Our Miracle Hartleigh

Since day one of Hartleigh being born I have shared her journey. As most of you know Hartleigh was born with a congenital heart defect called Hypoplastic Left Heart Syndrome, meaning the left side of heart didn’t develop in the womb. Not only was she born with a heart defect, she was also born with Malrotation of the intestines meaning her intestines are flipped the wrong way. Heterotaxy which is when your organs are not arranged where they should be. Asplenia meaning she has no spleen to fight off infections. Hartleigh is a child that has had three open heart surgeries, three heart cath, and two stomach surgeries. I’ve shared the happiest and some of the saddest and hardest days through out her life. There’s been days, we didn’t know what was next. One of those days being today. Hartleigh is a special needs child that has to have her medicines everyday being morning, lunch, and supper. Due to Wilkes (husband) being paid three times this month Hartleigh’s medicine will not be covered, it will be denied due to income increase. With that being said, she has just one medicine that is $17,000. I have attached a receipt below of the $17,791.59. Hartleigh is on eight medicines. This is why we have asked for any donations even if it’s just a $1 every little bit helps us and all the prayers. Please share with your friends! ♥️She goes to numerous appointments every month. It’s putting us in a financial situation. We are asking for prayers and any financial assistance/donations if you can donate to help our child.