Your Donation is Important!!

Some African Americans have rare blood types, such as U-negative, that are unique to the African-American community. Rare blood donors are special because they are desperately needed to help others with rare blood types survive. African Americans with diseases like sickle cell anemia, cancer, leukemia or kidney disease are less likely to have physical reactions to blood donated from other African Americans.



Many African Americans have become blood donors and donate blood regularly. However, there are far more African-American patients needing blood than there are African Americans donating blood. While African Americans comprise nearly 13% of the United States population, they represent less than 1% of eligible blood donors. The result is far greater demand for blood types O and B commonly found among African Americans.


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SCDAA, Oklahoma Chapter

Joined the

Sickle Cell Disease Association of America, Inc. for

ADVOCACY D AY ON CAPITOL HILL
Washington, DC
March 24, 2009

8:30 a.m. – 4:30 p.m.

 

SCDAA, Oklahoma and other Member Organizations outlined our request for full funding and reauthorization of the Sickle Cell Treatment Act (SCTA) programs, during the Fiscal Year 2010 appropriations cycle.

 

OUR KEY MESSAGES:

Thank you for supporting the Sickle Cell Treatment Act (P.L. 108-357). The SCTA allows states to receive federal funding for patient counseling, educational initiatives and community outreach programs. Patients can also receive federal matching funds for sickle cell disease-related services under Medicaid. The SCTA also sets the groundwork for the development of 40 sickle cell treatment centers located across the country and establishes a National Coordinating Center for Sickle Cell Disease. The SCTA expires in 2009 and remains seriously underfunded. However, as more and more individuals and communities learn about Sickle Cell Disease, the demand for more research and outreach increases.

More information about the Sickle Cell Treatment Act and more about the key messages that will be discussed can be found here.

New photos have been added here.







Gabriel George, right, met March 24, 2009 with President Barack Obama in

the Oval Office to talk about sickle cell disease. The National Poster Child

for the Sickle Cell Disease Association was accompanied by his mother,

Shelly. Obama was funny and joked about things, Gabriel said.





918 Riderz

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Copyright 2007 Sickle Cell Disease Association of America, Oklahoma Chapter. All rights reserved.

 
 
 

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