President Bush Signs Bill
to Ban Genetic Discrimination
After Pro-Life Language Added
-- Part One of Two
On Thursday
President Bush signed into law landmark legislation to ban genetic
discrimination by employers and health insurance providers.
The legislation
has been under consideration in Congress for more than a decade. Until
recently, it contained certain defects that made it impossible for the
National Right to Life Committee and other pro-life groups to support
it. But those defects were corrected in the current Congress due in
large part to the work of Congressman Bart Stupak (D-Mi.), the co-chair
of the House Pro-Life Caucus, resulting in a final bill that
substantially advances pro-life interests.
The main thrust of
the Genetic Information Non-discrimination Act (GINA) is to ban
discrimination in employment or health insurance on the basis of tests
that show a person's genetic makeup. Advocates for the bill argued that
as genetic information and testing becomes more prevalent, employers and
health insurance providers would be increasingly likely to use that
information to discriminate against persons with genetic predispositions
to costly and debilitating diseases.
However, for years
the legislation contained a fatal flaw--it defined "family member" to
exclude unborn children.
Specifically, the
original bill said that "the term 'family member' means with respect to
an individual ... a dependent child of the individual, including a child
who is born to or placed for adoption with the individual" [emphasis
added]. This definition left unborn children, their mothers, and their
entire families at risk of discrimination if the mother refused to
undergo an abortion at the request of her employer or health insurance
provider.
The risk of such discrimination is
very real. In 1998, Jeremy Gruber, legal director for the American Civil
Liberties Union, raised this concern in testimony before the Senate
Labor and Human Resources Committee. For example, he said, "Consider
further the pregnant woman whose fetus tested positive for cystic
fibrosis and whose managed-care health plan limited coverage for her
pregnancy and future child while offering full coverage should she
choose an abortion."
Prenatal genetic testing is becoming
increasingly common. In fact, in January 2007 the American College of
Obstetricians and Gynecologists (ACOG) issued guidelines recommending
prenatal screening for Down Syndrome for all pregnant women, and some
studies show that when women receive a prenatal diagnosis of Down
Syndrome, as many as nine out of ten abort. Already women who receive
test results showing a possible disability are pressured to abort. The
pressure to abort would become even more powerful if a decision not to
abort places a job in jeopardy or a health insurance company threatens
to withdraw health benefits.
Similar concerns arise in the context of in vitro fertilization (IVF).
Some IVF practitioners already employ "preimplantation genetic
diagnosis" (PGD) to eliminate embryos who carry genes that will produce
future disorders--a practice that would become more widespread if
insurance companies could demand such tests as a condition to funding
the IVF process.
Recognizing these serious defects in
the original GINA bill, Congressman Stupak last year announced his
intention to offer a pro-life amendment in the House Energy and Commerce
Committee. This led to an extended negotiation between Congressman John
Dingell (D-Mi.), who is the powerful chairman of the committee, GINA
prime sponsor Rep. Louise Slaughter (D-NY), and Stupak.
Eventually an
agreement was reached that addressed the full scope of the pro-life
concerns. The agreed-on language was inserted into the bill, and was
retained throughout the rest of the legislative process.
Under the
negotiated language, the final bill prohibits employers and insurers
from discriminating against a woman or her family on the basis of
genetic information about "any fetus carried by such pregnant woman."
For example, it would be unlawful for an insurer to exert financial
pressure on a mother to abort an unborn child who prenatal testing
revealed to have a serious genetic disorder.
Likewise, the
negotiated language prohibits discrimination on the basis of genetic
information about "any embryo legally held by the individual or family
member."
In
addition, the final bill provides full protection for any child who has
been placed for adoption, even if the adoption has not been finalized.
Deirdre McQuade, an official with the U.S. Conference of Catholic
Bishops, praised the legislation for extending protection against
discrimination to "some of the most vulnerable members of the human
family, whether born, yet to be born, or placed for adoption."
"No one should be
discriminated against on the basis of genetic testing," McQuade said.
NRLC Legislative Director Douglas Johnson explained that NRLC had
resisted earlier versions of the GINA, but was pleased to support the
legislation after the addition of the changes negotiated by Congressman
Stupak. The final bill, he said, "provides some very important
protections for all Americans who believe that the 'pick of the litter'
approach should not be applied to human beings."
Part Two -- An
Easy Way to Help Your Pro-Life Friends and NRL News