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Sue Mehl

[video src="https://vimeo.com/74149223" width="640" height="360"] Sue Mehl Sue Mehl shares how polycystic kidney disease (PKD) has affected her family and how she is hopeful for a treatment or a cure for future generations. [/video]

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Mike Pickett: Fighting the good fight for himself and his daughter

Mike Pickett plays golf for a living, so organizing a golf tournament to memorialize his mother, Mary, seemed the natural thing to do to honor her and to raise awareness for PKD. Though Mary quietly battled PKD most of her...

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Laverne Duvall’s Gift: A Legacy for Future Generations

[caption id="attachment_1450" align="alignright" width="400"] Laverne, center, with her family when she was crowned Miss Budweiser in 1956.[/caption] PKD is a disease that often devastates many members in one family. It's not unusual for several siblings to battle PKD together. This...

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Giving for a better future

[caption id="attachment_1452" align="alignright" width="500"] Harold's Walk for PKD team, Ivan's Investors for a PKD Cure.[/caption] During the estate planning process, Harold Saul determined it was important for him to include a contribution to the PKD Foundation in his will for...

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Young couple joins Founders’ Annual Giving Society to help move the needle

Dustin Williams and Bailey Jackson have been married for two and a half years. Both are getting ready to turn 25, and they have already become members of the PKD Foundation's Founders' Annual Giving Society. In 2014, they became Foundation...

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Living donor gives again, donates vehicle

Eight years ago, Bev Benson donated one of her kidneys to her mother who has PKD. Now, she's made another huge donation, this time to the PKD Foundation, to help others suffering from the disease. "Having two vehicles was more...

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Jill Riester

When Jill Riester found out she had PKD, she was a 23-year-old newlywed just home from a military stint in Germany with her United States Army husband…and she was absolutely shocked. No one else in her family had been diagnosed...

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Workplace giving proves to be a convenient way to give

Janice Wightman supports the PKD Foundation through payroll deduction Janice Wightman doesn't just donate to fight PKD through her employer. It's also where she found her kidney donor, Diane. Stuck at an airport with a friend and colleague from work,...

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Richard Pearson

[caption id="attachment_1454" align="alignright" width="500"] Richard Pearson (middle left with hat and sunglasses) with his Walk for PKD team, Pearson's Poly Psychos.[/caption] Richard Pearson had always known about his family's PKD genetic history. His great grandmother died from PKD complications, and...

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For Brock Nelson, it’s all about increasing his ability to donate to a cause he is passionate about

After developing a spontaneous mutation of polycystic kidney disease (PKD) five years ago, Brock is currently a PKD Foundation Board of Trustees member and donor. Among the many reasons he chooses to support the organization, Brock says, "The Foundation is...

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