FASD is the term used to describe the lifelong impairments that can result from brain damage caused by alcohol exposure before birth. These impairments might become evident as difficulties with physical activities, speech and language, memory, learning and behaviour issues.
Working towards a better future
Offering support, education, training, research and information on
Foetal Alcohol Spectrum Disorders (FASD).
WELCOME TO FASD AWARENESS
FASD can be the outcome in individuals whose parents were either not aware of the dangers of alcohol use during pregnancy or were not being supported to stay healthy and strong during pregnancy.
Our main aim is to support the prevention of alcohol exposed pregnancies and to improve the quality of life for those living with Foetal Alcohol Spectrum Disorders (FASD) and their parents and carers. Our vision is to be a strong and effective voice for individuals and families living with FASD, while supporting initiatives across the UK to promote prevention, diagnosis, intervention and management.
We are supported by individuals and companies alike, such as Lloyds, SEIB Insurance Brokers, Allied Fabrications Ltd, Tunstall Jubilee Foundation, and many more.
LAYLA'S LIFE, MY WORDS: AN INSIGHT INTO THE WORLD OF A CHILD WITH FOETAL ALCOHOL SPECTRUM DISORDER
Shushma Jain sheds light on ‘invisible disabilities’ such as FASD, Cystic Fibrosis, anxiety, sensory processing disorder and attachment parenting. She reveals what strategies she uses to support her child and why she took the decision to home-educate her indefinitely last year.
FASD AWARENESS appreciates all donations. Your donations help fund monthly FASD support groups and provide training within schools. In addition, we will be able to continue to grow awareness of FASD.
Welcome to The Oast Rainham
Welcome to The Oast Rainham our new #FASD place.
Come on over for a nose and a natter.
We will be Cake and Kettle ready.
Our Support Group meetings provide attendees with an opportunity to find understanding and support through group discussions and to access helpful resources.
Living life the FASD way
Hear from real people, living real lives that just happen to have FASD.
Postponed until further notice.