Stop ALL childhood vaccines?

I was thrilled to hear Dr Peter McCullough – a thoroughly mainstream cardiologist prior to the great covid reveal thrust upon the world beginning in 2020 – advise parents to forego all childhood vaccines.

This a a great step forward for medical professionals to be able to discuss the conflicts of interest long-held by regulatory bodies. The entire Covid event has overwhelmingly showed the world that there is a problem with vaccines, the regulatory bodies, and the companies that manufacture them. These facts have caused many extremely reputable doctors, like Dr Peter McCullough, to investigate the actual safety studies supporting the entire vaccine industry.

 It’s a wake up call.

“Growing international concerns about vaccine regulatory processes and vaccine safety have emerged following the widespread regulatory failure of Covid-19 vaccines. The Covid-19 crisis has demonstrated that regulatory bodies, once public watchdogs, are now at best incompetent and at worst have been deeply corrupted by pharmaceutical industry interests.”

You can read the well formulated statement by the World Council for Health here. You can watch the interview with Dr Peter McCullough and Dr Tess Lawrie here. Both doctors agree that ALL childhood vaccines should be halted. Dr McCullough is clearly NOT an ‘anti-vaxxer’ as he considers himself like a pin cushion – having received 69 vaccines in his life, including 40 flu vaccines! I don’t think he’ll be getting any more vaccines for himself.

https://worldcouncilforhealth.substack.com/p/health-revolutionary
https://worldcouncilforhealth.substack.com/p/a-common-sense-approach-to-childhood

Now many may say – ‘but who is the World Council of Health?’ You can expect that they will be attacked. But can anyone provide coherent arguments against their statement? All personal attacks are signals that there is no logical way to debate; no rationale to support their ideas, so they attack their opponents.

There have been many hundreds of doctors who have spoken out revealing the dangers of vaccines, but there is a huge tide overflowing to a greater number than ever before AND giving those who have researched the topic for many years ever greater validity.

A big win for truth. Let everyone you know with children, or soon to have children. You can bet this will not be on the news!

Becky Hastings collects information on health and tries her best to discover and share truth. By God’s grace, through Jesus Christ, I was saved, blessed with a husband of over 40 years, and five precious babies all grown up. I now get to delight as ten grandchildren grow! Together we can help each other discover a healthy path in this crazy upside down world.

DTaP and TDaP Nothing but Science

The link below should take you to a video produced by The Highwire where Del Bigtree creatively and passionately explains how the push for families to accept a TDaP vaccine in order to keep a new baby safe might NOT be giving the protection desired. From 14-25 minutes of this Hightwire episode, Del analysis a 2013 study of non human primates which compares the immunity of the old DTP vaccine, the DTaP vaccine and natural immunity. https://doi.org/10.1073/pnas.1314688110

https://thehighwire.com/ark-videos/big-pharma-propaganda-exposed/

Del’s passion and enthusiasm can be a bit over the top for some people. This is why I also collected several studies showing the impact of the DTaP/TDaP shot which explains why they do not give the hoped for protection of a new baby in a recent blog.

Becky Hastings collects information on health and tries her best to discover and share truth. By God’s grace, through Jesus Christ, I was saved, blessed with a husband of over 40 years, and five precious babies all grown up. I now get to delight as ten grandchildren grow! Together we can help each other discover a healthy path in this crazy upside down world.

Will getting a TDaP shot protect your baby?

Is my baby going to be at risk for developing whooping cough? Who will put my baby at risk?

The following information will help you navigate the pertussis/whooping cough shots. When assessing information that may contradict what you have been told by health professionals, keep an open mind. Seek the truth. Many times very well meaning people have been given false information and haven’t fully researched all the facts.

Did you know that the DTaP does not prevent colonization and transmission of Diphtheria and Pertussis? It only potentially reduces the symptoms in vaccinated individuals. A study done in 2000 concludes, “Vaccinated children may be asymptomatic reservoirs for infection.” http://wwwnc.cdc.gov/eid/article/6/5/00-0512_article

So the vaccinated can carry and spread the bacteria without feeling sick. That is part of the reason pertussis outbreaks are occurring in highly vaccinated populations. It also contradicts the idea that a healthy unvaccinated person is somehow more likely to spread the disease. The vaccine does not prevent against pertussis, it protects against the “whooping cough” symptom that comes along with pertussis. This may result in those who receive the vaccine being a “silent carrier” which is why pertussis is so prevalent. Grandma gets her TDaP shot and still gets pertussis but doesn’t have the number one sign of pertussis (the cough) and goes and smooches your baby – baby now has pertussis. Many scientific studies clearly acknowledge these facts.

