CANADIAN ORGANIZATION
INFORMATION
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
Canada?
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 :
andre.alorek@gmail.com with
the entitlement "KSA Canada".
Only serious applicants need apply, please.
Also, could all list owners who read this please pass this on to their
respective lists, please - Linda Morgan, Jim, and members of the other
KS&A lists - peds, etc., and anyone that I may have failed to
remember.
Andre Lorek & Vaughn Hambley
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Last updated on June 5, 2010