Welcome to the WHST wesbite!
Information will be updated regularly on this site with access to newsletters and links to other support groups worldwide, charities and medical information. Although the site is now on-line remember it is still a work in progress and we are adding new bits and pieces all the time at the moment. I would welcome any feedback you may have about the site. You can email me at enquiries@whs4pminus.co.uk
Above all this site has been created to ensure we are all up-to-date on the latest information regarding Wolf Hirschhorn Syndrome and to help us to stay in touch. Don't forget to visit the guestbook.
Stay in touch and make this site your own!
love to all
Susan Cooper
WHS Committee member/webmaster
Daughter of founder Chris Hilder
WHS UK newsletter May 2008
Tribute to Christine Hilder
WHS UK newsletter May 2007
WHS UK newsletter February 2007
WHS UK newsletter August 2006
WHS UK newsletter April 2006
WHS UK newsletter December 2005
The newsletters open as PDF. To install the software to view PDFs click here. This is free software to download and use.
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