In late
September of 2008, after approximately three years of advocacy, a victory
occurred when the Senate and House passed a unanimous law called the Prenatally
and Postnatally Diagnosed Conditions Awareness Act. This law will ensure that
pregnant women who receive a positive prenatal test result and parents who
receive the postnatal diagnosis will be more likely to receive up to date
scientific information about life expectancy, clinical course, intellectual and
functional development, and prenatal and postnatal treatment options.
Within the
Act, there are provisions that offer referrals to support services such as
hotlines, websites, adoption registries, and parent support networks and
programs. In the past, much of the information provided was outdated and
inaccurate. Many treatment options and opportunities were not provided, and
there were decades-old stereotypes still persisting.
Under this
new law, families and society will receive knowledge and information about
individuals with Down Syndrome. This is a major victory, as it is hardly a routine
occurrence with unanimous consent.
Senators
Edward Kennedy (D-MA) and Sam Brownback (R-KS) were the original co-sponsors of
the Bill, and they led this through the Congress for the ultimate benefit of
all families and their children. It is hopeful that many of the myths and
stereotypes will be dismissed, and that the future for these families and
people will be better served. If you need for further information please
contact the National Down Syndrome Society
or the National Down Syndrome Congress.
By: Hyman
G. Darling, Esq.
It's about time!!! Thank you to all involved in accomplishing this feat.
~A Proud parent
Posted by: Donna | January 31, 2009 at 09:37 AM