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
Now that our big day yesterday is over and we've been able to get a few hours of sleep, we are feeling rested and ready to give a p...
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Margaret has kept us all alert and aware of her every move (literally) over the last 24 hours. For the most part, she's been relaxing a...
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the look of pure exhaustion If there's one thing we all know about Margaret, it's that she likes to be the boss. Recovering aft...
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After meeting with the surgeon who is performing Margaret's procedure we find ourselves better understanding what they are aiming to do ...
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