“We know just how important the work of the Oxalosis & Hyperoxaluria Foundation is to patients’ futures. The medication that Jack is now receiving via home injections would not have been available to him even a few years ago. The work that OHF is doing is time sensitive and life-changing!” — Courtney
Let your voice create your destiny for the future of Hyperoxaluria!
SHARE YOUR STORY
The Oxalosis & Hyperoxaluria Foundation (OHF) is dedicated to supporting awareness, understanding, and treatment of primary hyperoxaluria, oxalosis, and related hyperoxaluria kidney stone conditions. When you donate to OHF, you support the research that will bring hope to the lives of people with hyperoxaluria and oxalosis and their families.
The Oxalosis & Hyperoxaluria Foundation is a non-profit 501(c)(3) organization, and all donations are tax deductible.
Young Executive Leadership Program (Y.E.L.P)
Why Become an OHF Young Executive Leader? To drive change to inspire the future!
The Young Executive Leadership Program (YELP) aims to elevate young voices, build confidence, develop leadership skills, and provide young people the tools to raise awareness of Hyperoxaluria. YELP is broken up into two age groups: “Future Leaders” for advocates between the ages of 12-18 and “Executive Leaders” for advocates between the ages of 19-30. Both groups will have opportunities to learn from each other and work together. We strongly encourage participants to be within this age range, but all are welcome!
Latest Past Events
Join patients, families, experts, researchers, and clinicians to connect, learn, and grow. Get ready for a day filled with inspiration, learning, and heartfelt connections. Renowned experts will share their wisdom, researchers will unveil exciting discoveries, and compassionate clinicians will be there to guide us. This is your chance to gain the latest insights on hyperoxaluria, […]
Join the 14th International Hyperoxaluria Workshop, the largest hyperoxaluria professional and patient event worldwide. The workshop is an unrivaled opportunity to network and exchange invaluable knowledge with all stakeholders in the hyperoxaluria community— patients, caregivers, researchers, clinicians, and industry representatives. People living with a rare disease have the right to reach their highest potential of […]
Follow the OHF on social media to connect with the hyperoxaluria community and to stay up to date with current OHF initiatives!