Support us now with your donation!

Support us now with your donation!

Thank you for supporting our projectūü§ć

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:

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Care4BrittleBones is an internationally recognized charity. Founded in 2012 by the parents of a child with OI, the foundation has grown rapidly. It is in contact with scientists, doctors and OI affected people in more than 80 countries worldwide and acts as both funder and coordinator of OI research projects. The goal: to enable a better quality of life for people with OI through research. For questions, contact: info@care4brittlebones.org