Mission and Vision

To identify the needs and priorities of under served families who have a family member with special health care needs.

We can help empower such families and individuals with the knowledge, skills, and assistance necessary for them to access services and support for their needs.

To provide advocacy training for them.

To provide for them referrals, information, and other assistance in regard to community resources and social services.

To provide families and individuals with networking support and activities enabling them to make positive changes when they feel overwhelmed by the barriers and experiences they face.

To provide such families and individuals with access to federal, state, city and local resources that will enhance their quality of life.

To promote public awareness and education re: sickle cell disorders, and to provide training and technical assistance for groups requesting it

To build collaborations amongst such families and individuals with concerned professionals, institutions, community groups, and other organizations