Félag um meðfædda ónæmisgalla

A patient advocacy association focused on congenital immunodeficiencies. The site includes a contact page inviting individuals to join as members by providing name, address, and email, and notes funding support from WIN-World Immunodeficiency Network to open the site. Félagið um meðfædda ónæmisgalla, also known as Lind, is an organization founded on May 11, 2002, dedicated to supporting individuals with primary immunodeficiency (Ónæmisgalla). Its objectives include promoting prevention, diagnosis, and treatment of congenital immunodeficiencies, raising awareness, providing education, facilitating experience sharing among affected individuals and families, improving social conditions, supporting research, and collaborating internationally. The organization is affiliated with NMPI (Nordic Meeting for Primary Immunodeficiency) and IPOPI (International Patient Organisation for Primary Immunodeficiencies). It is a member of Astma og ofnæmisfélagið and Umhyggja. The organization aims to support affected individuals and their families, promote research, and foster international cooperation.