Quest To Cure – Focus on Life, Not Pain

Providing public education to prevent genetic disorders from being passed on to newborns.

Inspiring healthy habits such as pain coping and healthy eating.

Where patients with genetic blood disorders transition from child-focused medical care to the adult care system.

A medical home focused on resources, referral and advocacy to those effected by genetic blood disorders.

About our foundation

Quest to Cure is continually present and provides much needed services to those battling sickle cell disease.

Because a community in crisis is a community that needs championing.

Despite public perception, Sickle cell disease still exists and continues to devastate the lives of so many individuals and their families.

Babies born globally every year with Sickle Cell Anemia/Disease

Experts predict this global birth rate will dramaticlly increase by 400,000 by year 2050

African-American babies are born with sickle cell trait (SCT)

Babies are born with hemophilia-A each year