Author name: Werner Kratz

Event, VAS

Strong networking at DiGGefa 2026

At the 7th DiGGefa annual meeting in Freiburg, radiology, paediatric surgery, genetics and psychosocial care came together at one table – with patient organisations right in the middle. What we are taking home for networking among Swiss centres.

Swiss Patient Forum 2026
RareDisease

Swiss Patient Forum 2026

How can co-creation with patients succeed in research and healthcare? Impressions from the Swiss Patient Forum 2026 in Bern – and why the lived experience of those affected is genuine expertise.

Tag der Seltenen Krankheiten in Bellinzona
RareDiseaseDay, VAS

Rare Disease Day 2026

On 27 February 2026, we will have our own stand at the national conference in Bellinzona. The theme of “collaboration” is exactly what we stand for: across specialties and on an equal footing with those affected.

VAS, Web

Multilingual Website

Vascular malformations know no language borders – and from now on, neither does our website. It is now available in German, French, Italian and English.

VAS

Statement on the BSKG

The Swiss Angiodysplasia Association welcomes the planned Federal Act on Rare Diseases (BSKG). In our statement, we argue for a publicly accessible data catalogue and special protection for sensitive images and medical findings.

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