WHAT IS THE IMPACT of injecting human DNA into our BABIES???

In the previous blog conclusive evidence was presented showing that some vaccines contain residual human fetal cell material from the growth mediums used in vaccine manufacture. Most people are unaware that the shots they inject into babies contain fragments of cells from human babies, and some even deny that this is true.

Four significant vaccines on the CDC recommended schedule [1] all contain human fetal tissue fragments, including both male and female DNA:

  • M-M-R®II: exclusively available in the USA since 1979 targeting measles, mumps, and rubella; 2 doses at 12 months and 5 years. [2]
  • Varivax®: the vaccine aimed to prevent chicken pox, added to the schedule in 1996; 2 doses at 12 months and 5 years.
  • Hepatitis A vaccine, approved in 1996, and added to the schedule for all babies in 2005; 2 doses given between 12 and 24 months. [3]
  • Pentacel® combined vaccine targeting diphtheria, tetanus, acellular pertussis, polio, Haemophilus influenza type b (Hib), introduced in 2008. Four doses given at 2, 4, 6, and 15 months of age. [4]

The average baby is injected with 10 different human tissue-containing shots before they go to school. Eight of them before the age of two years. Surely such widespread use of this growth medium – human fetal cells – was thoroughly demonstrated to be safe – right?

Since 40 years have passed since the first vaccine containing human cell debris was introduced, there has been ample time to study how this vaccine containing human DNA fragments could be impacting those that are injected with it.

But, how much DNA is really in a vaccine? Isn’t it just infinitesimally small amounts?

DNA residuals in human fetal cell line manufactured vaccines

In addition to the ingredients listed on the package insert for Meruvax II® (rubella), we detected significant levels of human ssDNA (142 ± 8 ng/vial) as well as dsDNA (35 ±10 ng/vial) fragmented to ~215 base pairs in length. The MMR II® package insert discloses the presence of human fetal residuals [sic] [but not] how much cell substrate dsDNA or ssDNA contaminates each dose. In each vial of Havrix® [Hepatitis A vaccine], we detected ssDNA (301 ± 153 ng/vial) as well as dsDNA (44 ± 24 ng/vial) unfragmented residual DNA more than 48.5 K base pairs in length. The Havrix® package insert discloses the presence of human fetal cellular residuals from the MRC-5 cell line, but not the DNA contaminant levels specifically.[5]

The Varivax® vaccine [chicken pox] is manufactured using the human diploid cell line MRC5, and is contaminated with 2 micrograms of cell substrate double stranded DNA. Single stranded DNA levels are not reported in Merck’s Varivax Summary Basis for Approval document nor are the length of the DNA fragments contaminating the vaccine (Merck 2011). [5]

Vaccines that have been cultured on or manufactured using the WI-38 fetal cell line such as MeruvaxII®, MMRII®, Varivax®, Havrix® and Pentacel® are additionally contaminated with fragments of human endogenous retrovirus HERVK (Victoria et al., 2010). Recent evidence has shown that human endogenous retroviral transcripts are elevated in the brains of patients with schizophrenia or bipolar disorder (Frank et al., 2005), [5]

According to EPA recommendations, birth year change points for prevalence of autistic disorder should drive consideration of environmental triggers, as for any disease (McDonald 2010).[5]

Scientists have been studying and learning that injected “human fetal DNA fragments are inducers of autoimmune reactions, while both DNA fragments and retroviruses are known to potentiate genomic insertions and mutations (Yolken et al., 2000; Kurth 1998; U S Food and Drug Administration 2011).” [5]

How has injecting male and female DNA fragments into ALL babies impacted their health? 

A detailed analysis of the data available and has found startling results. There are statistically obvious change points associated with the addition of fetal cell line vaccines and increased diagnosis of autism spectrum disorder: “Autistic disorder began to rise in the US after birth year 1978 (Newschaffer and Gurney 2005).” This corresponds to the introduction of the MMRII developed with two different fetal cell tissues. [5]

Additionally, “The US 1988.4 change point corresponded to the addition of a second dose of MMRII® to a measles vaccination campaign that increased compliance from ≤50 to 82% between birth years 1987 and 1989 (Centers for Disease Control 1989; Kaye and Jick 2001) as well as to the introduction of Poliovax in 1987. [5]

And, “The 1995.6 autistic disorder change point corresponded to the approval and introduction of the Varicella vaccine (Varivax®).” [5]

This chart summarizes the autism change points in relationship to the MMRII, the push for higher uptake of MMRII, and the chicken pox vaccine. [5]

Why aren’t the FDA (Food and Drug Administration), HHS (Federal Department of Health and Human Services), the CDC (Federal Center for Disease Control), or the ACIP (Advisory Committee on Immunization Practices) concerned about fetal cell contamination in vaccines causing harm?

The primary measure of effectiveness for the CDC, FDA, and vaccine makers is focused on “serologic evidence of immunity,” or a blood test showing raised antibody titers. No vaccine has ever been investigated for mutagenic or carcinogenic properties – tested and tracked long-term to see if they damage the genetic material of the recipient, if they could be implicated in causing cancer, or if they could be linked to infertility later in life. [6]

Even with all the advances in genetic understanding since the mapping of the human genome in 2001, the HHS has undertaken NO FURTHER SAFETY STUDIES on these vaccines known to contain human fetal DNA fragments. Further, the HHS has done no safety studies at all on any vaccine for 30+ years.

Isn’t that interesting.

