About KS&A

What began in 1989 as the effort of one concerned individual to locate information and support has grown into an international organization forcused on Knowledge Support & Action.  KS&A is the nation’s oldest and largest non-profit organization addressing the needs of the approximately 1 out of 500 individuals who were born with one or more extra X and/or Y chromosomes, as well as their families and the clinicians, educators and research scientists serving them. 

Currently in its fifteenth year of continuous operation, KS&A’s efforts have resulted in positive change. We have educated countless numbers of persons about X and Y chromosome conditions, ranging from expectant parents who just received news of a “genetic irregularity” to top medical professionals, educators, health writers and government officials.  We have helped to reduce the amount of mis-information and stigmatization concening these conditions, and helped advance efforts to find improved and more affordable diagnosis, treatment and intervention services.  As a result of our efforts, many children, adolescents and adults with these conditions enjoy more fulfilling and productive lives in their communities.

The conditions we address our present from our national headquarters in Southern California, and with a 100% volunteer staff and leadership team located all across the U.S. and Canada, include 47,XXY; Klinefelter syndrome; Trisomy X; 47,XYY syndrome and the approximately 20 additional variations involving additional X and/or Y chromosomes and mosaicism.

To learn more about KS&A, read our Mission Statement or get to know our Executive Officers, Board of Directors, Scientific Advisory Committee and Volunteer Staff.