A couple received distressing news from doctors about their newborn daughter potentially losing her eyesight permanently due to a rare disease. Petru and Natalia Obada are tirelessly working to help their daughter, Sophia, experience the world around her. Sophia was diagnosed with a rare condition called Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES), which affects her eyelids and eye placement.
Sophia, who has Type 1 BPES, faces challenges with her vision as her eyelids cannot fully open, posing a risk of permanent blindness. To address this, her parents are seeking medical treatment in Spain for specialized eyelid surgery. They have initiated a GoFundMe campaign to raise funds for Sophia’s medical expenses, travel, accommodation, and ongoing support.
Natalia’s pregnancy with Sophia was normal, similar to her first child, David, who is now three years old and healthy. Petru, an HS2 engineer, recalled the initial days after Sophia’s birth when they noticed her eye issues. Specialists at Oxford University Hospital diagnosed Sophia with BPES, explaining the condition and the surgical procedure that could potentially restore her eyesight.
With time being critical, Petru and Natalia are determined to take Sophia to Spain for treatment to prevent permanent blindness due to light deprivation. The couple created a GoFundMe page with photos of Sophia to seek financial support for her medical journey. To contribute to their cause, click on this link.