HANOVER, Md.—The Sickle Cell Disease Association of America will hold its 50th annual national convention virtually this year from Tuesday, Oct. 11, through Saturday, Oct. 15. The five-day multidisciplinary convention addressing sickle cell disease and sickle cell trait draws hundreds of health care professionals, patients, families, community-based organizations, leaders and advocates.
The convention this year, “Joining Forces for Our Future,” will be held jointly by the Sickle Cell Disease Association of America and Sickle Cell in Focus, a conference co-hosted by the National Heart, Lung, and Blood Institute and the University of West Indies.
“We’re thrilled to join with partners all over the world for the 50th annual sickle cell convention,” said Regina Hartfield, president and CEO of the Sickle Cell Disease Association of America. “The convention will facilitate a crucial exchange of ideas among health care professionals, support families living with sickle cell, strengthen advocacy efforts and move us forward toward a cure.”
Convention speakers and presentations will include:
Additional convention events include business and grant meetings, exhibit hall presentations, advocacy lectures, clinical trial updates, educational workshops, medical reports, panel discussions, award presentations and social events. Participants will have the opportunity to connect and interact virtually with health care leaders and professionals and gain new relationships, knowledge and resources.
To learn more and register for the convention, visit www.sicklecelldisease.org/get-involved/events/annual-national-convention.
Sickle cell disease is an inherited blood disease causing red blood cells to take a sickle shape, which leads to blockages that prevent blood from reaching parts of the body. As a result, people with sickle cell complications can experience anemia, jaundice, gallstones, stroke, chronic pain, organ damage and premature death. No universal cure exists. (sicklecelldisease.net)
Sickle Cell Disease Association of America advocates for people affected by sickle cell conditions and empowers community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure. The association and more than 50 member organizations support sickle cell research, public and professional health education and patient and community services. (www.sicklecelldisease.org)