New research from the Brittle Bone Disorders Consortium (BBDC)
Exploring Pharmacological Therapies for Fracture Risk Reduction in Adults with Osteogenesis Imperfecta
The IMPACT Survey
Living With Osteogenesis IMPerfecta: UnderstAnding Experiences Based On Community InsighT and Evidence Survey, the IMPACT Survey What is the IMPACT
OIF E-Newsletter: March 2023
  The OIF's March E-Newsletter is here! Click here to read about OIF Membership, an important Medicaid update, the Pain
**Important Medicaid Information!**
During the pandemic, state Medicaid programs were required to keep beneficiaries enrolled, even if they did not meet the eligibility
Using the ECHO Model® to Expand Professional Learning Opportunities for Osteogenesis Imperfecta
OIF Director of Education, Michael Stewart is presenting a poster at #RareDiseaseDay at NIH today. Using the ECHO Model® to
OIF E-Newsletter: February 2023
The February E-Newsletter is here! Check out this issue to learn about grants for OI community members, the Pain and
Complete the new OI and Pain Survey!
The OI Foundation and OI Federation of Europe (OIFE) have partnered on a new project investigating the experience of pain
OIF E-Newsletter: January 2023
The first OIF E-Newsletter of 2023 is here! Check out this issue to learn about the Impact Grant program, a
Edward D. Cranston College Scholarship Program
The OI Foundation is excited to announce that applications are available for the Edward D. Cranston College Scholarship. This scholarship
OIF Regional Conference: Washington, DC
  The OIF will host a Regional Conference in Washington, DC on June 10, 2023.