You might be asking, ‘But aren’t the vaccine manufacturers responsible for determining safety?’ Ever since the 1986 National Childhood Vaccine Injury Act, all liability was removed from vaccine manufacturers and the responsibility for vaccine safety was shifted to the HHS, who recently admitted, after being forced by a court order, that no safety testing of vaccines has been undertaken. [7]

In June 2018 I had three minutes during the public comment session at the ACIP meeting held three times a year at the CDC in Atlanta. I briefly presented some of the unintended consequences of the vaccine schedule, commonly known as “non specific effects.” It remains to be seen if this information will drive any change in recommendations.

The vaccine promoters have captured the media through controlling advertising revenue. Fear campaigns are promoted so that parents rush to stay up-to-date on vaccines without examining the ingredients. Doctors are busy and have confidence in the government regulatory agency recommendations. Has our cherished vaccine program helped children avoid short term infectious illness but caused an epidemic in longterm serious developmental impairment and auto-immune disorders?

If you have any fear of your child getting chicken pox, please read the description provided by the CDC: “The clinical course in healthy children is generally mild, with malaise, pruritus (itching), and temperature up to 102°F for 2 to 3 days.” [8]

Would you rather your child have a mild fever and have some itching, or inject them with human cellular debris containing DNA fragments – which has not been tested for whether or not it may adversely impact genetics, play a role in skyrocketing childhood cancers, or impact your future ability to have grandchildren?

So, today the public is pushed to continue to inject their babies with both male and female DNA, with no investigation of the possible mutagenic (genetic alteration) impact it might be having. We watch sky-rocketing rates of childhood cancer and donate money to those searching for ‘cures’. Many parents watch helplessly as their adult children struggle with infertility, but very few make any connection to vaccines. Vaccines were never studied to impact any of that.

Does this seem like “safe” science to you?

Please share this information widely.

I highly recommend that you read the full paper by Theresa Deisher on Impact of Environmental Factors on the Prevalence of Autistic Disorder after 1979 published in the Journal of Public Health and Epidemiology on 9 July 2014.

Author: Becky Hastings, wife, mother, grandmother, passionate follower of Jesus and truth. As a breastfeeding counselor for over 25 years, Becky is devoted to helping parents make wise decisions for the long-term health and wellbeing of their babies. As a member of a Vaccine Safety Education Coalition, Becky writes and speaks on the topic of vaccine safety. Becky also loves mountain biking and appreciates all comments and the rare donation which provides wonderful encouragement. 

[1] The 2018 (current) CDC vaccine schedule: https://www.cdc.gov/vaccines/schedules/hcp/imz/child-adolescent.html#f3

[2] Complete vaccine package insert for the M-M-R®II, exclusively used in the USA since 1979. https://www.fda.gov/downloads/BiologicsBloodVaccines/UCM123789.pdf

[3] Hepatitis Vaccine is manufactured by both Merck and GlaxoSmithKline. Havrix® by GSK was approved for use in the US in 1995; Vaqta® by Merck was approved in 1996. However, Hepatitis vaccine was for limited population groups and not part of the childhood immunization schedule nor recommended for use by any states. In 1999, 17 states began recommending/considering its use for children 24 months and older, and in 2005 it was included in the ACIP recommended vaccination schedule for children 12 months and older. http://soundchoice.org/scpiJournalPubHealthEpidem092014.pdf

“To produce each vaccine, cell culture-adapted virus is propagated in human fibroblasts, purified from cell lysates, inactivated with formalin, and adsorbed to an aluminum hydroxide adjuvant.” The GSK version also has a preservative, 2-phenoxyethanol. https://www.cdc.gov/vaccines/pubs/pinkbook/hepa.html

[4] Vaccine package insert for Pentacel combination vaccine https://www.fda.gov/downloads/biologicsbloodvaccines/vaccines/approvedproducts/ucm109810.pdf

[5] Deisher, Theresa A, et al. “Impact of Environmental Factors on the Prevalence of Autistic Disorder after 1979.” Sound Choice Pharmaceuticals, Journal of Public Health and Epidemiology, 9 July 2014, http://soundchoice.org/scpiJournalPubHealthEpidem092014.pdf.

[6] https://www.cdc.gov/vaccines/pubs/pinkbook/rubella.html

[7] https://www.icandecide.org/health-and-human-services/

[8] https://www.cdc.gov/vaccines/pubs/pinkbook/varicella.html

Are aborted baby parts in vaccines?

14 week gestation

The short factual answer is, YES.

Babies were specifically harvested from their mother’s wombs to provide living human cells as a desirable growth medium for vaccine development in the 1960s. Furthermore, the end product produced today contains some of the actual human DNA fragments used in the development of these products because it is impossible to fully purify a vaccine from all the human cellular debris. The DNA fragments are injected into the body with the rest of the components of the vaccines.

It’s true. While vaccines are pushed as a way to prevent infectious illness in children, most people are not aware that many vaccines are built on aborted human fetal tissue. Furthermore, parents are not told that this ‘preventative measure’ is known to kill some and harm countless numbers of others.

The rubella vaccine was the first vaccine derived from aborted human fetal cells. The rubella vaccine was added as the “R” to the MMRII licensed for use in 1979. This vaccine, exclusively used in the USA and used widely throughout the world, contains both RA27/3 cells (congenital rubella virus derived from an aborted baby) and WI-38 the first cell line used as a growth medium in vaccine development, derived from lung cells harvested from an aborted female baby.

MRC-5, the name of a second cell line used in vaccine development was developed in the U.K. using lung fibroblast cells from a male baby aborted at 14 week gestation (the size of the photo at the top of the page) for ‘psychiatric reasons’. Sometimes referred to as “human diploid cells,” MRC-5 is used in the manufacture of many vaccines, including Pentacle vaccine (since 2008), Hepatitis A and A/B combination vaccines (since 1995), polio vaccine (Poliovax, 1987), and shingles vaccine for adults (2006).

