Robert Kennedy Jr exposes the 1989 chronic disease surge
#1
Why was there an abrupt surge of chronic disease after 1989 among children? ADHD, diabetes, autism, etc



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#2
It’s Time to Pay Real Attention to Children’s Health
By Robert F. Kennedy, Jr.

Every year, the President of the United States issues a proclamation in honor of Child Health Day (the first Monday of October), which in turn launches Children’s Health Month. President Calvin Coolidge was the first president to dedicate a special day to children’s health, in 1928, recognizing that “the conservation and promotion of child health places upon us a grave responsibility.” The U.S. is not living up to that vital responsibility and, in fact, is failing children miserably. American children’s ability to develop and thrive is being sabotaged by an avalanche of chronic ailments, with pediatric rates of some chronic conditions among the highest in the world.




OCTOBER 05, 2017
It’s Time to Pay Real Attention to Children’s Health
By Robert F. Kennedy, Jr.

Every year, the President of the United States issues a proclamation in honor of Child Health Day (the first Monday of October), which in turn launches Children’s Health Month. President Calvin Coolidge was the first president to dedicate a special day to children’s health, in 1928, recognizing that “the conservation and promotion of child health places upon us a grave responsibility.” The U.S. is not living up to that vital responsibility and, in fact, is failing children miserably. American children’s ability to develop and thrive is being sabotaged by an avalanche of chronic ailments, with pediatric rates of some chronic conditions among the highest in the world.

Announcing the Campaign to Restore Child Health:




An abysmal children’s health report card

Nationally representative studies show that the chronic disease burden shouldered by children in the U.S. is not only heavy but has increased steadily over the past three decades. One of these studies, published in 2010 in JAMA, used national longitudinal survey data to examine the prevalence of four types of chronic conditions (obesity, asthma, behavior/learning problems and “other” physical conditions) in American children and youth from 1988 to 2006. The researchers found that prevalence of these conditions doubled—from 12.8% to 26.6%—over the 18-year-period.

The results of a second national study were even worse. Over two-fifths (43%) of children participating in the 2007 National Survey of Children’s Health had at least one of 20 chronic health conditions (see list of conditions in Table 1), and when the researchers added overweight/obesity and moderate or high risk for developmental/behavioral problems to their analysis, over half of all children (54%) suffered from at least one chronic condition.

Vaccination and chronic illness

American children also are the most highly vaccinated in the world. Since 1990, when the U.S. began substantially expanding its vaccine schedule, the number of vaccines required for school entry has increased by approximately 260%. There also has been a growing push to recommend certain vaccines (especially influenza and the Tdap vaccine for tetanus-diphtheria-acellular pertussis) to mothers-to-be, even though the package inserts for these vaccines openly state that “safety and effectiveness have not been established in pregnant women.” Currently, children receive repeated shots for 16 distinct illnesses (antigens). Counting vaccines administered during pregnancy, this adds up to as many as 73 total doses of the 16 antigens by the time children are 18 years old (Table 2).
I, being poor, have only my dreams;
I will do my utmost to keep them alive.
Against tyrants and adversity, I will strive.
Together, a better future, we will realise......
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#3
Toxic pathways to chronic illness

Increasingly, experts are studying how epigenetic factors contribute to the development of serious chronic diseases and disorders in children. Epigenetics looks at “de novo” genetic changes that “spontaneously arise within the child and are not present in the parents’ genes.” These changes control which genes switch on and off (gene expression). Many studies have described how environmental toxins prompt epigenetic changes that lead to developmental abnormalities and diseases. As the National Institutes of Health concedes, these environmental toxins include chemicals and medications.

