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Illinois Walk Team Chair Helps Build Community for Rare Kidney Diseases

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As a patient parent in Illinois, Cheryl LaBanco, is constantly raising awareness for Nephrotic Syndrome and FSGS. She is passionate about connecting with other local families and being a support system for those battling the same disease as her daughter. Cheryl is the Advocacy Lead and Local Walk Team Chair in her region. Learn more […]

Meet Northern California Regional Leader: Kara Jones

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Kara Jones is a patient parent in the Bay Area, her son suffers from Nephrotic Syndrome. She has been a dedicated NephCure volunteer for over 10 years, doing everything from supporting newly diagnosed families to creating the Silicon Valley Pig Jig event! You can connect with Kara directly at siliconvalleypigjig@gmail.com. What’s your personal connection to NephCure? […]

Meet Southern California Regional Leader: Christopher Windisch

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Christopher Windisch is an FSGS patient living in the Southern California area. His leadership has helped secure not only a great sense of support and friendship within the local kidney community, but his ingenuity and creativity constantly pushes him to think about what’s next. Christopher sits on NephCure’s Board of Directors. You can contact him […]

Meet Dallas Regional Leader: Tiffany Lievanos

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Meet Dallas Regional Leader, Tiffany Lievanos whose son suffers from Minimal Change Disease. Learn how she is working to help kidney kids understand the importance of their diet and how she is empowering other volunteers through the local events in her community. You can connect directly with Tiffany at nephcuredallas@nephcurevolunteer.org. What’s your personal connection to […]

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NephCure Kidney International’s ® mission is to accelerate research for effective treatments for rare forms of Nephrotic Syndrome, and to provide education and support that will improve the lives of those affected by these protein-spilling kidney diseases.

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