Join the Walk for PKD to support those with polycystic kidney disease. Lace up your shoes and make a difference.
Ready to reignite our Charlotte Region PKD Community connection. Please join us for a one hour kick off call to re-engage with our fellow PKDers and families. In addition to a speaker, we will plan upcoming meeting dates and in person meet ups around the region for the remainder of the year.
Join us for our upcoming community meeting via video conference!
Share your journey and hear from others within the PKD community who understand what you are experiencing. We'll share resources to help you manage living with PKD.
Join us for an informative and reassuring conversation with Dr. Roque Diaz Wong, Nephrologist, San Antonio Kidney, as he breaks down what to expect if kidney function declines. This session is designed to educate without overwhelming and will cover:
Share your journey and hear from others within the PKD community who understand what you are experiencing. We'll share resources to help you manage living with PKD.
Did you know that approximately 10% of ADPKD patients develop the disease due to a spontaneous genetic mutation, with no known family history of PKD? Dr. Juddith Maddatu, Clinic Director, Indiana University School of Medicine, will join us this month for an engaging discussion about the genetics of ADPKD, spontaneous mutations, and what this means for patients and families.
Our Phoenix Community meeting, hosted by Mayo Clinic, invites all who wish to engage in conversations about the best way to manage kidney and liver cysts, as well as suspected ruptures. Discussions will include patient experience with signs and symptoms, suspected triggers, infections, and pain management.
Join us at the Lakewood National Golf Club on October 27, 2025 for the PKD Applied Underwriters International Golf Event, to raise funds to help end PKD!
