Baby Jayson's Medical Fund

This fundraising account is for our newborn baby Jayson Robb Malicsi. He is a wonderful and cute baby boy with a head full of magical dreams and a heart full of love to give. He is our first born child, our bundle of joy and our source of strength.
November 20, I gave birth to our baby Jayson via C-section; Robert (my husband) and I are so humbled and blessed for having him. From the recovery room, our baby was supposed to be brought with me to our room, but due to his low blood sugar level, his pediatrician advised that he should be monitored at the NICU first. November 22 at around 9PM, i got a message from his pediatrician that our baby experienced tachypnea (abnormally rapid breathing) and will be referred to a pedia-cardiologist to perform 2d Echo. An hour after, we were called back again at the NICU, Jayson was already on oxygen; we met the cardiologist and he explained to us his 2d Echo findings: Atrial Septal Defect. Coarctation of the Aorta. Pulmonary Hypertension and Patent Ductus Arteriosus. He also discussed the immediate treatment needed as it is already affecting his lungs – Pulmonary Congestion. There will be medications to be given to treat his Pulmonary Hypertension, and treatment cycles for his Patent Ductus Arteriosus.

Next morning, Jayson was referred to a neonatologist to treat his other medical problems. He is being given antibiotic to treat his Pneumonia and Blood Infection. He was also placed under phototherapy to treat his Hyperbilirubinemia. He was intubated and is now hooked on ventilator to aid him in breathing; an orogastric feeding tube is also in place for the administration of his oral medications. His urine output started to decrease, thus, a catheter was inserted and is now being given diuretics. He is also experiencing tachycardia (fast heartbeat), so he needs to be sedated most of the time to keep him relaxed and stable.
November 30. His creatinine level was found to be higher than normal. A pedia-nephrologist is already onboard to help in Jayson’s treatment, and most especially to protect and save his kidneys. His ultrasound result revealed another congenital defect. Dialysis needs to be done to save his kidneys.

I already enrolled Jayson for insurance but he wont be eligible until he is one month old. I already asked for government financial assistance, but would only be able to help 5%-10% of the hospital bills. Remaining amount of the hospital bills and doctor’s fees will all be out of pocket. Jayson still needs to continue his medications, dialysis and treatment cycles for his heart, lungs, kidneys and blood infection. I am humbly asking your assistance to help our wonderful baby boy so he can get better, fulfill his dreams, enjoy and live his life to the fullest. Thank you from the Malicsi Family.