CdLS Foundation UK and Ireland
The Foundation is a registered charity in the UK (no 1054033) and part of the global federation of CdLS family support groups around the world.

CdLS Foundation
106 Lodge Lane
Grays
Essex. RM16 2UL

Tel: 01375 376439
Fax: 0207 536 8998
E-mail: info@cdls.org.uk
Web: www.cdlsoutreach.org

 
 

Board of Trustees
Chairman – Alan Peaford (Essex)
Vice chairman – Charles Maynard (Warwickshire)
Treasurer – Richard Simmonds (Shropshire)
Secretary – Alison Rich (Essex)

TRUSTEES
Lorraine Hawthorne (Staffordshire), Steve Penney (Essex); Tom OíNeill (Greater Manchester); David Axtell (Suffolk); Catherine Wantling (Cheshire); Heather Young (Berkshire); Sue Tennant (South Yorkshire); Carole Dickens (Kent); SAC Representative – Professor Chris Oliver (Birmingham); John Lennard (Dublin).

 
 
Scientific Advisory Council
Medical Director – Laird Jackson, Philadelphia, USA.
MEMBERS (All USA unless stated)
Genetics – Laird Jackson, Tom Strachan (UK) Ian Kranz, Angelo Selicorni (Italy) Antonio Baldini,
Development – Antonie Kline
Dental – Richard Mungo, Doug Clemens
Speech & Language – Marjorie Goodban, Cheri Carrico
Psychology – Eileen Ahearn, Chris Oliver (UK)
Psychiatry – Thomas Gualtieri, Doug Stockwell
Gastroenterology & dietary – Kevin Kelly, Annemarie Sommer
Radiology & Imaging – Mark Kliewer
Ophthalmology – Alex Levin
Education – Mary Morse
Orthopaedic – Thomas Renshaw
 
 
Mission
The CdLS Foundation is a family support organisation which exists to ensure early and accurate diagnosis of CdLS throughout the world, promoting research, and enabling individuals, families, friends and professionals make informed decisions and plan for the affected person’s
present and future.
 
 
CdLS Foundation UK and Ireland
 
Board of Trustees
 
Scientific Advisory Council
 
Mission
 
 
 
 
 
 
 
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