In an article entitled, “The 112-Year Odyssey of Pertussis and Pertussis Vaccines-Mistakes Made and Implications for the Future” in the Journal of the Pediatric Infectious Diseases Society, the author acknowledges: that the vaccine being given is making people more susceptible to pertussis: “Because of linked-epitope suppression, all children who were primed by DTaP vaccines will be more susceptible to pertussis throughout their lifetimes, and there is no easy way to decrease this increased lifetime susceptibility.” Cherry JD. The 112-Year Odyssey of Pertussis and Pertussis Vaccines-Mistakes Made and Implications for the Future. J Pediatric Infect Dis Soc. 2019 Sep 25;8(4):334-341. doi: 10.1093/jpids/piz005. PMID: 30793754.https://www.ncbi.nlm.nih.gov/m/pubmed/30793754/

The ‘baboon study’ may be the most significant explanation of how the vaccine may mask symptoms and instead of reducing transmission – may actually increase transmission to the non vaccinated. Acellular pertussis vaccines protect against disease but fail to prevent infection and transmission in a nonhuman primate model, https://www.pnas.org/content/111/2/787

Del Bigtree from The Highwire provides a detailed passionate video illustration of the findings of the baboon study here from 14 minutes – 25 minutes.

Additionally, TDaP vaccine recipients are more likely to get other strains. https://wwwnc.cdc.gov/eid/article/15/8/08-1511_article

Those who have natural immunity after contracting the disease naturally are protected. https://pubmed.ncbi.nlm.nih.gov/15876927/

Is there longterm protection for children who receive all five doses of the DTaP vaccine? Waning Protection after Fifth Dose of Acellular Pertussis Vaccine in Children. Nicola P. Klein, Joan Bartlett, Ali Rowhani-Rahbar, et al. The New England Journal of Medicine, Massachusetts Medical Society, Sep 13, 2012. https://www.nejm.org/doi/full/10.1056/NEJMoa1200850

Whooping cough in school age children with persistent cough: prospective cohort study in primary care states “Conclusions For school age children presenting to primary care with a cough lasting two weeks or more, a diagnosis of whooping cough should be considered even if the child has been immunised. Making a secure diagnosis of whooping cough may prevent inappropriate investigations and treatment.” BMJ 2006; 333:174 https://www.bmj.com/content/333/7560/174

So what’s a parent to do? Insisting that everyone that will come into contact with baby must be vaccinated will not offer protection from whooping cough and may, indeed, increase the risk that baby will be infected with and get whooping cough.

I believe breastfeeding is the number one immune boost your baby needs for protection against all infection. Breastfeeding is simple, but not always easy. Prioritizing successful breastfeeding means getting information and support in advance to understand and overcome potential challenges. Avoiding all nipple substitutes in the first six to eight weeks will help prevent nipple confusion and rejection by baby of the breast. The best way to become comfortable with breastfeeding is to spend time with mothers who successfully and happily breastfed their babies.

Close contact (holding, kissing, etc.) with recently vaccinated individuals should be avoided, as they are potential silent carriers, but there is no need to panic and stress. Wearing your baby in a carrier when out in public is a great way to keep baby close and protect from unwanted contact.

If baby does develop a pertussis infection, early treatment with a high dose vitamin C protocol has been highly effective. As a parent who experienced whooping cough with four of my children when they were young, I can encourage you that children do survive whooping cough.

One serious reason to be wary of the DTaP and TDaP vaccines is the high level of aluminum they contain. A deep dive into the potential harm of injecting aluminum shows that there are many possible ramifications from auto-immune disorders to neurologic (brain) injury. Parents are not given true informed consent when they are not told of the possible adverse events of injecting aluminum. The biggest question to consider is, do I want to avoid a lifetime illness, possible neurological injury, or an infection of short duration that can be treated?

Becky Hastings collects information on health and tries her best to discover and share truth. By God’s grace, through Jesus Christ, I was saved, blessed with a husband of over 40 years, and five precious babies all grown up. I now get to delight as ten grandchildren grow! Together we can help each other discover a healthy path in this crazy upside down world.

36 by 15 months?

A picture of a baby edited with needles sticking into it, illustrating how many shots a baby receives.
Evee Clobes

The CDC schedule is clear. Add them up for yourself. They want every child to receive 36 doses targeting 15 different diseases by the age of 15 months — in the hope that these injections will prevent illness in your baby. But, will following this recommendation produce a healthy baby?

I can’t show the entire schedule at once because it is so large, but take a look at this segment!

