Hi everyone, my 7 1/2 month old SWCAH daughter (Savannah Alexis) is probably going to have tubes in her ears within the next few weeks.  She has had the same ear infection for a couple of months with 4 different oral antibiotics (and one shot) that havent cleared it up, she never sleeps and we are all so tired.  We go to the ear, nose and throat doctor on the 27th. I am wondering if anyone else’s CAH child had to have tubes in the past?  I would love to hear some experiences .  My ped says she will be fine and the endo told us to let him know so he can increase the meds, but I am still sort of freaking out and I am scared for her.  Thanks for listening.