Osteogenesis imperfecta (OI) is a rare and complex genetic disorder that is often characterized by bones that break easily. While brittle bones are a major feature of OI, many other body systems are also affected. Individuals with OI may also experience dental issues, hearing loss, muscle weakness, joint hypermobility, cardiac, respiratory, gastrointestinal, and other health-related issues.

There is no cure for OI, but thanks to the efforts of the OI Foundation, there are now treatments available to manage symptoms, minimize fractures, enhance independent function, and promote general health.

The OI Foundation is committed to funding research, educating individuals and medical professionals about new treatments, enhancing independent function, and promoting general health. Donations made here benefit the OI Foundation’s Mission to improve the quality of life for 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 supporting people with osteogenesis imperfecta and their families. The Foundation’s mission is to improve the quality of life for people affected by OI through research, education, awareness, and mutual support. The OI Foundation began in 1970 by a small group of parents. At that time, they banded together to stimulate public and professional interest, support families and encourage research. Today, many of the people who serve on the Board of Directors and oversee the Foundation’s operations have OI themselves or are parents of children with OI.

Research

Since 1970, the OI Foundation’s funding for research has doubled every five years, for a total investment of more than $3.3 million. Funding is available for postdoctoral fellowships to encourage new investigators to begin a career in OI research, and seed grants for preliminary research. All applications are reviewed by the Foundation’s Scientific Review Committee, which includes many preeminent OI researchers and clinicians. Funding also supports the OI Registry and the Linked Clinical Research Centers. Funded research increases potential for advances in gene therapy, a new diagnostic test and drug therapies under study.

Education

The Foundation’s principal education event is the OIF National Conference, which provides more than 570 people with medical, research, and coping information. For many, it’s the first opportunity to meet others who are living with OI. In addition, the Foundation is continually developing new information resources in response to the needs of families, individuals, and professionals working with those affected by OI. Topics covered include schooling, pain management, psychosocial needs of the family, child abuse, fracture management, and osteoporosis.

Awareness

The Foundation strives to build public awareness and generate additional support among individuals, community organizations, public agencies, and medical professionals. Up-to-date information on OI- from medical issues to daily living strategies- is available via phone, Internet, fax, and mail. The Foundation also reaches out with print publications, press releases, DVDs, and the website.

Mutual Support

Improving quality of life is a continuing challenge that our small group of staff and enormous army of volunteers work constantly to achieve. From support and network groups to expanding resources or raising funds, the OI community and Foundation staff provide quality support services to OI community members.

OI Awareness Week 2026

Team Members