Welcome

EGS / GalNet Webinar 2020

In 2020, due to all COVID-19 measures, we decided to have an online Zoom Webinar for Galactosaemia patients, parents, family and professionals instead of our ‘normal’ EGS – GalNet Meeting for the EGS and GalNet Country representatives.

Click on the buttons below for the program and the recordings and presentations of the webinar.

Members

The EGS is an umbrella society of national Galactosaemia patient organizations.
Members are:
Austria, Belgium, Denmark, Estonia, Germany, France, Ireland, the Netherlands, Norway, Portugal, Spain, Switzerland, United Kingdom.
We represent more than 800 patients across Europe.

Aims and goals

Share information, promote awareness and stimulate research into Galactosaemia within Europe