
Hubby and I hugged little Caylah Bear so hard today. She is not getting better from this bought of pneumonia. She is weaker than she has ever been. She has not interacted with us this whole week- due to the paralytics she is being given to help keep her saturation levels up. I am so scared.
We had another meeting today with her team of doctors..the tone was different. We brought Macaylah to one of the best children's hospitals in the country in hopes of finding some answer, or a remedy to her lung issues. When I heard from one of their top pediatric lung practitioners that there is nothing more that they can do for our little girl...I died inside.
The meeting was greuling...question after question about what we want for little Caylah....unsolicited opinions on what we SHOULD do or what we SHOULDN'T. Being told that there are no right or wrong answers to any of their questions..but feeling like every time I feel like I'm making the right decision, they make me feel like it's wrong.
We are going to spend the day again with our little Caylah bear tomorrow..the docs are going to wake her up from her paralytic..all I wish for is another precious smile and for her to know that her mom and dad are so proud of her.




