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
13.8K views5 months ago
FacebookAngelman Syndrome Foundation
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
16.6K views8 months ago
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 views5 months ago
FacebookAngelman Syndrome Foundation
We want the whole world to know about Angelman syndrome and the tremendous impact it has on our loved ones and their families. The ASF is committed to families, research, clinics and community. #AngelmanSyndrome #Angelman #SupportingFamilies #DrivingResearch #CommittedCommunity #AngelmanAwareness #CureAngelman #ColinFarrell #RareDisease | Angelman Syndrome Foundation
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We want the whole world to know about Angelman syndrome and the tremendous impact it has on our loved ones and their families. The ASF is committed to families, research, clinics and community. #AngelmanSyndrome #Angelman #SupportingFamilies #DrivingResearch #CommittedCommunity #AngelmanAwareness #CureAngelman #ColinFarrell #RareDisease | Angelman Syndrome Foundation
6.1K viewsAug 7, 2024
FacebookAngelman Syndrome Foundation
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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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 views7 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 💙
941 views1 month 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
650 views6 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 views4 months ago
FacebookAngelman Syndrome Foundation
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Celebrate International Angelman Day with FAST! Around the world, families, researchers, advocates, and partners are raising awareness of Angelman syndrome and pushing research forward. This day reflects the strength of a global community united by progress, persistence, and shared purpose. Thank you to our global partners and affiliates for showing up and helping make Angelman syndrome visible today and every day. If you’re able, consider making a donation to support the research moving this fi
2.6K views4 months ago
FacebookFoundation for Angelman Syndrome Therapeut…
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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
2.5K viewsAug 9, 2024
FacebookAngelman Syndrome Foundation
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February 15 is International Angelman Awareness Day
58K views4 months ago
YouTubeIt's Our Wonderful Life
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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 views11 months ago
FacebookAngelman Syndrome Foundation
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Inspiring Journey: Overcoming Angelman Syndrome Challenges
4.6M viewsDec 2, 2023
TikTokashluv08
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Facing Loss: A Family's Journey with Angelman Syndrome
943.6K views8 months ago
TikTokashluv08
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Colin Farrell Foundation: Supporting Adults with Angelman Syndrome
1.1M viewsAug 7, 2024
TikTokpeople
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Colin Farrell Remembers His Son's First Steps with Emotion
1.1M viewsAug 7, 2024
TikTokcolinfarrellfoundation
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Supporting a Child with Angelman Syndrome
754.1K viewsJan 11, 2025
TikTokashluv08
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Empowering Angelman Syndrome: Makayla's Journey
523.4K viewsMay 6, 2025
TikTokashluv08
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A Friend with Angelman Syndrome #interview #truestories #motivation #fyp #foryou
1M viewsJul 28, 2023
TikToktruestories.doc
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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
190.6K views1 month ago
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