
Dream #1246

Born with Pontocerebellar Hypoplasia Type 2—an ultra-rare genetic disorder with only 81 confirmed cases worldwide—this beautiful 3-year-old requires constant care and support. PCH affects brain development, and she will never walk, talk, or feed normally. Yet, her joyful spirit shines through in every giggle, every soft curl, and every moment she connects with the world around her.
Though her vision is limited, she delights in sounds and sensations—music, flashing lights, chimes, laughter, birdsong, and the revving of engines from her brothers’ dirt bikes. She loves the taste of strawberries and watermelon, the minty freshness of toothpaste, and the feeling of floating in water with a breeze on her face and sand between her toes.
Alberta Dreams is honored to send this incredible family on a week-long vacation to the white sands of the Riviera Maya—where she can experience the sensory joys she loves most, surrounded by the warmth of her family.
