Our mission is to improve the lives of those living with osteogenesis imperfecta through research, education, awareness and mutual support.
The Osteogenesis Imperfecta Foundation, Inc.
(OI Foundation) is the only voluntary national health organization dedicated to helping people cope with the problems associated with osteogenesis imperfecta.
The OI Foundation is Here for You
Programs and resources of the OIF help individuals and medical professionals understand osteogenesis imperfecta.
Help Move OI Research Forward
Supporting research is an important part of the OI Foundation’s mission.
Participation in OI research helps advance the scientific understanding of OI so that more and better treatments can be made available to the OI community.
Once you are enrolled, you will begin to receive information on upcoming studies and online surveys about OI.
View a collection of published OI research.
Take Action
Support the mission of the OI Foundation by raising
OI awareness or hosting a fundraiser.
Raise OI awareness in your community, host an event, or create a Facebook fundraiser!
Members are the heart of our organization.
We are so thankful for your support!
Bringing OI community members together at OIF Conferences
OIF Conferences are educational and social experiences for families and individuals living with osteogenesis imperfecta.
OIF National Conference:
Orlando, FL: July 23-26, 2026
OIF Regional Conferences:
Atlanta, GA: February 22, 2025
Denver, CO: May 3, 2025
Portland, OR: TBD
Latest News & Updates
Edward D. Cranston College Scholarship Program
Jeanie Coleman Impact Grant Program
2024 Accomplishments
Quality of Life Findings from the IMPACT Survey!
Year End 2024: A Note From Our CEO
Donor Advised Funds Support the OIF Throughout the Year!
Helping our community stay up to date and connected.
Please sign up to receive updates from the OI Foundation including our monthly e-Newsletter, research updates, and upcoming event information.
