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Organisation:National Fetal AntiConvulsant Syndrome Support Group 

Comment:

It has long been realised that the frequency of various congenital birth defects is increased two to three times in babies of mothers who took anticonvulsant drugs in pregnancy. The major problems encountered are diverse, including spina bifida, cleft palate, congenital heart disease, kidney abnormalities and limb defects.
The National Fetal AntiConvulsant Syndrome Support Group aims to provide support and advice to families with children affected by the syndrome and professionals involved with children affected by the syndrome, raise awareness of the syndrome, and ensure that future mothers are aware of the potential risks.
The group provides information and support for affected families, and can put families in touch with each other for mutual support. To find a group close to your area contact Rheane O'Neill on 01158-406517 (e-mail: [email protected]). Information packs are available - any parents who would like to receive a parent pack, or professionals wishing to obtain a professional pack, contact head office. Any professionals who wish to obtain copies of research material should contact Ronnie Rutter on 01461-206870. 

Phone:01461-206870 
Fax:01461-206870 
Contact name:
C.R. Rutter 
Address:

PO Box 7416

Annan
Dumfriesshire
DG12 5YH
View map 

Internet:

www.facsline.org  

Email:
[email protected] 

Who is it for:

Families and children affected by the Syndrome 

How to Contact:

Contact the National Fetal AntiConvulsant Syndrome Support Group direct 

Opening Times: OpenCloseOpenClose 
Mon 0900 1700  
Tue 0900 1700  
Wed 0900 1700  
Thr 0900 1700  
Fri 0900 1700  
Sat    
Sun    
Ansaphone available at all times

Record updated:26 Jan 2007 


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National Fetal AntiConvulsant Syndrome Support Group phone: 01461-206870 or email: [email protected]