We are excited to announce that Guy’s and St Thomas’ Hospital in London has unveiled a beacon of hope for adults affected by complex lymphatic
From Left, Renè Haegerling (BIH Center for Regenerative Therapies and the Institute of Medical and Human Genetics at Charité – Universitätsmedizin Berlin.), Professor Miika Vikkula
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.
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La LGD Alliance Europe es una organización benéfica registrada en los Países Bajos.
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