around the world

Soft Bones
The US Hypophosphatasia Foundation and Soft Bones Canada provide both information and a community to educate, empower, and connect patients, families, and caregivers living with HPP.
Hypophosphatasie Deutschland
Written in German. Helps patients, families, and caregivers living with HPP better understand the illness.
Hypophosphatasie Europe
Written in French. Offers information about HPP, including patient stories, patient rights, and research in Europe.Rare disease and HPP advocacy
