Welcome to the Neonatal Hemochromatosis/Gestational Alloimmune Liver Disease (G.A.L.D.) Society

Hello and welcome to the Neonatal Hemochromatosis/Gestational Alloimmune Liver Disease Society. Whether you are researching this rare condition or have encountered it in your family, we are here for you. “We” are the families who have been on the rocky road of fear, frustration, many unanswered questions and many more blessings. This project is a combined effort of incredible women and men who dedicate their life and work to their beautiful babies and angels. We have been blessed with their love and life, however long and wherever far.

In loving memory of all the Angels, NH/GALD Society seeks to raise awareness of this rare condition by:

SPEAKING

We seek to bring attention and information to the public and the medical profession.

CAMPAIGNING

We actively campaign to promote fundraising for research of this rare condition.

CONNECTING

We provide a place and resources for those who need information about the experts in different countries and families who are willing to share their experiences.