Supporting families living with Sickle Cell Disease since 1994.
A Grassroots Organization
The Metropolitan Seattle Sickle Cell Task Force is a grassroots 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
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.
Education & Awareness
We provide workshops and outreach programs to raise awareness about Sickle Cell Disease and trait, partnering with schools and healthcare organizations across King County.
Community Outreach
Through collaborations with local nonprofits, hospitals, and institutions, we bring testing, resources, and support directly to those who need it most.
Family Support
We host family events, support groups, advocacy programs, and scholarships — including Sickle Cell Camps that offer encouragement and education for youth and adults alike.
Join Us in Making a Difference
Whether you’re volunteering, donating, or spreading awareness, your support helps sustain vital programs for individuals and families affected by Sickle Cell Disease.