The strength of the Angelman community is life-changing for individuals with Angelman syndrome. Every day, we lean on others for practical help, expert care, advancing science, and a network that never lets go. Your donation makes an immediate difference. It helps Angelman families access help they need today while building a stronger tomorrow for all of us living with Angelman syndrome. 💪 Donate 👉 support.angelman.org/strength #StrengthInCommunity #angelmansyndromefoundation #angelmansyndrome
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The strength of the Angelman community is life-changing for individuals with Angelman syndrome. Every day, we lean on others for practical help, expert care, advancing science, and a network that never lets go. Your donation makes an immediate difference. It helps Angelman families access help they need today while building a stronger tomorrow for all of us living with Angelman syndrome. 💪 Donate 👉 support.angelman.org/strength #StrengthInCommunity #angelmansyndromefoundation #angelmansyndrome
16.7K views9 months ago
FacebookAngelman Syndrome Foundation
Words shape how the world sees people with Angelman syndrome and how they see themselves. When we choose people-first language, we honor individuals for who they are, not a diagnosis. Behind every word is a person with personality, family, likes/dislikes, and a whole life being lived. ✨ Words matter. Choose them carefully. #angelmansyndrome #angelmansyndromefoundation #angelman #AngelmanStrong #StrengthInCommunity #WordsMatter #PeopleFirst #inclusionmatters | Angelman Syndrome Foundation
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Words shape how the world sees people with Angelman syndrome and how they see themselves. When we choose people-first language, we honor individuals for who they are, not a diagnosis. Behind every word is a person with personality, family, likes/dislikes, and a whole life being lived. ✨ Words matter. Choose them carefully. #angelmansyndrome #angelmansyndromefoundation #angelman #AngelmanStrong #StrengthInCommunity #WordsMatter #PeopleFirst #inclusionmatters | Angelman Syndrome Foundation
13.9K views6 months ago
FacebookAngelman Syndrome Foundation
The Angelman Syndrome Foundation is committed to supporting every individual, every step of the way. Introducing AS Grows Up: a movement dedicated to ensuring adults with Angelman syndrome have the resources they need to thrive. Growing up doesn’t mean growing out of support. It’s time to talk about what comes next. #angelmansyndrome #angelmansyndromefoundation #angelmanresources #angelman | Angelman Syndrome Foundation
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The Angelman Syndrome Foundation is committed to supporting every individual, every step of the way. Introducing AS Grows Up: a movement dedicated to ensuring adults with Angelman syndrome have the resources they need to thrive. Growing up doesn’t mean growing out of support. It’s time to talk about what comes next. #angelmansyndrome #angelmansyndromefoundation #angelmanresources #angelman | Angelman Syndrome Foundation
9.8K viewsApr 14, 2025
FacebookAngelman Syndrome Foundation
Angelman syndrome is a rare disorder that affects chromosome 15, resulting in intellectual and developmental delay. Common signs and symptoms usually appear in early childhood but despite these symptoms, people with Angelman syndrome have an overall happy and excitable demeanor. #InternationalAngelmanDay #angelmanday2024 | Angelman Syndrome Foundation
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Angelman syndrome is a rare disorder that affects chromosome 15, resulting in intellectual and developmental delay. Common signs and symptoms usually appear in early childhood but despite these symptoms, people with Angelman syndrome have an overall happy and excitable demeanor. #InternationalAngelmanDay #angelmanday2024 | Angelman Syndrome Foundation
3.2K viewsFeb 15, 2024
FacebookAngelman Syndrome Foundation
There’s something truly special about walking into a space where you don’t have to explain—because everyone just gets it. 💙 The ASF Family Conference is more than sessions and speakers. It’s hugs in the hallway, kids finding instant friends, siblings feeling seen, and families realizing they can relax and be their authentic selves. ✨ What to expect: • 1,300 attendees • 200 individuals with Angelman syndrome • 450 siblings • 250 researchers, clinicians & industry partners • 50 speakers over 30 s
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There’s something truly special about walking into a space where you don’t have to explain—because everyone just gets it. 💙 The ASF Family Conference is more than sessions and speakers. It’s hugs in the hallway, kids finding instant friends, siblings feeling seen, and families realizing they can relax and be their authentic selves. ✨ What to expect: • 1,300 attendees • 200 individuals with Angelman syndrome • 450 siblings • 250 researchers, clinicians & industry partners • 50 speakers over 30 s
