Layla Bug

Layla was diagnosed with a microdeletion of her chromosome 1. This disorder is rare. With little to no study Ms. Layla Bug has left everyone puzzled. In October 2016 she was place on life support and given only a few days to live..... She showed them.... 6 months later she was diagnosed with pneumonia, after spending 1 week in the hospital she was sent home. 24 hrs later she is now back in the PICU with acute respiratory failure.  Cheylan (laylas mom) made the quick decision to place her on life support yet again.  After hearing bad news after bad news (Bugs mother) has been faced with making one of the hardest decision any parent would hate to make, not once but TWICE she decided to take her off life support.
On 5/20/17 Drs gave Layla 1 hour to live marking this day as her last.... Guess what she is still here. All her vitals are at 100% and she is feeding well. Before this she celebrated her 2nd birthday surrounded by tons of family and friends. She is a fighter.
 Cheylan has left 2 other children home so she can spend every second of the day at Layas bed side. She has been looked at by doctors as the mother that cant let go. How she has done so twice. Layla cant let go, shes not ready, she has a purpose, the man above is not ready for her. With all of Cheylans bills piling up things have been very difficult for her.  This is why I ask if you can help her. Prayers, coins, bills they are all appreciated.