We care to improve the quality of life of our kids and their families.

1 in 12,000 people are diagnosed with Angelman Syndrome

Who We Are

We are a nonprofit parents’ association that brings together family members and friends of people affected by Angelman Syndrome.

Our mission is to improve the quality of life of our children and their families, driven by the belief that we can support those going through similar experiences by strengthening one another.

What We Do

01.

— We Find & Fund

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02.

— We Build Networks

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03.

— We Strengthen

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04.

— We Educate​

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05.

— We Provide Care​

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06.

— We Consult​

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Impact Stories​

Ella tiene la fuerza de una campeona…”

nos cuenta Adela sobre su hija Mercedes. http://angelmanargentina.com.ar/la-historia-de-mercedes/

Con Fran tenemos grandes desafĂ­os, y lo vamos a lograr, dĂ­a a dĂ­a, estoy segura”

nos cuenta Ramona, mami de Fran, diagnosticado recientemente con síndrome de Angelman. Conoce su historia: http://angelmanargentina.com.ar/la-historia-de-francisco/