In 1995 Varivax, manufactured by Merck, targeting the varicella or chicken pox virus, derived from aborted human fetal tissue was approved for the USA market and added to the Advisory Committee on Immunization Practices (ACIP) schedule. This vaccine was developed using both WI-38 cells harvested from a female baby, and MRC-5 cells harvested from the lung fibroblast cells of a 14 week gestation male baby.

Havrix, a Hepatitis A vaccine, propagated in human fibroblasts from the MRC-5 line was approved for use in limited populations groups in 1996. In 2005 ACIP expanded the recommendation for the Hepatitis A vaccine to include all babies in the USA. [1]

“Pentacel® contains inactivated polio viruses grown on the MRC-5 human fetal cell line. Since 2008, Pentacel® is recommended for children at 2, 4 and 6 months of age, and may account for the recent idea that scientists have become more adept at diagnosing autism at younger age. Diagnosis at younger age may more likely be the result of introducing human fetal cell vaccine contaminates to younger children.” [2]

Even today, the CDC confidently describes the rubella vaccine in their pink book:

“The RA 27/3 rubella vaccine is a live attenuated virus. It was first isolated in 1965 at the Wistar Institute from a rubella-infected aborted fetus. The virus was attenuated by 25–30 passages in tissue culture, using human diploid fibroblasts. It does not contain duck, chicken or egg protein.” Previous rubella versions contained duck embryo, dog kidney or rabbit kidney cells. [3]

The scientists were not concerned about the possible long-term impact of injecting foreign human DNA into a developing baby. The vaccine package insert for this vaccine continues to state, nearly 40 years later, “M-M-R II has not been evaluated for carcinogenic or mutagenic potential, or potential to impair fertility.” [4]

Surely, in 40 years there has been ample time to study how this vaccine, containing human DNA fragments, could be impacting those that are injected with it.

It has been suggested that there was only one abortion that provided the tissue necessary to produce the cell lines used in vaccine development. This is a side issue. But, a closer look reveals that a total of at least 80 separate, elective abortions recorded were involved in the research and final production of the present day rubella vaccine: 21 from the original WI-1 through WI-26 fetal cell lines that failed, plus WI-38 itself, plus 67 from the attempts to isolate the rubella virus. https://cogforlife.org/vaccine-abortions/

As a further attestation to the reality of the scientific use of aborted human fetal tissue, it is noted that these cells lines are still available to purchase on-line today:

RA27/3 congenital rubella virus infected cells: https://www.atcc.org/Products/All/VR-1359.aspx

WI-38 human female fetal lung cells: https://www.atcc.org/Products/All/CCL-75.aspx

MRC 5 cell line male lung fibroblast cells: https://www.atcc.org/products/all/CCL-171.aspx

WHAT IS THE IMPACT of injecting human DNA into our BABIES???

See the next blog….

The previous blog in this series examines the choice we make in using vaccines as a ‘preventative measure’.

Author: Becky Hastings, wife, mother, grandmother, passionate follower of Jesus and truth. As a breastfeeding counselor for over 25 years, Becky is devoted to helping parents make wise decisions for the long-term health and wellbeing of their babies. As a member of a Vaccine Safety Education Coalition, Becky writes and speaks on the topic of vaccine safety. Becky also loves mountain biking and appreciates donations which mainly encourage her. 

[1] Hepatitis A is manufactured by both Merck and GSK and was first approved in 1996 for limited population groups. “To produce each vaccine, cell culture-adapted virus is propagated in human fibroblasts, purified from cell lysates, inactivated with formalin, and adsorbed to an aluminum hydroxide adjuvant.” The GSK version also has a preservative, 2-phenoxyethanol. https://www.cdc.gov/vaccines/pubs/pinkbook/hepa.html

[2] Impact of environmental factors on the prevalence of autistic disorder after 1979. Theresa A. Deisher*, Ngoc V. Doan, Angelica Omaiye, Rumiko Toyama and Sarah Bwabye, Sound Choice Pharmaceutical Institute, 1749 Dexter Ave N, Seattle, WA 98109, USA.Received 13 May, 2014; Accepted 9 July, 2014 http://soundchoice.org/scpiJournalPubHealthEpidem092014.pdf

[3] CDC description and history of rubella vaccine https://www.cdc.gov/vaccines/pubs/pinkbook/rubella.html

[4] Complete vaccine package insert for the MMRII https://www.fda.gov/downloads/BiologicsBloodVaccines/UCM123789.pdf

A Choice

A song I heard recently resonated in my heart: “I need You to soften my heart. I need You to open my eyes, to pierce through the darkness, expose the lies and deception.” I think I added some words, but you get the idea! Here is the song in case you want to start worshipfully. It’s all about surrender and trusting that God loves you.

I’m just a mom, and now a grandmother, trying to figure out what is truly healthy for babies and children. I’ve been at this for a long time, since about 1982 when I found out God was blessing my husband and I with our first child.

Imagine this scenario:

There is a disease. It may make some people sick. A very small number of people may die if they get it. The disease can be spread from one person to another, but self-imposed separation can reduce the spread, and most people will recover fully and obtain lifelong protection and never get that disease again.

Now, some smart people didn’t want to see people suffering. They didn’t have confidence in the body’s self-healing mechanisms. They considered themselves able to circumvent God’s design. They developed a ‘preventative measure’ against the disease.

This ‘preventative measure’ may prevent someone from getting the disease, but it is known that it will kill some previously healthy people – we know that some percentage will die from receiving this ‘preventative measure.’ And, it will cause lifelong damage and suffering to an undetermined, but substantial, number of people.

Which do you choose?

Please bear in mind that there are other ways of helping to reduce the impact of the disease and shorten the duration of suffering – ways that are completely safe and beneficial.

