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Welcome to the FASD Trust
The FASD Trust was started in January 2007 in response to the growing number of requests for information on FASD being received by Simon & Julia Brown adoptive parents of a child with FAS.
However, please bear with us over the next couple of weeks, as we are currently updating our website significantly. If there are any items you wish to see appear on the website or you require further assistance, please contact us.
If you would like to download our Spring 2010 Newsletter, please click here. Also, if you would like to go on our mailing list for us to send our newsletters to you please click here
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The National FASD Clinic, which is run by Dr Raja Mukherjee, accepts referrals from across the UK......
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Spring Fever has certainly hit The FASD Trust! We are very excited about our new logo, our new newsletter and our new offices! The new logo will begin to appear on all our literature over the next few weeks - check out the preview for you to start getting used to it............
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Our Support Groups are an important part of our work, enabling families to meet with each other and for the children to play together. We have groups meeting throughout the year, including new groups staring this Autumn in Bristol, amongst other places....
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The FASD Trust has become a member of the Cotswold Connect, as our head office is located in this beautiful part of the UK.....
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In response to a large number of requests, we are pleased to announce that a series of books has now been written for children and young adults explaining what FASD is and how it affects a person. The first of these books, which are aimed at different age groups / levels of understanding, will be available from this summer.......
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