The Heart and Soul Family: Wigs for Kids

Thursday, July 14, 2011

Wigs for Kids

The other day Arianna and myself donated our hair to Wigs for Kids. This was something I have been wanting to do with her for a long time. She was so happy to be helping kids with cancer and she was finally old enough to understand and appreciate what we did! I am so proud of her!

Before

After
Arianna donated 12 inches
I donated 16 inches

Proud girl!

1 comment:

Nancy Jensen said...: Wow! I'm so proud of you both! I donated 11 inches after my nephew was diagnosed with his brain cancer (which he later died from). All the males in our family shaved their heads when Marcus had to shave his. His dad, brothers, uncles and male cousins shaved their heads and about 12 of his closest male friends shaved their heads too. what a great way to show support, huh?

I'm so glad that Arianna was able to understand that she was helping other kids. It's awesome. By the way... did you know that Arianna and Jessica share the same middle name? :); July 14, 2011 at 11:16 PM

Post a Comment

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

Thursday, July 14, 2011

Wigs for Kids

1 comment: