DTaP, Td, TDaP

See also:



What’s Really in the DTaP Vaccine? – Levi Quackenboss (cited, biased, blog with links – for scientific information and studies skip this link and scroll down this page)

whooping cough in vaccinatedGreat breakdown of DTaP Vaccine as it pertains to:

  1. Brain Damage
  2. Autism
  3. Neuropathies

“According to the testimony of the Assistant Secretary of Health, Edward Grant, Jr., before a U.S. Senate Committee on May 3rd, 1985, every year, 35,000 children suffer neurological damage related to the DTP vaccine. An even more recent figure on the reaction to the DTP vaccine indicates that 1 in every 100 children react with convulsions or collapse or high-pitched screaming and that one out of every 3 of these, that is 1 out of every 300 will remain permanently damaged.”
Treatise on “Vaccinations”

Adverse event reports after tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis vaccines in pregnant women.
“The most frequent pregnancy-specific AE was spontaneous abortion in 22 (16.7%)reports.”

Despite awareness of recommendations, why do health care workers not immunize pregnant women? (2017)
“In this study, approximately 26% of participants do not recommend the tetanus, diphtheria, and acellular pertussis and influenza vaccines to their patients, although being aware of the health ministry recommendations.”

Optic neuritis in pregnancy after Tdap vaccination: Report of two cases. (2017)
“Two pregnant women developed one-eye blurring vision within three weeks after Tdap vaccination. Neurophtalmologic and MR examination confirmed an unilateral optic neuritis without evidence of underlying disease. Both patients had a full recovery, one after intravenous metilprednisolone. This is the first report of optic neuritis related with Tdap vaccination in pregnancy.

Origins of and solutions for neonatal medication-dispensing errors.
“In 2008, there were five cases in which look-alike or sound-alike neonatal medication-dispensing errors occurred at our institution. A mix-up between neonatal and adult or pediatric products occurred in four of the five cases. Three of the five errors resulted in near misses with the potential to cause harm. The other two errors reached the patients but did not cause harm. The medication mix-ups involved adult and neonatal phytonadione injectable emulsion, sodium citrate injection and vancomycin-heparin combination injection, adult tetanus-diphtheria-acellular pertussis and infant diphtheria-tetanus-acellular pertussis (DTaP) vaccines, Haemophilus B and DTaP vaccines, and cisatracurium and vecuronium.”

These studies show that DTaP does not prevent transmission but likely decreases symptoms in a number of individuals.

Neurological Complications of Pertussis Immunization

The difference between TdaP, and DTaP:
“DTaP is approved for children under age 7. Tdap, which has a reduced dose of the diphtheria and pertussis vaccines, is approved for adolescents starting at age 11 and adults ages 19 to 64. (source)”


Lowered Consciousness Side Effect of the Pertussis Vaccine Explained – Health Nut News

DPT Vaccine and Chronic Nervous System Dysfunction: A New Analysis

Pertussis toxin is required for pertussis vaccine encephalopathy

Delayed DTaP associated with reduced risk of childhood Asthma

Effects of diphtheria-tetanus-pertussis or tetanus vaccination on allergies and allergy-related respiratory symptoms among children and adolescents in the United States

Effects of diphtheria-tetanus-pertussis or tetanus vaccination on allergies and allergy-related respiratory symptoms among children and adolescents in the United States

This chart shows that wide-spread vaccination actually led to an increase of pertussis.whooping cough resurges after vaccination

DTP and Autism:

CDC Releases New Data on the Prevalence of Autism Spectrum Disorders: First and Largest Multi-site Study Provides Baseline for Future Comparisons.

Megson5 proposed that autism is linked to the disruption of the G-alpha protein, affecting retinoid receptors in the brain. A study of sixty autistic children suggested that autism could be caused by inserting a G-alpha protein defect, particularly the pertussis toxin found in the DPT vaccine, into genetically at-risk children. This toxin separates the G-alpha protein from retinoid receptors. Those most at risk report a family history of at least one parent with a pre-existing G-alpha protein defect, including night blindness, pseudohypoparathyroidism, or adenoma of the thyroid and/or pituitary gland.

Megson proposed that natural vitamin A could reconnect the retinoid receptors critical for vision, sensory perception, language processing and attention.

Megson proposed that treating autistic children with natural cis – forms of Vitamin A could have the effect of reconnecting the hippocampal retinoid receptor pathways, critical for vision, sensory perception, language processing and attention.

Megson noted that many autistic children needed natural, unsaturated cis forms of Vitamin A found in sources such as cold water fish (salmon, or cod liver), kidney, and milk fat, foods not commonly available in the modern diet. Instead, children depend on Vitamin A Palmitate, found in commercial infant formula and low fat milk. Unfortunately, absorption of Vitamin A Palmitate requires an intact gut mucosal microvilli surface at the right pH, in the presence of bile for metabolism. Since many autistic children already had damaged mucosal surfaces due to unrecognized wheat allergy or intolerances, their capacity to absorb vitamin A is questionable.

Megson also argued that live viral measles vaccine depleted children of their existing supply of Vitamin A, negatively impacting retinoid receptors. Natural Vitamin A, in the cis form, is important for activation of T and B cells for long-term immune memory. Measles, mumps and rubella titers are either significantly elevated or negative, in spite of one or two doses of the vaccine given to many of these children. Fish oils contain one retinoid metabolite, alpha 14 hydroxyretroretinol that has a role in T-cell activation, vision and growth of lymphoblasts.