15/02/2026
Angelman Syndrome Awareness 💙
Angelman syndrome is a rare genetic condition, affecting around 1 in 12,000–20,000 people worldwide.
Children and individuals with Angelman syndrome may experience differences in:
• Development and learning
• Speech and communication
• Movement, balance, and coordination
• Sleep and epilepsy
Many are also known for their joyful, excitable personalities, with frequent smiles, laughter, and expressive movements.
Angelman syndrome is most commonly linked to changes in a gene called UBE3A, which plays an important role in brain development. When this gene isn’t working as expected, it can affect how the nervous system develops and functions.
At Ohana, we believe that awareness, understanding, and the right supports can make a meaningful difference. Every child deserves opportunities to move, play, connect, and participate in ways that work for them 💛