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

Appointment of 5 New Trustees

Appointment of 5 New Trustees

We are absolutely delighted to share the appointment of 5 new members to the FH Europe Board of Trustees The new Trustees, together with the existing ones, bring to the FH Europe Network a great diversity of experience and expertise areas. They represent understanding...

Heart Patient Groups Unite in Call to #JustGo in Cardiac Emergencies

Heart Patient Groups Unite in Call to #JustGo in Cardiac Emergencies

Heart Patient Groups Unite in Call to #JustGo in Cardiac Emergencies One of the unintended consequences of COVID-19 is that people suffering heart attacks and strokes delay seeking medical help, resulting in worse outcomes. Heart attack and stroke victims worldwide...

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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