Rosa’s Law: “Intellectual Disability” Applauded

WASHINGTON, D.C. – U.S. Senator Barbara A. Mikulski today introduced “Rosa’s Law,” a bill that will eliminate the terms “mental retardation” and “mentally retarded” from the federal law books. U.S. Senator Michael B. Enzi (R-Wyo

.), Ranking Member of the Health, Education, Labor and Pensions Committee, is the Republican sponsor of the bill.

Under Rosa’s Law, those terms would be replaced with “intellectual disability” and “individual with an intellectual disability” in federal education, health and labor law. The bill does not expand or diminish services, rights or educational opportunities. It simply makes the federal law language consistent with that used by the Centers for Disease Control, the World Health Organization and the President of the United States, through his Committee on Individuals with Intellectual Disabilities.


FOR IMMEDIATE RELEASE
November 17, 2009

Contact:
Annie Acosta
The Disability Policy Collaboration
(202) 783-2229/ acosta@thedpc.org

The Disability Policy Collaboration Applauds the U.S. Senate’s Introduction of Legislation to Use the Term “Intellectual Disability”

Washington, D.C. – The Disability Policy Collaboration (DPC), a partnership of The Arc of the United States (The Arc) and United Cerebral Palsy (UCP) to advance federal disability public policy, applauds today’s introduction of “Rosa’s Law,” a bipartisan bill introduced by U.S. Senators Barbara Mikulski (D-MD) and Michael Enzi (R-WY). Modeled after a recently enacted law in the state of Maryland, this legislation would substitute the outdated, stigmatizing terms “mental retardation” and “mentally retarded” with the terms “intellectual disability” and “individual with an intellectual disability” in federal health, education and labor policy statutes.

The term “intellectual disability” covers the same population of individuals who were previously diagnosed with the term “mental retardation,” and “mentally retarded.” Therefore, the change in terminology would in no way alter the eligibility requirements for services and supports.

“This bill is very important for people with intellectual disabilities who understand that language plays a crucial role in how they are perceived and treated in society and are actively advocating for terminology changes in federal and state laws. ‘Retard,’ ‘retarded’ and ‘retardation,’ once accepted medical terms, are now often used to demean and insult people,” stated Peter V. Berns, Chief Executive Officer of The Arc. “The Arc believes that changing how we talk about people with disabilities is a critical step in promoting and protecting their basic civil and human rights.”

According to Stephen Bennett, President and CEO, UCP, “By using the term ‘intellectual disability,’ we expect citizens of the U.S. and the world to understand and treat people experiencing this condition – whether it is a result of genetics, injury, illness or unknown causes – with dignity and respect. The descriptions of people are very important and imply how we value people, and the Senate’s introduction of ‘Rosa’s Law’ is aligned with the aim of UCP and its nationwide network of affiliates to ensure the inclusion of persons with disabilities in every facet of society.”

Senator Mikulski’s statement to the U.S. Senate upon introduction of the bill is available at: http://mikulski.senate.gov/record.cfm?id=319975&.

While the DPC supports the U.S. Senate’s introduction of Rosa’s Law, it is only the first step in a lengthy process towards enactment. The Arc and UCP will continue to work together to ensure the bill’s introduction in the U.S. House of Representatives and its progression through the entire legislative process.

About the Disability Policy Collaboration

The Disability Policy Collaboration (DPC) is a partnership of The Arc of the United States (The Arc) and United Cerebral Palsy (UCP) to advance federal disability public policy through a merged government affairs office, which combines resources and talent from both organizations. Begun in 2003, the collaboration assures cost-effective performance for its parent organizations, while combining for a more powerful voice for people with disabilities. The DPC leads efforts in mobilizing chapters, affiliates, self-advocates, families and other supporters to become active players in national public policy.

The Arc is the largest community-based nonprofit working through a network of 732 state and local chapters and their members to advocate on behalf of and serve people with intellectual and related developmental disabilities and their families. The Arc works to improve systems of supports and services, connect families, inspire communities, and influence public policy. It is the only organization that supports persons from pre-natal care through end-of-life issues and over 100 diagnoses that may include the effects of intellectual and developmental disabilities, including Autism. For more information, please visit www.thearc.org.
UCP is a leading service provider for adults and children with disabilities. UCP’s mission is to advance the independence, productivity and full citizenship of people with disabilities through an affiliate network, and its services reach over 176,000 adults and children daily through its network of approximately 100 affiliates in the U.S., Canada, Scotland and Australia. For more information, please visit www.ucp.org.

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The Disability Policy Collaboration of The Arc and UCP
1660 L Street, NW
Washington, DC 200136
p. 202.783.2229 | f. 202.783.8250