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

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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

Join our Board of Trustees

Join our Board of Trustees

May 4, 2020

FH Europe is a young yet very successful, energetic and ambitious Patient Network. We represent 24, soon to be 25, patient organizations across the whole of Europe and are still growing. As a Network, we are actively working together to secure early identification and...

FH Europe joins the World Heart Federation and EURORDIS

FH Europe joins the World Heart Federation and EURORDIS

Apr 17, 2020

We are pleased to announce very positive and important updates. On April 17, 2020, FH Europe had been welcomed as an official member to the World Heart Federation - powerful global community of organizations dedicated to the treatment, prevention and control of...

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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