Ella Anderson was born on the 21st of March 2019 at 1:43 pm weighing 6lbs 11.9oz . She was born with an extremely rare condition known as Giant Omphalocele. It is an abdominal wall defect noted in babies. In this condition, a hole (hernia) is present in the muscles and skin around the child’s belly button,where the stomach, liver or intestines of the baby protrude outside the body through an opening. In other words,some of Ella's internal organs developed outside her body.This wasn't known before birth but was only seen after her birth. This prognosis normally involves other issues or birth defects and Ella was unfortunate.Apart from her Omphalocele, she has recently been diagnosed with acute lung failure which makes it difficult for her to breathe
Ella has started oxygen therapy and is currently fighting for her little life.
With the help of family & friends,we have taken care of every medical cost since Ella was born until now and it hasn't been easy at all :( The cost of treatment has become unbearable for us and we are afraid we might Lose Ella if we do not act quickly.
We've run out of funds due to medical expenses and appealing to the generous public to help us save Ella's life. All raised funds will go into her prolonged oxygen therapy and surgery to correct her Omphalocele.
We need as much help as we can get ,so any amount will go a long way to help Ella Live.
Thank you for your support
updates will be posted as treatment progresses.