Birth to 15 months vaccine schedule published by CDC

To inspect the entire schedule, as published by the CDC, go here.

Please note that the number, 36, is reached by

  • counting the DPaT and MMR as THREE because both of these shots contain 3 different concoctions added together.
  • does not include the number of injections recommended by the CDC for children in the hope of preventing influenza (aka flu). If you accept all of those (most parents do not) add three for a total of 39 by 15 months. After that, the recommendation is for an additional shot each and every year.
  • This chart only shows injections recommended up to the age of 15 months. There are plenty more the CDC recommends to get after that time. For the next portion of recommendations, go to this link and scroll down.
skeptical baby

Studying this schedule creates many questions in my mind. How did children survive before receiving such a barrage of shots? Prior to 1986 there were far less shots being promoted. See the following chart comparing shots given in s1962, 1983 and 2018.

Doses of Vaccines for US Children from Birth - 18 years

Another important question – and one that should be OBVIOUS: Has anyone ever studied in detail how this combination of shots will impact a baby? Has each shot added been tracked and followed in its entirety since it is given in combination with so many others? Searching for this information on-line has become challenging. Every search I tried brought me to yet another page by the CDC. The following diagram shows that the testing of every vaccine is based on the assumed safety of a vaccine that was older. Each vaccine added was not tested against a true placebo, but was tested against an older vaccine. When challenged by ICANdecide.org the CDC was unable to produce any safety trials showing that vaccines were tested by a true placebo. Additionally, CDC was unable to produce any evidence that the entire combination schedule of shots had been tested and proven to be safe.

Placebo Pyramid Scheme
‘Safety’ trials for all the vaccines added to the schedule built on supposed safety of previous shots

Another critically important question: Has the total amount of aluminum and other potential neurotoxins been considered in this bloated schedule? Aluminum is just one of the ingredients. There is no evidence of safety of aluminum in shots because it has never been tested for safety. Aluminum has been added to vaccines because it enhances the body’s response. It is called an adjuvant. From early days it that has been “GRAS” meaning, generally regarded as safe, despite no testing or evidence to support this categorization.

And finally, as a parent that is most concerned about a healthy happy baby who grows up to be a healthy teen and adult: Has there ever been a longterm thorough study of fully vaccinated, partially vaccinated and non vaccinated children in regards to total health outcomes? Does accepting the vaccine schedule by the CDC lead to a longer, healthier life? Since we live in a time with skyrocketing allergies, neurologic disabilities of many types, and other serious health issues in childhood, this is a vitally important question to consider. It would be very easy for the CDC to do such a study — if they truly wanted to know the results.

Here is an idea to consider. If I offer you a milkshake — in your favorite flavor — how many rat turds can I put into it before you will reject it? If I put in one rat turd, and you can easily remove it with a spoon, will you still drink the milkshake? What about a handful of rat turds, mixed around? At what point will you refuse the milkshake?

Delicious milkshake

The milkshake represents the CDCs credibility. Maybe they made a couple mistakes in the past. But how can they continue to recommend so many shots TO HEALTHY BABIES to this day? If any of their recommendations cannot stand — and the Hepatitis B shot for newborns is a great example – can I trust ANY of their recommendations?

You decide. Your baby’s health is in your hands. The most important part of your baby to protect is their brain.

Becky Hastings collects information on health and tries her best to discover and share truth. By God’s grace, through Jesus Christ, I was saved, blessed with a husband of over 40 years, and five precious babies all grown up. I now get to delight as ten grandchildren grow! Together we can help each other discover a healthy path in this crazy upside down world.

Buyer Beware

Have I been impacted by LIES?

If car seats had warnings about causing my child encephalitis, anaphylactic shock, SIDS, febrile seizures, chronic illness, lifelong neurological impairment, etc., I wouldn’t use them.

If my doctor told me to use the same car seat for newborns, toddlers, older children and adults, regardless of size or medical status, I would remember we don’t treat other products or medications as one-size-fits-all and I wouldn’t try to put an infant into a seat too large for an adult.

If my doctor said the exact compilation of harnesses, the direction the car seat is facing, and the type of car it fits into, all make the car seat not only safe and effective but necessary to prevent death, and then I found out they’ve NEVER studied the multiple factors together, AND that the car seat manufacturers had no liability WHATSOEVER for their products, I would question the knowledge and loyalties of my doctor and not follow the recommendation.

If I asked for more information on the car seat and my doctor gave me two pages that said the car seat works great, but failed to give me the full data sheets that showed the car seats were actually quite dangerous, haven’t been studied in babies, and have contraindications in many of the groups doctors use them in, I would at the very least find a new doctor.

