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Wolf Hirschhorn Syndrome

Welcome to the official site of the Wolf Hirschhorn Syndrome Trust for the UK and Ireland.

The Trust achieved charitable status in 1994 however the original support group was founded in 1978 by the late Chris Hilder who wanted to ensure families caring for someone with WHS could access information - both medical and practical. The primary aims of the Trust remain the same as Chris' and over the years the group has grown and made important links with doctors and other families all over the world.

A national meeting is held once every two years and a newsletter is sent to members quarterly. The group offers advice, support and friendship to anyone with an interest in Wolf Hirschhorn Syndrome and we hope to hear from you soon.


First time here?

First time here?
Our newsletters are here read moreRead More

The latest medical research results

National Meeting 2007- keynote speech

Dr John Carey's Powerpoint presentation

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Take time to visit our guest book

Visit our message board

Have you got a question? Do you have a suggestion? Maybe you could give some advice...

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Make a donation to the Wolf Hirschhorn Syndrome Trust online by clicking on the justgiving logo

 

Welcome to whs4pminus.co.uk

First Time here? read morearrow

Latest booklets are here read morearrow

Latest medical articles read morearrow

Launch of our web site read morearrow

NEW LINKS ADDED

 

 

UKC BEHAVIOURAL STUDY INITIAL FINDINGS - presentation shown by peter McGill at National Meeting 2009 - DOWNLOAD

 

SPRING 2009 NEWSLETTER

CLICK HERE TO DOWNLOAD

 

Click here to leave a comment on the message board

 

 

Click HERE to see the Twitter run-down of what happened at the 10th WHS UK National Meeting held in Northampton May 1 - May 3, 2009

 

MORE FROM THE NATIONAL MEETING TO BE ADDED SHORTLY

 

Wolf Hirschhorn Syndrome