from one of the highest-ranking whistleblowers to date, Rost has also claimed that Big Pharma is purposely keeping the public unhealthy so they can make a fortune from continual treatments of illnesses rather than curing them. Dr. Rost made the revelations during an interview for the “One More Girl” documentary in which he candidly discussed how the main objective for vaccines and pharmaceutical drugs is to keep the public in a constant state of disease.
READ MORE…

101 Million dollars paid to child victim of MMR vacine

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$101 Million Dollar Vaccine Injury Award for Encephalopathy from MMR Vaccine

(July 17th, 2018 – SARASOTA, FL) — Attorneys at Maglio Christopher & Toale, P.A. negotiated a $101 million dollar settlement for an infant who suffered a severe reaction to the Measles Mumps Rubella (MMR) vaccine.

O.R.* was a one-year-old healthy baby girl who was already walking and climbing.  On February 13, 2013, she received vaccinations for Measles Mumps Rubella (MMR), Hepatitis A, Haemophilus Influenzae type B (Hib), Prevnar (pneumonia), and Varicella (chickenpox).  That evening, the mother noticed baby O.R. was irritable and feverish. After a call to the pediatrician, the doctor advised Mom to give her Tylenol and Benadryl. The fever continued for several days and on the evening before the baby’s scheduled pediatrician visit, O.R. began having severe seizures. She was rushed to the emergency room.  Baby O.R. went into cardiac and respiratory arrest and doctors placed her on a ventilator.

The seizures and cardiac arrest left O.R. with a severe brain injury, encephalopathy, cortical vision impairment, truncal hypotonia (low muscle tone), and kidney failure. After months of treatment at the hospital, baby O.R. finally went home, but her disabilities require specialized medical care and supervision around the clock for the rest of her life.  READ MORE…

 

 

Vaccine Court:(New) Attorney Fees-may not be paid if vaccine injury case is lost

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Good Faith and a Reasonable Basis

The answer to the third question to compensate attorneys, even when their clients were not compensated by the NVICP, is a devilish debate and where the special masters try to hold a hammer over the attorneys.

I wonder how many times the following statement has been whispered or inferred within the discussion of attorney fees, “You must play ball, or we will not compensate you for your work now and possibly in the future?” The statute allows for payment, yet the devil is in the details.

Within the NVICP, attorneys shall be compensated for fees and expenses when a client is successful with their petition for compensation from an injury or death. [6]

When a petitioner is not successful, the Special Masters can award attorney fees and expenses at their discretion. [7]

And this is where it gets very tricky, and recently, this is where we start to lose our ability to obtain legal counsel to represent our claims within the NVICP.

The Special Master uses his/her discretion to award fees using the Good Faith and Reasonable Basis standard.

Even if a petitioner is not awarded “compensation,” the special master “may award an amount of compensation to cover petitioner’s reasonable attorneys’ fees . . . if the special master or court determines that the petition was brought in good faith and there was a reasonable basis for the claim for which the petition was brought.”[8]  READ MORE…

Samoa Seizes All MMR Vaccines After Two Infants Die Minutes After Receiving the Vaccine

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TV1 in Samoa is reporting that two infants have died within minutes of receiving the measles, mumps, and rubella (MMR) vaccine.

Tala Fou brings you breaking news on the death of two young children both aged 1-year-old from the villages of Safotu and Sasina in Savaii. Both children died within minutes of being vaccinated with the MMR vacine at Safotu Hospital on Friday morning the 6th of July.

Our News Reporter Alisa Faamaoni met with both families in Savaii today. The parents of the first child Marietta and Samuelu Tuisuesue of Sasina explained in detail to Tala Fou that within three minutes of their 1-year-old daughter Lannacallystah Samuelu being injected with the MMR vacine by a nurse she was dead. (Source.)

What is so tragic, and has this island nation in such an uproar, is that the parents of the second child who died had reportedly already learned about the first infant’s death a couple hours earlier and declined to have their child receive the same vaccine. The mother reports that the nurse administered the MMR vaccine against her consent, leading to the child’s immediate death upon receiving the vaccine.  READ MORE..

INFERTILITY UNEXPLAINED: Vaccines- Polysorbate 80 metabolized by Cytochrome P450, HPV vaccine

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Are we sterilizing or genderbending the population between hormonal disrupting agricultural herbicides and vaccines and pharmacuetical drugs?

Research paper (Polysorbate 80)

Effects of non-ionic surfactants on cytochrome P450-mediated metabolism in vitro

Author links open overlay panelAnneChristiansenabThomasBackensfeldaKarstenDennercWernerWeitschiesb

 

Biotransformation XXXIX. Metabolism of testosterone, androstenedione, progesterone and testosterone derivatives in Absidia coerulea culture

Read study Abstract

FULL TEXT PDFsurfactants_suppress_CYP_enzymes_2011

VLA comment: Re: “Non-ionic surfactants like polysorbate 80 inhibit the CYP3A4 mediated hydroxylation of testosterone”.  I am wondering if Polysorbate 80 in vaccines considering it needs to be metabolized by Cyp 450 family of enzymes, involving hydroxylated testosterone, has a gender tweaking or has a precocious puberty effect that we find in Autism.

