Scarlett McFeeley was born on June 12, 2020 and was diagnosed shortly afterwards with Noonan Syndrome, a genetic disorder that has wreaked havoc on this sweet little girl's body by directly affecting her lymphatic system and causing serious issues with her heart.  JP, Ashley, and big sister Ava, along with the team of doctors at Pittsburgh Children's Hospital have been fighting at Scarlett's side over the past four months to try and build her strength so that doctors would be able to perform life-saving heart surgery.  It was discovered this week that Scarlett's condition has worsened, and the life-saving heart surgery is not going to be possible.  The McFeeley family will continue to fight with Scarlett, but the doctors are now looking for solutions that may or may not exist.  Their situation is dire, and they need our love and support.  Having a critically ill child is beyond difficult.  Please help to support the McFeeley family with a donation so that we can help take the burden of any financial hardships away from them.  Thank you, and may God be with  Scarlett and the McFeeley family.