Mental Health Series
Register Now! Join our insightful webinar series focused on empowering patients and their families with valuable knowledge and self-help techniques to address mental health issues
Tracy Milne
24 Agosto 2023
Register Now! Join our insightful webinar series focused on empowering patients and their families with valuable knowledge and self-help techniques to address mental health issues
The International Scientific Conference on Complex Lymphatic Anomalies brings together leaders in the field to discuss the latest research on CLAs. It will also foster
LGD Awareness Day is an opportunity to raise awareness of complex lymphatic anomalies (CLAs). To help connect patients and their families to peers, networks of
Lymphatic Malformation Institute and the LGDA welcome LOIs for the Alfie Milne Young Investigator grant. It is a one-year award designed to support early career researchers,
Support Team CLA Warriors Since 2015, the LGDA have partnered to participate in UPenn Orphan Disease Center’s annual Million Dollar Bike Ride (MDBR) event –
Celebrating Rare Disease Day We are Many – We are Strong – We are Proud Having something wrong with you, feeling ill, facing a difficult
Rare Disease Day is the globally-coordinated movement on rare diseases, working towards equity and access to diagnosis and therapies for people living with a rare disease.
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
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LGD Alliance Europe è un ente di beneficenza registrato (ANBI) nei Paesi Bassi.
Registrazione della Fondazione: 63159333
RSIN o codice fiscale: 855117540