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My name is Larissa, and I am Lorenna's mother. I want to share my daughter's story to raise awareness about congenital glaucoma and show how early diagnosis and continuous treatment can change a child's life.
Shortly after Lorenna was born, we noticed that something was different about her eyes. What followed was a difficult journey of medical appointments, examinations, and uncertainty. After about fifteen days, we finally found a glaucoma specialist who confirmed the diagnosis of congenital glaucoma.
The pressure inside Lorenna's eyes was dangerously high, and she needed emergency surgery immediately. Since then, she has undergone four eye surgeries and continues to require lifelong follow-up care to preserve the vision she still has.
Today, at three years old, Lorenna attends school, participates in classroom activities with the support of dedicated caregivers, and faces every day with joy and determination. Although her low vision limits her independence, it has never diminished her curiosity, her love of learning, or her desire to explore the world.
As her mother, I hope Lorenna's story helps more people understand congenital glaucoma and reminds them that early diagnosis and access to continuous treatment can change a child's future.





















