For Parents / Carers
As several of us are parents of children with FASD we share and understand your daily tears, smiles, frustrations and joys!
One of our main aims as a charity is to continue to increase awareness of FASD thereby making your lives easier, as people begin to understand the condition and, hopefully, you will find yourself gradually having to explain less and less what FASD is!
We hope you will find lots of helpful and useful information in these web pages, but please do come to our support groups, call our helpline or
e-mail us with any queries or suggestions; we are always looking to improve our services to you.
Remember, we are always willing to travel to your locality and give training / information sessions at your child's school, place of worship or even in your workplace. We can act as expert witnesses in Educational Tribunals. We can also signpost you to other organizations whom we work with to give you further information or assistance. Please look at our Partners & Sponsors page for some initial details.
The FASD Trust Team
Support Groups
We aim to start more groups nationwide, as demand arises. For now we have groups in Oxfordshire, Kent / Sussex Cornwall and Hertfordshire. For more information
click here.
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Wigan/N West |
Our sister organisation, FAS Aware UK, run a group in Lancashire; for details go to www.fasaware.co.uk or call 01942-223780. |
Informal E-Mail Support Groups & Other Assistance
We have several informal e-mail support groups that exist between parents / carers and those with FASD, where we share experiences and information.
