Category Archives: Government experimentation on the public

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

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

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

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…

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

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…

MAYO CLINIC: Anti-depressant and Pregnancy – and current protocol of Shock treatments

According to Mayo Clinic “generally, these antidepressants are an option during pregnancy:”

VLA comment: The list below are the recommended options that however come with risks.  What is not listed are the rest of the pharma madness drugs given to women approaching child bearing age and therefore compelled to continue the regimen during pregancy.  Other drugs are not listed because they are so risky for birth defects that they are not even considered.  However, how many young women have been prescribed these medication since teenagers?

  • Certain selective serotonin reuptake inhibitors (SSRIs). SSRIs are generally considered an option during pregnancy, including citalopram (Celexa), fluoxetine (Prozac) and sertraline (Zoloft). Potential complications include an increased risk of heavy bleeding after giving birth (postpartum hemorrhage), premature birth and low birth weight. Most studies show that SSRIs aren’t associated with birth defects. However, paroxetine (Paxil) appears to be associated with a small increased risk of a fetal heart defect.
  • Serotonin and norepinephrine reuptake inhibitors (SNRIs). SNRIs also are considered an option during pregnancy, including duloxetine (Cymbalta) and venlafaxine (Effexor XR). However, research suggests that taking SNRIs at the end of pregnancy is associated with postpartum hemorrhage.
  • Bupropion (Wellbutrin). This medication is used for both depression and smoking cessation. Although bupropion isn’t generally considered a first line treatment for depression during pregnancy, it might be an option for women who haven’t responded to other medications. Research suggests taking bupropion during pregnancy might be associated with heart defects.
  • Tricyclic antidepressants. This class of medications includes nortriptyline (Pamelor). Although tricyclic antidepressants aren’t generally considered a first line or second line treatment, they might be an option for women who haven’t responded to other medications. The tricyclic antidepressant clomipramine might be associated with fetal birth defects, including heart defects. Use of these medications during the second or third trimester might also be linked with postpartum hemorrhage.     READMore

SHOCK TREATMENTS

Electroshock is also known by the euphemism electroconvulsive therapy or ECT. Many electroshock patients receive the treatment against their will. Psychiatrists also claim that electroshock is safe during pregnancy and give the treatment to pregnant women.

Pregnancy and Electroconvulsive Therapy: A Multidisciplinary Approach  

STUDY: SHOCK TREATMENTS PREGNANCY 786178

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877273/
by SL Ray-Griffith – ‎2016 – ‎Cited by 7 – ‎Related articles

Electroconvulsive therapy is a safe and effective treatment during pregnancy and of particular benefit in the acute treatment of suicidal ideation.

VLA COMMENT: Suicidal ideations are a result of anti depressants and other drugs not being metabolized properly.  These drugs need Cytochrome P450 to metabolize.  If the patient does not have the activity of this family of liver enzymes and are prescribed drugs that are contra-indicated, as per the package inserts, adverse reactions such as “compelling” suicideal ideations (and heinous ideations of homicide) are likely to occur.

As the statement above refers to “acute treatment of suicidal ideation” it signals that the pregnant patient may be on medication that cannot be metabolized by his/her system of liver enzymes. Hence…the apparent solution to pregnant women who have been on anti depressants and psyche drugs for years and must continue during pregancy, is to top it all off with SHOCK TREATMENTS.  This allows the women to remain on psyche drug medication during her pregnancy.  However as noted in our posting Glyphosate, Drugs and Vaccines....the Cytochrome P450 metabolism is also found in the placenta.

Washington University in St. Louis Shocks Pregnant Women

According to the Citizen’s Commission on Human Rights (CCHR), Approximately 150,000 people get ECT every year in the US, with 2,000 shock treatments being done every year by WUSTL psychiatrists at Barnes-Jewish Hospital. Complications after treatment usually increase with the age of the patient; small surprise there. WUSTL psychiatrists say that, “ECT is considered a safe treatment modality in pregnant women in whom a number of medications may be associated with risk to the fetus.” READ MORE…

Article: ELECTRO SHOCK THERAPY WHILE PREGNANT

 

 

Glyphosate , Psyche Drug and Vaccines: THE CONNECTION

CCHR Newsletter: Overview of Cyp 450, Pharmacogenetics, Psyche Drugs, vaccines.

AGRICULTURE

Read Study glyphosate_rats_CYP_enzyme_suppression_2006

Syngenta Patent shows that the Genetic Engineering of our nations food supply is based on Cytochrome P450 technology whereby the genetically engineered seed is manipulated to be an ultra rapidmetabolizer while the “weeds” who are normal metabolizer dies in the presence of Glysophate.  Cytochrome P450 Gene Conferring herbicide resistance PATENT

MENTAL ILLNESS DIAGNOSIS –

PHARMA DRUGS, STREET DRUGS & MEDICATION AND METABOLIZING OPIOIDS

Plants and humans share the same detox mechanism involving Cytochrome P450.  In humans Cytocrome P450

90% of today’s modern drugs are metabolized by Cytochrome P450.

