For those of you who don't know, my brother has Smith Magenis Syndrome. This syndrome was only recognized in the 1980s. My brother was not diagnosed until he was 8 years old, but only because his doctors did not have a name to attach to his pattern of physical, behavioral, and developmental features. Even 30 years later, there is still much to learn about this chromosomal disorder.
The other day I stumbled upon an album called Do Fun Stuff, Vol. 1. This album was put together (by Ryan Marshall) for the sole purpose to raise money to fund research of SMS. The songs are written for children, since SMS kids are forever children, and 100% of the proceeds go to SMS research. I can get behind this effort completely and I encourage you to as well.