Network 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.

Network 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.

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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.

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Our NETWORK

The network is made up of organisations and individuals that represent FH patient groups within their specific European country.

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Latest News

Call for EU Plan on CVD

Call for EU Plan on CVD

FH Europe joins forces with European and international health organizations to call for action to address the increasing burden of cardiovascular disease (CVD). Rochester, UK 16 June 2021: Today, 12 European and international health organizations signed a joint...

FH Europe Heart Beat News – May 2021

FH Europe Heart Beat News – May 2021

Welcome to FH Europe’s very first edition of Heart Beat, a monthly newsletter from the European patient community sharing updates from the network, events, patient support information, clinical research news, and industry updates. This month we reflect upon FH...

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
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