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Our Research2021-01-13T01:00:49+00:00

It is well understood scientifically that primitive human DNA fragments when injected into a person could 1) activate the immune system and potentially trigger and autoimmune reaction in genetically susceptible people and 2) insert into the genome of blood forming stem cells causing mutations. As the DNA in the genes govern the function of the cells, such DNA insertions can seriously disrupt the function of the mutated cell. Sound Choice Pharmaceutical Institute (SCPI) researches the potential health risks of the residual human DNA found in some vaccines and other products.

Scientists have now hypothesized some cancers and other childhood neurological disorders such as Autism Spectrum Disorder (ASD) may be caused by mutations in the child’s DNA.  This conclusion is based upon finding numerous mutations in the brains and/or blood of such children which cannot be found in their parents. Some mutations occur at or soon after conception and are called de novo. Others are acquired mutations that occur after birth due to environmental factors or exposures and are called somatic mutations. One such event could be exposure to residual human DNA from childhood vaccines. SCPI researchers have extensively reviewed the potential health risks posed by this residual human DNA.

Based upon those findings, SCPI does ongoing research and seeks to raise awareness of the potential health risks of manufacturing medical products on human cell lines.

Sound Choice Published Papers

Insertional Mutagenesis and Autoimmunity Induced Disease Caused by Human Fetal and Retroviral Residual Toxins in Vaccines

This published paper aims to inform vaccine manufacturing and cell substrate residual contaminant levels, insertional mutagenesis and autoimmunity and the relationship these pathological processes to current childhood disease epidemics including autistic disorder, leukemia, lymphoma, intellectual disability, schizophrenia and bipolar disorder.

Sociological Environmental Causes are Insufficient to Explain Autism Changepoints of Incidence

This study confirms the 1988 changepoint detected by EPA and adds 1981 and 1996 as additional changepoints. AD birthyear changepoints, particularly 1981 and 1996, cannot be explained by predicted birthyear changepoints based on altered thimerosal content in vaccines nor on revised editions of the DSM. Based on changepoint anaylses, environmental factors introduced universally to children in the US according to the schedule in the table below should be investigated. A prime environmental suspect is the introduction of human DNA contaminants in vaccines introduced to the US in 1979-1983, 1989 and 1995.

Impact of environmental factors on the prevalence of autistic disorder after 1979 (Journal of Public Health and Epidemiology)

The aim of this study was to investigate a previously overlooked, universally introduced environmental factor, fetal and retroviral contaminants in childhood vaccines, absent prior to change points in autistic order prevalence with subsequent dose-effect evidence and known pathologic mechanism of action.

Sound Choice Research

Sound Choice is dedicated to researching the dangers of using aborted fetal material in biologics and seeks alternative treatments and products which are ethically acceptable.

Insertional Mutagenesis and Autoimmunity Induced Disease Caused by Human Fetal and Retroviral Residual Toxins in Vaccines

This published paper aims to inform vaccine manufacturing and cell substrate residual contaminant levels, insertional mutagenesis and autoimmunity and the relationship these pathological processes to current childhood disease epidemics including autistic disorder, leukemia, lymphoma, intellectual disability, schizophrenia and bipolar disorder.

Sociological Environmental Causes are Insufficient to Explain Autism Changepoints of Incidence

This study confirms the 1988 changepoint detected by EPA and adds 1981 and 1996 as additional changepoints. AD birthyear changepoints, particularly 1981 and 1996, cannot be explained by predicted birthyear changepoints based on altered thimerosal content in vaccines nor on revised editions of the DSM. Based on changepoint anaylses, environmental factors introduced universally to children in the US according to the schedule in the table below should be investigated. A prime environmental suspect is the introduction of human DNA contaminants in vaccines introduced to the US in 1979-1983, 1989 and 1995.

Spontaneous Integration of Human DNA Fragments into Host Genome

Not only damaged human cells, but also healthy human cells can take up foreign DNA spontaneously. Foreign human DNA taken up by human cells will be transported into nuclei and be integrated into host genome, which will cause phenotype change. Hence, residual human fetal DNA fragments in vaccine can be one of causes of autism spectrum disorder in children through vaccination. Vaccine must be safe without any human DNA contaminations or reactivated viruses, and must be produced in ethically approved manufacturing processes.

Applying Atomistic Modeling to Predict NLGN3 Isoform Binding to Neurexin 1- Beta

Autism spectrum disorders have been associated with over 300 genetic mutations. As a polygenic disease, ASDs require at least one additional insult in addition to the underlying genetic susceptibility in order for manifestation of the disease phenotype (Caldwell, 2010). This work was funded by the M.J. Murdock Charitable Trust and private donations.

Impact of environmental factors on the prevalence of autistic disorder after 1979 (Journal of Public Health and Epidemiology)

The aim of this study was to investigate a previously overlooked, universally introduced environmental factor, fetal and retroviral contaminants in childhood vaccines, absent prior to change points in autistic order prevalence with subsequent dose-effect evidence and known pathologic mechanism of action.

Open Letter to Legislators

Other Supporting Publications

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