When I thought about writing this post, the title was going to be "Two months and a tongue tie later." As you can see, I failed in my timing. We also got a diagnosis contrary to what I was somewhat expecting.
A few weeks ago I wrote a post detailing all that we've been through with breastfeeding. Toward the end I mentioned that a lactation consultant thought Little Man might have a tongue tie, but one that no surgeon might touch. The very next week our pediatrician agreed and told us to go see a specialist to find out if anything could be done.
If you haven't heard of a tongue tie, you aren't alone, though I bet you've heard the phrase "tongue-tied." If you want to know more or see pictures, google it, but it basically means there's a piece of tissue or something that attaches the tongue to the floor of the mouth. Unless clipped, it won't let the tongue move as freely, thus causing nursing problems as well as speech impediments.
Some babies have a posterior tongue tie that is harder to operate on, and since I had been told Silas's was not as pronounced I thought maybe this was the case. I knew he had a high palette (sign of a tongue tie) and he tends to lose suction, but his tongue does move out over his teeth, something that doesn't happen with most tongue tie cases.
I went into our appointment with the pediatric surgeon secretly hoping for a true tongue tie just because it would "solve" my nursing problems. (Me, looking for another solution, trying to control...story of my life!) The pain is pretty much gone now, but Little Man is still an inefficient feeder. He just takes so stinkin' long!
Well, that didn't happen. The surgeon said he doesn't see one at all, that Silas is perfectly fine. I know this is great--who wants their child to go through the agony of having something clipped in his mouth?--but it basically means that until Silas gets big enough to figure it out (or maybe never) he will just take his time.
And that has to be okay. I'm trying to remind myself that one day he won't let me hold him for 30 minutes several times a day. I also just have to organize things so that when he takes a long time to eat, I don't get stressed that we can't go here or do this, etc. And besides, he only eats five times a day now, so things are improving!
Now, funny/could have been not so fun story about our pediatric surgeon appointment. After waiting for 20-30 minutes, we were called back. Little Man was weighed, and we were put in a room. Just as the nurse was walking out of the door, the fire alarm goes off. This was not a normal fire alarm. It was SCREECHING, and for people with epilepsy, seizures would have ensued with the flashing lights.
No one moved at first, but finally the nurse tells me we have to evacuate. I get Silas in one arm, his car seat and bag in the other, and we walk down the stairs outside. We trekked across the parking lot because if this was a real fire I wasn't going to be standing just outside the front door with all the other inconvenienced people.
After several minutes, the fire department arrived. I could tell by the length of time nothing bad was actually happening. At least I hope if there had been a fire they would've responded more quickly. The building was checked, and we were allowed back in.
The entire time we were in the building with the insane screeching, Silas didn't make a peep. He was awake, and I did my best to shove one of his ears into my side while trying to put my arm (that was holding him) over the other ear. Apparently that was unnecessary because my son just looked around, frowning, knowing very well that this was taking more time out of our day than anticipated. Thankful for that, and I really hope his hearing wasn't harmed!
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