Most of you know Cecelia aka Cece was born with a rare liver disease known as Glycogen Storage disease (GSD) she is type 1a. http://www.liverfoundation.org/abouttheliver/info/... Cece has to take cornstarch mixed with soy milk or a sugar free juice every 4 hours including interruptions during the night and eat every 2-3 hours to maintain normal blood sugar levels. Unlike a diabetic she cannot have anything with sugar as this will send her into hypoglycemic shock and could cause a seizure and or possible death. For 16 years we have managed this disease with round the clock care. Until now, we have never had the option to get a liver transplant. Though we have health insurance there is still such a financial strain due to co-pays and deductibles for lab work, MRI's, CT scans as well as consult visits with the team of doctors caring for her. We are now on the transplant list and hoping to find a donor within the coming months. I am reaching out to each of you with the hopes that you can help my family More so my daughter. This surgery means the world to Cece as well as myself so she can experience the quality of life each and everyone one of us take advantage of. Cecelia is a junior in high school she is in her third year of AFJROTC, on the drill team and this year became the comander of her team.. She works at Whataburger on the weekends and still maintains excellent grades. It would mean so much if you would donate any amount to help my daughter achieve a life long goal that will in the end give her a much better outlook on her life as well as open so many doors. My family thanks you in advance for your donations and prayers as we hope for the best quality of life for Cece. Please share! Thank you and God Bless!