Not a lot to report, but we have learned to appreciate that!
After having flu & Synagis shots & getting his feeding tube changed, Mitchell isn't too fond of going to the doctor. His cardiologist decided to wait until his next visit (mid Dec.)to do an echocardiogram. His weight is creeping up- 19 lbs. 3 oz. Although, not on the charts; his weight/length ration is proportionate. He does have Huff genes, so he may just be small.
His oxygen saturation remained mid to high 80s while monitored (for about 10 minutes). This is quite typical during the post Glenn phase. We will probably see an increase following his next surgery. Many people have been asking about his next surgery. We just don't know when it will be. They will continue to monitor his heart; and at some point, he will require additional blood flow to his lungs. Textbook says 18-24 mos. but we have noticed that other children have had the surgery around age 3. Given that he is small, I would think later might be more likely. He does have a stent in his pulmonary artery that may require a trip to the cath lab for dilation at some point. For now, he is doing well; and for this, we are very thankful!
Mitchell has started to walk (while pushing things). He is getting stronger, and doing more and more. He stays very busy, and is repeating a lot of words. He is identifying body parts; some letter sounds- really becoming quite vocal! It is very exciting to see. He LOVES his daddy and goes racing to the kitchen as soon as he hears the door open. He points in the morning and asks for his "Mi Mi". He has gotten into the routine of visiting grandma around the corner. When you ask him questions, he usually responds with a "yeah"; but shakes his head no- if you want him to eat something, or doesn't want to do what you ask. He has quite a bit of spunk, which is good- he's had to fight through a lot during his 17 months.
Thank you for your continued support & interest in Mitchell.
We feel so blessed to have him with us and try to enjoy every minute.
We hope you all enjoy this time of year & can rejoice in God's blessings.
Monday, November 1, 2010
Cardiology Update
Posted by The Holz Family at 9:32 PM
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1 comments:
I AM A COUSIN OF THE CRISAFULLI'S THAT ARE CONNECTED TO YOU THROUGH THE AUSK'S. I KEEP TRACK OF MITCHELL AND YOUR FAMILY THROUGH YOUR BLOG, AND PRAY DAILY FOR YOU ALL, HAVE NOT SEEN A BLOG SINCE NOV AND AM WONDERING HOW EVERYONE IS DOING? HOPE ALL IS WELL. PRAYING FOR YOU ALL! NICOLE CRISAFULLI
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