(Washington, D.C.) Today, Congresswoman Cathy McMorris Rodgers and other members of the Congressional Down Syndrome Caucus held their first briefing. Today’s briefing marks the first official event of the bipartisan caucus since its launch last week.

McMorris Rodgers co-chairs the caucus. She and her husband Brian have a one-year-old son, Cole, who has Down syndrome.

“The news of Cole’s Down syndrome was at first difficult to get our arms around and we were eager to learn all we could,” McMorris Rodgers said. “I’m often asked how being a mother has changed my life and changed my priorities, and I can assure you that it’s all been for the better. I have a new passion and a new energy for everything that I do. We have every intention of doing everything possible to ensure Cole has every opportunity to reach his full potential. I believe the Congressional Down Syndrome Caucus will be a vehicle to help bring this information to the forefront so all families of children and adults with Down syndrome can lead happy lives.”

There are more than 350,000 people with Down syndrome in the U.S., but past and current funding at the National Institutes of Health (NIH) is disproportionately low when it comes to finding treatments and increasing understanding of secondary disorders that often afflict people with Down syndrome, like Alzheimer’s disease and atherosclerosis.

Today, the Congressional Down Syndrome Caucus held its first briefing on what research is being done at the National Institutes of Health (NIH). The NIH updated us on its 10-year research plan which calls for increased research on the medical, cognitive, and behavioral conditions that occur in people with Down syndrome.

Contact:
Destry Henderson
202-225-2006
202-279-0418