They call him non-verbal. But right now, in his bed, laughing and refusing sleep he’s having a full conversation with me. Mendy is 12 years old and has Angelman syndrome. This isn’t just a bed, it’s a Knut safety bed, designed to keep him safe at night while still giving him comfort, freedom, and dignity. And moments like this laughter, connection, pure joy are everything. Endless gratitude to Variety the Children’s Charity @varietyvic for a gift that truly keeps giving 💙 #AngelmanSyndrome #Non
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FacebookMagical Mendy
They call him non-verbal. But right now, in his bed, laughing and refusing sleep he’s having a full conversation with me. Mendy is 12 years old and has Angelman syndrome. This
Magical Mendy. John Pattern & Jonah Kest · glow. They call him non-verbal. But right now, in his bed, laughing and refusing sleep he’s having a full conversation with me. Mendy is 12 years old and has Angelman syndrome. This isn’t just a bed, it’s a Knut safety bed, designed to keep him safe at night while still giving him comfort ...
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Angelman Syndrome
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
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Cadence is diagnosed with a rare genetic disorder known as Angelman syndrome. She is nonspeaking and very social. Cadence and her family want others to know that a person can be nonspeaking and still love to be around others and interact in their own way. | Special Books by Special Kids
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Cadence is diagnosed with a rare genetic disorder known as Angelman syndrome. She is nonspeaking and very social. Cadence and her family want others to know that a person can be nonspeaking and still love to be around others and interact in their own way. | Special Books by Special Kids
FacebookSpecial Books by Special Kid
85.4K viewsJun 27, 2024
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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
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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
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