Our Mission
Our mission is to generate awareness, promote advocacy, and support research treatment options for CACP syndrome and other related, rare and joint disorders.
Our Team
Co-founders, David and Kari have put fourth a lot of effort making CACP Research Foundation a reality. However, they have received a lot of invaluable help from friends and colleagues and welcome interested parties to also become part of the team.
Get Involved
Ask us how to become an ambassador of CACP Research Foundation and host a Rare Disease Day event or other fundraiser.
Volunteer opportunities
Become an ambassador and be a part of the CACP Research Foundation team.
Make a Donation
Choose to give, all donations are tax deductible and go to support awareness, education, and research.