[News from Congressman Chris Smith - 4th New Jersey
 

                                                         Saturday, December 17, 2005

                       Congressional Passage of Stem Cell Therapeutic and Research Act of 2005

 

Mr. SMITH of New Jersey. Mr. Speaker, I thank my friend for yielding
me the time.
Mr. Speaker, it occurred to me on the way to work this afternoon thatit is especially 
fitting that during this season of holiness and faith
and surpassing religious
significance that Congress send to the
President a bill designed to effectuate cures
of some of the most
devastating diseases and cancers on earth.
Not only has God in His wisdom and goodness created a placenta and umbilical cord to 
nurture and protect the precious life of an unborn
child, but now we know that another
gift awaits us immediately after
birth. Something very special is left behind, cord blood
that is
teeming with life-saving stem cells. Indeed, it is one of the best kept secrets
in America that umbilical cord blood stem cells and adult stem
cells are curing people of
a myriad of terrible conditions and disease
and are now showing the plasticity and
pluripotency that my previous
colleague just mentioned. So I would hasten to correct the
gentlelady
from Colorado that cord blood stem cells are not just for blood-related diseases,
it also has the capability increasingly, as research shows, t
o do other miraculous things as
well.
Let me just remind Members that we passed this legislation 6 months ago. Many things have 
happened since those 6 months. Much progress has
been made. This bill law will establish a
national program to collect
upwards of 150,000 units, with great diversity, so that most
Americans
who suffer from anomalies that could be cured by cord blood will be able to get it.
Let me thank so many people, the Speaker, Tom DeLay, Roy Blunt, Joe Barton whom we all pray 
for and wish a very speedy recovery. Let me
thank my friend on the other side of the aisle,
the gentleman from
Alabama (Mr. Davis) and the Congressional Black Caucus for the yeoman's
work that they expended in getting this legislation first passed in the House, then passed
over on the Senate side, because there was a
Democratic hold on it regrettably, Tom Harkin,
but then he lifted it.
Let me especially thank Senator Frist for the good work he did; Sam
Brownback; Mike Enzi; Orrin Hatch; Jon Kyl; so many others as well as so many here; the
gentleman from Florida (Mr. Weldon); the gentleman
from Pennsylvania (Mr. Pitts); the
gentleman from California (Mr.
Daniel E. Lungren); the gentleman from Indiana (Mr. Pence)
and I could
go on and on. I have a list of three pages of people who have been instrumental
in getting this legislation to the point where it will be
passed and sent down to the
President for signature.
Let me especially thank Cassie Bevan in the Majority Leader's Office who has worked so hard. 
She is amazing. John Cusey, on September 11,
2001, put together our first drafting meeting
on this legislation. He
too is amazing. That is how far back it goes. It has been a long time
coming, and so many others. Cheryl Jaeger, Chuck Clapton, Kikki Kless in the Speaker's Office,
Nicole Gustafson and Autumn Fredericks in the
ProLife Caucus, Eric Euling in Senator Frist's
office and Doug Branch
with Senator Brownback and some of the others were outstanding. I will
put the full statement in regarding all the many, many fine people who worked on this.
I will insert the remainder of my statement and the material I referred to previously at this 
point in the Record.
 
Cord-blood stem cells are, as we speak, treating and curing patients. Amazingly, we are on 
the threshold of systematically turning medical
waste, umbilical cords and placentas, into
medical miracles for huge
numbers of very sick and terminally ill patients who suffer from such
maladies as leukemia and sickle cell anemia. And because this legislation promotes cord-blood
research as well, we can expect new and
expanded uses of these very versatile stem cells.
For the first time ever, our bill establishes a nationwide stem cell transplantation system. It 
also authorizes the national bone marrow t
ransplant system and combines both under a new program,
providing an
easy, single-access point for information for doctors and patients and for the
purpose of collecting and analyzing outcomes data.
The cord blood stem cell portion of this bill will provide federal funding to increase the 
number of cord blood units available to match
and treat patients. The goal is to reach a
total inventory of 150,000
units so that matched stem cells will be available to treat more
than
90 percent of patients, especially focusing on providing genetic diversity. The
legislation would also link all the cord blood banks
participating in the inventory program
into a search system that would
allow transplant physicians to search for cord blood and bone
marrow
matches through a single access point. The national program would promote stem cell
research by requiring any participating cord blood
banks to donate units not suitable for
transplant because of disease or
size to researchers who are working on new applications for
cord blood
stem
cells. The National Bone Marrow Registry authorization expired on
September 30, 2003.
The bill reauthorizes an updated program through fiscal year 2010 for $34 million in FY06 and 
$38 million for each
additional year of the program. In the more than 6 months since we passed
this bill, even more
advances have been made in the field. Peer-reviewed studies have been
published showing increased plasticity and flexibility. In August, it was released that cord
blood stem cells are as flexible as embryonic
stem cells.
Two young Maryland siblings have been cured of severe combined immune deficiency syndrome by 
cord blood from unrelated
donors. Victims of Krabbe's and Hurler's diseases have found new hope
in cord blood treatments -- these are severe genetic neurological diseases that kill most of
their victims before they reach 2 years old.
A Duke University group treated newborns with cord blood--the lead author, Dr. Maria Escolar, 
now reports of the oldest survivor that the
seven-year-old is ``now running, jumping and doing
well in school.''
Earlier this month, Michelle Farrar from Leesburg, Virginia, traveled to South
Korea
to be treated for her spinal cord injury. True hope
exists for countless other medical
conditions, ranging from heart
attacks to muscular dystrophy to diabetes.
Just over a month ago, Dr. Brian Mason, an OB/GYN at Detroit's St. John Hospital, 
explained that "People literally are dying on the
transplant list who could be cured with
this." I am so happy that for
those people, delayed action on this bill has ended. No longer
will
they be denied access to the cures that are out there. Those suffering from the nearly
70 often terminal diseases will now get the cures that
the legislation will make available
to them. The door to the treatments
that have cured people like Keone Penn, Steven Sprague,
and Jacklyn
Albanese will now be opened for thousands of others.
As I mentioned before, there are so many people who deserve thanks in helping get this bill
moved through the legislative process on both
sides of the Hill. Among those people are
Rich Doerflinger and Mark
Gallagher from the U.S. Conference of Catholic Bishops, Dr. David
Prentice and David Christensen from the Family Research Council, the staff of the New York
Blood Center
including Pablo Rubenstein, Cladd
Stevens, and Kathleen Reichert, Sue Ramthun
who has been so personally
invested in this issue, Dr. Edward Guindi at Cordus and NBA Hall
of
Famer Julius ``Dr. J'' Erving, Richie Weiblinger with the Senate Budget Committee, and
the folks at Concerned Women for America, Focus on the
Family, and the Susan B. Anthony List.
I am ecstatic that we are
passing it through here today and getting it to the President, so
that
we may set up this network that will absolutely save thousands of lives.
###
For Immediate Release: December 18, 2005