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 Long Island 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.

Gillian Kolodny
PKD Connect Ambassador
Walk for PKD Ambassador
My family and PKD have a long history. Starting with my grandfather and possibly his father, it has stolen family members way before their time. It is also quite prevalent. The last two generations have seen the disease pass down to 100% of the children in the family. In 2003, I began volunteering with the PKD Foundation as we began the Long Island Chapter. It’s been an incredible journey so far! I feel quite blessed to have met so many wonderful people through the Foundation. We affectionately call ourselves “The Little Chapter That Could”. Since joining together, we have had a PKD awareness news program, were able to get the local and state legislature to reserve a day as PKD Awareness Day, and continue to support countless families as they begin to understand and move through their own journeys with PKD. We have members in all stages of PKD which makes it helpful when others need support. Banding together to raise funds and awareness to stand up to PKD is our focus. Being here to support one another is paramount! We hope to meet you soon. Please reach out if you’re living on Long Island, and if you’re interested in speaking with others living with PKD.

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