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Latest announcements and gatherings
The Sickle Cell Community Consortium is pleased to announce the 2017 Leadership Summit & General Assembly of Advocates and Community-based organizations (CBOs). The Consortium is a 501(c)(3) not-for-profit collective of Sickle Cell Community-Based Organizations (CBOs), Community Partners, Sponsored Patient Organizations, Patient/Caregiver Advocates and Healthcare/Research Advisors- each dedicated to sickle cell advocacy, education, research, community awareness and patient support throughout the country.
The Consortium was created to provide an organizing arm to enable our communities to identify and address local and national needs. Patterned after the United Nations, and following a model of Collective Impact, we provide a platform to “amplify the power of the patient voice”. As part of this collaborative effort, we are excited to host the 2017 Leadership Summit and General Assembly, March 16-19, 2017 in Atlanta, Georgia. This meeting is open to the public. You are invited to join us as we continue to effect patient-powered change in our community.
news & events64th American Society of Hematology (ASH) Annual Meeting & ExpositionThe 64th ASH Annual Meeting and Expositi...
news & eventsThe University City Turkey TrotCome celebrate the 8th year of the Unive...
news & eventsNational Sickle Cell Awareness MonthSeptember is National Sickle Cell Awaren...
news & eventsA Conversation With a Twist: Mental Health and Sickle Cell DiseaseOur goal is to help raise awareness abou...
Community CenterLocal Blood Drives & Donation Centers Near YouOne person can help save hundreds of liv...
news & eventsInaugural Event, World Cord Blood Day 2017, Highlights Non-Controversial Source of Stem CellsWorld Cord Blood Day (November 15th) wil...
news & eventsCamp Sunshine – Program Schedule2021 Fall program schedule to be determi...
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This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.