Polysorbate 80 in Vaccines:

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The U.S. Centers for Disease Control and Prevention (CDC) Vaccine Excipient and Media Summary lists 11 vaccines that contain polysorbate 80:

  • DTaP (Infanrix);
  • DTaP—IPV (Kinrix);
  • DTap-HepB-IPV (Pediarix);
  • DTaP-IPV-Hib (Pentacel);
  • Gardasil
  • Influenza (Agriflu);
  • Influenza (Fluarix);
  • Meningococcal (MenB-Trumenba);
  • Pneumococcal (PCV13—Prevnar13);
  • Rotavirus (RotaTeq);
  • Tdap (Boostrix)5
  • HPV

INFANTS INABILITY TO METABOLIZE VACCINE EXCIPIENTS

Studies: Cytochrome P450 and failure of infants to metabolize vaccine excipients

Top Medications with this excipient

Hypersensitivity reaction to human papillomavirus vaccine due to polysorbate 80.

Read study polysorbate_80_reaction_to_HPV_vaccine_2012

Badiu I1, Geuna M, Heffler E, Rolla G.
Abstract

A 17-year-old girl reported generalised urticaria, eyelid angioedema, rhino-conjunctivitis, dyspnoea and wheezing 1 h after third intramuscular administration of quadrivalent human papilloma virus vaccine (Gardasil). She was treated with antihistamine, and corticosteroids with prompt relief of rhinitis and dyspnoea, while urticaria and angioedema lasted 24 h. Intradermal test with Gardasil, which contains polysorbate 80 (PS80), resulted positive, while skin tests with the bivalent vaccine were negative. Prick test performed with PS80 resulted positive in the patient and negative in ten healthy controls. The CD203 basophil activation test result was negative for PS80 at all the tested dilutions and specific IgE was not found. As flu vaccine was recommended, the authors skin tested two flu vaccine, one containing PS80 (Fluarix, GSK), which resulted positive and another flu vaccine with no adjuvant or preservative (Vaxigrip, Sanofi Pasteur MSD), which gave negative results. The patient then received Vaxigrip without adverse reactions.

A lowered probability of pregnancy in females in the USA aged 25–29 who received a human papillomavirus vaccine injection

NEW STUDY (2017) LOWERED PREGNANCY RATES

Results suggest that females who received the HPV shot were less likely to have ever been pregnant than women in the same age group who did not receive the shot. If 100% of females in this study had received the HPV vaccine, data suggest the number of women having ever conceived would have fallen by 2 million. Further study into the influence of HPV vaccine on fertility is thus warranted.

VLA COMMENT: Lots of vaccines (see above) contain Polysorbate 80.  Does Polysorbate 80 considering its effect on testosterone have a negative hormonal effect on woman after years of being injected with the stuff.   Could the HPV vaccine with Polysorbate 80 providing the direct target to the reproductive system be the tipping point?  Or is there some other component  interfering? I believe in-vitro technology was rising prior to the Gardasil shot due to some interference in fertility.  January 1979 in Glasgow.[12] A team led by Ian Johnston and Alex Lopata were responsible for Australia’s first baby conceived by IVF, Candice Reed, born on 23 June 1980 in Melbourne.[13]   Hormanal disruption via agriculture chemicals came into being after WW II, (such as Atrazine, Alachlor and DDT).  See Peter Montague’s work such as Sperm in the News.

 

SPERM IN THE NEWS (1996)

This must be the year of the sperm. The NEW YORKER magazine ran a long story [1] January 15th called “Silent Sperm” –a wry reference to Rachel Carson’s SILENT SPRING, which made its debut in the NEW YORKER 35 years ago. “Silent Sperm” describes the 50% loss in sperm count that has occurred in men worldwide during the past 40 years. Furthermore, the January issue of ESQUIRE features an article on sperm loss, [2] titled “Downward Motility.” MOTHER JONES magazine [3] also began the new year with a sperm story, titled “Down for the Count.” And the nation’s newspaper of record, the NEW YORK TIMES, ran a 4-part, front-page series on increasing infertility in the U.S. January 7-10.

VLA Comment: The hormonal disrupting DDT was introduced in the 1940s (WWII era). In Vitro started gain steam in the 1980/90s. Study showed that Male sperm count was down 50% in 1996. How long before the study was there a consistently reduceing sperm count in males? How long have Vaccines contained polysorbate 80 that inhibits the CYP3A4 mediated hydroxylation of testosterone?.

 

 

 

Glaxo Smith Kline (GSK) responds to Pandemrix and Narcolepsy

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GlaxoSmithKline’s full statement to W5 on Pandemrix

1. A. Studies in Sweden, Finland, Ireland, Norway and Britain have also shown the risk of developing narcolepsy is between seven and 13 times higher in children who were immunized with Pandemrix than in those who were not – What is your response to these findings?

B. Can Pandemrix trigger narcolepsy in children?

Epidemiological data currently available to GSK suggest an increased risk of narcolepsy following vaccination with Pandemrix™ (H1N1). Due to the methodological limitations of the studies, which are retrospective observational studies, further research is needed to determine whether the observed risk is related to the vaccine, environmental effects, genetic factors, other factors or a combination of them. Further research also is needed to evaluate whether there are biologically plausible mechanisms by which vaccination with Pandemrix™ (H1N1) may have triggered narcolepsy in some individuals as no such mechanism has been demonstrated to date.

GSK remains committed to the pursuit of additional research to understand the potential role of Pandemrix™ (H1N1) in those who developed narcolepsy after vaccination and continues to support the research of others who are investigating the reported cases of narcolepsy.

2. In some jurisdictions Pandemrix is no longer used in people under 20 – what do you think of that decision? Is it justified? Why? Why Not?

READ MORE…

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