[Congressional Record Volume 165, Number 52 (Tuesday, March 26, 2019)]
[House]
[Pages H2822-H2824]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]
COMMEMORATING WORLD DOWN SYNDROME AWARENESS DAY
The SPEAKER pro tempore. Under the Speaker's announced policy of
January 3, 2019, the gentleman from Kansas (Mr. Estes) is recognized
for 60 minutes as the designee of the minority leader.
Mr. ESTES. Mr. Speaker, on March 21, our country and the world
celebrated World Down Syndrome Awareness Day.
This afternoon, I am happy to lead my colleagues in recognizing this
important day and all of the contributions individuals with Down
syndrome make each day to families, businesses, schools, and
communities. From brothers and sisters to employees and businessowners,
to artists and models, people with Down syndrome have an incredible
impact on every part of society. They deserve our support,
understanding, and full acceptance.
Thankfully, there are many groups and programs that have made it
their mission to support individuals with Down syndrome and their
families.
As Kansas State treasurer, I advocated for passage of the Federal
ABLE Act and led the effort to implement it in Kansas.
It is kind of one of those things that, several years ago, I didn't
necessarily expect that I was going to be standing here today; so I was
going through the process of how do we lobby, how do we make sure that
a good program gets passed through the Federal legislative process that
benefits so many people, and then having to take that initiative in my
home State of Kansas and work through the legislature and making sure
that we implemented it to help people's quality of life and enable them
to live the lives that they wanted to live and make it more beneficial
for them.
This important law created tax-free savings accounts for individuals
with disabilities to cover expenses like healthcare, education,
housing, and transportation. It is important for parents raising a
child to be able to help provide their care.
Obviously, the concern on the part of parents is that, over years,
particularly as the parents age, they want to make sure that their
children, in some cases when they are in their adult life, are able to
enjoy the life that they want and the life that they deserve. A program
like ABLE is able to help make that dream come true.
These programs are similar to the 529 college savings programs,
health savings accounts, and individual retirement accounts. The ABLE
accounts
[[Page H2823]]
give people with Down syndrome and other disabilities the opportunities
to live the life they deserve.
The Kansas ABLE Act went into effect in January 2017. I was proud to
be part of that effort because it is the right thing to do.
In Congress, I have been humbled to work with organizations like the
National Down Syndrome Society to build upon the progress of the ABLE
Act. Last year, I was honored to receive the 2018 National Down
Syndrome Society Impact Award and look forward to supporting the
mission in this Congress.
This year, I am also honored to be on the honorary committee for the
AcceptAbility Gala, hosted by the Global Down Syndrome Foundation, an
annual event in Washington, D.C., that supports lifesaving research and
medical care for children and adults with Down syndrome.
Back home in Kansas, I am also inspired by groups like the Arc of
Sedgwick County, which supports individuals living with intellectual
and developmental disabilities, including Down syndrome.
Just as each of these groups, among numerous others, supports those
with Down syndrome, it is my hope that, in Congress, we can do the same
thing.
Mr. Speaker, I look forward to discussing this more today, but, at
this time, I am happy to yield to the gentleman from Minnesota (Mr.
Stauber).
Mr. STAUBER. Mr. Speaker, I rise in honor of World Down Syndrome
Awareness Day, which was Thursday, March 21.
One of the greatest blessings in my life is my 16-year-old son,
Isaac, who has Down syndrome. Each day, he brings joy to our lives, and
I am so proud of everything he has accomplished.
World Down Syndrome Awareness Day is an excellent opportunity to
raise awareness about the challenges that Down syndrome brings, but it
is also a chance to celebrate just how incredible people with Down
syndrome truly are. It absolutely breaks my heart--just breaks my
heart--when I hear some people say that they would rather get an
abortion than have a child with Down syndrome.
The sheer ignorance of those individuals is disheartening to me. They
do not see what a blessing all of God's children are, even if they are
different, and that is unfortunate for them. If they met my son Isaac,
I know they would have a change of heart.
When we talk about disabilities, I want us to talk about the
abilities of those like my son Isaac. Instead of focusing on what they
can't do, let's focus on what they can do.
The limit to what people like Isaac can accomplish is not determined
by their condition but by how much we love them and give them the
empowerment so they can navigate the world of work, education, and
public life.
As Isaac's dad and now as a Member of Congress, I am committed to
strongly advocating for the inclusiveness of those who live with
disabilities and the protection of their lives, always.
Mr. ESTES. Mr. Speaker, I thank Representative Stauber for those
comments.
