The Tristan Project is the continuing journey of my child with Albright Hereditary Osteodystrophy (AHO). He has osteoma cutis, developmental (severe speech delays associated with PDD-NOS, a form of Autism Spectrum Disorder (ASD)) and growth delays, and pseudohypoparathyroidism type 1a. Many of you accompany me on this journey, and what I put together now on my blog is a pictorial sequence of events from the beginning. The story is pulled from emails and Facebook updates I provided along the way. The Tristan Project in this blog is a way to share what my husband and I encountered related to Tristan’s condition. My hope is this journey will help others who could be at the beginning or an early stage of a similar journey. It also helps me see just how far Tristan and our family have come as a team. I am indebted to my friends and family for their generous and encouraging support along the way.