Queens Sickle Cell Advocacy Network, Inc.
Copyright 2005 - 2006 All rights reserved
Who we are
The Queens Sickle Cell Advocacy Network, Inc. is a non-for-profit broad based community organization, servicing children and families with special needs. Established in 1989 as the Queens Sickle Cell Community Network, we subsequently became incorporated in 1997 and changed our name to the Queens Sickle Cell Advocacy Network, Inc. (QSCAN).
Our mission and vision are a deep sense of commitment; it focuses on those with Sickle Cell conditions. We provide a clear sense of direction for families and individuals, enabling them to participate actively in their communities and health care needs.
Our goals and objectives
To serve and support families and individuals affected by Sickle Cell and other chronic disorders
To identify the needs and priorities of neglected families
To empower such families and individuals with knowledge, skills and assistance by providing, training, referrals, information and other assistance to access services and support to meet their needs
To provide an awareness and educational system through community outreach
To collaborate with health care professionals, government agencies and programs, private institutions and interested community groups for the management and eventual eradication of the Sickle Cell disease
