The Heart and Soul Family: In the newspaper!

Sunday, June 22, 2008

In the newspaper!

I was contacted by the local newspaper last week wanting to do an article on Mended Little Hearts. I have already been contacted for a possible fundraising opportunity which I'll tell you more about at a later time. Here is a link to read the article.

http://www.azstarnet.com/allheadlines/244892.php

3 comments:

mina said...: Vanessa, you're doing a great job spreading CHD awareness while reaching out to other families that need support. Way to go!; June 22, 2008 at 2:31 PM
Tina:0) said...: What a great article & picture! I'm so proud of all that you've done to get Mended Little Hearts going! What a super mom you are! Hope you had a good weekend!; June 22, 2008 at 3:23 PM
Samantha said...: Bravo my friend! What a great thing you are doing! I love the picture of the two of you...so cute!

Keep up all your amazing work!

Love ya!
Samantha; June 22, 2008 at 4:05 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!

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Sunday, June 22, 2008

In the newspaper!

3 comments: