Sarita Edwards is the CEO & President at the E.WE Foundation, a global healthcare advocacy organization for families impacted by Trisomy 18 and other rare diseases. Sarita began her advocacy and public policy efforts after receiving a rare genetic diagnosis for her unborn son. Sarita is recognized as a world’s top patient expert and social health ambassador. She is an award-winning advocate, global speaker, and host of the Being Rare Podcast. Sarita holds a certification in Mental Health First Aid Instruction, a Bachelor of Science in Health Science, a Master’s in Healthcare Administration, and she’s in the final months of completing her Doctorate in Health Science and Research. Sarita lives in North Alabama with her husband and five children.
