•  
  •  
FEDERG
  • Donate
  • Menu Canvas
    • HOME
    • ABOUT FEDERG
      • WHAT WE DO
      • OURS MEMBERS
      • GOVERNANCE, STATUES & FINANCIAL STATEMENTS
      • COLLABORATIONS
    • RARE/GENETIC KIDNEY CONDITIONS
    • NEWS & EVENTS
      • UPCOMING EVENTS
      • EVENTS
      • FEDERG REPRESENTATIONS
      • MEMBERS ACTIVITIES
      • USEFUL LINKS
    • CONTACT
    • Sidebar

      Tags

      CKD Congress COVID-19 empowering patients ERN-Erknet EURORDIS HIPOFAM kidney diseases Patients Day Rare Disease trasplantation
FEDERG
Send us
an email
  • ABOUT FEDERG
    • WHAT WE DO
    •  Why our name matters
    • OURS MEMBERS
    • GOVERNANCE, STATUES & FINANCIAL STATEMENTS
    • FEDERG Strategic Plan 2026 – 2029
  • COLLABORATIONS
  • NEWS & EVENTS
    • UPCOMING EVENTS
    • FEDERG REPRESENTATIONS
    • MEMBERS ACTIVITIES
    • USEFUL LINKS
  • CONTACT
  • TESTIMONIALS
  • SEARCH

Patients Day

Homepage Patients Day

AIRG, 21st Annual Meeting in Madrid, January 17, 2026
News, Rare Disease
empowering patients, kidney diseases, Patients Day, Rare Disease

The Association for Information and Research on Genetic Kidney Diseases (AIRG-Spain) will hold its 21st Annual Meeting on Saturday, January…

11 January 2026
0
320

About Us

FEDERG is the non-profit federation of European associations of patients affected by rare and/or genetic kidney diseases.

FEDERG Homepage

Upcoming Events

  •
    World Kidney Day 2026 Thursday, 12, Mar
  • FEDERG at the European Parliament event “Safe Hearts, Safe Kidneys: Elevating Kidney Health on the EU Agenda” Friday, 27, Feb
  • Together, 20 patient organizations raise their voices for hope — better diagnosis, treatment, and research for rare genetic kidney diseases on RARE DISEASE DAY 2026 Friday, 27, Feb

Member activities

   

FEDERG Representations

   

 

Copyright ©2021-2025 FEDERG. All Rights Reserved
SearchPosts
Thursday, 12, Mar
World Kidney Day 2026
Friday, 27, Feb
FEDERG at the European Parliament event “Safe Hearts, Safe Kidneys: Elevating Kidney Health on the EU Agenda”
Friday, 27, Feb
Together, 20 patient organizations raise their voices for hope — better diagnosis, treatment, and research for rare genetic kidney diseases on RARE DISEASE DAY 2026
Wednesday, 14, Jan
Alport Syndrome Patient Information Day on September 6th, 2026!
Sunday, 11, Jan
AIRG, 21st Annual Meeting in Madrid, January 17, 2026
Tuesday, 16, Sep
Members activities Newsletter, volume 2.