The ASF Walk is next week. Who do you walk for? Show us in the comments. Support or find more information at www.angelman.org/walk #walkforangelman #angelmanstrong | Angelman Syndrome Foundation
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If you recently received a diagnosis of Angelman syndrome, the ASF and our network of Angelman families are here for you at every step of your journey. Complete the ASF Contact Registry to receive information and get connected. More info here: www.angelman.org/for-parents/newly-diagnosed | Angelman Syndrome Foundation
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Wishing Peace, Joy, and Love to the entire Angelman Community. We're honored to stand beside you on this journey. 🎁❄️💙 | Angelman Syndrome Foundation
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Angelman Syndrome doesn’t take breaks — and neither do caregivers. This is what 24/7 care really looks like. On February 15, wear blue and help us make Angelman Syndrome impossible to ignore. Awareness changes lives. 💙 #AngelmanSyndrome #WearBlueForAngelman #RareDiseaseAwareness check out my link in my bio the Windy City Angels to donate to the Angelman Syndrome foundation | Emily Wallace
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You are the Strength of the Angelman Community 💪 Your support makes everyday life better for individuals and families who live with Angelman syndrome. Give today: support.angelman.org/strength #angelmansyndrome #AngelmanSyndromeAwareness | Angelman Syndrome Foundation
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What does Angelman Strong mean to you? Never giving up—no matter the challenge? Fighting for treatments and a cure? Believing in the potential of every individual with Angelman syndrome? No matter what Angelman Strong means to you, join us on May 17 (in most locations)—at your local event or virtually. Find details at angelman.org/strong #angelman #AngelmanSyndromeAwareness #angelmansyndrome #walkforangelman #angelmansyndromefoundation #AngelmanSTRONG | Angelman Syndrome Foundation
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Here's what you need to know about Angelman syndrome, a rare genetic disorder that is sometimes misdiagnosed as cerebral palsy or autism. Sponsored by Ovid Therapeutics Inc. | Rare Disease on The Mighty
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