About the Association of Peyronie’s Disease Advocates

Working together to provide support and find a cure. That’s what inspired us — two men with Peyronie’s disease and a woman whose husband had the condition — to establish the Association of Peyronie’s Disease Advocates (APDA) in 2002. (Read a message from the founder.)

The APDA is a nonprofit organization dedicated to Peyronie’s disease sufferers and their families. Our Medical Advisory Board is made up of renowned physicians and leaders in the medical field who share our commitment to advance the understanding and treatment of this condition. Our mission is to provide sound information, comprehensive support, and relevant referral services to patients, partners, and physicians seeking Peyronie’s disease resources. At APDA, it is our sincerest intention to become your primary resource for honest, direct information and to connect you with others who face the physical and psychological effects of Peyronie’s.

As a representative of Peyronie’s disease sufferers and their partners, our commitment to finding a cure for Peyronie’s disease is unwavering.
Learn more about the APDA.

Get more from APDA

Join now.

How You Can Help

Make a donation or become a volunteer.