My son was born with P.R. diagnosed at birth. 3 months later he had jaw distraction surgery. We are now embarking on the dreaded palate surgery. I dread this because my sons Dr. Has already warned us that he will be unable to drink from a bottle, sippy cup it use a spoon, and absolutely nothing hard in his mouth for 3 wk after the surgery. Now my question is, can anyone out there who has already been through this process recommend any cups, techniques words of advise for successful feeding to help us through this next / last stage.
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