If I knew the U.S. Supreme Court clearly declared car seats ‘unavoidably unsafe’ I would wonder why they aren’t making car seat manufacturers accountable for injuries and death, and I certainly wouldn’t make usage mandatory.

If I knew car seat manufacturer whistleblowers had come forward to expose data manipulation that implicated the manufacturers and the government agencies that recommended them, I wouldn’t use them and I’d call for a federal investigation rather than allowing the complicit parties to ‘investigate’ themselves.

If car seat ads accounted for 85% of mainstream media ad revenue, I would understand that they can’t be impartial with their reporting, I wouldn’t blindly trust their recommendations, and I would question all information supplied by mainstream media.

If car seat manufacturers continually paid out billions in civil and criminal fines for manipulating safety data, injuring and killing people with their products, yet the products were not recalled, I wouldn’t use them.

If car seat manufacturers used aborted babies in their manufacturing process, I wouldn’t use them.

If car seats caused the accidents they were meant to protect against, I wouldn’t use them.

If my child had a worsening reaction and decline in health every time I put them in a car seat, I wouldn’t use them.

If my doctor got paid an additional $400 every time I used a car seat, couldn’t tell me anything specific about the car seat, and saw these negative reactions following car seat exposure, but said it was ‘just a coincidence’, I wouldn’t use them and I’d get a new doctor.

If the available car seats used ingredients and schedules that were​ banned in other safer/healthier countries, I wouldn’t use them.

If I knew that after using a car seat my child might seem fine at first, but that car seats may cause infertility, cancer, mutagenesis, neurological damage and autoimmune diseases, I wouldn’t use them.

If people who didn’t use car seats were consistently healthier, I would at least do my own research.

If we weren’t allowed to do actual thorough standard scientific tests for car seat safety or ask ANY questions about them, if all dissenting views on car seats are censored — even personal accounts from parents who are direct eye-witnesses to the car seat damage — but the public is still urged, coerced and/or forced to use them, I would think maybe I should do some digging for myself instead of blindly accepting the research of the companies profiting from products known to injure or kill and for which they face no liability at all.

You can bundle the healthiest ingredients with the best of intentions, wrap them in poison and they’re still just poison. When you make an extremely profitable product liability-free, the result is that there is no incentive to make sure the product is safe or effective.

Don’t exchange liberty for a fallacious sense of security, especially at the expense of our children.

Based on writing attributed to Kristi Miller

Becky Hastings collects information on health and tries her best to discover and share truth. By God’s grace, through Jesus Christ, I was saved, blessed with a husband of over 40 years, and five precious babies all grown up. I now get to delight as ten grandchildren grow! Together we can help each other discover a healthy path in this crazy upside down world.

Vaccine Ingredients

You’ve been told – probably many times – that vaccines are safe. So, what exactly is in that syringe being injected into the body of someone you love? Do you know? Does your doctor know? The following is a list directly from the CDC of the ingredients in all vaccines. The color coding will help you determine which vaccines contain human cell derivatives such as aborted fetal cell debris (including male and female DNA fragments), animal proteins, possible allergy irritants, and antibiotics.

Orange: Animal-derived 💗 Pink: Derived from humans cells 💛 Yellow: Toxic to humans 💚 Green: Allergy irritant 💙 Blue: Antibiotic

I always urge parents to double check all information – regardless of the source. Don’t believe me, but be sure to spend more time researching vaccines than you do any other item you may purchase for your baby – such as a car seat. Your baby’s health is too valuable to take any chances. Too many parents have learned the hard way that the risk of vaccines is actually quite high.

If you do decide your baby needs a vaccine, please research whether a Hepatitis B vaccine on the first day of life is a necessity for YOUR baby. Is YOUR baby truly at risk for Hepatitis B – an infection primarily shared through sexual promiscuity and the sharing of needles?

Before giving any vaccine at any time, take 3 minutes to read through these steps you can take prior to getting vaccines to help protect your baby. One of the biggest things you can do is to be aware that giving Tylenol (acetaminophen) in conjunction with vaccines greatly increases the risk of a vaccine reaction.

I have no vested interests in this topic. I write to educate and share information to empower parents to make wise choices for the life-long health and wellbeing of their family. Vaccine makers are 100% liability free. If their products cause any harm for any reason you cannot sue them or make any claim against them. Pause. Think about that.

Compiled by Becky Hastings, wife, mother, grandmother, health seeker and reporter. Seeking truth can be challenging, and sometimes confusing, but far more rewarding than staying ignorant!


