Amazon Removed Anti-Vax Documentaries

Last weekBuzzfeed News reports that Amazon “appears to have removed” anti-vaccination documentaries like Vaxxed from Amazon Prime.

On the first of this month, California Rep. Adam Schiff published an open letter to Amazon CEO Jeff Bezos asking that Amazon remove anti-vax content to from its website.

Related: How To Heal Your Gut 
https://twitter.com/ThunderTheiss/status/1101581110436421632

As the largest online marketplace in the world, Amazon is in a unique position to shape consumption. The algorithms which power social media platforms and Amazon’s recommendations are not designed to distinguish quality information from misinformation or misleading information and, as a result, harmful anti-vaccine messages have been able to thrive and spread. The consequences are particularly troubling for public health issues.”

Schiff Sends Letter to Amazon CEO Regarding Anti-Vaccine Misinformation

Schiff also wrote letters to Google and Facebook. Soon after YouTube banned advertising on some of the anti-vax videos and added additional pro-vaccine information. Google also said in a blog post that it will down-rank conspiracy theory videos.

Facebook says it’s “currently working on additional changes.”

Related: Facebook Planning To Censor Anti-Vaccination Posts

We have paid more than $4.03 billion dollars for vaccine damage lawsuits with our tax dollars.

https://www.youtube.com/watch?v=6hL2aO4Pd4U



FDA Has Removed Restrictions on Genetically Modified Salmon

Genetically modified fish will soon be sold in the United States. The Food and Drug Administration lifted the import restriction on AquaBounty’s genetically engineered salmon eggs on Friday, March 8th.

In late 2015 the FDA approved AquaBounty’s genetically modified salmon, but shortly thereafter Congress had the FDA block the GM salmon from entering the U.S. until labeling standards were issued. Last December the former U.S. Secretary of Agriculture Sonny Perdue announced the National Bioengineered Food Disclosure Standard. The GM salmon will be labeled as “Bioengineered.”

AquaAdvantage GM Salmon eggs will be imported to the company’s land-based facility in Indiana where the eggs will be raised into salmon and sold as food. The AquaAdvantage Salmon grows year-round and grows faster than farm-raised Atlantic salmon. The salmon will take more than a year reach the market if everything goes according to plan. Aquabounty chief Sylvia Wulf told the AP certification for an Indiana growing facility is expected in a few weeks. The facility will then receive the genetically modified salmon eggs and it will then take approximately 18 months for the salmon to reach their target weight.

Related:
Recommended:
https://www.youtube.com/watch?v=ssRQqno_Xjw



Tylenol Side Effects You Should Know About

You have probably heard that Acetaminophen may damage the liver. But a recent study showed that Acetaminophen may also damage the heart, the gastrointestinal bleeding, and the kidneys. The study also shows increased mortality for those who take Acetaminophen as well. As Acetaminophen use increases the risks increase as well.

There are also risks to using Acetaminophen while pregnant:

  • In a Norwiegan cohort, mothers were surveyed for acetaminophen exposure in weeks 17-30 of gestation, and 6 months postpartum. Children evaluated at 3 years were found to have dose-related effects from up to 28 days of cumulative acetaminophen exposure. These effects included motor, communication, and behavioral parameters.
  • Acetaminophen depletes the body’s primary antioxidant, glutathione, and interferes with the imperative function of fever to resolve infection and inflammation.
  • This study did not control for vaccination status, but there is empirical evidence that combining vaccines and acetaminophen may set vulnerable children up for a diagnosis of autism.

Another study linked prenatal acetaminophen use with an increased likelihood of ADHD.

Kelly Brogan, MD also reported in another article that after swallowing 1000 mg of Tylenol people showed less empathy.

Be sure to visit Kelly Brogan’s website and check out her YouTube channel as well.

Related:



FDA Admits That Flu Vaccine Vaccines for Pregnant Women Untested, Unlicensed

The CDC and other government agencies are recommending the FLULAVAL and Tdap vaccines for pregnant women. The manufacturers of FLULAVAL and Tdap vaccines have not had any clinical safety trials with pregnant mothers and the vaccines are not licensed for use with pregnant mothers, according to the Children’s Health Defense.

The manufacturers warn against against vaccinating pregnant mothers:

There are insufficient data on FLULAVAL QUADRIVALENT in pregnant women to inform.”

Package Insert for FluLaval Quadrivalent

There are no controlled data in human pregnancy. Diphtheria/pertussis, acellular/tetanus is only recommended for use during pregnancy when benefit outweighs risk.”

