My Nonprofit Reviews

Because of MAGIC, my son is thriving today. He was one of the first members with Russell-Silver Syndrome and, now, Growth Hormone Deficiency. We have all learned so much about his syndrome and found support from people all over the world. The yearly convention used to be a great way for him to see others just like him. (He is older now, so he does not want to attend anymore.) There have been many ups and downs, but the people at MAGIC and its members are like a big family to us. And the guidebook from the RSS/SGA Research and Education Fund is a timeless resource with everything we need to know. MAGIC will always be a part of our lives.