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Georgene' Glass, founder and Executive Director of Nevada’s first Sickle Cell Disease (SCD) nonprofit, Dreamsickle Kids Foundation, is a tireless advocate for SCD and rare diseases. Her leadership brings critical support, advocacy, and awareness to the forefront in Nevada. With a patient-first approach, Georgene is recognized as a Global Award-Winning Rare Disease Advocate.

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As a mother of two—one angel and one strong SCD warrior—Georgene channels her personal experiences into her work. She is a Community Health Worker and Health Equity Champion dedicated to improving health outcomes and crafting legislation specifically targeting SCD. Her efforts include authoring a children’s book focused on SCD to promote health literacy and representation in minority communities.

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Using social media effectively, Georgene networks and amplifies Sickle Cell awareness, making significant strides in grassroots nonprofit sustainability. She serves on several boards including the Nevada Minority Health and Equity Coalition, is the Vice Chair of the Nevada Rare Disease Advisory Council (NVRDAC), a board member for Angel Aid Cares, and the Legislative Chair for the Sickle Cell Community Consortium.

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Georgene's advocacy extends to fighting for fair compensation in the rare disease space, ensuring that voices like hers lead the charge in creating meaningful change. Her insights are her own as she continues to be an impactful speaker and nonprofit consultant, dedicated to fostering a supportive and well-informed community.