Can you please join us in praying for Miss Pear's cardiology appointment October 22?
This is the follow up to the one a year ago where they discovered she may need to be referred to a pediatric cardiothoracic surgeon. Actually, the doctor said it was more of a case of when she was referred, not if. But we have been praying for a miracle, a miracle that would defy all medical odds that the membrane would either shrink or disappear completely, both completely unheard of medically.
But God is still in the miracle business, and it is Him that we put our trust in.
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3 comments:
God can do all things. Prayers offered up. :)
I'm praying for you and Miss Pear. In Him all things are possible
Prayers for you and your precious daughter. I have a son that was diagnosed at 1 1/2 with a membrane growing under his aorta valve. The first cardiologist told us he would have to have it removed before he started kindergarten. We got a second opinion and our new cardiologist said she just needed to monitor it to make sure it didn't get larger and damage the valve. It is now 12 1/2 years later. He is a healthy, happy freshman in high school with a membrane in his heart that has never been a problem. We go to the cardiologist every two years just to make sure everything is still "good". Hopefully this will be the same thing that happens with your daughter. Please email me if you would like to "talk" about it.
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