About US
The Metropolitan Seattle Sickle Cell is a grass roots community based organization empowered to seek knowledge, support for people with Sickle Cell Disease.  The Task Force was Established in 1994 as a private non-profit organization. We are professionals, families and individuals making a difference in the community.

Our Mission
Our mission is to provide education and support to the community and to enhance the overall well-being of those afflicted with various forms of sickle cell disease and their families. We  work to disseminate information and provide support to people with sickle cell disease, young and old.

  Community Outreach
  The Task Force works in partnership with 
  schools, institutions, non-profit
  organizations, and  health care providers to 
  provide sickle testing and education about
  sickle cell disease and trait to the community.



Support
We desire to support individuals and families  affected by sickle cell disease and trait.  We offer family nights for families and friends. We also provide support groups for teens and adults affected by sickle cell.  We want to be advocates for individuals and families in any way possible to enhance their well being. Please contact us if you have particular questions, concerns, or needs.
 


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Contact
Metropolitian Sickle Cell Task Force
PO Box 20194
Seattle, WA 98102
mssctf@hotmail.com
Community Coordinator
253-226-5578

The Metropolitan Seattle Sickle Cell Task Force (501(c)3) is committed to helping local people effected by Sickle Cell Anemia through the Gertrude Dawson Scholarship Fund, Sickle Cell Camp and educating the community.
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