ABOUT US
About The Luca Hill Acrania and Anencephaly Foundation
The Luca Hill Acrania and Anencephaly Foundation was created by the parents of Luca Joseph Hill in honor of their son. Luca was diagnosed with Anencephaly and Acrania in 2014. He lived a life of celebration and graced everyone with his bright beautiful light on February 11, 2015. You can read more about Luca's amazing life and his parents journey with their son by visiting their blog and the Luca Hill page.
Our Mission
The Luca Hill Acrania and Anencephaly Foundation is dedicated to the families and communities affected by Acrania and Anencephaly. Our mission is to create an environment for families, communities, and medical professionals to seek accurate information on Acrania and Anencephaly, find a wealth of support, understand the joy and impact of carrying to term, and raise much-needed funding to further Anencephaly and Acrania research.
