The Faces of HAE

This unique tool provides helpful tips and advice direct from people living with and supporting those with hereditary angioedema (HAE) in the UK. From motivational messages to practical everyday information, the interactive wall collectively provides HAE Know How – the real life experience of the HAE community.

To view a tip, simply click on a photograph. You can submit your own tip by following the instructions below. This resource is jointly supported by CSL Behring and HAE UK.

Want to share your tips on HAE?

Please provide your tip in no more than 100 characters, and complete your details and image (optional) using the online form. Please note that your tip will be reviewed before it is accepted and displayed.*

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  • All About HAE helps with information on recognising, treating and managing this rare disease

  • HAE UK

    Online support from the association of HAE patients, which aims to improve the situation for all HAE patients in the UK

  • CSL Behring

    CSL Behring is committed to improving the quality of life for patients with rare and serious diseases. The company develops, manufactures and markets a range of products including HAE therapies.

*Tips should not mention any specific product or convey any positive or negative opinion on a company or their products. The tip is not intended to replace the advice and recommendations given by healthcare professionals. The information you provide will only be used for the purposes of this website and will not be disclosed to third parties.
Date of preparation: February 2017