Vivians new heart

Vivi Warrior princess was born August 20th. She has Turner Syndrome,  restricted interatrial septum,  and Hypoplastic left heart syndrome.  We were told she would never take a breath.  That comfort measures only was a good option.  She came out screaming.  She's endured more in 5 weeks than most will in a lifetime.  She had her first open heart surgery at 2 weeks old.  It's been a battle since to get her stable enough to come home.  She is listed on the transplant list because no surgery other than a transplant will ensure that she lives.  She gets her fight from her daddy. He was injured 2 years ago in Afghanistan  and was told he'd never hold more than a bottle of water.  He continues to prove them wrong.  And so does Vivi.  Every day.  She had a 2 percent chance of maKing it past 13 weeks in utero.  She is our miracle.  But with this comes expenses.  Daddy has to go back to work.  I will stay here with V until she is ready to go home,  however long that may take.  Anything helps,  prayers,  donations,  sending good energy, etc.  Thank you to everyone who has reached out to us during this time.  And thank you for loving our girl so much.  She's a fighter and she's our angel.