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Our events and conferences bring together patients, families, advocates, healthcare professionals, and community partners to share knowledge, raise awareness, and strengthen support for those impacted by Sickle Cell Disease. From educational forums to community gatherings, these opportunities foster connection, learning, and meaningful dialogue. |
Webinar: Advocacy, Access & Action “It’s Not Just a Diagnosis — It’s a Life” Why Social Services Are Essential in Sickle Cell Care Supporters of Families with Sickle Cell Disease, Inc. invites you to join an important and empowering webinar focused on the critical role social services play in improving the lives of individuals and […]
“It’s Not Just a Diagnosis — It’s a Life” Why Social Services Are Essential in Sickle Cell Care Supporters of Families with Sickle Cell Disease, Inc. invites you to an […]
Rare Disease Town Hall Meeting A Virtual Community Conversation Supporters of Families with Sickle Cell Disease, Inc., in collaboration with Oklahoma Rare, invites you to join us for an important […]