Tdap Vaccine Information

A Freedom of Information Act (FOIA) lawsuit was filed by Children’s Health Defense attorney, Robert F. Kennedy, Jr. on behalf of Informed Consent Action Network to obtain clinical trial data used by FDA to approve influenza vaccines for pregnant women.

The FDA’s response:

We have no records responsive to your requests.”

The FDA is admitting that these vaccines being recommended for pregnant women have not been licensed for such use by the FDA or tested for safety for pregnant mothers in clinical trials.

As a nation, we can no longer pretend our trusted agencies are protecting our children. It is time to hold federal agencies accountable.”

Robert F. Kennedy, Jr.

Recommended:
How To Heal Your Gut
How To Detoxify and Heal From Vaccinations – For Adults and Children

From Children’s Health Defense:

WASHINGTON, D.C., Feb. 11, 2019—In response to a Freedom of Information Act (FOIA) lawsuit, the FDA has admitted, for the first time, that government agencies, including the CDC, are recommending vaccines for pregnant women that have neither been licensed for pregnant mothers by FDA nor tested for safety in clinical trials. The lawsuit, filed by Children’s Health Defense (CHD) attorney, Robert F. Kennedy, Jr. on behalf of Informed Consent Action Network(ICAN), a vaccine safety advocacy group, sought all clinical trial data used by FDA to approve influenza vaccines for pregnant women. The FDA’s terse reply: “We have no records responsive to your requests.”

The manufacturers of flu and Tdap vaccines warn against their use for pregnant mothers since their safety has never been established. Package inserts state that it is “not known” whether the vaccines “will harm an unborn baby” and there are “insufficient data” on use in pregnant women to inform vaccine-associated risks. FDA regulations strictly prohibit pharmaceutical companies from marketing products for “off-license” uses. Noncompliant companies are routinely prosecuted criminally and civilly, paying billions in lawsuits and settlements.

The CDC nevertheless has actively recommended influenza vaccination during any trimester of pregnancy since 2004 and has told pregnant women to get Tdap shots (for tetanus, diphtheria and pertussis) since 2011. The FDA is responsible for vaccine safety and licensing, but, in the just-released court documents, it admits that it has no safety data to back up the CDC’s “off-license” pregnancy recommendations. FDA’s website states that it has never formally approved any vaccines “specifically for use during pregnancy to protect the infant.”

Blanket recommendations for vaccination during pregnancy are a dangerous proposition due to vaccination’s ability to activate a maternal immune response that can damage the developing fetal brain—just as infections during pregnancy sometimes do. In 2008, neuroscientist Paul Patterson warned, “Even if it happens less than 1% of the time, vaccinating an entire population of pregnant women could affect thousands of children.”

Long-term safety studies have not been designed to detect vaccine-related fetal injuries, but a 2017 Kaiser study of over 45,000 women (published in JAMA Pediatrics) showed an elevated risk of birth defects and a 20% higher risk of autism in children whose mothers received a first-trimester flu shot. After the authors applied a statistical correction that lessened the significant association, renowned UCLA statistician Sander Greenland criticized the methodologically “inappropriate” decision, noting that pharmaceutical researchers use the technique when they don’t like a result and “want to see if they can get rid of it.”

Click here to read the rest of the article on Children’s Health Defense’s website.

Thanks to Health Impact News for bringing this story to our attention.




Facebook Planning to Censor Anti-vaccination Posts

Facebook is being pressured to censor misleading or “fake” information.

Officials believe information discouraging people from getting vaccines may have contributed to the recent outbreaks of measles. Adam Schiff, U.S. Representative for California’s 28th congressional district, sent a letter to Facebook’s  Mark Zuckerberg and Google’s Sundar Pichai, asking the companies to address the problem.

Facebook curates content based on the user’s interests. Recommended posts are displayed on the Facebook wall, based on what the Facebook algorithm deems most likely to engage the reader.

Bloomberg reports that Facebook responded to Adam Schiff’s letter by saying the company is “exploring additional measures to best combat the problem.” The company says it is considering removing anti-vaccine information from the recommendations feed, which will severely limit the post reach, “while also ensuring that higher quality and more authoritative information is available.” The company also says it may stop recommending groups with questionable content.

Recommended: How To Heal Your Gut

YouTube is often criticized for pushing misinformation and has recently come under fire for promoting flat earth theories. Last month, Google’s YouTube algorithm adjusted how it recommends videos. The company says said it will stop recommending videos with “borderline content” that “misinforms users in harmful ways,” for example, videos that promote “a phony miracle cure for a serious illness.”

