About Us

A Grass Roots Organization

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.

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.

Donate Now

We rely on donors like you to continue to help our community. Each donation is tax-deductible and goes directly to helping our efforts.

Community Outreach

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.


We desire to support individuals and families who are affected by Sickle Cell Disease or who have the sickle cell trait. We offer family education events, support groups social events, advocacy, scholarship, and Sickle Cell Camp. 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.

Tim Jerris

Founder & CEO

Erica Browser

Marketing Manager

Jack Nolston

Technology Manager

Jane Austin

Products Lead

Get In Touch

Want to volunteer or have questions about resources? Contact us!