Do you need to talk to someone? 0845 603 5338

 

 

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. 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

Dr John Carey's Research

read moreRead More

 

 

 

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...

read moreRead More

 

 


 

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

Our web site read morearrow

NEW LINKS ADDED

 

 

 

Email your photos and news for the next newsletter to...

enquiries@whs4pminus.co.uk

 

 

Click here to leave a comment on our forum

***PLEASE NOTE***

If you register to use the forum you will not be able to post until your account is activated. Each post is also moderated before it is published. This is usually done within 24 hours.

 

 

 

Wolf Hirschhorn Syndrome