Yesterday we met with the neurosurgeon and his team. We shared all of our frustrations with Olives' care so far, and our concern with her remaining here without a better plan in place.
The neonatologist had training in the States before and she has agreed to do tapping every two days to remove fluid. This seems to be a good option, better than having residents without much experience doing it, or waiting for the neurosurgeons to come who are extremely busy.
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