Mr. Speaker, it is important for us, as Representatives, to actually
stand up for what we think is important. Obviously, as parents, we all
care about our children. We want to make sure they get the best
opportunities that they can, and, as elected Representatives, one of
the reasons I ran for office was to make sure that we could have an
impact and make sure that we could make a difference in people's lives.
When I look at the role of the Federal Government, one of the things
that is most important for us is making sure that we can help those
individuals live out the life that is embedded in our Constitution and
Declaration of Independence and having the right to life, liberty, and
the pursuit of happiness, people having that opportunity to live and
enjoy all the blessings of this great country.
We can talk a lot about different issues, and there are, obviously,
lots of us here in the Halls of Congress who want to talk about some of
those issues. Mr. Speaker, I yield to the gentleman from Arkansas (Mr.
Hill), my good friend, who wants to weigh in on this subject as well.
Mr. HILL of Arkansas. Mr. Speaker, I thank my friend from Kansas for
yielding. I appreciate him organizing an opportunity to come to the
House floor and talk about this important issue.
As the father of two children, I have been committed to policies for
a safe and enduring future for all kids and understand that we have to
ensure the protection of kids no matter what their walk in life,
particularly those with developmental disabilities.
Mr. Speaker, over 200,000 in the United States live with Down
syndrome, and one in 792 babies is born with this genetic disorder.
While there have been great advances in medical research and public
policy to enhance the lives of those affected by Down syndrome, there
is still much work to be done.
Individuals with disabilities face many challenges, and I understand
the need to ensure access to vital services and medical equipment to
support independent and active lives. This is critical to help
effectively live with Down syndrome. Getting our kids the proper
development path at a young age helps them ensure they will be
healthier adults with a bright future.
For over 20 years, I have watched with such pleasure young people
begin to build that proper developmental path at Access Academy in
Little Rock or Easter Seals Academy at Riverdale.
As a former member of the board of directors of Arkansas Children's
Hospital, I saw firsthand how important it was that parents are given
the tools they need to keep their children healthy. This is
particularly important for families who have a child with a disability.
Back in 1990, President George H. W. Bush signed the ADA into law,
the Americans with Disabilities Act. I was proud to have been working
on President Bush's staff at that time. It was an amazing piece of
legislative work that brought this Congress together and that has
benefited thousands and millions of Americans and families since.
I look forward to working with my colleagues to build upon that
legislation so that all Americans can reach their full potential, no
matter what challenges they face. I will continue to support efforts
that provide services to individuals and families who are impacted by
Down syndrome.
Regardless of political ideology, I think we can all agree that every
single child deserves protection. When I think about the kids over the
past two decades whom I have watched grow up, who had incredibly
nurturing parents who got them on that developmental path in the right
way, who sacrificed so that they had that opportunity to talk about
what my colleague did, the pursuit of happiness, and I see them smiling
at workplaces when I visit in Conway, North Little Rock, and Little
Rock, that they have a job, that they are out working, that they have
that self-sufficiency and excitement of the work they do, it gives me
such a warm feeling to see their success with all the hard work they
have put into that pursuit of happiness.
Finally, Mr. Speaker, I have to say, and I don't think it should be
left unsaid today, that a right to abortion should not extend to
children with traits deemed undesirable or inconvenient. Would we throw
away a life so casually if a child had the wrong color eyes or off-
texture hair? Of course not.
If a child does not fit the physical or developmental ideals of their
parents, they should be treated with the same degree of medical
attention, love, and care as any other child. As a proud Catholic and
proud pro-life Member of Congress, I believe we need to value life.
Mr. Speaker, I thank my friend from Kansas for hosting this important
event today to talk about Down syndrome, the love we have for our
American citizens who live with Down syndrome, and the affection we
have and support we have for their families.
{time} 1545
Mr. ESTES. Mr. Speaker, I thank the gentleman from Arkansas (Mr.
Hill).
It is tremendous to be able to work with representatives like him
that have a goal to focus on: how do we make life better? How do we
provide opportunities for individuals?
You touched on a sad part in society today where so many people seem
to think that it is right that just because of some particular trait
that the parents don't necessarily like, that they are able to kill
individuals because of that through abortion.
[[Page H2824]]
When we are talking about Down syndrome and awareness of that, you
know, it is a sad fact that we have got to address this issue. We have
got to address that extreme discrimination that some individuals that
want to impress upon those people who may have Down syndrome even
before they have a chance to live a life.
In the United States, two-thirds--67 percent--of babies diagnosed
with Down syndrome while in the womb are aborted.
In Europe, it is even worse. In France, the rate is 77 percent. In
Denmark, it is 98 percent. And in Iceland, it is nearly 100 percent,
where late-term abortions are allowed if the baby has a deformity,
which includes Down syndrome, to quote a CBS News article.
