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

NEWS

Homepage NEWS
Read More
Uncategorized

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…
Read More
Read More
News, Rare Disease

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…
Read More
Read More
News, Rare Disease, Uncategorized

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…
Read More
Read More
Education, Rare Disease, Uncategorized

FEDERG support the adoption of the WHA Resolution on Rare Diseases.

Earlier this year, a Coalition was formed to support the adoption of the WHA Resolution on Rare Diseases. As we…
Read More
Read More
Education, Enviroment, News, Rare Disease, Uncategorized

FEDERG strongly support the WHA Resolution on rare Diseases

May 2025 was a landmark month for RDI and the global rare disease community. The WHA Resolution on Rare Diseases was adopted, affirming…
Read More

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