The Hong Kong Angelman Syndrome Foundation is a charity organisation for Angelman patients. Our website is designed to be a positive and uplifting online knowledge resource to assist these individuals and families overcome the difficulties of living with Angelman Syndrome - a complex genetic disorder that primarily affects the nervous system. The responsive design ensures that visitors have access to information on a diverse range of mobile devices as well as desktop computers.

Hong Kong Angelman Syndrome Foundation (HKASF) is a new Non-Governmental Organization in Hong Kong founded by Angel Chloe’s parents, Mr Joson Chan & Ms Joe Ng in Jun 2015. Our core theme is to assist individuals and their families living with Angelman Syndrome to develop themselves and to overcome the difficulties in life in any aspect on a non-profit making basis.