What do you choose? The man-made ‘preventative measure’ that WILL kill and harm some? Or, the potential risk of getting the disease, and using known safe measures to treat it?

What number of healthy people dying will it take before the ‘preventative measure’ is unthinkable?

There are many ways of reducing the duration and severity of the illness, which do not result in death or life-long impairment. Would you choose these? Or would you choose the ‘preventative measure’ that will kill and seriously harm some?

Your child could be one of the ones harmed.

But, the plot thickens…

What if you knew that this ‘preventative measure’ is built on the lives of aborted babies, and the final product contains DNA fragments from the cells of those babies?

More on that in the next blog

Before we choose a ‘preventative measure’ that has the known capacity to kill some, we need to research that preventative measure extremely carefully, paying close attention to who is providing the information, and what they may possible gain from their connection to the ‘preventative measure’.

Author: Becky Hastings, wife, mother, grandmother, passionate follower of Jesus and truth. As a breastfeeding counselor for over 25 years, Becky is devoted to helping parents make wise decisions for the long-term health and wellbeing of their babies. As a member of a Vaccine Safety Education Coalition, Becky writes and speaks on the topic of vaccine safety. Becky also loves mountain biking and appreciates donations which mainly encourage her. 

A Loving Entreaty

I seek to lovingly make my case for why a person thoroughly convinced that vaccines are absolutely essential “because they have saved the lives of millions of children,” should re-evaluate their firmly held ideas about vaccines.

I am absolutely convinced. You are also absolutely convinced. One of us is wrong.

I am not accusing you of causing harm to children. I am not trying to load you with a burden of guilt. I am not assaulting your character, your competence, or your training. I am simply asking you to reexamine your stance on vaccines and ask yourself before God, “Is it possible that I could have been deceived?”

I come to this topic not as a doctor, but as a mother, a grandmother, a breastfeeding counsellor eager to help moms raise a healthy baby, and as a citizen journalist seeking to uncover the truth.

But mostly, I come to this topic as a devoted follower and believer in Jesus Christ. The Holy Spirit opened my eyes in 1980 to accept God’s grace and salvation though Jesus. As a thoroughly rebellious individual, I wholeheartedly dived into grace, seeking God’s direction, through the Holy Spirit, towards truth in every area of my life. Hard decisions were made easier because of my past wrong choices that were primarily guided by adhering to cultural norms. I questioned every culturally accepted practise, especially where it pertained to the babies God blessed my husband and I with.

Trying to change the mind of a resolute vaccine proponent is a huge assignment for which I need some help. I am not a doctor. That doesn’t make me less able to read and understand science and statistics, but it may make me less able to understand how thoroughly entrenched vaccine thinking is amongst those who have undertaken medical training. Thus, I have chosen a doctor who explains in detail his journey as he began asking questions about vaccines, and what he discovered as he explored with an inquiring mind.

Sam Eggertsen, MD

I’ve been accused of not understanding physiology and seeking to benefit from the fact that most of the population is vaccinated, thus keeping myself, my children, and my grandchildren safe from infectious disease even though we refuse vaccines. However, I believe the science that has been uncovered in the last 15 years presents facts showing the foundation for injecting vaccines is faulty. Dr Suzanne Humphries has done more research on vaccines than any medical professional known and does a brilliant job explaining both the physiology of the human body, detailed analysis of the most recent science available, and the mechanism of vaccines in light of the latest understanding of the gut microbiome, the blood brain barrier, aluminum safety, and many other topics. It will take some time to listen and comprehend her lectures. Some of her lectures I have watched and taken notes four times or more. If you are honestly interested in finding out the true state of vaccine safety and efficacy in light of all the recent science discovered, you can find a lot more of Dr Humphries’ videos for free on Youtube. She has also written two excellent books, Dissolving Illusions (a detailed historical analysis of polio) and Rising From the Dead (a fantastic autobiography reflecting on her training in medicine and her journey to question her training) both available on Amazon. One of the most exciting aspects of Dr Humphries’ story is her coming to find a relationship with Jesus Christ after she began her search for truth in the vaccine realm which she describes in her autobiography.

Suzanne Humphries, MD

There are so many reasons to be skeptical about vaccine safety. Each topic could be a complete book. I will list some of the most powerful, compelling points which convinced me that vaccines deserve to be questioned:

