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!

2016 Raise Your Wings Dinner Event
The Fighting Angels Foundation would like to cordially invite you to the 3rd annual "Raise Your Wings" dinner event on March 12th at Testo's Ristorante in Bridgeport. You can click here for ticketing and sponsorship information.

Make a Donation
You can submit a donation to the Fighting Angels Foundation via Paypal by clicking the button below. Every donation makes a difference!
 

2015 Raise Your Wings
Fighting Angels Foundation

2014 Angel Run


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