PKD Connection Blog

Kevin McDonald, captain of Team Lucy D, is ready to get moving in the Detroit Walk for PKD. With the event just a few weeks away, we reached out to Kevin to learn more about his family’s experience with PKD […]

This Walk for PKD season, we saw the return of an event spearheaded by a volunteer who is passionate about connecting with his PKD community. We recently reached out to Parker Burns of the Salt Lake City Chapter to hear […]

This post is part of a special series in honor of the 2017 fall Walk for PKD season. As the season progresses, a PKD Foundation staff member will share their experience at a local Walk event. This week’s featured contributor […]

This post is part of a special series in honor of the 2017 fall Walk for PKD season. As the season progresses, a PKD Foundation staff member will share their experience at a local event. This week’s featured contributor is […]

Paula Browning, captain of team InCYST a Cure, is ready to get moving in the Baltimore Walk for PKD. With the event just a couple weeks away, we reached out to Paula to hear more about her family history with […]

Our researchers are hard at work to find treatments and a cure for PKD, but with the first Walk for PKD event only two weeks away, they’re also working on fundraising! We recently reached out to Dr. Rachel Gallagher, head […]

Walk season is underway, which means our researchers are gearing up to win the title of top fundraising team in the Researcher Challenge! We recently spoke with Dr. Robin Maser, head of The Renal Avengers from KU Medical Center, about […]

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