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

FEDERG REPRESENTATIONS

Homepage FEDERG REPRESENTATIONS

 

About Us

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

FEDERG Homepage

Latest News

  •
    Alport Syndrome Patient Information Day on September 6th, 2026! Wednesday, 14, Jan
  • AIRG, 21st Annual Meeting in Madrid, January 17, 2026 Sunday, 11, Jan
  • Members activities Newsletter, volume 2. Tuesday, 16, Sep

Tags

CKD Congress COVID-19 empowering patients ERN-Erknet EURORDIS HIPOFAM kidney diseases Patients Day Rare Disease trasplantation
Copyright ©2021-2025 FEDERG. All Rights Reserved
SearchPosts
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.
Tuesday, 16, Sep
FEDERG support the adoption of the WHA Resolution on Rare Diseases.
Monday, 9, Jun
FEDERG strongly support the WHA Resolution on rare Diseases
Thursday, 19, Sep
Fighting for our federation Federg f2f Members meeting September 14 Martorell