This is historical material “frozen in time”. The website is no longer updated and links to external websites and some internal pages may not work.

overrule the FDA's decision to bar 23andMe from selling their potentially life-saving diagnostic kits.

Created by R.S. on November 25, 2013

We, the healthcare consumers of America, demand that we maintain access to genomics testing services like 23andMe's, which serve as a 100% privately purchased complement to government-regulated healthcare.

The FDA grossly overstates the risks associated with 23andMe's assessments. Statements such as those suggesting that dangers like false positives may "lead a patient to undergo prophylactic surgery, chemoprevention, intensive screening, or other morbidity-inducing actions” are outrageous and patently false.

Risks associated with services like 23andMe's are understood by private consumers, while the benefits of these services (such as early diagnoses for chronic diseases) are significant. The price of over-regulation is lengthy delays in potentially life-saving medical innovations.

Health Care
Government & Regulatory Reform
Technology & Innovation
Return to top