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A new vaccine study published in Molecular and Genetic Medicine is bringing to the forefront the disturbing connection between the dramatic expansion in the quantity of routine childhood vaccines administered and a corresponding increase in inflammation-associated disorders.
Titled, "Review of Vaccine Induced Immune Overload and the Resulting Epidemics of Type 1 Diabetes and Metabolic Syndrome, Emphasis on Explaining the Recent Accelerations in the Risk of Prediabetes and other Immune Mediated Diseases," the study argues that vaccine-induced immune overload is a driving factor in a number of rapidly accelerating childhood epidemics including:
- Type 1 diabetes
- Food allergies
- Many autoimmune diseases
- Type 2 diabetes
- Non-alcoholic fatty liver disease (NAFL)
- Metabolic disease.
The paper sought to provide a theory of vaccine induced immune overload to explain many observations about the changes in the epidemics. The fundamental problem, according to the study, is that vaccinology assumes a 'one size fits all' approach that results in the majority of the vaccine recipients having overstimulated immune systems:
"One major problem with vaccines is the concept of one size fits all. Package inserts of almost all vaccines recommend a dose based on age. In order for a vaccine to be a commercial success it is expected to induce a protective immune response in well over 90% of children. In order for this to happen a dose, based on age, must stimulate a protective immune response in those with the weakest immune system. In the process of doing this, the other 90% or more of children have their immune system over stimulated. The process of over stimulating the immune system time and time again increases the risk of inflammatory diseases like autoimmune diseases, and allergies which cause even more inflammation."
The result of the over stimulated state of the body following vaccination varies, but depends entirely on bio-individuality, namely, the unique physiological response an individual has to inflammation. The inflammatory cascade has other adverse downstream effects:
"Inflammation causes the release of cytokines which can trigger autoimmune diseases but also stimulate cortisol production, the major negative feedback loop of the immune system. According to the theory inflammation induced cortisol production varies based on race  which can be explained by the presence of genes that alter cortisol production. Individuals who produce a lot of cortisol in response to inflammation have a tendency to develop a Cushingoid like response that includes obesity, type 2 diabetes/insulin resistance, hypertension, and dyslipidemia which is called metabolic syndrome."
As the dominant meme perpetuated by stakeholders in the vaccine agenda over the past 15 years has been 'the more vaccines the better,' today's vaccine schedule is loaded to the hilt with vaccines, each new addition increasing with mathematical certainty the chances of immune overload:
"Since 1999 the routine pediatric immunization schedule [9,10] increased by 80 vaccines. This number is derived by the fact that multivalent vaccines contain specific vaccines to each separate strain. The following have been added, pneumococcus (13 valent), meningococcus (4 valent), human papilloma virus (4 valent), hepatitis A (1 valent), rotatavirus (4 additional valent), influenza (3 valent per year x 18 years=54)."