The mission of the SMS Research Foundation is to advance scientific research leading to innovative treatment options for people living with Smith-Magenis Syndrome...
We fund only the best, most comprehensive SMS research projects along with the best and brightest scientists focused in this area. Through this science, SMS Research Foundation is committed to improving the lives of children around the world...
…live births in the US are affected by SMS. Identified only in 1982, the SMS Research Foundation is working tirelessly to fund research to improve the treatment options and lives of SMS children.