Working to raise awareness of Klinefelter's Syndrome

and to provide help and advice to all those affected

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My KS Story My KS Story

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Date added:07/04/2011
Date modified:01/31/2012
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Iain W McKinlay 2010

The KS Story
You are not alone

AN INFORMATIVE GUIDE & FURTHER STUDY

The KS Story is the culmination of twelve years ongoing study and an emotional journey through the workings of the congenital chromosome condition Klinefelter’s Syndrome (KS).

The book was created primarily as a conduit to respected support groups, medical specialists and research units, with a chapter devoted to further study, including a comprehensive support address and online section and a selection of books, research papers, medical journals and scientific magazines.

The book also offers a glimpse into the various aspects of Klinefelter’s Syndrome; showing how it affects individuals and those who love, care and treat them.

The KS Story has been compiled by a person with Klinefelter’s Syndrome (karyotype: 47,XXY), from reputable medical, research and support group sources, and with the help and support of several UK and international scientists in the fields of biology, cytogenetics, endocrinology, neuroscience and sexology.

To balance the overwhelming amount of data there is a degree of comic relief in the writing, with a sprinkling of cartoons.

All that is asked, is that you please put aside any preconceived ideas or stereotypes and view the guide with a respectful and open mind.

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2012 Annual Conference & AGM

When: Eaxct date still to be confirmed probably third Saturday in September 2012
Venue: The South of England.
Cost: tbc
Speakers: tbc

More information will be added as soon as we have agreed on a location, venue and date. 

KSA Activity Weekend 2012

 

For forms please contact Alison Bridges on 01629 534402 or by email: activityweekends@ksa-uk.net

When: 2 nights, 3 days 2012
Venue: Dukes Barn, Derbyshire.
Cost: £75 for those with KS or under 19, £130 for other Members, £300 for Non-Members.

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