The Heart and Soul Family

Tuesday, July 14, 2009

This is a video I took of Ari eating the other day.

Make video montages at www.OneTrueMedia.com

6 comments:

The Portas said...: Cute girl! I just love watching videos of her and hearing that sweet voice. Macaroni, yum!!; July 14, 2009 at 5:52 AM
jencooper said...: Could she please be any cuter?? She is so adorable!

I am glad that she is feeling better. I hope that you are having a terrific week!

<3,
Jennifer; July 14, 2009 at 1:51 PM
Anderson Family said...: Eating is so much fun when you get to eat the same piece over and over again.; July 16, 2009 at 6:54 AM
Unknown said...: Glad she is doing better, She is so cute and eating again that is great.; July 16, 2009 at 7:41 AM
Tina:0) said...: What a cutie pie?!?! Isn't it such fun to take little one's out to eat?! I always seem to forget the bib, though!

Hope you're having a nice weekend!; July 18, 2009 at 8:00 PM
Kathy said...: OH...I can't wait!!!
I love watching Ari hit all these awesome milestones...I'm showing Isaac...asking him to PLEASE pay attention!!; July 21, 2009 at 9:51 PM

Arianna Marie

Arianna was born on 11/26/06. 4 weeks premature, and weighing 4lbs 13ozs. She was born with a congenital heart defect called Tetralogy of Fallot, which is actually 4 heart defects, and was later diagnosed with an ASD. She had open-heart surgery on 5/22/06. Her surgery was to patch the VSD, patch the ASD, widen her pulmonary artery, and attempt to fix her pulmonary valve. They created a man-made pulmonary valve out of myocardium to avoid a conduit placement, which would require multiple surgeries. On September 21st, 2012 we got the news that Arianna's right ventricle pressures are too high and she needs a pulmonary valve placed. When we meet with the surgeon we found out she also has pulmonary branch stenosis and a possible defect in her tricuspid valve. He will be addressing all of these issues at the time of surgery. On October 18th, 2012, Arianna had her 2nd open-heart surgery.

At 5 weeks old she was diagnosed with a genetic disorder called 22q11.2 Deletion Syndrome, which is caused by a deletion of a small segment of the long arm of chromosome 22. This disorder has many names such as 22q Deletion syndrome, Velo-Cardio-Facial syndrome, DiGeorge syndrome, Shprintzen syndrome, and Catch 22. So far there has been more than 180 anomalies reported in this syndrome, which is highly variable from person to person and no individual has all of the anomalies. Arianna has overcome many obstacles and we find peace in knowing that God is working miracles in her life. We set this site up to share our family journey. We know that God has a special plan for Arianna and our family!

Pages

Tuesday, July 14, 2009

6 comments: