Fighting Epilepsy with Development Delays

My name is Alba Radici and I am raising money to help my niece Ema fight against epilepsy.

Ema is a 4 year old girl from a small town in Albania. Ema was born 07/15/2018 and was diagnosed with facial deformity, psychomotor retardation, and epilepsy when she was just four months old. Ema takes a drug called Depakine to help control her epilepsy.

Ema has never been able to walk or talk, her family has tried to help her with speech and physical therapy. Ema lives with her mother, father, little brother, and grandmother. To pay for her speech, physical therapy, and housing. Her father was forced to sell the house where they all lived. For the past several years, the parents and Ema have been in and out of hospitals and seen by numerous doctors. This has been a long, frightening, and expensive journey for them all. Ema requires daily speech and physical therapy, as well as an MRI every 6 months to assess her progress. We are asking everyone to help Ema's parents with their financial burden. Any contributions would be greatly appreciated. This fundraiser will help offset Ema’s medical costs and associated costs with both speech and physical therapy.

Any contributions at all would be greatly appreciated.