Walk for PKD - Your Way! is an opportunity to join the nationwide Walk for PKD community in a way that caters to your schedule and interests while keeping things simple. Walk for PKD - Your Way! offers you the freedom to choose – how, when, and where you Walk for PKD. Participate as an individual or a team of loved ones, select a date and decide how you are going to Walk for PKD Your Way. How you raise awareness and funds for PKD research is up to you!
If you have questions, or would like to help with next year's walk, please reach out to us at walkforpkd@pkdcure.org.

Are you interested in helping us grow the South Florida Community?
We are looking for volunteers to help us offer more opportunities in your local area. If you are interested in this opportunity to volunteer and further our shared vision to #endPKD, please complete our volunteer form and let us know how you would like to get involved.
If you have questions, please email us at volunteers@pkdcure.org.
If you have questions, or would like to help with next year's walk, please reach out to us at walkforpkd@pkdcure.org.
Now, as always, the PKD Foundation is committed to our mission of giving hope, advocating for patients, and building a community for all impacted by PKD. We'll continue supporting our community by providing important resources and timely updates on social media. If you have questions or need help navigating this unprecedented health crisis, we are here for you. Email or call (844) PKD-HOPE.

If you’re looking for a shoulder to lean on or want to help others from the safety of your home, our Peer Mentor Program is a great resource:
- Interested in connecting with a mentor? Please take a moment to fill out our mentee survey and our team will follow up with you via email or by phone.
- Interested in becoming a peer mentor? Please complete our mentor application and a member of our staff will follow up with you by email or by phone.

Justin Greene
PKD Connect Ambassador
After graduating from Johns Hopkins University in 2021, I moved to San Francisco to work at a drug discovery startup called Octant, where I had the opportunity to conduct research on various rare disease drug programs. I experienced how important patient advocacy is in informing therapeutic research and was inspired by the people and communities with whom I interacted.
Last year, I learned that my own family carries a dominant mutation for Polycystic Kidney Disease. Because PKD is one of the most common rare diseases, the patient population is markedly diverse. My goal as a Connect Ambassador is to help as many voices be heard as we make advancements in PKD research and care, and to ensure that no patients are left behind. I moved back home to Boca Raton, Florida, this past Spring and am excited to learn from and contribute to the South Florida PKD community.
I am also an aspiring physician-scientist. Throughout my career, I hope to stay involved with the PKD Foundation and continue contributing as I gain more experience in clinical research and care.

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