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

Vote for Thanos at the EURORDIS Black Pearl Awards!

Vote for Thanos at the EURORDIS Black Pearl Awards!

Marking Rare Disease Day 2021, the Eurordis Black Pearl annual awards event will take place on the 24th February to recognise the outstanding achievements and celebrate the exceptional work of people making a difference for the rare disease community. The black pearl...

Welcome to our new Chair – Giovanni Nisato

Welcome to our new Chair – Giovanni Nisato

We are delighted to welcome our new Chair, Giovanni Nisato. Giovanni is passionate about health, sustainability, and human-centric innovation. He holds a PhD in physics and gathered 20 years of international experience working at NIST (US), Philips Research (NL), CSEM...

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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