Dreamsickle Kids Foundation

Our Story

Founded in 2018 by Executive Director Gina Glass, Dreamsickle Kids Foundation emerged from a personal experience that revealed the urgent need for resources and awareness surrounding Sickle Cell Disease in Nevada. The foundation is dedicated to celebrating, educating, and supporting families impacted by Sickle Cell Disease and Rare Diseases, while advocating for improved healthcare access.

Impact

Dreamsickle Kids Foundation has become a beacon of hope for the Sickle Cell community in Nevada. Through advocacy and education, the foundation has significantly improved the quality of life for individuals and families affected by these conditions.

Why Donate?

Your generous donations to Dreamsickle Kids Foundation provide essential resources for children and families affected by Sickle Cell Disease and Rare Diseases. Support the mission to raise awareness, provide education, and advocate for better healthcare access.

Get Involved

Join the movement to empower families and transform lives. Donate cryptocurrency or cash today to help Dreamsickle Kids Foundation continue its vital work in the community!