The FH Early Logo

Survey and focus groups

Help improve future care and support for people living with FH

For Patients

Do you live with Familial Hypercholesterolaemia (FH)?

Share your experience of living with Familial Hypercholesterolaemia

As part of the EU-funded FH-EARLY project, we invite people living with FH to take part in a short questionnaire about their experiences, needs, and daily life with FH.
 
Your input will help develop new tools and approaches to improve the management of FH and support the prevention of cardiovascular disease.
20 min
To complete
6
Languages
Private
Research use only

The questionnaire takes up to 20 minutes to complete. Your responses will remain confidential and will be used for research purposes only.

You can skip any question you do not wish to answer.

Help us reach more people

If you know someone living with FH, please share this page or the survey links with them. Every response helps strengthen the FH community and improve future support for people and families affected by FH.

Help us spread the word by sharing the message below on your social media channels:

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Do you live with Familial Hypercholesterolaemia?

FH-EARLY is inviting people living with FH to complete a short questionnaire about their experiences, daily management, healthcare support, lifestyle, and information needs.

The survey takes up to 20 minutes and is available in several languages. Responses are confidential and will be used for research purposes only.

Your experience can help improve future care and support for people living with FH and their families.

Take the survey here:- https://fh-early.eu/survey-and-focus-groups/

#FamilialHypercholesterolaemia #FH #FHEARLY #PatientExperience #CardiovascularHealth #InheritedLipidDisorders

For Healthcare professionals and lipid clinics

Support the FH-EARLY Survey

Healthcare professionals, lipid clinics, and patient organisations can support the FH-EARLY survey by sharing the information with eligible patients.

These materials can be displayed in clinics, shared during consultations, circulated by email, or posted on social media to help reach more people living with FH.

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The project is funded by the EU
Funded by the European Union. Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or HaDEA. Neither the European Union nor the granting authority can be held responsible for them.
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