  1. Absolute immunity. The makers of vaccines were granted absolute immunity from lawsuits for any type of damage caused by their products in 1986. This has seriously reduced the motivation for manufacturers to ensure the safety of vaccines. It is a business plan to die for: a product recommended to millions, yet no liability.
  2. Acknowledged harm. Since 1988, after vaccine makers received protection, nearly $4 billion has been paid by the HHS to victims of vaccine injury and death. HHS was charged with the mantel of vaccine safety by the same act of Congress, which gave protection to the makers, and the VICP (Vaccine Injury Compensation Program) was set up to compensate for known and expected vaccine harm.
  3. Lack of safety studies. In July 2018 HHS confirms they have not conducted any safety reports or studies on the improved safety of vaccines in over 30 years, as they were charged by Congress to do in 1986.
  4. Bloated schedule. In 1986 children were recommended to have a small number of vaccines. Since the makers have been protected from liability, the recommended vaccine schedule has ballooned. Children are now recommended to receive 72 vaccines by 18 years for 18 different infectious illnesses.
  5. Manufacture and delivery errors. Vaccine manufacture in inherently unsafe. Cold supply delivery chain is essential for many vaccines. Unsafe batches and unsafe delivery is a very real risk. The Cutter Incident and the Wyeth memo reveal some history of unsafe vaccines in the USA. Additionally, today many vaccines are made in China and the USA FDA has no jurisdiction over the safety. Chinese vaccines have had several serious wide-spread problems. An Italian study in 2017 demonstrates serious contamination in most vaccines analysed. [http://medcraveonline.com/IJVV/IJVV-04-00072.pdf]
  6. Administrative errors become increasingly problematic with the bloated schedule of vaccines given. In Texas a 4-month-old baby was given her recommended vaccines and was also injected with the HPV vaccine intended for her older brother. All the vaccines were put on a tray and all injected into baby. The doctor received no disciplinary action. The mother struggled with baby’s health. All connection to vaccines was denied, and CPS was called to initiate the removal of baby from the mother’s care. Sheila Ealey recounts how in 2000 her son, a twin, was given both MMR vaccines, as well as the DTaP and HIB at their routine one-year doctors visit. Somehow the office staff intended to give MMR shots to each twin, but injected her son with two MMR vaccines. He is severely neurologically impaired, while his twin sister excels in many areas. Administrative errors happen.
  7. Aluminum. There are many questionable ingredients in vaccines, perhaps in small amounts, too many to focus on in this list. One of the more troubling ingredients in vaccines is aluminum, added purposefully as an adjuvant in much larger quantities to ramp up the body’s immune response. If an infant receives all the vaccines on the CDC recommended schedule, the will be injected with 4,925 mcg of aluminum  by 18 months of life. The FDA stipulates a safe limit for intravenous feeding of 25 mcg per day. The aluminum content and quantity in vaccines has never been studied for safety or long-term impact. Current aluminum ‘studies’ are based on ingested aluminum in an adult. More on aluminum, by world renowned aluminum expert, Dr Christopher Exley, Keele University: [https://www.sciencedirect.com/science/article/pii/S0946672X17308763]
  8. Human DNA fragments. Many vaccines are derived from the use of aborted human fetal cells. While attempts are made to remove these cells from the final vaccine product, there remains residual contamination of DNA fragments of both male and female aborted babies. The practise of developing pharmaceutical products from aborted fetal tissue may be abhorrent to many, but purposefully injecting DNA into infants with no long-term safety testing is proving to be extremely problematic and perhaps contributory to a host of issues, including auto-immune disorders and NDD. “In the US, autism has spiked up in 3 distinct years, called changepoints. The first changepoint occurred in 1981, the second in 19881, and the third in 1996. These spikes coincide with the introduction of vaccines that are produced in human fetal cells.” Dr Theresa Deisher
  9. Deception and Greed. Jeremiah warned us thousands of years ago, “the heart of man is deceitful above all things, and desperately wicked, who can know it.”Many of the NT writers also warn of deception based on greed. Here is just one example: “But there were also false prophets among the people, just as there will be false teachers among you. They will secretly introduce destructive heresies, even denying the sovereign Lord who bought them – bringing swift destruction on themselves. Many will follow their depraved conduct and will bring the way of truth into disrepute. In their greed these teachers will exploit you with fabricated stories. Their condemnation has long been hanging over them, and their destruction has not been sleeping.” 2 Peter 2:1-3. Throughout history people with power have sought to control, gain wealth, and gain more power through taking advantage of others. The reality of companies seeking profit over health is just as real today and can be easily verified by the track record of pharmaceutical companies and prescription drugs – for which lawsuits can be brought. If pharmaceutical manufacturers have pled guilty, or been fined billions of dollars in cases of purposefully perpetuating harm on a population in order to profit through the sale of a specific drug, why do we trust them absolutely in the area of vaccine manufacture? Jesus told us to judge by the fruit. Is the fruit of the pharmaceutical company above reproach? “Beware of false prophets. They come to you in sheep’s clothing but inside are ferocious wolves. By their fruit you will recognize them.” Matt 7:15
  10. Unavoidably unsafe. The US Supreme Court ruled that vaccines were unavoidably unsafe, yet the media, the CDC, local pharmacies, doctors, and nurses continue to tell the public that “vaccines are safe and effective.” Somewhere, somehow, there is a disconnect. Both statements cannot be true. [https://www.supremecourt.gov/opinions/10pdf/09-152.pdf]
  11. VAERS. While the Vaccine Adverse Events Reporting System is a passive reporting system and cannot be an absolute marker of true vaccine reactions, the NIH estimates it accurately reflects only 1% of actual vaccine adverse events because most cases are not reported. https://healthit.ahrq.gov/sites/default/files/docs/publication/r18hs017045-lazarus-final-report-2011.pdf
  12. Media slant. Orchestrated campaigns and the full weight of media seek to drive home one message. Why can’t their be rational discussion and honest questions on the topic of vaccine safety?
  13. Legislative Onslaught driven by Pharmaceutical companies. In the name of ‘safety for the children’ nearly every state is facing rabid lawmakers seeking to push through obviously pharma favorable bills.
  14. Fraud. Admitted fraud by the CDCWhistleblower, Dr William Thompson and the two scientists working on the MMR vaccine for Merck. Paul Thorsen is a major author of papers promoted by the CDC as proving vaccine safety, yet is wanted on many criminal counts by the FBI. See this 22 page report on the criminal activity of this CDC researcher: https://worldmercuryproject.org/wp-content/uploads/world-mercury-project-report-on-poul-thorsen-9-7-17.pdf
  15. Myth of Herd Immunity. Disease rates and vaccine rates in 1980 were low. Most adults were not up-to-date on vaccines, thus did not posses vaccine acquired immunity. Basically, because the overall vaccine rate in the population there was no ‘herd immunity’, yet there were not widespread outbreaks of disease. Herd immunity is a term that only accurately applies to the immunity acquired via natural exposure to diseases such as measles.
  16. Hepatitis B shot given to newborns on the first day of life. Please investigate this one vaccine. Why are mothers who test negative for Hepatitis B still encouraged to give their babies the Hep shot on the first day of life? This disease is well known to be primarily transmitted through sharing needles and sex. Why does a 24 hour old baby get injected? This vaccine contains 250 mcg of aluminum and has never been studied for long-term safety. Recent studies show a potential increase in neurological developmental disorders in animals who received the vaccine equivalent for their weight. These studies were repeated and the team found a latency period suggesting that greater neurological harm develops over time. This finding needs urgent attention. Until conclusive results are found, vaccine recommendation for babies of Hepatitis B negative mothers should be halted immediately. [https://www.ncbi.nlm.nih.gov/pubmed/29751176]
  17. SV40. Polio vaccines administered in the 1960s were contaminated with a cancer causing virus, simian virus 40. [https://www.ncbi.nlm.nih.gov/pubmed/?term=Italian+vaccine+contaminated+2017]
  18. Vibrant health of non-vaccinated individuals. It is so obvious and it speaks for itself. Doctors who have a large non-vaccinated population note they are the healthiest of all the children they see by far. Non vaccinated individuals with adequate nutrition, clean water, and a healthy life-style are utilizing their God-given innate immune system for protection against illness. Additionally, breastfeeding is the designed method to feed babies and passes on immunological benefits that last a life-time.

