Morning routine with my 9-year-old, Griffin, who has Angelman Syndrome 💙
2:57
YouTubeIt's Our Wonderful Life
Morning routine with my 9-year-old, Griffin, who has Angelman Syndrome 💙
Morning routine with my 9-year-old, Griffin, who has Angelman Syndrome. 💙 Angelman Syndrome is a rare genetic disorder that affects chromosome 15. Griffin lives with seizures, a balance disorder, is nonverbal, and has global developmental delays. His journey isn’t easy, but his joy is contagious. Watching him reminds me every day that ...
19.9K views2 weeks ago
Angelman Syndrome Symptoms
Angelman Syndrome - A Basic Explanation
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Angelman Syndrome - A Basic Explanation
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Prader-Willi Syndrome | Angelman Syndrome | Genomic imprinting #neetpg #biochemistry
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Prader-Willi Syndrome | Angelman Syndrome | Genomic imprinting #neetpg #biochemistry
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Traveling with a child who has Angelman Syndrome means safety is always a priority
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Traveling with a child who has Angelman Syndrome means safety is always a priority
YouTubeIt's Our Wonderful Life
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Some days with Angelman syndrome are harder than others
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Colin Farrell's Heartwarming Journey Raising Son with Angelman Syndrome ❤️
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Today we worked on getting my son with Angelman Syndrome a new adaptive stroller
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Today we worked on getting my son with Angelman Syndrome a new adaptive stroller
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19 days until the Angelman Syndrome Family Conference in Denver! 💙
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19 days until the Angelman Syndrome Family Conference in Denver! 💙
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February 15 is International Angelman Awareness Day
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My son has Angelman Syndrome and struggles with mobility, toe walking, and being pigeon-toed
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YouTubeIt's Our Wonderful Life
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
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FacebookAngelman Syndrome Foundation
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Griffin has Angelman Syndrome and struggles with balance + being pigeon toed 💛
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Sensory regulation with my son who has Angelman Syndrome 💙
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Waking up my 9-year-old son Griffin, who has Angelman Syndrome💙
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We built a safe space in our home for our son with Angelman Syndrome
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My son with Angelman Syndrome loves timers
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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
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I have a story for you… the pajama saga continues 😅
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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
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FacebookAngelman Syndrome Foundation
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Griffin has Angelman Syndrome. Griffin and Betty have always had a special relationship
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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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Today is International Angelman Syndrome Day
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New episode of the ASF Podcast. CEO Amanda Moore is joined by Bryan LaScala, CEO of the NAPA Center. Bryan shares the inspiring story of how his mother’s determination to help her son led to the founding of the therapy center. Bryan dives into the benefits of intensive therapy, the individualized approach at NAPA, and how the center supports families navigating complex care journeys. Listen on Spotify, Apple Podcasts and YouTube Podcasts. | Angelman Syndrome Foundation
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Honest Confession: Her Son Saved Her from Alcohol
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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
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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
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TikTokweb21104
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