Welcome to the website of PH-Europe!

An independent advocacy group for patients with Primary Hyperoxaluria (PH)

We’re a European support network powered by the compassion and dedication of patients, parents, medical professionals, translators, artists, IT specialists, and friends. This website is built entirely through voluntary contributions, driven by a shared commitment to make life with PH a little easier and a little less lonely. 

All content you’ll find here is independent and free of commercial influence — with the sole exception of a grant kindly provided by the German PH Self-Support Group. No one has received payment or compensation for their contributions. This is a project built on idealism, care, and community spirit — and that’s what makes it so special. 

This website serves as a first source of information for those newly diagnosed, looking for guidance, or wanting to connect with others across Europe. Your stories, your voices — especially those of patients and caregivers — are at the heart of what we do. 

Thank you to everyone who has contributed so far. Let’s keep building this together — and please, continue to support us on this journey.

What is Primary hyperoxaluria?

Contact

Please contact us

Address

PH-Europe, c/o.
David Attar,
Franzensbaderstrasse 23,
14193 Berlin,
Deutschland

Phone:

+49 (0) 163 4000 987

Email Address:

info@ph-europe.net