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• name: description content: FEDERG is the non-profit federation of European associations of patients affected by rare and genetic kidney diseases.
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• https://federg.org/contact/
• http://federg.org/tel:24268688888
• https://federg.org/
• http://federg.org/#
• Learn more about our work
• Find out who our members are
• https://federg.org/about-federg/governance/
• https://federg.org/about-federg/collaborations/
• https://federg.org/rare-genetic-kidney-conditions/
• https://federg.org/news/
• https://federg.org/events/
• https://federg.org/federg-representations-newsletters/
• https://federg.org/members-activities-newsletters/
• https://federg.org/useful-links/
• CKD
• Congress
• COVID-19
• empowering patients
• ERN-Erknet
• EURORDIS
• HIPOFAM
• kidney diseases
• Patients Day
• Rare Disease
• trasplantation
• https://federg.org/why-our-name-matters/
• https://federg.org/federg-strategic-plan-2026-2029/
• FEDERG
• World Kidney Day 2026
• FEDERG at the European Parliament event “Safe Hearts, Safe Kidneys: Elevating Kidney Health on the EU Agenda”
• Together, 20 patient organizations raise their voices for hope — better diagnosis, treatment, and research for rare genetic kidney diseases on RARE DISEASE DAY 2026
• https://federg.org/wp-content/uploads/2026/02/Summerfederg-members-activities-Newsletter-no2.pdf
• https://federg.org/wp-content/uploads/2026/02/RREPRESENTATIONS-2026-1.pdf
• Search
• Posts
• Alport Syndrome Patient Information Day on September 6th, 2026!
• AIRG, 21st Annual Meeting in Madrid, January 17, 2026
• Members activities Newsletter, volume 2.

• https://www.linkedin.com/company/federg/
• https://www.facebook.com/federg
• https://twitter.com/FedergAisbl
• https://www.instagram.com/federg2025?igsh=MW85bTM5N3FIMmFheA==
• https://www.facebook.com/profile.php?id=61560101372996

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