To all Canadians:

Is there anyone interested in being a part of a new organization that
deals with all issues pertaining to Klinefelter syndrome/47,XXY within

The KSA organizations have existed for many years in the UK and the
United States. They deal with governmental aspects including the medical
systems, social aspects, and conferences with guest speakers.

As the United States and the UK have their different systems, Canadians
also need a system whereby all aspects of 47,XXY/Klinefelter syndrome is
addressed along with a a good list of Doctors and Endocrinologists that
give a fair diagnosis and treatment based on xxy alone and not on a male
or female template.

If anyone is interested in joining this team and helping create this
Canadian vision please let us know through this email : with the entitlement "KSA Canada".

Only serious applicants need apply, please.

Andre Lorek

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Last updated on January 11, 2015