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

An update about the FH Europe Board

An update about the FH Europe Board

Dec 18, 2020

A message from Jules Payne, Chair of FH Europe, and CEO of HEART UK “The time has now come for me to step down as Chair of FH Europe, a role I have been so very proud to fulfil these past four years.  I would like to thank all fellow Trustees, past and present in...

Community webinar – “Global FH Registry: ….”

Community webinar – “Global FH Registry: ….”

Nov 18, 2020

Join us for a community webinar Ever wondered what a #registry was? Curious to find out how FH registry can impact you and your family? #FamilialHypercholesterolemla (FH) is one of the most common and life-threatening inherited conditions. If you have FH, at least...

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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