FACS Syndrome Association (FACSA)

All original content copyright Emma4facs 2012 – 2014

The FACS Syndrome Association was established in November 2012.

Founded by myself and colleague Janet Williams, FACSA are a not for profit support group providing information, support and help to children and their families diagnosed with the medical condition FACS-SYNDROME. FACSA is a sister organisation to IN-FACT both working together to ensure children with a diagnosis of FACS get the best care, support and advice.



Leave a Reply

Your email address will not be published. Required fields are marked *