Margaret's o2 levels are starting to slowly decline but her cardiologist said that's exactly what he expects considering her specific
❤️defect and the severity of it. For peace of mind, we now have or very own pulse ox to spot check at home. As the numbers go down (and mom & dads anxiety about them goes up!) we will begin to talk about further tests that will need to be done in a couple of months (all depends on her sat level). Then we will have a better idea of when her "full repair" will need to happen. For now we get to keep on keepin on and continue to pray that her levels decrease slowly and she doesn't give us anymore surprises. 
Our family blog documenting our life as a Heart Family. Spreading CHD Awareness and living life to the fullest!
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OHS #2
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