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

Publication of FH Global Call to Action

Publication of FH Global Call to Action

FH Europe, the European FH Patient Network, and the European Atherosclerosis Society (EAS) collaborate with global stakeholders to tackle the global burden of Familial Hypercholesterolaemia (FH) FH Europe and the EAS announced today the publication of a Global Call to...

Announcing Magdalena Daccord as FH Europe new Chief Executive

Announcing Magdalena Daccord as FH Europe new Chief Executive

We are pleased to announce that Magdalena Daccord has been appointed as our new Chief Executive. She officially started on Nov 1st 2019. Chair of the Board of Trustees, Jules Payne commented: "On behalf of myself and the Board of Trustees, we very much welcome...

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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