cureangelman.orgFAST (Foundation for Angelman Syndrome Therapeutics) | Cure Angelman Now
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Title:FAST (Foundation for Angelman Syndrome Therapeutics) | Cure Angelman Now
Description:The Angelman journey. Most people have never heard of Angelman syndrome (AS), but scientists believe that AS has the greatest potential for being cured when compared to other neurogenetic disorders.
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× Site Navigation Home Newly diagnosed Newly diagnosed Register Talk to Paula Educate yourself Meet other parents Letters from AS parents Video message from actor and AS dad Colin Farrell Video message from FAST for AS parents and family members Helpful resources About FAST Welcome Paula’s story Our role & mission Priorities Funding philosophy Board of directors Scientific advisory board Audited financials Tax returns Understanding Angelman syndrome What is Angelman syndrome Types Characteristics Behavioral traits Causes Tests & diagnosis Resources Our research & impact Our research & impact FIRE team Penn team Roadmap to a cure Impact FAST-funded research Funding forecast Scientific advisory board Apply for grants 2019 Global Summit & Gala Media coverage FAST news FAST blog CAN (Cure Angelman Now) CAN home Welcome from Paula Fundraise for a cure Donate Take action Join Register Fundraise Donate Other ways to give Find my CAN page Skip to content 2020 FAST Virtual Summit & Mini-Gala Fundraise Menu Breaking News A BRAND NEW cureangelman.org website experience coming January 2021. Angelman Syndrome Most people have never heard of Angelman syndrome (AS), but scientists believe that AS has the greatest potential for being cured when compared to other neurogenetic disorders. Learn Join Donate Newly Diagnosed You’ve found your way to our website and a support system that will help you understand Angelman syndrome and make sense of your child’s diagnosis. Here are two things we want you to know right away: THERE IS HOPE FOR TREATMENT AND A CURE. Angelman syndrome has been cured multiple ways in mice, and the progress our scientists are making is nothing short of thrilling. YOU ARE NOT ALONE. We are all parents of children with Angelman syndrome, and we’re standing by to answer questions and assist you. Next Steps Understanding Angelman Syndrome Angelman syndrome (AS) is a rare neurogenetic disorder that affects approximately one in 15,000 people – about 500,000 individuals worldwide. Symptoms typically include difficulty suckling and eating, gastrointestinal issues, delayed crawling and babbling, balance and motor impairment, and seizures. Learn More Join Donate Causes Testing Diagnosis Research & Impact Our sole mission is to cure Angelman syndrome. That’s why FAST brought together a multidisciplinary team of more than two-dozen scientists from top research universities and pharmaceutical companies. These men and women are the nation’s foremost authorities on Angelman syndrome (AS), and they have joined forces on a focused path to a cure. Latest Developments Donate Join Our Community Connect with other people who have a child or loved one with Angelman syndrome. Facebook Instagram FAST League Register ^ Cure Angelman Now As diverse as our Angelman community is, we are all united in one goal: a better future for our children. FAST is committed to bringing life-changing treatments to clinical trials within two years, but we need your help. Fundraise Donate FAST Blog Gene Therapy 101 When we refer to gene therapy in Angelman syndrome (AS), we are typically referring to a “viral delivery” or “virus vector” of the missing gene (UBE3A) or the missing protein (UBE3A protein) into the brain. Read More Contact Us PO Box 608 Downers Grove, IL 60515 Phone: (630) 852-FAST Fax: (630) 852-3270 Toll Free: (866) 783-0078 Email: info@CureAngelman.org © FAST 2018 FAST. All rights reserved....
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