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Just who is Molly?

Molly Kate is a daughter, a sister, a friend and an inspiration.  Molly is a tenacious, inquisitive & beautiful child. Angelman Syndrome is something she has - not who she is.

Molly was diagnosed with Angelman Syndrome shortly after her first birthday.

Our Mission

The website started with a number of goals in mind, and a great deal of those have been realised; teams rallied and groups set up to advance the mission we set out to achieve (see the links to the left for Rare Disease Awareness and Foundation for Angelman Syndrome Therapeutics Australia).

Angelman Syndrome research is advancing at breakneck speed and the consensus is that a treatment is not only possible ~ but likely.

As we approach 100,000 thousand visits to this website it has been a fantastic platform for Angelman Syndrome awareness.

By viewing this website, and passing it on to friends and colleagues, you help to create a voice for Molly.