The Isaac Foundation was formed to find a cure for my son's progressive and very rare disease, MPS VI. For more information, please visit us at www.theisaacfoundation.com.
Mom and Gabriel snuggling for our movie (and Gabe’s Teddy Bear!) (Taken with instagram)
-
mimimph liked this
-
anaritacardoso liked this
-
theisaacfoundation posted this
