Abigail suffers from a rare degenerative disease that causes progressive loss of sight called Leber Congenital Amaurosis (LCA) with mutations in the RPE65 gene.

She also has Nictalopia. The most common cause of nyctalopia (referred to as "night blindness") is retinitis pigmentosa, a disorder in which the rod-like cells of the retina gradually lose their ability to respond to light.

The cloudy and dark days are terrible for her because she cannot see and she gets a little sad but still she tells us that it does not matter because I have magic hands and I can see with them.

Abigail needs specific treatment for her condition. The medicine is called Luxturna (https://luxturna.com/) and one dose should be applied to each eye. Only authorized hospitals with the necessary training and equipment can apply this treatment. Children's Hospital of Philadelphia (CHOP) in the United States is one of them. In that hospital, Abigail's case was evaluated in October 2019 and they gave positive results for said treatment.

The application of it in each eye has a value of USD $ 425,000, for both eyes a total of USD $ 850,188.54 + Hospitalization Expenses ($ 86,700.00) + transfer.

Help us to restore the illusion to princess Abigail