{"id":27390,"date":"2024-03-26T14:46:16","date_gmt":"2024-03-26T18:46:16","guid":{"rendered":"https:\/\/nephcure.org\/?page_id=27390"},"modified":"2025-03-21T08:58:22","modified_gmt":"2025-03-21T12:58:22","slug":"la-red-de-accion-nephcure","status":"publish","type":"page","link":"https:\/\/nephcure.org\/es\/get-involved\/advocacy\/the-nephcure-action-network\/","title":{"rendered":"La red de acci\u00f3n NephCure"},"content":{"rendered":"
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Home<\/a><\/span> \/ Get Involved<\/a><\/span> \/ Advocacy<\/a><\/span> \/ The NephCure Action Network<\/span><\/span><\/div>\n\n
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Join the NephCure Action Network<\/h1>\n\n\n\n

The NephCure Action Network (NCAN)<\/strong> is a movement of patients with rare kidney disease and their caregivers, physicians, and partner organizations who all have one goal: to save kidneys and save lives through lasting legislative and policy improvements.<\/p>\n\n\n\n

We believe that activated, educated, and empowered patients, families, and allies are powerful voices in developing policies and procedures that optimize care and treatment for the rare kidney disease population.<\/p>\n\n\n\n

By joining this coalition, you\u2019ll be invited to attend various educational opportunities to learn how to effectively fight for rare kidney disease patients, stay informed on our latest advocacy work, and receive time-sensitive action alerts for opportunities to raise your voice and help policymakers understand what\u2019s important to those directly impacted by rare kidney disease.<\/p>\n\n\n\nJoin NCAN today<\/a>\n\n<\/div>\n<\/section>\n\n

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Sign up to get NephCure\u2019s latest updates.<\/h2>\n\n\n\nSIGN UP<\/a>\n\n\n
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