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Hong Kong Angelman Syndrome Foundation (HKASF) is a non-governmental organization founded by Angel Chloe’s parents, Mr Joson Chan & Ms Joe Ng in June 2015 in Hong Kong and registered as charity organization since Jan 07, 2016. HKASF’s mission is to build a bi-lingual platform to share learnings through education, information exchange and researches; as well as providing support to individuals with Angelman syndrome, their families and people in concern. By organizing series of networking activities, HKASF aims to connect angel families in the region and cater their emotional and practical needs. Their goal is also to gradually raise public awareness and gain more community supports. Acting as the hub for Angelman Syndrome related organizations across the global, they are also committed in collecting cases in the Greater China region for medical research among the Chinese community.
To encourage and support patients of AS and their families
To connect related community organizations and government departments for addressing needs and concerns
To facilitate cross-sector collaboration
To raise media and social awareness with latest information released about AS
To provide or assist to provide care, cure, and support to individuals and their families living with Angelman Syndrome on a non-profit making basis
To facilitate self-development of Angelman and assist their families to overcome difficulties in life through experience sharing
To organize regular activities such as seminars, training and forums, in connection with Angelman Syndrome organizations from overseas, facilitate information exchange and encourage care to the Angel Families
To generate topics for discussions regarding the syndrome and its related issues, as well as the supports and well-being of the individuals and their families. This can be done through researches and studies, education and training, publications and releases of new findings in Hong Kong and overseas authorities. All of these are to be conducted on a non-profit basis
To connect to Angelman Syndrome Foundation and relevant international organizations; translate and share latest findings and information for local families to keep up with the global trend
To prepare promotion materials and publications for HKASF
To sponsor or provide financial assistance to related organizations or individuals with Angelman Syndrome and their families in Hong Kong and overseas, including payment of school fees, transportation, living allowance and other incidental expenses
Patient who diagnosed with Angelman syndrome
Patient's families and caregivers of Angelman Syndrome
Suspected patient of Angelman Syndrome
People caring for the Angelman Syndrome
If you are interested to help, please send your contact details to info@hkasf.org
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