Dr. W. John Martin
MD, PhD
Certifications/Credibility
PhD. Medical Director, Institute of Progressive Medicine, a component of MI Hope Inc., a non-profit public charity based in South Pasadena CA.
Research on viruses, which normally fail to evoke inflammation because of an immune evasion mechanism called stealth adaptation. Characterization of the alternative cellular energy (ACE) pathway as a non-immunological anti-virus defense mechanism, as well as a source of cellular energy different from that obtained from the metabolism of food. Investigation on a natural force termed KELEA, an abbreviation for Kinetic Energy Limiting Electrostatic Attraction. Studies on the therapeutic uses of KELEA activated water.
"Perspective" on Health
Key Resource: Biological understanding of the role of viruses in mental illnesses, neurodegenerative diseases, chronic fatigue syndrome, autism. Therapeutic uses of KELEA activated water.
Videos
Renegade Sequences in Stealth Adapted Viruses: Introduction to Dr. Martin's Research Program
This video provides a scientific foundation to the research leading to the detection of stealth adapted viruses. These viruses are not effectively recognized by the cellular immune system. They can also transmit genetically unstable cellular and bacterial genetic sequences. Emphasis is given to the use of low stringency polymerase chain reaction (PCR) to detect stealth adapted viruses iin patient’s blood samples and in brain biopsies. Subsequent videos will discuss the published molecular data relating to these viruses.
Renegade Cellular Sequences in African Green Monkey & Rhesus Monkey Derived Stealth Adapted Viruses
This is a continuing video on the research leading to the detection and characterization of stealth adapted viruses. These viruses can acquire and transmit potentially pathogenic, genetically unstable cellular sequences from monkeys to humans and also between humans. Stealth adapted viruses are proposed as the primary cause of many major neurological and psychiatic illnesses. Monkey derived steralth adapted viruses are a consequence of producing polio vaccines in kidney cells obtained from cytomegalovirus infected rhesus and African green monkeys.
Stealth Adapted Viruses: 2019 Presentation to Interagency Autism Coordinating Committee (IACC)
Information on Stealth Adapted Viruses presented by Dr. W. John Martin, MD, PhD. to the Interagency Autism Coordinating Committee (IACC) in April 2019. The video underscores the need to quickly re-establish a laboratory to culture and to further characterize stealth adapted viruses. Some of these viruses arose from the cytomegaloviruses ihat nfected monkeys used to produce polio vaccines.
African Green Monkey Simian Cytomegalovirus Origin of Stealth Adapted Virus Infecting a CFS Patient
This video describes the initial DNA sequencing data, which unequivocally determined that the stealth adapted virus cultured from a patient with the chronic fatigue syndrome (CFS) had originated from an African green monkey simian cytomegalovirus (SCMV). Portions of the virus genome were amplified using the polymerase chain reaction (PCR). They werre used as molecular probes and were also cloned into plasmids. The cloned DNA was genetically sequenced.
Bacterial Genetic Sequences in the Monkey-Derived Stealth Adapted Virus Cultured From a CFS Patient
This video describes the identification of bacteria-derived genetic sequences in the stealth adapted virus isolated from a patient with the chronic fatigue syndrome (CFS). The predominant source of the bacterial sequences are from the Brucella-Ochrobactrum genus of alpha-proteobacteria, and more specifically from the Ochrobactrum quorumnocens species.
Training & Qualifications of Dr W John Martin in Support of Research on Stealth Adapted Viruses
This video is about the research career of Dr. W. John Martin. it is presented in support of the research on stealth adapted viruses, alternative cellular energy (ACE) & KELEA activated water. Public Health authorities have essentially ignored the research on stealth adapted viruses. This is partly due to the originality of the research, but also because of political reluctance to acknowledge shortcomings in safety concerns with the polio vaccines.
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