My Nonprofit Reviews

Our son is 8 years old and was diagnosed with Alagille Syndrome at just 2 months old. He has undergone two transplants and also has pulmonary stenosis. From the moment of his diagnosis, we began searching for support and discovered the ALGSA. Since day one, they have been an incredible source of help for our family. Today, I am an active member of the ALGSA and a witness to the tremendous impact it has had—economically, emotionally, and educationally—on a global scale and within the Spanish-speaking community. Their immense support has transformed countless lives, including ours.