Member Organisations

The European FH Patient Network actively working together to secure early identification and diagnosis of FH patients to prevent early cardiovascular disease.

Countries

The European FH Patient Network actively work together to secure early identification and diagnosis of FH patients to prevent early cardiovascular disease.

Member Organisations

Countries

who we are

FH Europe consists of multiple FH patient groups across Europe. By sharing information & best practice we aim to secure early identification and diagnosis.

More info

about fh

Familial Hypercholesterolaemia (FH) is an inherited genetic condition that leads to levels of cholesterol that are much higher than that of the general population.

More info

Our members

Our members are made up of organisations and individuals that represent FH patient groups within their specific European country.

More info

Latest News

FH Europe E-Flash : December ’18

FH Europe E-Flash : December ’18

The December edition of the FH Europe e-Flash rounds up the latest news Stories include: FH Europe Third Annual Network Meeting – Paris, November 2018 New members’ area on FH Europe website launched News of FH Foundation Global Summit FH Global Call to Action...

Anhet’s awareness video now launched in English

Anhet’s awareness video now launched in English

At FH Europe's annual meeting in Paris in November 2018, members were moved by the awareness-raising video that Anhet, the French FH patient association, produced. English sub-titles were added to the video which you can view below: 

FH Europe is registered as a charity; Charity number 1170731, registered in England and Wales.

FH Europe is registered as a charity; Charity number 1170731, registered in England and Wales.

FH Europe is supported by an educational grant from Amgen Limited, Sanofi, Regeneron, Akcea Therapeutics Inc. and Amryt
Site by: Vovi Web Design