Our Partners

These organizations are ones that we have partnered with in order to make the impact of your donations and support as large as possible. The work being done by the organizations listed here is saving lives and improving patient outcomes all over the world.

  • The Sickle Cell Adult Provider Network (SCAPN) was established in 2002 with a mission to establish a network for healthcare providers who serve adults with sickle cell disease. This was the first and remains the only national organization that offers a home for healthcare professionals from multiple disciplines who focus on adult-oriented research, clinical care, provides education/training, mentorship, and advocacy.

  • The Sickle Cell Disease Association of America's mission statement 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.

  • The Sickle Cell Disease Association of America's mission statement is: The Society's mission is to further the understanding, diagnosis, treatment, and prevention of disorders affecting the blood, bone marrow, and the immunologic, hemostatic and vascular systems, by promoting research, clinical care, education, training, and advocacy in hematology.

  • The Center For Disease Control and Prevention's Sickle Cell Data Collection (SCDC) program collects health information about people with sickle cell disease (SCD) to study long-term trends in diagnosis, treatment, and healthcare access for people with SCD in the United States. The program helps to inform policy and healthcare standards that improve and extend the lives of people with SCD.