This website provides readers an historical perspective on the evolution of various healthcare laws and regulations affecting healthcare freedom and privacy.
For updated information about healthcare freedom and privacy issues, visit Citizens' Council for Health Freedom's website www.healthcarefreedom.us
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Genetic Ownership Rights

Americans overwhelmingly support genetic privacy and control over their genetic information. A 2000 Gallup survey found that most adults (86%) believe a physician should ask permission first before running tests for genetic factors. . . (continue reading)

Related articles
Jun. 2008 Minn. Governor Protects Genetic-Privacy Rights; Vetoes “DNA Warehouse” Bill
May 2008 Federal Anti-Discrimination Bill Inadvertently Legalizes Sharing of Genetic Information Without Patient Consent
Apr. 2008 CCHC Urges President Bush to Veto Newborn Genetic Screening Bill (S. 1858); Says Bill Lacks Privacy, Property Rights and Informed Consent Safeguards
Apr. 2005 Should a Federal Committee Recommend Making Your Family’s Genetic History Available on the Internet?
Feb. 2005 Who’s Shaping Our Genetic Health Policies?
8/12/2002 Individuals Lose But Government and Corporations Gain Control over Personal Health & Genetic Information - Bush administration grants data-processing companies and other health care industries new federal regulatory authority to collect and share individuals' personal health information—including genetic information—without individuals' consent.
6/4/2001 Testimony Before the Pennsylvania Senate Communications and High Technology Committee - Simply because we have new technology that facilitates the exchange of medical information electronically does not mean that we should eliminate the important legal concept of informed consent.
4/3/2001 Who Owns Your Genetic Information? - Americans concerned about genetic privacy and ownership rights should carefully read consent forms when undergoing medical procedures and treatments.
1/4/2001 IHF Hosts Roundtable Discussion of Patients' Rights (Including Genetic Privacy) - The first principle of the Nuremberg Code is "The voluntary consent of the human subject is absolutely essential."
9/26/2000 Gallup Survey Finds Americans' Concern About Medical Privacy (Including Genetic Privacy) Runs Deep - Key findings include: 91 percent oppose a federal requirement to assign everyone a medical identification number.
Sept. 2000 Public Attitudes Toward Medical Privacy (Including Genetic Privacy) - This report is based on the results of a survey conducted by The Gallup Organization on behalf of the Institute for Health Freedom.
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