"An important point is the fear of liability (at the legal and moral level) which perpetrates attitudes and actions. The protective psychological mechanism that comes into action when one knows deeply other people have been harmed, because of their negligence, or because they have been hiding behind the presumed lack of science, because they have minimized, belittled the issues, this mechanism which hides behind denial, camouflage, or aggression needs to be uncovered. Consequences need to be brought to the conscious level, for healing to take place, and prevention to take its role.
This report's 244 page annotated bibliography on environmental effects on health includes articles about reactions affecting the central nervous system dating back to 1908. The report and bibliography were written by Bruce Small and Associates for Health and Welfare Canada in 1988.
The daily unnecessary killing of persons with sensitivities is, in duration, numbers affected, and extent of injury, one of the top five human rights abuses in Canadian history. It is the most ignored by civil health authorities, the most invisibilized by journalists, and the most betrayed by Canadians who are normally concerned about social justice and human rights. The Advocacy Gateway for Environmental Sensitivities was created to document the long mainstream history, and the contribution of various parties to the exclusion, injury and unnecessary killing of Canadians with sensitivities. The documents on the site were collected during more than thirty years of confronting abusers and enablers, lobbying, consumer leadership, case advocacy, civil disobedience, and human rights complaints. Scientific, clinical and consumer experience date back centuries. A 1985 Ontario Ministry of Health report identified an existing, publicly insured method of diagnosis. Various parties have misled the public about the availability of this diagnostic method for more than a quarter century, despite legal ramifications concerning consequent preventable harm. Between 1988 and 1993, CMHC, Health and Welfare Canada and the Chief Commissioner of the Canadian Human Rights Commission, along with several other federal departments and Ontario ministries, were working to reduce preventable harm being caused to persons with sensitivities, work that public servants and politicians are now invisibilizing. In contrast to their position in the early 1990's, the CHRC is now eclipsing the actual history of sensitivities behind a revisionist version provided by so-called “doctors of environmental medicine.” Canadians are being injured and killed daily as a result of human rights violations that health and human rights officials ignore. Protections that Health Canada had been encouraging were abandoned after the 1993 election. The response of abusers to being confronted about this negligence says a lot about governance in Canada. Mapping the prevalence of sensitivities against statistics on adverse drug events provided by Terence Young, MP, in his book, “Death by Prescription,” suggests that more than a dozen Canadians with sensitivities are being unnecessarily killed in health care daily. This is a significant portion of Canada's 55 daily adverse drug event deaths. Instead of protecting people in high risk groups, as they were ecouraging in the late 1980s, Health Canada is merely counting the dead. Agencies of remedy, journalists and civil society trivialize the issues, join in the bullying or turn a blind eye.
Children with undiagnosed sensitivities, along with other vulnerable people, are being injured and killed in health care. Canadian authorities and Canadian political parties invisibilize protective measures Health Canada was encouraging prior to 1993.
Agencies of remedy exploit peoples' terror, telling persons with diagnosed sensitivities that they will be shunned unless they they help cover up agency mistakes that are contributing to the ongoing killing of persons with undiagnosed sensitivities.
Researchers at the University of Toronto accepted money and pretended that things already known were not known. They accepted money to research things they knew or ought to have known were impossibly defined. They allow the damaging misinterpretation of their work by funders.