MEMBERS

“Not just an OI community, a true OI Family”

Interview with Agnieszka Czoch-Tokarczyk from the Polish organization. She agreed to share the story of her family with a child with OI for Rare Disease Day Campaign 2026. After getting to know the OI community, what has surprised you the most and what has helped you as a parent? “I first met the OI community…

READ MORE
Group photo of the members of Association of People with Brittle Bone Disease in Poland, there's people standing and others in wheelchairsMEMBERS

Welcome to new Polish OI-Association!

Interview with Agnieszka Czoch-Tokarczyk, President of Association of People with Brittle Bone Disease – Poland Who are you? My name is Agnieszka Czoch-Tokarczyk, I am the president and one of the founders of the new Association of People with Brittle Bone Disease-Poland (together with Karolina, Ewa, Magda and Izabela). In Polish they are called Stowarzyszenie…

READ MORE
Translate ยป