According to the CDC, vaccines contain an astounding variety of ingredients, including preservatives and antibiotics to prevent contamination, adjuvants to stimulate a stronger immune response, stabilizers to enable transportation and storage, cell culture materials to grow antigens and inactivating ingredients to kill viruses or inactivate toxins. It is disingenuous to deny that these vaccine ingredients—both “chemicals” and “medications”—carry a sizeable toxic load straight into children’s bodies. Vaccine-friendly celebrity doctor Robert Sears acknowledges that parents are right to worry about the developmental impact of the “chemicals and metals and artificial things” harbored in vaccines. To name just four ingredients:

The neurotoxic ethylmercury-based preservative thimerosal is present in seasonal influenza and Tdap vaccines and can lead to accumulation of inorganic mercury in the brain in vaccine-relevant concentrations.
Aluminum adjuvants contribute to chronic neuropathology via multiple mechanisms, including through direct and indirect reductions in mitochondrial performance and integrity.
Formaldehyde, used as an inactivating agent, is both neurotoxic and a known carcinogen.
As an excitotoxin, monosodium glutamate (MSG) overstimulates nerve cells; neonatal exposure to MSG can produce “a significant pathophysiological impact on adulthood,” including increased permeability of the blood-brain barrier.
The ingredients of the Pediarix (DTaP-HepB-IPV) vaccine further illustrate the toxic soup injected into infants. They include formaldehyde; three different types of aluminum adjuvants; bovine, calf and monkey products; the inflammatory emulsifier polysorbate 80; and two different antibiotics. The complete list is as follows: “Fenton medium containing a bovine extract, modified Latham medium derived from bovine casein, formaldehyde, modified Stainer-Scholte liquid medium, VERO cells, a continuous line of monkey kidney cells, calf serum and lactalbumin hydrolysate, aluminum hydroxide, aluminum phosphate, aluminum salts, sodium chloride, polysorbate 80 (Tween 80), neomycin sulfate, polymyxin B, yeast protein.”

Neurodevelopmental experts have described a number of biologically plausible mechanisms whereby the heavy metals in vaccines may trigger neurodegenerative processes by prompting chronic microglial activation and excessive immune stimulation; interacting with autoantibodies (which are associated with higher blood mercury levels); impairing detoxification pathways; and causing mitochondrial dysfunction. Both thimerosal and aluminum harm astrocytes, which play an important role in higher neural processing.

Questions that need to be answered

The parallel timing of the increased vaccination schedule in the U.S. and the chronic disease epidemic in children cannot be dismissed as a coincidence. Moreover, there are many additional vaccine-related questions that urgently demand answers. For example, what are the synergistic effects of multiple toxins such as thimerosal and aluminum, and what happens when these toxins build up over time? What is the association between the timing and spacing of vaccination and subsequent health outcomes? Is there a down side to tinkering with the innate immune system so early in life? On this latter point, Dr. Suzanne Humphries comments that aluminum adjuvants “create a red-alert situation forcing the infant’s innate immune system to respond in the opposite manner to the way it should function in the first year of life.”

Finally, it is important to remember that vaccines have been associated not only with morbidity but also with mortality. Infants in the U.S. receive more vaccines in their first year of life than anywhere else in the world, yet the U.S. infant mortality rate is much higher than in other high-income countries. A group of researchers examined reports to the U.S. Vaccine Adverse Event Reporting System (VAERS) following Haemophilus influenzae type b (Hib) vaccination (1990–2013) and found reports of 896 deaths (median age=6 months); 749 records cited a cause of death, and 51% of these (n=384) listed the death as sudden infant death syndrome (SIDS). Although the vague SIDS moniker often has made it difficult to definitively pinpoint a causal role for vaccines, in July 2017, the U.S. Court of Federal Claims handed down a decision ruling that the parent-petitioners put forth “preponderant evidence” that vaccines “actually caused or substantially contributed” to their son’s SIDS death. Corroborating a vaccine-mortality association, a study in the African country of Guinea-Bissau found that infant mortality in children who received the diphtheria-tetanus-pertussis and polio vaccines was roughly double (10%-11%) the infant mortality observed in the no-vaccination group (4%-5%).
I, being poor, have only my dreams;
I will do my utmost to keep them alive.
Against tyrants and adversity, I will strive.
Together, a better future, we will realise......
Quote
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