Saturday, May 23, 2009

Our family went to the upper midwest annual Williams Syndrome Picnic. We went last year when Hazel was 7 months old. We had a great time visiting with the kids and talking with the other parents. It's wonderful to see all the kids a year older and that everyone is doing well. We hope to make it a yearly outing.

Time....

The hope was to move Hazel's caringbridge site over to this blog, but we were a little side tracked with health issues. A quick update on Hazel since last Oct. 4th's post. She had successful Open heart surgery to fix her SVAS. She was switched over to Calcilo formula and has since started to go off of it. She has been put on Propranolol and Diuril to control her blood pressure due to her hypoplastic renal arteries (Kidney arteries). Hazel is now eating real food and cruising around. All in all we are really happy with how she has progressed since surgery. We hope to never have to go through a surgery like that again.