They decided to wait to do an echo cardiogram until a cardiologist from Primary Children's could do it on the spot instead of just getting a report and then needing to see us anyway. Sooooo, we waited a month for that appointment.
About 3 days before the appointment, Ashlie started having chest pains and complaining her chest felt like it was going to explode. We took her into Community Care, had another chest x-ray and was told it didn't look good. The diagnosis was congestive heart failure.....a very scary, scary moment for me as a mom. After telling Alan, completly losing it, I calmed down enough to call the pediatric clinic in Poky who had seen her the month earlier. That doctor, bless his heart, assured me congestive heart failure can mean many things, mainly that her heart is not functioning properly but most likely could be fixed.
Anyway, we went to the cardiology clinic, met with Dr. Williams, who let us know from the echo that she does have a hole between her atriums about 2cm big (ASD, same as Garrett, only his closed up and was tiny.) She does need surgery, open heart, to fix the hole and most likely the heart will go back to its normal size and start functioniong properly. **Much better news than previously diagnosed** Her surgery is scheduled for October 2nd and it will be a huge relief to get this over with. 2 1/2 months is much too long to wait. It's been difficult preparing for and of course its been hard on Ashlie waiting, wondering and worrying.
Oh yea, NO cystic fibrosis!!!!!
Oh yea, NO cystic fibrosis!!!!!




Garrett, Justin and Hallie LOVED football this year. Yes, Hallie got to play also. They all finally were able to catch the ball and actually knew which way to run. They all 3 were able to make touchdowns.








