Survey Opportunity: Help Orthopedic Surgeons Learn About OI
The OI Foundation would like to bring your attention to a new survey to help orthopedic surgeons learn more about
OI Community Call: Mental Health during COVID-19
On Thursday, September 3, 2020, Dr. Kara Ayers (Associate Director of the University of Cincinnati Center for Excellence in Developmental
Reflecting on 50 Years
Read a special message from OI Foundation CEO Tracy Hart highlighting the OIF’s milestones and accomplishments over the past 50
OI Foundation PCOR Project Approved for Supplemental Funding Award
OI Foundation Project, Improving Patient-Centered Outcomes: Expanding Engagement of the Osteogenesis Imperfecta Community, Approved for Supplemental Funding Award The Osteogenesis
Celebrating 50 Years!
The OI Foundation was officially incorporated on August 21, 1970! We will be celebrating the OIF's 50th Anniversary on our
OIF Young Investigators Symposium
OIF Young Investigators Symposium Basic, Translational and Clinical Aspects of Osteogenesis Imperfecta and Other Rare Bone Disorders The Osteogenesis Imperfecta
Remembering Gemma Geisman
“Hope lies in dreams, in imagination and in the courage of those who dare to make dreams into reality.” —Jonas
OIF E-Newsletter: August 2020
The August issue of the OIF E-Newsletter is HERE! Read more about the OIF's 50th Anniversary celebrations next week, OIF
It’s not too late to support your favorite Walk-n-Wheel participant!
Thank you so much to everyone who participated in the first-ever Virtual Unbreakable Spirit® Walk-n-Wheel! Across the United States, Canada,
Rare Bone Disease TeleECHO Program: Year 2 Begins Thursday
Rare Bone Disease TeleECHO Clinic Series: Year 2 The Osteogenesis Imperfecta Foundation and the Rare Bone Disease Alliance are excited