Children with Angelman Syndrome (AS) do not talk and many struggle to walk. They have difficulty eating and sleeping. Every year, individuals with AS die due to complications from seizures, however large pharmaceutical companies are not focused on the search for a cure. Despite the rarity of AS, a cure for this disorder is not only possible, but probable. We know what causes Angelman Syndrome. We know that, despite its devastating effects, it's an incredibly simple disorder involving only one gene. And we know that curing AS will have a profound impact on other related and rare disorders, such as Prader-Willi, Rett and Fragile X Syndromes, as well as much more common disorders such as autism and Alzheimer's.

Fighting Angels Foundation, Inc, is an organization, dedicated to support and fund research and raise awareness of the rare neuro-genetic disorder Angelman Syndrome as well as serving and protecting the needs of the 1 in 15,000 individuals affected by this disorder. Our inspiration is Joseph (Joey) Paul Moretti Jr. FAF focuses its activities through yearly fundraising events and the support of public donations from generous individuals and companies to help fund its cause. Fighting to Talk, Fighting to Walk, Fighting for a Cure is our motto!

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