In related news, Pinterest blocked our website. When asked why this was their response:

 




Glyphosate May Increase Risk of Non-Hodgkin Lymphoma by 41%

Glyphosate raises the risk of Non-Hodgkin lymphoma in heavily-exposed individuals by 41 percent, according to a study by former EPA advisors. This is part of a growing body of evidence against Monsanto’s Roundup, now owned by Bayer, that may influence the new wave of lawsuits against the company. The study was a meta-analysis published in Mutation Research that analyzed the results of six earlier studies on glyphosate.

All authors claim to have no financial conflicts of interest.

Glyphosate is the most widely used broad-spectrum systemic herbicide in the world. Recent evaluations of the carcinogenic potential of glyphosate-based herbicides (GBHs) by various regional, national, and international agencies have engendered controversy. We investigated whether there was an association between high cumulative exposures to GBHs and increased risk of non-Hodgkin lymphoma (NHL) in humans. We conducted a new meta-analysis that included the most recent update of the Agricultural Health Study (AHS) cohort published in 2018 along with five case-control studies. Using the highest exposure groups when available in each study, we report the overall meta-relative risk (meta-RR) of NHL in GBH-exposed individuals was increased by 41% (meta-RR = 1.41, 95% CI, confidence interval: 1.13–1.75). For comparison, we also performed a secondary meta-analysis using high-exposure groups with the earlier AHS (2005), and we determined a meta-RR for NHL of 1.45 (95% CI: 1.11–1.91), which was higher than the meta-RRs reported previously. Multiple sensitivity tests conducted to assess the validity of our findings did not reveal meaningful differences from our primary estimated meta-RR.”

Recommended: How To Heal Your Gut

Lianne Sheppard is a former scientific adviser to the EPA on glyphosate.  In 2016 an advisory panel was instructed to determine the safety of glyphosate. Sheppard and to more of the study’s authors served on that panel. After reviewing multiple studies indicating a high likelihood that the herbicide is carcinogenic, the panel declared glyphosate to be noncarcinogenic. Bayer uses the panel’s findings as proof that their product is safe, but Sheppard criticized the EPA for “not following their own rules.

Together, all of the meta-analyses conducted to date, including our own, consistently report the same key finding: exposure to glyphosate-based herbicides are associated with an increased risk of non-Hodgkins lymphoma.”

Bayer AG is facing more than 9,000 lawsuits in the US brought by people suffering from cancer. Plaintiffs blame Monsanto’s glyphosate-based herbicides for their cancer. Dewayne Johnson was the first plaintiff to go to trial; he won a unanimous jury verdict against Monsanto in August. A judge reduced the verdict, and of course, Monsanto is appealing. The next trial is set for February 25th, and with many more to follow.

Related: Foods Most Likely to Contain Glyphosate



Massive Study Links Diet Soda To Major Heart Problems

A new study shows that women who drink two or more diet drinks a day are 30% more likely to have heart problems, including heart attack and stroke, and 50 percent more likely to die from related disease. The University of Iowa included nearly 60,000 women, making it the largest study of it’s kind.

The study looked at diet soda and diet fruit drink intake and heart health for women participating in the Women’s Health Initiative Observational Study, comparing women who never or only rarely consume diet drinks to those who consume two or more a day.

This is one of the largest studies on this topic, and our findings are consistent with some previous data, especially those linking diet drinks to the metabolic syndrome.” – Dr.Ankur Vyas, lead investigator of the study

Recommended: How To Heal Your Gut

Diet drinks were defined as a 12-ounce beverage of diet soda or a diet fruit drink.

After an average follow-up of 8.7 years, the primary outcome—defined as a composite of incident coronary heart disease, congestive heart failure, heart attack, coronary revascularization procedure, ischemic stroke, peripheral arterial disease, and cardiovascular death—occurred in 8.5 percent of the women consuming two or more diet drinks a day compared to 6.9 percent in the five-to-seven diet drinks per week group; 6.8 percent in the one-to-four drinks per week group; and 7.2 percent in the zero-to-three per month group.

The association persisted even after researchers adjusted the data to account for demographic characteristics and other cardiovascular risk factors, including body mass index, smoking, hormone therapy use, physical activity, energy intake, salt intake, diabetes, hypertension, high cholesterol, and sugar-sweetened beverage intake. On average, women who consumed two or more diet drinks a day were younger, more likely to be smokers, and had a higher prevalence of diabetes, high blood pressure, and higher body mass index.” – Iowa State

Related:  If You Drink Soda, It’s Probably The Worst Thing You Do To Yourself (even worse than smoking!)