V3 has been fighting in the hospital for 11months.

Hi everyone! Most of you know but if you didn’t, I had to give birth at 29 weeks. When V3 was born, we found out he has EA/TEF. That means when he was born his esophagus was attached to his windpipe. He had a surgery at 3 days old then had another major surgery in December to attach it back to his stomach. He’s been in the NICU for the last 7 months. He’s not able to eat through his mouth, he gets all his food through a G tube in his stomach. He is also having a lot of breathing issues & he keeps aspirating liquid into his lungs which gives him pneumonia. Last week we got word that he will need to be life flighted to a children’s hospital in California for better care. Once he gets to California, he will need 2 more surgeries. We’re not sure when he is able to come home. A couple days ago, I was let go from my job because they didn’t want to let me take leave so I could follow V3 to California. Since we have to up & leave our home in Las Vegas and relocate to LA, we have nowhere to stay until the Ronald McDonald’s house has a room available. We have to spend our money on booking hotel accommodations while we’re there for a few months or longer. Vick and I don’t ask for a lot but we have been through so much dealing with V3’s health. Right now we’re asking if you could donate whatever amount of money you can to go towards all of his hospital bills and our bills at home since we will be out of work for awhile. Anything helps & we greatly appreciate it! Blessings xoxo We love you guys!