The Mikayla Sarai Foundation is dedicated to addressing the critical need for health equity in Sickle Cell Disease care. We work tirelessly to raise awareness, provide education, and advocate for better healthcare access and treatment options for individuals affected by Sickle Cell Disease.

Through community outreach, educational programs, and partnerships with healthcare providers, we strive to bridge the gap in understanding and care delivery. Our foundation believes that everyone deserves access to quality healthcare and accurate information about Sickle Cell Disease, regardless of their background or circumstances.