Newsletter February 2023
Celebrating Rare Disease Day We are Many – We are Strong – We are Proud Having something wrong with you, feeling ill, facing a difficult
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
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
Sign up for our newsletter and receive news and other important information.
We don’t use a postal address or telephone number. Please use the contact page to get in touch with us.
LGD Alliance Europe is a registered charity (ANBI) in the Netherlands.
Foundation registration: 63159333
RSIN or tax nummer: 855117540