Kayla was born three weeks early with an 80% heart blockage and had a surgical repair at 2 months weighing only 6 pounds. She was diagnosed with Failure to Thrive as an infant and then with Epilepsy by 2 years of age. By 2.5 years, she was diagnosed with a rare genetic metabolic disorder which caused many severe metabolic crises in her young life. By the time she was 4, Kayla had survived two cardiac arrests, liver and kidney failure, pancreatitis and severe fluctuations in her blood sugar levels. With the diagnosis of Mitochondrial Disease, a Mediport and G-Tube were surgically implanted. We have since been able to more effectively manage her medical conditions. However, social and behavioral concerns continue to exist and in 2010, Kayla was diagnosed with Autism Spectrum Disorder and learning disabilities. She is TRULY our miracle child!