|
|
President Bush Signs Genetic Information
Nondiscrimination Act of 2008
Wed., May 21 2008 — The President has signed into law the
Genetic Information Nondiscrimination Act (GINA) that will protect
Americans against discrimination based on their genetic information
when it comes to health insurance and employment. The bill had passed
the Senate unanimously and the House by a vote of 414 to 1. The
long-awaited measure, which has been debated in Congress for 13
years, will pave the way for people to take full advantage of the
promise of personalized medicine without fear of discrimination.
The US Senate passed earlier versions of the bill twice before,
but they were blocked from coming up for floor votes in the House
of Representatives. This year, the House passed it by a bipartisan
landslide, but Sen. Tom Coburn (R-Oklahama) had single-handedly
stalling legislation in the Senate, saying it could place too much
strain on businesses. "We're not really clear on what Coburn
wants, because his excuses don't make sense," said the bill's
original sponsor, Rep. Louise Slaughter (D-New York). "But
if this bill got to a floor vote in the Senate, I think it'd pass
almost unanimously."
A Congressional Research Service report notes that
"S. 358 and H.R. 493 are supported by consumer groups, the
medical profession, researchers, the medical products industry (including
pharmaceutical companies), and President Bush, and are opposed primarily
by the U.S. Chamber of Commerce. Since the first bills were introduced
in the 103rd Congress, many of the arguments and positions supporting
and opposing genetic nondiscrimination legislation have remained
largely unchanged. Supporters of nondiscrimination legislation feel
that current laws are not sufficient to protect individuals from
discrimination in health insurance or employment. Supporters of
the legislation further contend that without protection, individuals
are hesitant to seek potentially beneficial genetic services or
participate in much needed clinical research. Opponents believe
that current law provides sufficient protection. They are primarily
concerned that new legislation will provide further incentives and
additional opportunities for litigation against employers."
Retail Genomics is certainly
no fan of frivilous lawsuits, but it is great to see this legislation
finally pass in 2008. The public must be enabled to use the new
medical tools provided by the Retail
Genomics industry without fearing that it will lead to discrimination
against them by employers or insurers. Furthermore, a person's genetic
code must remain their own property and must remain a private matter
unless they choose to disclose it. Unauthorized disclosure or discovery
of such information must be prosecuted.
|