Lydia was sent off the the OR at 7:30 EST this AM with Dr. Foker and Dr. Jennings who I am confident are one the best pairs to tackle the challenge that her esophagus presents. As of now, almost 8 hrs later, she’s doing well, stable and tolerating the procedure. Not sure what all is being done, but we trust she’s in good hands and are hoping for the best.
January is EA/TEF awareness month and as this is such a rare birth defect we are trying to help raise awareness of this defect and help other families avoid the nightmarish surgical path we have been on. Here is video montage put together of one of our EA moms. Pay close attention when you get to the L’s – there’s a super cute baby on there.
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