Kid Delegates Meet Elected Officials, Testify at Senate Hearing, and Urge Legislators To Request Fund Research
WASHINGTON, June 23 /PRNewswire-USNewswire/ -- More than 150 children and teenagers throughout the U.S. with type 1 diabetes are in Washington, D.C. this week to advocate for funding for type 1 diabetes research. They'll be joined by JDRF International Chairman Mary Tyler Moore, Nick Jonas of the Grammy nominated multi platinum group The Jonas Brothers, boxing legend Sugar Ray Leonard, and other advocates at the sixth Children's Congress of the Juvenile Diabetes Research Foundation.
Children's Congress, the largest grassroots advocacy event held in support of research for type 1 diabetes, will include a visit with President Barack Obama at the White House, a Town Hall panel of athletes and celebrities impacted by diabetes, and a hearing on Wednesday before the Senate Committee on Homeland Security and Governmental Affairs to request federal funding for diabetes research and remind Congress about the urgent need for a cure for the disease.
The Senate hearing, "Type 1 Diabetes Research: Real Progress and Real Hope for a Cure," will include testimony from Ms. Moore, Mr. Jonas, Mr. Leonard, Dr. Griffin Rodgers, Director of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), and four children with type 1 diabetes. The hearing will be chaired by Senator Susan Collins (R-ME). Following the Senate testimony, the delegates and their families will visit individually with their respective Members of Congress to educate for a cure.
A Town Hall panel, "Role Models in Diabetes," on Tuesday will enable delegates to interact with athletes, musicians and doctors who also live with type 1 diabetes - and share their experiences on how they're managing the disease and fulfilling professional careers at the same time. Panelists will include professional concert cellist Alisa Weilerstein; Miss Black USA 2007 Kalilah Allen-Harris, NFL player Jared Allen and Dr. Aaron Kowalski, JDRF's Research Director for the Artificial Pancreas Project. ESPN broadcaster Brian Kenny will moderate the forum.
The 150 children - ranging in age from 4 to 17 years old - represent each state. Joining the children in Washington, D.C. are five International Delegates from Australia, Canada, Denmark, Israel, and the United Kingdom.
"The day that you or your child is diagnosed with type 1 diabetes is a day you will never forget," said Ms. Moore, who has had type 1 diabetes for almost 40 years. "Members of Congress will now have the chance to give these children and their parents another day they will never forget. Instead, this time will be a day of hope instead of a day of fear."
The Senate Co-Chairs of Children's Congress 2009 are Sen. Collins and Sen. Lincoln, and the House Co-Chairs are Rep. Diana DeGette (D-CO) and Rep. Mike Castle (R-DE).
Cynthia Ford, of Grosse Pointe Farms, Michigan is Chair of Children's Congress 2009. Ms. Ford, her husband Edsel and son Albert, who has type 1 diabetes, serve as the designated Chair Family.
"Our entire family understands what a vital role this event plays in the furthering of our mission to cure diabetes. We are honored and excited to be leading such an extraordinary group of delegates who truly will have all the Washington leaders knowing they need to 'Promise to Remember' all of us who crave a true cure for diabetes and its complications."
Children's Congress, held every other year since 1999, has become the largest media and grassroots advocacy event held in support of finding a cure for type 1 diabetes. A once-in-a-lifetime experience, the delegates help raise awareness about type 1 diabetes, and participating in personal advocacy at the highest level of U.S. government.
In type 1 diabetes - the most serious and complicated form of the disease that accounts for at least $174 billion in annual health care costs in the U.S. alone - a person's pancreas stops producing insulin, the hormone that enables people to get energy from food. To survive, people with type 1 diabetes must test their blood sugar levels up to four or more times a day by pricking their fingers to draw blood, and then administer insulin through multiple daily injections, or the use of a continuous infusion insulin pump.
While trying to balance insulin with the amount of food eaten (which raises blood sugar) and exercise (which lowers blood sugar), people with type 1 diabetes must constantly be prepared for potential life-threatening low or high blood sugar levels. Just as devastating, the long-term complications of diabetes include blindness, heart attack, kidney failure, stroke, nerve damage and amputations. While usually diagnosed in childhood, type 1 diabetes can also be diagnosed in adults.
JDRF is the leader in research leading to a cure for type 1 diabetes in the world. It sets the global agenda for diabetes research, and is the largest charitable funder and advocate of diabetes science worldwide.
The mission of JDRF is to find a cure for diabetes and its complications through the support of research. Type 1 diabetes is an autoimmune disease that strikes children and adults suddenly, and can be fatal. Until a cure is found, people with type 1 diabetes have to test their blood sugar and give themselves insulin injections multiple times or use a pump - each day, every day of their lives. And even with that intensive care, insulin is not a cure for diabetes, nor does it prevent its eventual and devastating complications, which may include kidney failure, blindness, heart disease, stroke, and amputation.
Since its founding in 1970 by parents of children with type 1 diabetes, JDRF has awarded more than $1.3 billion to diabetes research, including more than $156 million in FY2008. In FY2008, the Foundation funded more than 1,000 centers, grants in laboratories, hospitals, and industry, and fellowships in 22 countries.
For more information, visit the JDRF web site at www.jdrf.org or call 800-533-CURE.
For more information on Children's Congress, visit www.cc.jdrf.org.
|SOURCE Juvenile Diabetes Research Foundation|
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