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Susana Carvajal Arjona

Homepage Susana Carvajal Arjona

FEDERG BOARD 2024-2026

Uncategorized

This is the Board of Directors team that continues the work of FEDERG management from 2024 to 2026 after the…

1 August 2024
0
3899

Representation of FEDERG at the ERA Congress, Stockholm from May 23 to 26.

Rare Disease
CKD, EURORDIS, Rare Disease

From May 23 to 27, the ERA European Renal Association Congress took place in Stockholm. Representatives of patients and members…

23 June 2024
0
1916

FEDERG at the 47th Congress of the AENP Spanish Association of Pediatric Nephrology, May 2024.

Education, Rare Disease
CKD, kidney diseases, Rare Disease, trasplantation

Susana Carvajal Arjona (FEDERG, hipofam) Mireya Carratalá (FEDERG ASHUA)

25 May 2024
0
2359

FEDERG in 53rd Congress of the Spanish Society of Nephrology 2023.FEDERG in

Education, Rare Disease
EURORDIS, HIPOFAM, Rare Disease

From November 11 to 13, Palau de Congresos Palma de Mallorca 2023. Within the framework of the 53rd Congress of…

11 November 2023
0
2040

FEDERG participation at ERA Congress 2023

Rare Disease
EURORDIS, HIPOFAM, Rare Disease

Date:               15-18 June 2023Venue:            MICO, MilanAttendees:      Tess Harris (President, FEDERG) and Susana Carvajal (Secretary of FEDERG) Tess Harris, FEDERG President,…

18 June 2023
0
1195
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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

   

 

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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.