Understanding Complex Lymphatic Anomalies
An introduction to complex lymphatic anomalies. A guide for patients and families (January 2023 Version)- download your copy here.
Tracy Milne
24 janvier 2023
An introduction to complex lymphatic anomalies. A guide for patients and families (January 2023 Version)- download your copy here.
Hello! My name is David Williams. I have been appointed as the Chair of the Board. I am British, with a Welsh name, but
Our 2021 Annual Report is out now. It highlights our accomplishments and new projects that further our mission. Read it here. Annual Report 2021
News from the LGDA Europe community Celebrating LGD Awareness Day 2022! LGD Awareness Day is an opportunity for the community to celebrate this special day.
Our communications team is looking for new volunteers Are you the person we are looking for? Do you have any expertise (or interest) in one
Join our cause and support us. Help us to continue supporting the patient’s community of rare lymphatic diseases in Europe. Today and in the future.
We are very pleased to introduce a brand new publication: the VASCA Magazine! A co-operation of five patient organisation in Europe representing patients with rare vascular anomalies. Download the PDF
Sirolimus has been used in a number of studies as an experimental drug for the treatment of vascular malformations. Especially for patients with lymphatic and
The VASCERN Vascular Anomalies (VASCA) Working Group has formulated a statement concerning SARS-CoV-2 vaccination for patients with vascular malformations General statement: Follow the national safety
The VASCERN (European Reference Network on Rare Multisystemic Vascular Diseases, specifically the VASCA working group) wrote a statement on Covid-10, initated by patient advocacy groups
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LGD Alliance Europe est une organisation caritative enregistrée (ANBI) aux Pays-Bas.
Enregistrement de la fondation : 63159333
RSIN ou numéro d’identification fiscale : 855117540
