Paislee Rose

Hi my name is Irish I am Paislee's grandma. This is our story. My daughter Bailey had Paislee at 32 weeks. Because Bailey had Preeclampsia and she had high amniotic fluid. They had to give Bailey 2 shots of steroids to help Paislees lungs develop faster. They said if Bailey didn't have her very soon that she could have uncontrolled seizures that to cause both of them to die. So Bailey had paislee's on Feb. 1st, 2023. We found out that Paislee was diagnosed with Esophageal Atresia with TEF ,Bronchomalacia and 17Q12 Duplication. She just turned 3 months and is having surgery to fix her esophagus. When she is done she will still be in the NICU for another month. She has been in the NICU since she was born. When she gets out of the hospital she will come home with a Mickey button for up to 2 years. She will have to be on continuous feeding for a while. She will have a home nurse come out as also pt and someone to help Paislee to learn how to swallow. This will take a while I mean on Paislee time they say. We have been going back and forth to the hospital. This has been very hard for my family, Martin and myself going back and forth to the hospital. We could use the help for getting Gas to go back and forth and to get the medical stuff that paislee would need.

we want to thank you all for everything. And Prayer will help