IV 112th CONGRESS 1st Session H. RES. 256 IN THE HOUSE OF REPRESENTATIVES May 10, 2011 Mr. Peters (for himself, Mr. Young of Florida, Ms. Lee of California, and Mr. Bartlett) submitted the following resolution; which was referred to the Committee on Oversight and Government Reform RESOLUTION Expressing support for designation of the week of May 8, 2011, through May 14, 2011, as Williams Syndrome Awareness Week.

Whereas Williams syndrome is a rare genetic condition that is present at birth, affects more than 25,000 individuals in the United States, and is characterized by lifelong medical problems, including cardiovascular disease, developmental delays, and learning disabilities; Whereas the Williams Syndrome Association (WSA), founded in 1982, is a nonprofit organization and the most comprehensive resource for people and families living with Williams syndrome as well as for doctors, researchers, and educators; Whereas through its efforts, from raising public awareness, to funding critical new research, and providing valuable information and support to families, the WSA has improved the quality of life and futures of those affected by Williams syndrome; Whereas to generate awareness about Williams syndrome and raise funding for critical WSA programs and initiatives, the WSA has organized Williams Syndrome Awareness Week which includes the Walk for Williams and will encompass 45 walks across 30 States; Whereas the WSA and the families and friends of those with Williams syndrome should be commended for their hard work, compassion, and courage for educating the country about this rare disorder; and Whereas the week of May 8, 2011, through May 14, 2011, would be an appropriate week to designate as Williams Syndrome Awareness Week: Now, therefore, be it

That the House of Representatives supports the designation of Williams Syndrome Awareness Week.