Learn About Callie's Journey with CHD

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Callie was born with an extremly rare, complex congenital heart defect, Hypoplastic Right Heart, Pulmonary Atresia with an Intact Ventricular Septum, MAPCA’s, Pulmonary vein stenosis. Currently she has had 11 heart surgeries,15 heart caths & over 30 blood transfusions.All of her surgeries have been performed at Lucile Packard Children’s Hospital in California by one of the best surgeons in the world, Dr. Frank Hanley.This blog is dedicated to her and her journey as a survivor with Congenital Heart Disease.Her battle is by no means over but we take one day at a time and rejoice in ALL the good times. Please join us in praying for our sweet girl.

Tuesday, January 17, 2012

Heart cath tomorrow.....

So, tomorrow is Callie's heart cath. Everything is riding on the results of this cath to determine whether or not she can have her Glenn she so desperately needs.

Please everyone pray for a safe, easy cath with GREAT results. Callie's cath is scheduled for 930am our time. So, everyone back at home that 1230pm is your time. Please take a minute and stop to pray for Callie around then, we need all the prayer warriors we can get, praying for our little girl.

I will update as much as I can tomorrow to keep everyone up to speed.

Also, I have been asked by a few people if it is okay for them to share Callie's story and the blog....100% YES;) Please feel free to share, it never hurts to have an extra person praying;) Also, Callie's story helps spread Congenital Heart Defect awareness to people!

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