Gavin Bryant CHD Journey to Recovery

Baby G will be our third boy and is due to come out August 13,2020 via C-Section due to his condition(originally Sept 3,2020)!  We were told at 20 weeks during our gender "reveal" via ultrasound, that our baby has a congenital heart defect known as Transposition of the Great Arteries with VSD. It was the most devastating news any parent had to hear. Baby G's condition is where his pulmonary artery and aorta are reversed and has a hole in the heart.  Because of this condition, he would have to go through Open Heart Surgery immediately or a few days after birth. TGA requires lifelong visits to the cardiologist for continuous care. As parents, our world crashed and hearts sunk as we were dealing with this news during the most difficult time(Covid-19). We were trying to figure out how we can stay afloat since our business was forced to shut down. My income was not enough to cover our housing, food, and medical expenses. We were referred to Stanford's Children's Hospital to be with the best neonatal Cardiologist in the Bay Area. I'm not one to ask but any help would be greatly appreciated and put to pay for his surgery and stay in the NICU. The costs associated with Baby G's cardiac surgery and medical care are something I'm trying hard not to think about right now. Any amount will help!Prayers for Baby G are much appreciated as well. Our little man is destined for great things in this world, we just know it <3.Thank you from the bottom of our hearts!