If after investigating each of these 18 points, you are still absolutely convinced of the necessity and goodness of vaccines, we may just have to agree to disagree. I do not believe we should expose even one healthy child to harm in the hope of protecting many. The reality is that we may be exposing a far higher percentage to harm than we every thought possible.

I am absolutely convinced. You are absolutely convinced. One of us is wrong. One day, before God, we will find out.

This decision – whether to question vaccine safety and history or accept the mainstream point of view – is critically important to your personal health, your family’s health, generations to come, and our culture as a whole. Paul’s admonishment to the Ephesians seems appropriate to keep in mind as we delve into this topic:

Let no one deceive you with empty arguments, for God’s wrath is coming on the disobedient because of these things. Therefore, do not become their partners. For you were once darkness, but now you are light in the Lord. Live as children of the light (for the fruit of the light consists in all goodness, righteousness and truth) and find out what pleases the Lord.

Have nothing to do with the fruitless deeds of darkness, but rather expose them. It is shameful even to mention what the disobedient do in secret. But everything exposed by the light becomes visible – and everything that is illuminated becomes a light… Be very careful, then, how you live – not as unwise but as wise, making the most of every opportunity, because the days are evil. Ephesians 5:6-13; 15-16

Author: Becky Hastings, wife, mother, grandmother, passionate follower of Jesus and truth. As a breastfeeding counselor for over 23 years Becky is devoted to helping parents make wise decisions for the long-term health and wellbeing of their babies. As a member of a Vaccine Safety Education Coalition, Becky writes and speaks on the topic of vaccine safety. Becky also loves mountain biking and appreciates donations which mainly encourage her. 

 

Vaccines and Eczema

Are we going backwards or forwards? Keep in mind as you read this precautionary policy from 1958 that they were only talking about a few vaccines, smallpox, polio and diphtheria. Today babies are given 36 vaccines against 14 different infections before they are two years old. The CDC has quite a lot of information about who should NOT get each vaccine, but nowhere do they mention eczema as a reason NOT to get vaccines.

In 1958 the American Academy of Pediatrics made the following statement:

1) No child with atopic eczema or other skin disorder should be vaccinated.
2) No child should be vaccinated if any member of his family has eczema or other skin disorder.
3) Parents of children with eczema should be notified at the onset of the disease of the danger from vaccination contact.
4) If a sibling of a child with atopic eczema is vaccinated, he must be completely separated from that child for at least 21 days.
5) Forms used by state and local health departments for parents’ consent to vaccination should include an appropriate warning of the contraindications.
6) Eczema vaccinatum should be a reportable disease.
7) Patients recently vaccinated must be excluded from pediatric wards containing patients with atopic eczema, other diseases of the skin, burns or healing surgical incisions.
8) Vaccination may be recommended at 2 months of age, especially for babies from strongly allergic families.

Received December 18, 1957.
Accepted February 18, 1958.
Copyright © 1958 by the American Academy of Pediatrics. Read the abstract and access the full paper here.

It is somewhat comforting to know that the CDC recognizes there are some people who should NOT get a DTaP shot:

However, rarely have I ever heard of pediatricians expressing hesitancy about administering this shot or asking about these adverse events. Also, many times a “life-threatening allergic reaction after a dose of DTaP” is denied as having been connected to the vaccine.

The bottom line is, in 1958 eczema was recognized as a signal that the immune system could not handle a vaccine. Today, it’s up to parents to educate and inform themselves on the true risk of vaccines in order to have a healthy baby. Parents will bear all the weight and responsibility for any vaccine harm.

Author: Becky Hastings, wife, mother, grandmother, passionate follower of Jesus and truth. As a breastfeeding counselor for over 23 years Becky is devoted to helping parents make wise decisions for the long-term health and wellbeing of their babies. As a member of a Vaccine Safety Education Coalition, Becky writes and speaks on the topic of vaccine safety.

Addendum. Helpful information if you have experienced eczema. https://thinkingmomsrevolution.com/thinking-moms-guide-red-flags-eczema/

This 2004 study purports to study vaccines and allergic responses such as eczema, but does not use a non-vaccinated control group. They compare DPT to MMR vaccines and make ‘adjustments’ for various factors. The ‘science’ seems to be designed to squelch all true understanding of the real risk of vaccines. Studies that have compared completely non vaccinated to vaccinated children show the non vaccinated to be significantly healthier. These studies have mostly been privately funded and are not recognized by government agencies who refuse to do their own study.

