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Host Carla Lewis and Rae Blaylark are mother’s of children born with sickle cell disease. We welcome you to join a forum created to support, educate and share resources with parents/caregivers of a child/children or young adult with sickle cell disease/ trait or thalassemia. The forum will provide a safe place for parents to share & ask questions bridging the gap to important conversations.
Upon completion of this activity, participants should be able to:
• Increase knowledge about sickle cell & treatments
• Identify current evidence-based practices to improve care of individuals with sickle cell disease
• Identify resources available to caregivers
• Identify treatments & resources available to individuals with sickle cell or chronic blood disorders
Date and Time:
Saturday, July 24, 2021
7:30 PM – 10:30 PM IST
This event has ended.
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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.