So we went for our first of many appointments at Primary Children's Medical Center regarding Max's heart.
This is Georgia saying goodbye as we left at 9:30am for our {8 hr} appointment.
Max's oxygen levels were really low after the sedation, especially when he would eat.
{they wanted them above 80 and his would drop into the 60's and 50's when eating}
We spent a couple of hours just hanging out trying to get the numbers up, but he was really groggy. {these pictures are from today, not the groggy little guy}
Our cardiologist, Dr. Saarel, thought Max was doing fine and thought he should wait until he's 4 months old to do the open heart surgery. So we didn't get it scheduled. I am kind of bummed about that. I really want to get it over with. Maybe after she looks over the echo she'll change her mind :)
We also went to our first Utah Down Syndrome Foundation event last night. Actually, just Max, my mom, & I went. Piper crashed after a full play day at a friend's, so she and Steve didn't make it. It was great to meet a few 'blog commentors' and others who have gone through this whole process before.
3 comments:
I'm so sorry I missed the luau! I am sick. You guys would have ran me out of the park :-) I'm happy to read that Max is doing fairly well considering all things!
It was so good to meet you! Little Max is darling! I feel like Justin's sedated echo and PDA closure was just yesterday. Time flies by. Let's keep in touch!
Emily
What you describe is exactly what we experienced the first few days of his life at the hospital. Eating was a huge inhibitor and he had to have frequent forced breaks to "catch his breath".
Overjoyed to hear that it was short lived like before and also that he is as tough as I knew.
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