Our beautiful daughter Mia was born with a light in her eyes that touched everyone around her. But as she grew, we noticed she wasn’t reaching the milestones most children do. She wasn’t babbling, wasn’t sitting up on time, and struggled to control her movements. We felt something was wrong, but nothing prepares a parent for hearing the words Angelman syndrome — a rare neurological condition that affects development, speech, balance, and learning.

Mia cannot speak to tell us what she needs or how she feels. She faces global delays that make daily life a challenge. She works harder than most children just to do things others take for granted. Yet despite everything, she smiles, she laughs, and she fills our home with a strength and joy that inspires us every day.

Angelman syndrome has no cure, but therapy can change Mia’s life. With the right support — speech therapy to help her communicate, occupational therapy for daily skills, and physiotherapy to strengthen her body — Mia can achieve more independence, more comfort, and more opportunities to connect with the world around her.

These treatments, however, are expensive, ongoing, and often not fully covered. As parents, all we want is to give Mia the best chance at a bright future. That’s why we’re reaching out for help.

Your support will fund the therapies and specialist care Mia urgently needs. Every contribution, no matter the size, directly impacts her ability to grow, learn, and overcome the challenges she faces.

Mia may have Angelman syndrome, but she also has determination, courage, and a family fighting for her. With your help, she can reach her full potential.

Thank you for standing with Mia and giving her the chance she deserves.

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