2.3K views6 months ago
FacebookAngelman Syndrome Foundation
Today is our annual Angelman Syndrome Foundation Walk & 5K 💙
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Today is our annual Angelman Syndrome Foundation Walk & 5K 💙
927 views2 months ago
YouTubeIt's Our Wonderful Life
Strength in community means no family faces Angelman syndrome alone. 💙 For families living with Angelman syndrome, it means guidance, connection, and care when it matters most. Donate today and be part of the strength we rely on: https://support.angelman.org/strength | Angelman Syndrome Foundation
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Strength in community means no family faces Angelman syndrome alone. 💙 For families living with Angelman syndrome, it means guidance, connection, and care when it matters most. Donate today and be part of the strength we rely on: https://support.angelman.org/strength | Angelman Syndrome Foundation
674 views7 months ago
FacebookAngelman Syndrome Foundation
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It's #InternationalAngelmanDay. We're celebrating our loved ones with Angelman syndrome, raising awareness & creating a more inclusive world. #angelmanday2026 #AngelmanSyndromeAwareness #AngelmanStrong #angelmansyndrome | Angelman Syndrome Foundation
21.1K views5 months ago
FacebookAngelman Syndrome Foundation
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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
1.1K views8 months ago
FacebookAngelman Syndrome Foundation
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These are a few of the faces of Angelman syndrome and we are so proud to be #AngelmanStrong. #AngelmanSyndrome #AngelmanSyndromeAwareness | Angelman Syndrome Foundation
2.6K viewsAug 9, 2024
FacebookAngelman Syndrome Foundation
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Xavier, a recent high school graduate living with Autism, will take on his first marathon this Sunday at the Bank of America Chicago Marathon in honor of his friend Sam, who lives with Angelman syndrome. A powerful story of friendship, inclusion, and strength in community - Angelman style! #Autism #AutismAwareness #Neurodiversity #InclusionMatters #AngelmanSyndromeFoundation #AngelmanSyndrome #ChicagoMarathon #BankofAmericaChicagoMarathon #StrengthInCommunitya | Angelman Syndrome Foundation
16.6K views9 months ago
FacebookAngelman Syndrome Foundation
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Save the date! The 2026 ASF Family Conference will be July 30 - August 1, 2026. We're heading west to Aurora, Colorado at the Gaylord Rockies Resort & Convention Center. To be added to the invitation list, go here: https://mindfulmeetings.swoogo.com/2026asfconference/savethedate The 2026 theme, Soar, celebrates the limitless spirit of our community and a future full of possibility, where every individual is empowered to rise beyond limitations. 💙 Stay tuned for more info on sessions, registrati
2.1K viewsJul 14, 2025
FacebookAngelman Syndrome Foundation
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Creating a Safe Haven for Son with Angelman Syndrome
778.8K views2 months ago
TikTokwhatilovetodo
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Inspiring Journey: Overcoming Angelman Syndrome Challenges
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Understanding Angelman Syndrome: A Special Needs Girl's Emotional Response
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Facing Loss: A Family's Journey with Angelman Syndrome
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Supporting Makayla Through Angelman Syndrome Challenges
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Makayla's Inspiring Growth with Angelman Syndrome
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TikTokashluv08
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I’m not gonna lie… some of the hateful comments hurt. But if those comments help push Brett’s story farther and teach more people about Angelman Syndrome (chromosome 15 deletion), then maybe some good can come from it ❤️ The more people who learn, the more compassion, understanding, and awareness families like ours receive. So thank you for helping spread awareness… even if it wasn’t your intention ❤️ #AngelmanSyndrome #DisabilityAwareness #SpecialNeedsParent #RareDisorder #SpreadAwareness
319.6K views2 months ago
TikTokweb21104
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Understanding Angelman Syndrome: Makayla's Journey
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TikTokashluv08
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