Georgene' Glass is a visionary leader, devoted mother, and passionate advocate who has transformed her personal journey into a powerful force for change. As the founder and executive director of Dreamsickle Kids Foundation, she pioneered the landscape of Sickle Cell Disease (SCD) advocacy in Nevada, establishing the organization in 2018. Georgene's unyielding commitment to her cause was ignited in 2015 with the birth of her second child, who was diagnosed with SCD. This pivotal moment propelled her into the world of SCD education, advocacy, and community building.
A dedicated caregiver and a fervent speaker, Georgene has become a sought-after authority on SCD and rare diseases. She fearlessly leads by example, leveraging her experience as a mother, caregiver, and advocate to motivate others. Georgene's impactful speaking engagements span a range of platforms, from panels for nonprofits, pharmaceutical companies, colleges, and universities, where she addresses vital topics including health equity, SCD, and legislative advocacy.
Georgene's influence goes beyond the stage. Her dedication to legislative advocacy has brought about significant change, resulting in the passage of a pivotal SCD bill in Nevada. In collaboration with partners, she has successfully established the state's first SCD community center, offering a hub of support and resources for those affected by the disorder. Additionally, she authored "The Tale of the Cell," a heartwarming children's book featuring her daughter Gia, which serves as a source of inspiration and empowerment for young individuals living with SCD.
Certified as a Community Health Worker and equipped with a Healthcare Leadership certificate from Duke University, Georgene is a multifaceted advocate who brings both passion and expertise to her work. She holds positions on various boards within the SCD community and other organizations, including the Nevada Minority Health and Equity Coalition, demonstrating her commitment to broadening the reach of health advocacy.
Georgene's impact extends beyond her role with Dreamsickle Kids Foundation. She generously shares her knowledge as a nonprofit consultant, aiding individuals in establishing and nurturing nonprofit organizations, writing grants, and building solid foundations for their causes.
Through her dedication, Georgene continues to make a profound impact on the SCD community, inspiring positive change and ushering in a brighter future for those affected by this rare genetic disorder.