Google
Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Metropolitan Seattle Sickle Cell Taskforce
PO Box 20194Seattle, Washington, United States
Email Phone Web
The Metropolitan Seattle Sickle Cell Task Force is a grass roots community based organization committed to helping people with Sickle Cell Disease in our local community. The Task Force was established in 1994 as a private non-profit organization. The Task Force works in partnership with schools, institutions, non-profit organizations, and health care providers to provide sickle cell testing and education about sickle cell disease and trait to the community. The mission of this organization 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. It also works to disseminate information and provide support to people with Sickle Cell Disease, young and old.
The task force desires to support individuals and families who are affected by Sickle Cell Disease or who have the sickle cell trait. It offers family education events, support groups social events, advocacy, scholarship, and Sickle Cell Camp. The members of the organization advocates for individuals and families in any way possible to enhance their well-being.
+myBinderRelated Content
-
Rae BlaylarkRae Blaylark is a passionate and genuine...
-
Chief executive of the Sickle Cell Society is awarded an OBEJohn James, Chief Executive of t...
-
The Nazhi Thee Baker Angel Foundation Inc.The Nazhi Thee Baker Angel Foundation In...
-
Mental Health Resources for Black, Indigenous and People of Color (BIPOC)In addition to COVID-19, recent events h...
-
North Alabama Sickle Cell Foundation (NASCF)North Alabama Sickle Cell Foundation's (...
-
Pfizer’s Kevin Williams to Pen Health Column on Sickle Cell Disease for the Black PressDr. Kevin Williams, the Chief Medical Of...
-
Cynthia Gipson, MACynthia Gipson is a family advocate for ...
