Aubrey's Blog Launch!
Friday, September 01, 2006
Hello everyone and thank you for visiting!
We have implemented yet another way to keep our visitors, just like you, informed on events taking place, news, and a way for families and supporters to reach out to other people.
Please use this blog to express anything you would like. We'll have more topics very soon!!
Thank you from the bottom our hearts and double lungs!
~ The Aubrey Rose Foundation
We have implemented yet another way to keep our visitors, just like you, informed on events taking place, news, and a way for families and supporters to reach out to other people.
Please use this blog to express anything you would like. We'll have more topics very soon!!
Thank you from the bottom our hearts and double lungs!
~ The Aubrey Rose Foundation


2 Comments:
At Friday, September 01, 2006 11:03:00 PM,
Nancy Hollenkamp said…
This comment has been removed by a blog administrator.
At Saturday, March 01, 2008 8:13:00 AM,
Anonymous said…
I think what you are doing is wonderful. When our son Kenton had a Tetralogy of Fallot repair done at Cincinnati in 1991, there was very little external support. We were very fortunate to have Dr. Bailey perform his surgery. Kenton is now 17 years old. He is a fine young man who gives back to his community, is a good student, and has been able to play varsity golf and wrestle, reaching the Fairfield District Tournament before being eliminated. He has exceeded the expectations were given at the time of his surgery, and talking to his cardiologist, I know there are improved methods being used today. So, if you are a parent with a child diagnosed with a congenital heart defect, know that there are good outcomes, and take heart.
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