A family received distressing news from doctors regarding their newborn daughter’s potential loss of eyesight due to a rare disease. Petru and Natalia Obada are now tirelessly working to ensure their daughter, Sophia, has the opportunity to see the world she brightens up. Sophia was diagnosed with a rare condition known as Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES), which affects her eyelids and vision. This specific type of BPES has hindered Sophia’s eyelid movement, posing a risk of permanent sight impairment.
To address Sophia’s condition, her parents are seeking specialized eyelid surgery in Spain, as it is crucial for her visual development. The family has initiated a fundraising campaign to cover the medical expenses, travel costs, and accommodations required for Sophia’s treatment. Natalia had a smooth pregnancy similar to her first child, David, who is now three years old and healthy. Petru, an HS2 engineer, noticed Sophia’s eye abnormality shortly after her birth, prompting medical evaluation and the subsequent BPES diagnosis.
Sophia’s case is unique, with only one in 50 babies in the UK diagnosed with BPES annually. Specialists at Oxford University Hospital confirmed her condition and explained the surgical procedure that could improve her vision significantly. Time is of the essence for Sophia’s parents as prolonged lack of light exposure could worsen her condition. With determination and hope, Petru and Natalia are determined to take Sophia to Spain for the necessary treatment.
The couple has set up a GoFundMe page to raise funds for Sophia’s medical journey and have shared their story to garner support. Those willing to contribute to Sophia’s cause can do so by visiting the GoFundMe page.