CYP1A2, CYP2C9, CYP2C19, CYP2D6, CYP3A4, and CYP3A5 enzymes metabolize 90 percent of drugs. these enzymes are predominantly expressed in the liver, but they also occur in the small intestine (reducing drug bioavailability), lungs, placenta, and kidneys.2

One out of every 15 white or black persons may have an exaggerated response to standard doses of beta blockers (e.g., metoprolol [Lopressor]), or no response to the analgesic tramadol (Ultram). This is because drug metabolism via CYP450 enzymes exhibits genetic variability (polymorphism) that influences a patient’s response to a particular drug.3

Every person inherits one genetic allele from each parent. Alleles are referred to as “wild type” or “variant,” with wild type occurring most commonly in the general population.

For example, 7 percent of white persons and 2 to 7 percent of black persons are poor metabolizers of drugs dependent on CYP2D6, which metabolizes many beta blockers, antidepressants, and opioids.7,8 One in five Asian persons is a poor metabolizer of drugs dependent on CYP2C19, which metabolizes phenytoin (Dilantin), phenobarbital, omeprazole (Prilosec), and other drugs.

The Effect of Cytochrome P450
Metabolism on Drug Response,
Interactions, and Adverse Effects 
READ STUDYCyp Study

VACCINES

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

Early Childhood Vaccines contain excipients that need Cytochrome P450 to metabolize.

VLA Comment: Cytochrome P450 is not mature in infants and children under the age of three years old yet we are giving vaccines with excipients that must be detoxed out of the body by Cytochrome P450 family of liver enzymes which infants do not have. These enzymes are predominantly expressed in the liver, but they also occur in the small intestine (reducing drug bioavailability), lungs, placenta, and kidneys.

Note in cases of Autism and vaccinating pregnant women:

Cyp 450 are found in the “Small intestines and placenta”

READ more…

RFK, jr. THE CDC IS A SUBSIDIARY OF THE PHARMACEUTICAL INDUSTRY

“The CDC is a subsidiary of the pharmaceutical industry. The agency owns more than 20 vaccine patents and purchases and sells $4.1 billion in vaccines annually.” 

Robert F. Kennedy Jr. claims the CDC owns patents on at least 57 different vaccines, and profits $4.1 billion per year in vaccination sales. 

According to RFK Jr., the CDC is not an independent government agency but is actually a subsidiary of Big Pharma.

“Upon cursory review of the patents, I found that one did not seem applicable to vaccination, but merely referenced an article on vaccination.  That leaves us with 56 CDC patents to scrutinize.  Here is what I found.

There are CDC patents applicable to vaccines for FluRotavirusHepatitis AHIVAnthraxRabiesDengue feverWest Nile virusGroup A StrepPneumococcal diseaseMeningococcal diseaseRSVGastroenteritisJapanese encephalitisSARSRift Valley Fever, and chlamydophila pneumoniae.

Goldman: Chicken Pox/ SHINGLES? (story of CDC obstruction and denial)

Review of the United States universal varicella vaccination program: Herpes
zoster incidence rates, cost-effectiveness, and vaccine efficacy based primarily on the Antelope Valley Varicella Active Surveillance Project data

In a cooperative agreement starting January 1995, prior to the FDA’s licensure of the varicella vaccine on March 17, the Centers for Disease Control and Prevention (CDC) funded the Los Angeles Department of Health Services’ Antelope Valley Varicella Active Surveillance Project (AV-VASP). Since only varicella case reports were gathered, baseline incidence data for herpes zoster (HZ) or shingles was lacking.

Goldman VaricellaAntelopeValley

VLA COMMENT:  The near eradication of the early childhood Chicken Pox has resulted in people who have had natural wild chickenpox as children are not getting their”subtle” exongenous boosters from the subsequent generation of our children or our grandchildren who unfortunately  are prevented from getting  wild chicken pox, They  are getting vaccinated with a different strain that can’t boost us. So, in essence, the CDC has simply brought another chicken pox strain into existence.  Now we have two. However, the wild typeis not prevelant enough to give us the necessary booster so we don’t get shingles.

Dr. Gary Goldman:  The reason why we are getting SHINGLES

The only reason that “children who get the chickenpox vaccine APPEAR to have a much lower risk of shingles” is that the live vaccine has provided these children with a recent boost to their immunity. However, the vaccine-strain of varicella zoster virus (VZV)–also known as the Oka strain–is genetically different from the wild-type U.S. strain. When a vaccinated child is exposed to an adult with shingles or a child with wild-type varicella, if the strains are sufficiently heterologous, the vaccinated child will break out in chickenpox. It is also possible for the weakened vaccine-strain to revert to a more virulent strain that manifests wild-type pathology. This means when children are exposed to the wild-type strain, even though they may not have a breakthrough infection with chickenpox, they now harbor two heterologous (genetically different) strains of VZV–both of which are at a later time subject to reactivation as shingles. Thus, as they age, they will be even more likely to reactivate with shingles (unless periodically administered booster vaccine doses for life in order to maintain the immunity)–especially if they do not receive exogenous (outside) boosts to their cell-mediated immunity which, in the pre-vaccine era, came from expostures to other children infected with wild-type varicella which provided the adult with a subclinical boost that helped to suppress or postpone reactivattion of shingles.