In the 20 minute video below Dr Shiva Ayyadurai provides a helpful informed explanation of the modern immune system and compares it to what was known about the immune system at the time of the development of vaccines. The truth is, doctors today are still operating under the old understanding and many will not associate auto-immune disorders like eczema to vaccines.

MIT PHD Explains the Reality of the Modern Immune System https://t.co/XHZhY17RXh— Dr. Shiva Ayyadurai, MIT PhD. Inventor of Email (@va_shiva) January 2, 2020

Easy Immune Boost

This is a recipe for a simple, economic, tasty way to combat nearly any type of illness in the initial stages. It is far more effective than a flu shot or most common over-the-counter medications. While pharmaceutical medications may reduce some symptoms, they generally do not assist and support the body towards wellness. Each ingredient in this Immune Boost has properties that support the body’s ability to mount a response to offending pathogens.

  • local raw organic honey (not for babies under 12 months), preferably produced by bees who do not have access to pesticide laden fields!
  • coconut oil (raw, organic)
  • powdered vitamin C either sodium ascorbate or ascorbate acid
  • cayenne pepper
  • turmeric powder
  • cinnamon
  • ginger powder

Mix equal parts of honey and coconut oil in a jar. You can either mix a Tablespoon of each, or 1/4 cup, or more. You might want to start with a smaller amount to try it!

Add all the other powdered ingredients in as large a quantity as you think you (or your child) will be able to tolerate. You can always start small, and add more. Usually you can put quite a large amount of vitamin C (remember you will only be giving a small amount of this mixture at a time) without it being too noticeable. Start with just a sprinkle of the spices. The honey and coconut oil are a great aid to masking the flavors of the vitamin C and spices.

Give a 1/4 – 1/2 teaspoon at a time. Give frequently until symptoms disappear!

What is it good for? Allergies, sore throat, cold sores (at the first sign), upset tummy, cold or flu, headaches, etc. Try to allow the mixture to sit in your mouth, under your tongue for as long as possible so it can be absorbed quickly sublingually.

Try it – you may be astounded!

Why? All of these spices have amazing properties of antibacterial, anti-inflammatory, and provide immune stimulation/activation. It really works. And it tastes great – even for children. Elderberry syrup is another great immune booster to have on hand, but can be a little more work to prepare from the dried berries, or expensive to purchase.

CBD Oil is another natural supplement that provides excellent immune boosting benefits. Make sure your CBD Oil is organic, tested for purity and potency, and safely extracted. I have found a great product and am happy to answer any questions you may have about it. You can learn more and order CBD at http://healingplant.org.

Author: Becky Hastings, wife, mother, grandmother, passionate follower of Jesus and truth. As a life & wellness coach, Becky seeks to inspire and motivate others to find increased energy, joy, and longevity. Navigating information to achieve long-term health goals in every area of life is a passion!

Choosing a Good CBD Oil

Now that you are convinced to try CBD Oil derived from hemp because it is legal, safe, and highly effective as a health supplement, how do you decide which product to choose?

Dr. Rachna Patel, a medical marijuana expert, states there are three key questions to help you choose a quality product.

  1. Is the manufacturer/supplier of the oil accountable to anyone?
  2. Is the product lab tested?
  3. What method was used to extract the CBD oil?

I’m confident to report that the company I have been repping passes these tests with flying colors.

  1. They are accountable to you, the customer, and to their thousands of affiliates. They are so confident of their product, that they offer a 30 money back guarantee.
  2. Every batch is 3rd party tested for potency and purity. You can find certificates verifying the CBD content on their website.
  3. The CBD oil is extracted from organically grown hemp in the USA using a CO2 extraction method that does not leave behind any harmful residue.

Additionally, the prices compare very favorably with other quality brands AND there are no ‘fillers’ or unwanted ingredients – only full spectrum CBD and hemp oil.

Please leave your name and email address below if you would like more information on this product, or refer back to the person who shared this blog with you.

Author: Becky Hastings, wife, mother, grandmother, passionate follower of Jesus and truth. As a life & wellness coach, Becky seeks to inspire and motivate others to find increased energy, joy, and longevity. Navigating information to achieve long-term health goals in every area of life is a passion!

Healing Plant

Most people have heard of medical cannabis. Most are aware of a recreational plant that is smoked, known by a variety of names: pot, weed, marijuana, cannabis, etc. Many have heard of CBD and perhaps CBD oil.

CBD is the abbreviated name for cannabidiol, an active cannabinoid found in cannabis. Cannabis is a plant that has been cultivated for both medicinal and industrial properties for thousands of years. Hemp is the word used for the cannabis plant which contains very low levels (< 0.3%) of THC (tetrahydrocannabinol) which can produce a psychoactive effect in the brain. Extensive research studies reveal the benefits of CBD, which has no psychoactive or harmful side effects. Hemp is legal to be grown and CBD oil is legal in all 50 states.

CBD oil has been found to reduce pain and inflammation, lower blood sugar levels, and protect the brain and nervous system from degeneration. These widespread benefits result because of the Endocannabinoid system in our bodies. In our body we have Cannabinoid type 1 receptors (CB1) concentrated in our central nervous system (CNS: brain, cranial nerves, and spinal cord). Supplementing with CBD oil can restore balance to many detailed chemical processes in the body.

Additionally, CBD successfully stimulates the release of 2-AG, an endocannabinoid that stimulates both CB1 and CB2 (Cannabinoid receptor type 2). These receptors play a key role in regulating mood, memory, appetite, sleep, and reduction of inflammation within the human body.

Watch this video which discusses the benefits of CBD oil.

