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Home - About VASCERN - Structure and Governance - Working Groups - Rare Disease Working Groups - Hereditary Haemorrhagic Telangiectasia (HHT-WG) - Training and Education - Webinars
Hereditary Haemorrhagic Telangiectasia (HHT-WG)
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Training and Education
E-Learning Pills of Knowledge Webinars
Based on Evidence European (BEE) Meeting
First Edition | 25th May, 2023

Webinars

Our webinars are a unique opportunity for healthcare professionals and patients or caregivers to learn about rare vascular diseases from leading experts in the field. They provide an interactive forum for participants to ask questions and get answers. The webinars are recorded and can be consulted at a later date on our YouTube channel.

Results (2)
VASCERN Webinar: HHT and Nosebleeds
February 13 2023

This webinar consists of a informative presentation followed by an interactive Q&A session. Involving clinicians and patient advocates from our Hereditary Haemorrhagic Telangiectasia Working Group (HHT-WG): Prof Anette Kjeldsen, Prof Urban Geisthoff, Dr Freya Droege, Dr Ruben Hermann, Christina Grabowski.

Video in English.

VASCERN Webinar: HHT and the lungs
February 13 2023

This webinar consists of a informative presentation followed by an interactive Q&A session. Involving clinicians and patient advocates from our Hereditary Haemorrhagic Telangiectasia Working Group (HHT-WG): Dr. Hans-Jurgen Mager, Prof. Marco Post, Claudia Crocione, Christina Grabowski and Ria Blom.

Video in English.

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