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.
Take Action
Support the mission of the OI Foundation by raising
OI awareness or hosting a fundraiser.
Bringing OI community members together at OIF Conferences
OIF Conferences are educational and social experiences for families and individuals living with osteogenesis imperfecta.
Latest News & Updates
In Memory of Tracy Mulroy
The Osteogenesis Imperfecta Foundation is saddened to share the passing of Tracy Johnson Mulroy. ...
OI Treatment Survey
The OIF is asking adults with OI and parents/caregivers of children with OI to ...
Rune’s OIF Conference Experience
Thank you, Rune, for sharing your Conference experience! This article was published in the ...
OIF E-News: August 2026
The August issue of the OIF E-Newsletter is here! Read about the 2026 National ...
Thank You for Attending the 2026 OIF National Conference
Thank you for attending the 2026 OIF National Conference! Please check out the recap ...
OI Factsheet & Toolkit Chatbox (updated 2026)
The OI Factsheet & Toolkit Chatbox is an AI-powered assistant created by the Osteogenesis ...
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.
