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.

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