Arianna Marie
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This site was created to keep family and friends up to date with Arianna's progress. Arianna was born with a congenital heart defect called Tetralogy of Fallot and was diagnosed with DiGeorge Syndrome, a genetic disorder. If you read through "My Story" it tells you the beginning of our journey. Thank you for taking the time to visit our site.

Vanessa, Robert & Arianna

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  WEDNESDAY, FEBRUARY 27, 2008 10:38 PM, CST
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I have decided to stop posting on this caring bridge site. I am finding it redundant to just copy and paste my posts from the blog over to here. I am keeping it active because I want to print out our journal and guestbook signings for Arianna to have when she gets older.

If you want to keep up with whats happening with Arianna you can do so through our blog. There is a way to get update notification for our blog so you will know when a new post is added. Just go to the blog and on the top right section there is a place to enter your email address.

Thank you everyone for all your messages and support we have received through caringbridge. Please continue to do so on our blog, as you all have made this journey much more brighter just knowing you all care.
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Thank you for stopping by and checking on Arianna. Please feel free to leave a message, we love to hear from you all!

You can also check out our blog at http://ariannamarie.blogspot.com
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EMAIL AUTHOR
nessa1880@yahoo.com
HOSPITAL INFORMATION
University Medical Center
1501 N. Campbell Ave
Tucson, AZ 85724
United States