Help us to Raise Money and Awareness for Osteogenesis Imperfecta (OI for short)
Our daughter Molly was born with OI, which means her bones break easily. We would love to raise money to fund research and treatment options for Molly and the OI community.
Molly will be participating in the Walk and Wheel-a-thon in Baltimore, MD on 7/12/18. We would greatly appreciate any donation you are able to make. OI is a rare condition and funds raised will help fund research for treatments as well as help provide resources for families. Please click the DONATE button on the right :)
A little about OI from the OI Foundation:
50,000 people in the United States are affected by osteogenesis imperfecta (OI), a rare genetic disease that makes bones fragile and easily broken. A person living with OI may experience hundreds of painful fractures over a lifetime. Infants with OI are often born with multiple broken bones. In severe cases of OI, a cough can break an adult’s rib. Each person with OI is unique, with different fracture rates, a varied range of related health issues and his or her own path through life. Yet there is one thing every person living with OI has in common… an Unbreakable Spirit®!
Please help us to provide answers to families, fund research, and maintain a network of support groups for families dealing with the daily realities of OI by making a gift and even joining us for this fun event.
You can improve lives! To support the important work of the OI Foundation, simply click on the Donate Now button at the top of this page.
I truly appreciate your time, consideration and generosity!