So, Nate is part of the 10% of children whose tear duct blockages do not resolve on their own. I am not surprised considering his other craniofacial abnormalities and mid-line defects.
Has anyone's child had this procedure? I know what it entails, I was just curious regarding any "inside information" that would be helpful. He has been under general anesthesia before, so we are well prepared in that arena.
Re: Tear Duct Obstruction surgery
Thanks everyone for the tips!!
Our ophthalmologist is Dr. Feirgang. He does his procedures at GBMC. I did hear from him that the Wilmer folks are not fans of piggybacking. They don't even want Hopkins ENTs piggybacking.
I was trying to think of doing a two-fer with Nate, but they only thing I can come up with is scoping his nose and throat for breathing obstructions. He still has his mouth open about 70% of the time. SLP thinks that if we can get him to close his mouth more he may gain on some bilabial sound making. *shrugs*
I think his open mouth is more a muscle tone thing than a breathing thing since he seems to have it closed most of the time while sleeping....Anywhooo, the procedure is scheduled and frankly, I am not in the mood for the hassle of a two-fer for only an information gathering procedure. We may pursue a swallow study in the future...hmmm...that reminds me of another question I have for you ladies....
I can't wait to get rid of the goopy eye!!!
I am always worried school will send him home thinking he has conjunctivitis.
It is entirely possible that piggybacking could be an option at this time. I have no idea how current Dr. F's impression is regarding how Wilmer operates.....