Patient Advocate Spotlight: Tracy Hart
Rare Diseases Clinical Research Network Patient Advocate Spotlight  Tracy Hart, chief executive officer of the Osteogenesis Imperfecta Foundation, serves as
Sunday is #RAREDISEASEDAY
THIS SUNDAY - #RAREDISEASEDAY Rare Disease Day, which takes place on the last day of February each year, improves knowledge
Impact Grant Application Deadline Extended!
The Children’s Brittle Bone Foundation / Osteogenesis Imperfecta Foundation Jeanie Coleman Impact Grant helps individuals living with OI fund projects,
Impact Grants 101
Impact Grant Applications are due on MONDAY (3/1/21)! Impact grants may help cover the cost of items such as a
OIF E-Newsletter: Feb 2021
The February E-Newsletter is here! CLICK HERE Read about COVID-19 resources, upcoming virtual events, updates from the OIF, and more!
Virtual Northeast Regional Conference
Virtual Northeast Regional Conference The OI Foundation is hosting the first Virtual Northeast Regional Conference on Saturday, February 27 from
COVID-19 Vaccines Statement from the MAC
The following is a statement from the OIF’s Medical Advisory Council regarding COVID-19 vaccines.  As with any health decision, it
OI Love You!
OI Love You! This month only! Make a gift to the OIF in honor of a special someone and will
COVID-19 Vaccine Update Session
The OI Foundation hosted a second COVID-19 Vaccine Q&A on Thursday, February 11, 2021 at 6:00pm ET. Drs. Bottazzi, Lee,
Rare Disease Day at the NIH
On March 1, OIF CEO Tracy Hart and OIF Medical Advisory Council member Robert A. (Sandy) Sandhaus, M.D., Ph.D. will