For Parents / Carers
 
NEW Section:  Information on Events you can get involved in to influence the way care is provided to you and your family.  For more information click here.  Also Dr Mukherjee is carrying out some new research; details of how you can participate are here
 
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 - for more information click here.   We are really excited about the new groups in Yorkshire and we are also looking at Bristol for the New Year. 
  • we have a regular "spotlight" section, this week it is Cornwall (click here);
  • ask us to send you a copy of our latest family Newsletter
  • 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 also signpost you to other organisations whom we work with to give you further information or assistance.  
 
We look forward to hearing from you. 
 
The FASD Trust Team
 
 
 
 
 

 

 

 
 
  

Providing a Lifeline to those affected by FASD