EKHA–European Kideney Forum — Kidney Health Disparities, Adresssing the Gender Gap, October 13, 2026
FEDERG at the European Kidney Forum: Addressing the Gender Gap in Kidney Health FEDERG, the Federation of European Associations of…
EKPF Annual Summit, October 7 and General Assembly October 8, 2026
EKPF Annual Summit 2026 | EKPF The EKPF Annual Summit 2026 will take place in Krakow, Poland, on October 7,…
58th ESPN Annual Meeting, September 30 – October 03, 2026
FEDERG, the Federation of European Associations of Patients with Rare and Genetic Kidney Diseases, will participate in the 58th European…
EKHA Webinar From Care to cure, an EU wide Network, Advancing Rare Kidney Disease healthcare and research, July 7, 2026
FEDERG at the EKHA Webinar: From Care to Cure – An EU-wide Network Advancing Rare Kidney Disease Healthcare and Research…
World Kidney Day 2026
The Importance of World Kidney Day for European Rare Genetic Kidney Disease Patient Associations World Kidney Day is a key…
FEDERG at the European Parliament event “Safe Hearts, Safe Kidneys: Elevating Kidney Health on the EU Agenda”
A High-Level World Kidney Day Event at the European Parliament “Safe Hearts, Safe Kidneys: Elevating Kidney Health on the EU…
Together, 20 patient organizations raise their voices for hope — better diagnosis, treatment, and research for rare genetic kidney diseases on RARE DISEASE DAY 2026
Across communities and countries, 20 patient organizations have come together with one shared purpose: to change the future for people…
Alport Syndrome Patient Information Day on September 6th, 2026!
We are delighted to invite you to a special Alport Syndrome Patient Information Day on September 6th, 2026! This day…
AIRG, 21st Annual Meeting in Madrid, January 17, 2026
The Association for Information and Research on Genetic Kidney Diseases (AIRG-Spain) will hold its 21st Annual Meeting on Saturday, January…
Members activities Newsletter, volume 2.
We are proud to present the latest newsletter from FEDERG, the federation uniting European associations of patients affected by rare…