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Angelman syndrome (AS) is a rare neurogenetic disorder that affects about one in 15,000 people, or approximately 500,000 individuals worldwide. Some say it could be as frequent as one in 8,000 people, or over 1,000,000 individuals worldwide.

Children and adults with AS typically have impaired motor and balance, and debilitating seizures. Some individuals never walk. The majority do not speak. Disrupted sleep cycles also can be a serious challenge to the individual and caregivers. Individuals with AS require continuous care and are unable to live independently. They have a normal life expectancy. People with Angelman syndrome have some distinct behavioural traits, including a happy demeanour, characterised by frequent laughing, smiling and excitability. Many individuals with AS have a fascination with water and take great pleasure in activities like swimming.

This is life today for people living with Angelman syndrome.

But it won’t be for long.

Scientists believe that AS is now the neurogenetic disorder with the greatest potential to be cured. FAST is the reason why, and the force making it happen.

Ready to know more about Angelman syndrome? You can start with the basics from the menu at the left.

For more about FAST, head on over here.

FAST is committed to assisting individuals living with Angelman syndrome to realise their full potential and quality of life.

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PO Box 689

Bungalow QLD 4870

info@cureangelman.org.au

1300 078 108

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