The Moon Family

Jacob, his parents Bill and Christine, sister Ella, and brother Matthew.

"Join Jacob’s journey filled with innocence, laughter, and triumph."

The Moon Family

Jacob Moon

Current Age:
Home State:
New York
Diagnosis Date:
October 3, 2016
MPS/Sanfilippo Type:
Bill and Christine
Ella and Matthew

What it felt like when we learned our child has Sanfilippo Syndrome…

When our geneticist told us that Jacob had Sanfilippo Syndrome, we could not believe what we heard. Once we were told more about the disease, we were both filled with a deep, profound sadness. Our lives would be altered forever.


Jacob loves to jump on the trampoline and sing songs. He loves Toy Story, especially Buzz Lightyear. Jacob also enjoys eating and some of his favorite foods are pancakes, bacon, pepperoni pizza, Korean BBQ, spaghetti and meatballs, raw peppers, and nearly any type of fruit!

The hardest part of being a Sanfilippo parent is …

Seeing the judgments of other parents when Jacob is having a difficult time. Giving up some part of our normal lives either socially or professionally. Never feeling comfortable that we could leave anyone with Jacob. Knowing that every day, Jacob gets farther away from us.

Why are we asking you to donate to Cure Sanfilippo Foundation?

Cure Sanfilippo Foundation is providing hope to the thousands of Sanfilippo children across the world by funding research to find a cure for this rare disease. Join Jacob’s journey and provide us with hope that our lives can change one more time.


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Cure Sanfilippo Foundation

501c3 non-profit
(Tax ID: 46-4322131)

P.O. Box 6901
Columbia, SC 29260