Thus we see how CBD oil is able to bring so many different benefits to a wide range of people. Additionally, CBD oil is being studied for its ability to protect from cancerous cells and tumor formation. CBD may lower blood pressure, indirectly promote bone growth, and act as a natural antibacterial.

CBD oil is now legal in all 50 states, and many other countries in the world. It is safe. It is effective. It can be used by everyone from children to pregnant women. A detailed analysis and understanding of the cannabis plant and the Endocannabinoid system leads many to realise that this plant is uniquely designed as a primary ‘medicine’ for our body. CBD oil has also been found to bring benefits to many animals.

I am thrilled to have found a company that provides CBD oil from 100% organic, grown in USA, non GMO, hemp. This CBD oil is formulated with hemp seed oil, contains no other filler ingredients, and every batch is 3rd party tested for purity and potency. All this AND at an affordable price. If you have any symptoms at all, if you are currently using prescription medications and would like to reduce them, or if you would just like to protect your brain from degeneration due to natural ageing, this is a supplement for you. I will benefit in a small way from any purchase you may make, but, by far, the greatest benefit I receive is hearing the wonderful stories of pain relieved, medication reduced, and lives reclaimed because of this amazing product.

If you received this link from a friend, be sure to contact them so they can continue to share this incredible product and opportunity with you.

Author: Becky Hastings, wife, mother, grandmother, passionate follower of Jesus and truth. As a life & wellness coach, Becky seeks to inspire and motivate others to find increased energy, joy, and longevity. Navigating information to achieve long-term health goals in every area of life is a passion!

Speaking Truth to Power

I was privileged to be able to attend the ACIP (Advisory Committee for Immunisation Pratices) held in June 2018 at the CDC (Centre for Disease Control) in Atlanta, Georgia.This appointed committee is responsible for the recommended schedule of vaccines for children and adults in the USA and now includes 18 different vaccines given in about 62 doses during a child’s first 18 years of life. By 18 months of age this committee recommends a child receive 34 vaccines.[1]

As part of the agenda, time is allowed for Public Comment at the end of each day. The two day meeting is available to live stream. Someone kindly recorded my comments from the two sessions and put them together in a video.

I share with you, not because I think I did a great job or to get your congratulations. This is absolutely essential information that needs to be delivered to every parent making vaccine decisions. There are complex non-specific effects from vaccines. For the lay person, that means, there are unintended consequences. Yet, the ACIP, the CDC, the FDA, the NIH, the HHS, the IOM, the AAP, the AAFP, ACOG, and other esteemed institutions, which claim to promote and protect health, ARE ALL IGNORING powerful evidence of harm. This behaviour has been well entrenched. More and more solid research and evidence is being reported and should be raising serious concerns about the combination of vaccines given, the amount of aluminum in the schedule, the role of human fetal cell contamination, and the serious consequences of giving vaccines to premature babies, etc. Yet all these austere bodies continue to support this enormous toxic burden foisted upon the bodies of babies and children.

It truly must stop. It must be re-evaluated. Yet I felt as if the 14 members of ACIP barely listened to my comments. Will they continue to remain wilfully ignorant of the harm being inflicted on far too many children?  Their two day agenda included discussions of many more vaccines they want to introduce, including a 3rd MMR vaccine because they admit that the vaccine is NOT WORKING! Cutting back or analysing their current recommendations seems far from a priority.

New efforts to push vaccines are particularly disturbing, especially the one from the Americal College of Nurse-Midwives Resources on Immunizations pronouncing “Vaccines are SAFE for you and your baby, even during PREGNANCY!”, a blatant falsehood since vaccines have never been studied for safety during pregnancy and all ingredients are known to cross the placenta and the blood brain barrier of the vulnerable developing infant.

Please share. Please pray. Please protect your baby, and your neighbours’ baby.

Author: Becky Hastings, wife, mother, grandmother, passionate follower of Jesus and truth. As a breastfeeding counselor for over 23 years Becky is devoted to helping parents make wise decisions for the long-term health and wellbeing of their babies. As a member of a Vaccine Safety Education Coalition, Becky writes and speaks on the topic of vaccine safety.

 

[1] If you have never looked at the details of the CDC schedule, I highly recommend you review for yourself this 8 page document with many notes on each vaccine. Every time I review the contents, count the number of shots and doses, my chest grows tight.

Doctors Learn Vaccine Risk

Struggling to understand how good doctors can advise parents to follow dangerous medical practises? Dr Moss, highly qualified practising physician, and Professor teaching young doctors, has a unique understanding.

Another doctor explains his viewpoint of the direction of our country, especially the medical system and the desire for total control. His childhood experience of being forced to flee from Vietnam gives him insight into the direction of medical care and practice in this country.

Thank you to the Vaxxed Team for their tireless collection of real life stories of vaccine injury and awakening to the truth.

Dr Neides from Ohio was fired after writing a blog post in which he explains his adverse reaction to a flu vaccine and began asking questions about vaccine safety. The way he was treated by the medical establishment launched him into a detailed investigation of the history and safety of vaccines. In this segment of his talk, he makes 8 specific points regarding why he now questions vaccines.

Dr Neides warns us that Pharma is now racing to bring 140 new vaccines to the public. In many states there are campaigns to mandate vaccines for school attendance, as was passed by California in 2015. What are you doing to learn and share the truth?

What is your story?

Author: Becky Hastings, wife, mother, grandmother, passionate follower of Jesus and truth. As a breastfeeding counselor for over 23 years Becky is devoted to helping parents make wise decisions for the long-term health and wellbeing of their babies. As a member of a Vaccine Safety Education Coalition, Becky writes and speaks on the topic of vaccine safety.