Helpline 0300 111 4748
Helpline 0300 111 4748
Helpline 0300 111 4748
The Klinefelter’s Syndrome Association (KSA) was formed on 21st December 1990 by parents, Sue and David Cook, and a KS/XXY adult, Steve Hammett.
It was incorporated as a charity in 1996. Sue and David remained as very active trustees until 2018. All are still members.
The KSA is run by trustees who make up a National Executive Committee (NEC). They are helped by non-trustee volunteers. It has no paid workers.
The KSA is funded mainly through membership fees and donations.
The aims of the KSA are:
The KSA vision is of universal recognition, support and understanding of KS/XXY.
Through our website and helpline, we provide information and support for all affected by KS/XXY including families, medical professionals, teachers and anyone else who comes into contact with people diagnosed with KS/XXY.
National Helpline: 0300 111 47 48
Our very grateful thanks to Childline for allowing us to link extensively to their website.
© 2022 Klinefelter’s Syndrome Association
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