Phew! That was some lengthy surgery! (NOT) OK! Seriously by the time I posted the "in surgery" blog update we were meeting with the surgeon discussing how the surgery went and meeting Hayleigh in the recovery room. Since the nasal drainage is much improved and almost non-existent in the past 3-4 days. We were supposed to follow up with Dr. Scalf yesterday, but he was not feeling well so we rescheduled for next week. More to come later.
We are scheduled for the first of next month to have genetics counseling and testing done. Dr. Helder (pediatrician) is concerned for her lack of height and the fact that she is not communicating. Not so much that she is not talking (which she is not doing at all) but more concerning is that she is not pointing at things and gesturing for things like her cup or toy that she wants. Some things I have researched on my own makes me concerned for Turner's Syndrome. We shall see!
Kids are back in school which equals boredom for Hayleigh and a little less chaos for mommy! Hope this update finds all of you well.
Until next time...
Wednesday, September 16, 2009
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1 comments:
Hey Alber family! I'm glad Hayleigh is doing better! She has been through alot, but I know her strenght. She was tough, and brought through! See ya guys later and may God bless you all!
Your neighbor, Jenna
P.S. Rebekah told me about this website! Pretty cool!
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