Thank you for supporting our project🤍
About the project
The Initiative Unique is a fundraising project to support the resarch of therapy and treatment options for the rare brittle bone disease/ Osteogenesis Imperfecta (OI).
The project was initiated by Lena & Nicklas, whose son Theo was born with the disease in December 2020.
Where do the donations go?
All donations go directly to carefully selected research projects in the field of OI through our partner, the Care4BrittleBones Foundation.
Where can I find more information?
If you want to learn more about OI, you can find more info here: