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  1. Voices of PKD - Nicole Harr


    from PKD Foundation Added 293 1 0

    Nicole Harr describes the emotions of being diagnosed with polycystic kidney disease (PKD) and the impact it has on her family. The PKD Foundation provides her information and support as she lives…

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    • Voices of PKD - Jason Baldwin


      from PKD Foundation Added 210 0 0

      Jason Baldwin shares what it was like to hear his daughter has autosomal recessive polycystic kidney disease (ARPKD). Jason and his wife have been able to find support, community and encouragement…

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      • Voices of PKD - Sue Mehl


        from PKD Foundation Added 164 0 0

        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.

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        • Voices of PKD - Sue Full


          from PKD Foundation Added 116 0 0

          Sue Full talks about the honor of supporting her long-time friend, Nicole Harr. Sue became involved with the PKD Foundation after she found out Nicole had been diagnosed with polycystic kidney disease…

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          • Voices of PKD - Dr. Jim Calvet


            from PKD Foundation Added 111 0 0

            Dr. Jim Calvet explains the importance of polycystic kidney disease (PKD) research and the role the PKD Foundation has played in funding research. He says meeting patients fuels his interest in doing…

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