Abstract

Stealth adapted viruses elude recognition by the cellular immune system due to the loss or mutation of genes coding the relatively few components typically targeted by the cellular immune system. Political barriers to accepting the existence of these viruses arose when it became apparent that some of the viruses had originated from the cytomegaloviruses that commonly infected monkeys used to produce poliovirus vaccines. Many virologists are seemingly unaware of the restricted targeting of viral components by the cellular immune system or that genetically defective viruses can continue to replicate and cause cellular damage. Immunologists may also be somewhat reluctant to acknowledge possible nonimmunological virus defense mechanisms. There are growing concerns regarding the increasing incidence of major chronic illnesses. Patient support groups are continually advocating for more research on the cause of specific disease entities. There is also a growing sense that special interests may have unintentionally imposed toxic exposures on the public leading to chronic illnesses. Relief from such exposures is being demanded by various Health Freedom movements. This article is intended to better inform the Health Freedom movements and various chronic illness support groups about the existence of stealth adapted viruses. A broader understanding of these viruses and their incorporated renegade cellular and microbial sequences will facilitate therapeutic endeavors, especially those based on the Alternative Cellular Energy (ACE) pathway.

Keywords

Alternative cellular energy (ACE) pathway, chronic fatigue syndrome, chronic Lyme disease, autism, PANDAS, amyotrophic lateral sclerosis, Gulf War syndrome, Health Freedom, SCMV, vaccine safety, polio vaccine, Mycoplasma fermentans, Ochrobactrum, Porphyromonas gingivalis, SV-40, FDA, GenBank, public health