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

#FHaware2020 – one week to go

#FHaware2020 – one week to go

A multi-stakeholder collaboration is critical to resolving the burden of FH. Our community is very pleased to partner with national and international stakeholders – from patient organizations to policy makers, societies and medical communities.

FH education for young medical community

FH education for young medical community

Determined to raise awareness about Familial Hypercholesterolemia among medical community, FH Europe partners with MEDizzy, an online international community of young health care professionals.

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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