Babies Get Injections

These two graphics are published on a CDC website illustrating where to inject multiple vaccines to a baby at one visit.

A screen shot from Merck shows conflicting information:

The conflicts:

Point one says don’t use with other live virus vaccines, but give MMR one month before or after live viral vaccines. Varicella is a live virus vaccine. Point two contradicts point one: “MMR II has been administered concurrently with VARIVAX”… using separate injection sites and syringes – but no mention is made of safety tracking. Point four says the ACIP declares that simultaneous administration causes “no interference”. No mention is made of any study of the safety of giving all these vaccines at one time.

I did find an encouraging document linked on the same CDC link that addresses procedures to follow if there is a vaccine adverse reaction.

“These reactions can vary from trivial and inconvenient (e.g., soreness, itching) to severe and life threatening (e.g., anaphylaxis). Vaccine providers should be familiar with identifying immediate-type allergic reactions, including anaphylaxis, and competent in treating these events at the time of vaccine administration. Providers should also have a plan in place to contact emergency medical services immediately in the event of a severe acute vaccine reaction.

Parents, please research vaccines more than you research any other item or decision you make for your baby. All vaccine manufacturers have been given a liability free product. When their vaccine is added to CDC’s ACIP recommended shots for all babies and children, there is a LOT of money involved. If your baby/child experiences any vaccine reaction or death, you will bear the responsibility on your own. There is a cumbersome process to receive compensation through VICP which has paid $4 billion since 1988 to those injured or killed by vaccines. This represents a small fraction of the true harm vaccines have caused.

At the very least ask your vaccine provider if they have an emergency plan in place in the event of severe acute vaccine reaction. If they don’t have one, chances are, they lack information on administering vaccines and recognizing adverse reactions. If you do decide to give vaccines, please read this piece which has many helpful tips for reducing any potential reaction.

Becky Hastings, wife, mother, grandmother, avid reader, health promoter, and seeker of truth through Jesus Christ. Navigating health information can be confusing. Becky writes and speaks to educate parents on the anomalies and contradictions in many aspects of modern medical recommendations.

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

Does TDaP protect Newborns?

It is an incredible shame that doctors are urging parents to do the exact opposite of what will protect their precious newborn from pertussis exposure.

Since the parents and the doctor are primarily interested in protecting their newborn baby from exposure to pertussis, according to the science, allowing anyone contact with the baby who has been recently vaccinated with TDaP is contraindicated. That is the science. Here are 2 studies every doctor should respect AND READ, because they are published in well respected journals.

Regarding Bordetella pertussis, Stanley Plotkin wrote: “we are far from a full understanding of the organism, the disease, the correlates of protection…immunity after vaccination is more or less transient. Therefore, it is not surprising that control of pertussis is relatively poor…The result is the continued circulation of the bacterium in family contacts, regardless of their vaccination history, resulting in exposure of vulnerable newborns.”

Plotkin, Stanley A. “The Importance of Persistence.” Advances in Pediatrics., U.S. National Library of Medicine, 1 Dec. 2016, www.ncbi.nlm.nih.gov/pmc/articles/PMC5106615/.

Even more importantly, the following study, funded by the FDA presents facts in direct opposition to the recent advertisements seen on television by GSK.

The title of this paper makes the conclusion abundantly clear: “Acellular pertussis vaccines protect against disease but fail to prevent infection and transmission on a human primate model.”

Warfel, Jason M., et al. “Acellular Pertussis Vaccines Protect against Disease but Fail to Prevent Infection and Transmission in a Nonhuman Primate Model.” PNAS, National Academy of Sciences, 14 Jan. 2014, www.pnas.org/content/111/2/787.

For those of us who are not experienced in analysis the details of scientific papers, Del Bigtree from ICAN, Informed Choice Action Network, has long experience as a medical journalist. This 4 minute video explains the details found by Dr Jason Warfel and his team in their study of pertussis transmission in animal primates. [Edited 2020: the original video in which Del describes the baboon study and it’s important has been removed by YouTube along with the entire Highwire channel. I found a clip (below) from another episode where Del Bigtree explains clearly how the pertussis vaccine does not stop transmission and could be the culprit in spreading whooping cough to the vulnerable. The abstract of Dr Warfel’s study here.]

For more information on vaccines, I have prepared a “Table of Contents” page for new parents, or anyone interested in vaccine safety, and protecting their precious baby from infectious illness.

Every parent wants to protect their precious child from any potential harm. Most grandparents are thrilled with the idea of seeing their new grandchild. In this world of vast information, it can be challenging to navigate to the truth.

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.