FASD (Foetal Alcohol Spectrum Disorder) can have a serious, long-term impact on a baby’s growth and development. Around 7,000 (1 per cent) of UK babies have FASD. It’s important that foster carers are aware of the condition and how it may affect a child’s development, learning and behaviour.
FASD is a spectrum disorder or umbrella term for a range of defects which a baby can suffer if their mum drank alcohol while pregnant. It is one of the leading causes of learning disability in the UK and one of the leading causes of birth defects in newborn babies. The individual conditions under this umbrella term are:
Sometimes FASD is detectable at birth, especially if severe and life-threatening.
FASD is often compared to autism because of the scale of different defects within the spectrum. Some babies with FASD may have severe, life-shortening symptoms which can be detected at birth, while others will show the effects much later in life. If parents and foster carers know the signs to look out, it means a child can be properly diagnosed. Early diagnosis limits the impact the condition will have on their long-term learning and development.
FASD can have a wide-ranging impact on a newborn’s health and development. When alcohol passes into the foetus, it circulates through the bloodstream, killing brain cells and damaging the nervous system. It can also cause abnormal growth defects and facial disfigurement – all through exposure to alcohol.
Some of the most common defects and symptoms caused by FASD include:
Not all children will have the same symptoms and, even if they do, it may still affect their quality of life differently. Among the most difficult FASD defects to spot are neurological problems, which could hinder a child’s learning, development, behaviour and relationships in later life.
If FASD isn’t detected at birth, the condition gets more difficult to spot and diagnose correctly as a child gets older. An accurate and timely diagnosis can vastly improve a child’s chances of living a normal life, so it’s important that foster carers know some of the signs to look for.
If you have concerns about your child, it’s always worth speaking to their doctor, as well as their social worker. They are best placed to look into the child’s family and medical history.
Given the number of children now born with FASD, there is a growing number of support groups and resources. Providing help and advice for children and their families, these support networks are invaluable in helping a child cope with their condition.
|The National Organisation for Foetal Alcohol Syndrome is the UK’s leading organisation dedicated to supporting people affected by FASD. It advocates for better public awareness about the dangers of drinking while pregnant, and provides a support network for people living with alcohol-related birth defects. NOFAS also offers free and comprehensive online training for parents and carers on how to provide help for a child suffering from FASD.
|FASD Network UK
|FASD Network UK is a social enterprise which works with local authorities to offer training and support to foster carers, adoptive parents and birth families who are raising children with FASD. It can provide local training and information to foster carers across the north of England.
|An FASD learning resource, offering essential information on the various alcohol-related birth defects caused by the condition, as well as links to additional resources and accredited training courses.
|A support network for those affected by FASD, as well as their parents and carers. The FASD Trust runs a confidential helpline for those living with FASD or looking for information on the condition. Just call 01608 811599.
FASD can have a significant impact on a child’s life, both physically and psychologically. National Fostering Group provides excellent training and support for carers of children with special needs, empowering them to provide the help and support their child’s needs both now and in the future. We’re also here for you every step, providing 24/7 support to all our foster families.