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.
When: 2 nights, 3 days 2013
Venue: Dukes Barn, Derbyshire.
Cost: £80 for those with KS or under 19, £135 for other Members, £310 for Non-Members
Please book early as the weekend is filling up fast!! Our April Weekend was a great success – and the sun shone as us!
There is more information about Activity Weekends under the Read more.... link below.
Contact me as soon as possible if you want further information or wish to book a place by phone on 01629 534402 or email@example.com
When: 2014 Date to be confirmed.
Venue: To be confrmed.
Friday night pre-conference get-together: To be confirmed.
Conference Organiser wanted
Voluntary post - for more details contact WebAdmin@ksa-uk.net