I would also like to clear up the point that shingles has always been increasing–even prior to the licensing of the varicella vaccine. This statement is true; however, the increases were on the order of 2 to 4% per year (which were likely due to an aging population, or greater access to healthcare). Once a community had widespread distribution of varicella vaccine, increases in herpes zoster were on the order of 20% per year. For example, this source [Yih WK, Brooks DR, Lett SM, et al. The incidence of varicella and herpes zoster in Massachusetts as measured by the Behavioral Risk Factor Surveillance System (BRFSS) during a period of increasing varicella vaccine coverage, 1998-2003. BMC Public Health 2005; 5:68.
32. Schmid DS, Jumaan AO. Impact of varicella vaccine on varicella-zoster virus dynamics. Clin Microbiol Rev 2010; 23(1):202–217] found a 90% increase in shingles over 5 years (1999-2003).

CDC Varicella/shingles Vaccines: Insider tells of CDC censorship and cover up

Abstract

Introduction: A Research Analyst insider reports findings that the Universal Varicella Vaccination Program alters the epidemiology of herpes zoster (shingles); and details ways in which the CDC, in collusion with the Los Angeles Department of Health Services (LADHS)—the Acute Communicable Disease Control unit—apparently manipulated data to conceal unwanted outcomes that supported an immunologically-mediated link between varicella and herpes zoster(HZ) epidemiology.

Read Journal

EASY SUMMARY REVIEW

Dr. Gary Goldman:  The reason why we are getting SHINGLES

The only reason that “children who get the chickenpox vaccine APPEAR to have a much lower risk of shingles” is that the live vaccine has provided these children with a recent boost to their immunity. However, the vaccine-strain of varicella zoster virus (VZV)–also known as the Oka strain–is genetically different from the wild-type U.S. strain. When a vaccinated child is exposed to an adult with shingles or a child with wild-type varicella, if the strains are sufficiently heterologous, the vaccinated child will break out in chickenpox. It is also possible for the weakened vaccine-strain to revert to a more virulent strain that manifests wild-type pathology. This means when children are exposed to the wild-type strain, even though they may not have a breakthrough infection with chickenpox, they now harbor two heterologous (genetically different) strains of VZV–both of which are at a later time subject to reactivation as shingles. Thus, as they age, they will be even more likely to reactivate with shingles (unless periodically administered booster vaccine doses for life in order to maintain the immunity)–especially if they do not receive exogenous (outside) boosts to their cell-mediated immunity which, in the pre-vaccine era, came from expostures to other children infected with wild-type varicella which provided the adult with a subclinical boost that helped to suppress or postpone reactivattion of shingles.

I would also like to clear up the point that shingles has always been increasing–even prior to the licensing of the varicella vaccine. This statement is true; however, the increases were on the order of 2 to 4% per year (which were likely due to an aging population, or greater access to healthcare). Once a community had widespread distribution of varicella vaccine, increases in herpes zoster were on the order of 20% per year. For example, this source [Yih WK, Brooks DR, Lett SM, et al. The incidence of varicella and herpes zoster in Massachusetts as measured by the Behavioral Risk Factor Surveillance System (BRFSS) during a period of increasing varicella vaccine coverage, 1998-2003. BMC Public Health 2005; 5:68.
32. Schmid DS, Jumaan AO. Impact of varicella vaccine on varicella-zoster virus dynamics. Clin Microbiol Rev 2010; 23(1):202–217] found a 90% increase in shingles over 5 years (1999-2003).

LEEP Surgery: Electro surgery on the Cervix for “Abnormal Cells

 

This Cervical Procedure to Prevent Cancer Is Causing Complications

Many women are experiencing severe and long-lasting side effects after getting a LEEP. So why isn’t the medical community listening

Five months ago, I received a phone call from my OB-GYN informing me I had abnormal cells on my cervix and that a loop electrosurgical excision procedure (LEEP) would be necessary to remove the cells and prevent cervical cancer.

Sarah also experienced a loss of sensation in her labia and overall vagina, which culminated in her loss of feeling during an orgasm, which she believes is a direct result of the surgery.

“It was like something had been removed surgically from my body. It was so frightening. I can’t even begin to say how it affected me sexually,” she explained, adding that her ability to experience an orgasm was also greatly diminished following the LEEP. “I had lost my entire sense of sexual identity and connection to my body. I was in a really terrible place. I couldn’t even cry. I was so numb.”

After my surgery and during my research, a doctor  explained to me that the “cervix brain connection is severed [during a LEEP], and that results in the inability to transfer critical sensory afferent information from the cervix to the critical brain areas.”