Forum to get advice on Foetal Alcohol Syndrome (From Banbury Cake)
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Forum to get advice on Foetal Alcohol Syndrome
2:00pm Saturday 28th July 2012 in News
Julia Brown and daughter Niamh
AN online forum for parents of children with a rare condition caused by drinking while pregnant has been launched in Oxfordshire.
Julia Brown founded the Foetal Alcohol Spectrum Disorder Trust after her adopted daughter Niamh was diagnosed.
Foetal Alcohol Syndrome (FAS) is caused by drinking during pregnancy and can cause lifelong brain damage.
In extreme cases, such as Niamh’s, sufferers are unlikely to be able to live independently.
Mrs Brown, from Finstock, said she was inspired to set up the forum – which she hopes will one day be as popular as patenting site Mumsnet – after her own early Internet searches for help drew a blank.
She said: “These days the first thing people do when they are looking for help and advice, is turn to the Internet.
“That is what we wanted to do – offer a place for people to share experiences and offer advice.”
Mrs Brown and her husband Simon adopted Niamh when she was a baby.
Niamh was five when her adopted parents realised she was slow in doing things for her age, such as crawling and walking.
After an arduous process, Niamh, now 13, was eventually diagnosed with FAS.
The forum can be reached at fasdtrust.healthunlocked.com
Comments(4)
goshua
says...
11:08am Tue 31 Jul 12
lots of excellent advise . Teaching and support resources from this are
now available free from this workshop, can be downloaded at www.fasaware.co.uk . They also have a National FASD Parent/ Carers support forum and facillitate lists of all FASD Support Groups in the UK
Surfboy
says...
9:14pm Wed 1 Aug 12
goshua
says...
10:20pm Wed 1 Aug 12
much focus on posotive solutions, early intervention's 0 too 7 , My two are Adults now , yes i had too use Canada some 23 years ago www. fasdoutreach.ca. and home tutor our children . Not much in the UK except
volantry groups , Bit of education just out . I am retired now it's been hard
that i agree on . wish you all the best for you and your family , our's even as Adults will always have FAS / FASD but have learnd control and how too live
with it, make know asumptions it's still like walking on egg shells.
All FAS/ FASD Children are different .
goshua says...
12:23am Tue 31 Jul 12
think posotive all our Children are effected in different ways.
We have Two Children one with full FAS and one FASD , both now adults
both in full employment and independant., with good parenting and support
mainly schools understanding teaching methods and support services.