In a society where Down syndrome individuals can have a wonderful
quality of life and pursue their dreams, this discrimination needs to
be brought to light.
We live during a time when there is so much medical innovation, so
many opportunities, so many brilliant things that our doctors are
developing, we need to make sure that we capitalize on that innovation,
make sure that we allow people the opportunity to live a full life and
live the opportunities that they enjoy.
This innovation, unfortunately, has been used by individuals to
determine the sex, determine if the child is healthy, determine if the
child has certain traits; and in some cases, for positive reasons, to
determine whether there is some medical necessity to operate while in
the womb to make sure that that individual--that child--enjoys quality
of life.
However, we need to make sure that that testing process never gets
corrupted, never gets used in a discriminatory way, and it is never
used to justify abortion.
It is a sad fact that we are seeing so many things being talked about
in the abortion arena nowadays, and so many people beating that drum.
We have got to stand up, you know, in our country. We want to be able
to stand up for people's rights and we want to be able to stand up for
the opportunities for babies to live and have the opportunity to live a
life that we all will enjoy as well.
I now yield to the gentleman from Texas (Mr. Babin), my fellow
colleague, the opportunity to speak and talk about this very important
issue.
Mr. BABIN. Mr. Speaker, I thank my great colleague from the State of
Kansas.
Mr. Speaker, on March 21, we celebrated World Down Syndrome Awareness
Day. What an appropriate thing to celebrate as folks with Down syndrome
make incredible contributions to society every single day that should
be acknowledged and appreciated.
I, for one, am thankful for all of those with Down syndrome that I
have had the great pleasure and honor of knowing and learning from.
With the rise of prenatal screening tests across the United States,
the number of babies born with Down syndrome every year has
significantly decreased. And while we do not know the exact number of
Down syndrome children who are aborted each year, it is estimated that
approximately two-thirds of children diagnosed in the womb are aborted.
Two-thirds of children who would go on to make a significant impact
in this world are murdered before they are given a chance to even be
able to have that opportunity.
Iceland, in particular, has almost completely eradicated Down
syndrome births.
Statistics show that they have an almost 100 percent termination rate
of Down syndrome children.
France has a 77 percent termination rate; while Denmark is at 98
percent.
I pray that the United States will reject the idea that Down syndrome
children somehow are less than other children. As a society, we should
move away from any idea that advocates killing any child in its
mother's womb. And as a pro-life Congressman, I believe that all life
is valuable, especially the lives of those who cannot speak for
themselves.
Aborted Down syndrome children are just that, they are children who
have their own hopes and dreams for a future and to live a long,
healthy life. To take away their right to life is inconceivable to me
and abhorrent.
I will continue to fight for legislation that protects every single
unborn child, regardless of whether or not they have an extra
chromosome.
Mr. ESTES. Mr. Speaker, I thank Representative Babin, and I
appreciate those words.
Mr. Speaker, we, as fellow colleagues, have such an important role
trying to work on how we bring forth those American principles and
opportunities for everybody.
In recent months, we have seen politicians from States around the
country embrace late-term abortions and openly discuss infanticide.
Individuals with Down syndrome would be among the most severely
impacted by these tragic policies.
To help respond to that, my colleagues and I have repeatedly called
to bring forward the Born-Alive Abortion Survivors Protection Act to
the floor for a vote.
This straightforward bill would require healthcare practitioners to
give the same care to a child who has survived a botched abortion just
as they would any other newborn child.
Apparently, the bill has 182 cosponsors.
Unfortunately, a vote on the bill has been blocked 21 times now by
the majority.
However, as we rise to commemorate World Down Syndrome Day, I call on
my colleagues to consider this bill and any other one that would
protect life and support those with Down syndrome.
There are 250,000 people in America with Down syndrome. They live
healthy, productive, happy lives, just like you and I do, and want to
have the same hopes and dreams and goals.
We need more awareness of what a diagnosis of Down syndrome really
means. It means that a child simply has an extra chromosome and that
nothing else about their life is different from you or me.
They have so much to contribute to this world, and they deserve that
chance.
Last year, I had the chance to meet David Egan. David is a fellow
working for the National Down Syndrome Society, and previously worked
for the House Ways and Means Committee.
When I met him, he told me how much he wanted to help others with
Down syndrome accomplish anything they wanted to do, just as he has
done in his own life and career.
I am inspired by people like David, and I want to thank my colleagues
who join me today for this Special Order recognizing World Down
Syndrome Day.
Mr. Speaker, I look forward to working with Congress to support those
with Down syndrome, and with that, I yield back the balance of my time.
____________________