Queens Sickle Cell Advocacy Network, Inc.
Copyright 2005 - 2008 All rights reserved
On behalf of the Board Of Directors of the Queens Sickle Cell Advocacy Network, Inc. I wish to thank all of the families, staff, volunteers and the community at large for your continued support in helping us to accomplish our goals. We continue to respond to requests for presentations at schools and community Health Fairs which offer the opportunity to distribute educational materials to raise the level of awareness of Sickle Cell Disease, Thalassemia and the Trait. We collaborate with The Sickle Cell Disease Association of America, the Newborn Screening Program, Hospitals and other national and international community organizations to access state and city programs to match these services to the needs of the unserved and the undeserved. QSCAN is working tirelessly to ensure quality services to children, families and individuals to meet their needs. Much more remains to be done, but with the help of everyone in the community we will continue in our quest to find a cure for this deadly disease. QSCAN will be a beacon of light to all those who feel hopeless in coping with the disease. With us working together we WILL make a difference.
