Hipofam is pleased to invite patients, families, and professionals to the 7th edition of the annual conference on hereditary hypomagnesemias. The…
The Cystinosis Group Netherlands & Flanders celebrates its 25th anniversary with a family event bringing together children and adults with cystinosis,…
Join Us in Heidelberg!
Dear friends and families living with aHUS, C3G, or IC-MPGN –
We warmly invite you to a special Family Weekend full of…
This webinar will be on March 20th, 2024 from 15.00 -16.00 CET
Exploring Patient Journeys: Enhancing healthcare services through patient-centered…
Speakers: Alexandra Cambier, Canada Josh Storrar & United Kingdom Patient’s Perspective
The FEDERG F2F Meeting marks ten years of progress in supporting and researching rare and genetic kidney diseases across Europe.
Únase a Hypofam en Valencia el 28 de septiembre para debatir sobre la hipomagnesemia hereditaria.
An opportunity for the Alport community to connect, update and discuss the latest research.
Join AIRP in celebrating 20 years of progress, knowledge, and community!
Nephie e.V. lädt zum Patientenkongress nach Dachau ein. Sie erwartet ein Programm mit Vorträgen und Austausch mit anderen Betroffenen und Experten.