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The founder, Arya Reddy, was born with a mild case of OI, a rare genetic disorder that affects bone strength and quality. Despite his condition, Arya was determined to live a full and active life. However, this proved to be a challenge as he suffered multiple fractures during his first 13 years of life, with his first fracture occurring at just 15 months old.

Through his experiences, Arya became passionate about raising awareness and funds for OI research and support. He was inspired to create a non-profit organization that would give children with OI the resources and hope they need to thrive.

Arya's vision and dedication have been the driving force behind our organization's mission. His personal experience with OI has given him a unique understanding of the challenges faced by those living with this rare genetic disorder. Arya's commitment to improving the lives of children with OI is reflected in every aspect of our organization's work.

In 2023, Arya founded our organization, which is growing into a thriving community of supporters and volunteers. We are committed to raising awareness and funds for OI research and support, and to giving children with OI the hope and resources they need to live full and active lives.

Thank you for taking the time to learn more about our organization. We invite you to join us in our mission to make a difference in the lives of those affected by OI.

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