FH Europe News

Can you imagine living on no more than 20 grams of fat a day? This is the reality for people living with Familial Chylomicronaemia Syndrome (FCS), as it represents a crucial way for managing their disease and symptoms. On 19 January 2023, FH Europe, in partnership...

Welcome to the new member of the Network, Action FCS from the UK, who support and advocate for people with familial chylomicronaemia syndrome (FCS). As we kick off the new year with a long awaited webinar on FCS, we have some exciting news to share. After a very...

This year is very important to FH Europe. On the horizon, we have some key structural changes and significant potential for growth for which we have been preparing for some time … while ensuring that after 3 years of external factors affecting what we do and how we do...

In the December edition of FH Europe’s Heart Beat newsletter you’ll find news of the following: FH Europe President´s review of the year. Important information about “FH and Women” Survey. Interview with Vlastimil Válek, Czech Health Minister, on a European Action...

As the year draws to an end, we are entering the festive season. Before we start considering resolutions for the New Year, we are delighted and proud to share with you some of our achievements over the past year. Read the message from FH Europe’s President, John...