The Angelman Syndrome Collections Showcase was founded by Joanna Marcella to raise awareness and funds for Angelman Syndrome. This is a new site that will be used over the coming months to document in image format the journey of this Angelman Syndrome campaign. The slide show includes images the AS Creative Arts Events and the London and New York City Angelman Syndrome Collections Showcase.
Contact: [email protected]
Contact: [email protected]
I’m inspired to raise awareness of Angelman Syndrome by my grandson 12 year old Manasseh he has Angelman Syndrome (AS), and he’s is such a joy to be around. As a designer and the relative of a little 'Angel' I and other members of the arts and fashion industry can use this showcase to raise awareness and funds which will lead to treatments and eventually a cure.
I’m honoured to be an awareness representative for this cause I fundraise for ASSERT the Angelman Syndrome Support Education & Research Trust
and FAST Foundation for Angelman Syndrome Therapeutics and individuals with AS. I will also be selling some of my own work to raise funds for Manasseh’s speech therapy.
I’m honoured to be an awareness representative for this cause I fundraise for ASSERT the Angelman Syndrome Support Education & Research Trust
and FAST Foundation for Angelman Syndrome Therapeutics and individuals with AS. I will also be selling some of my own work to raise funds for Manasseh’s speech therapy.
I’m also encouraged by Colin Farrell’s mission to raise more awareness about Angelman Syndrome. As a celebrity he is able to catch the attention of the media with the story of his own son James who has Angelman Syndrome.