Poor little Logan has had issue after issue with ear infections, like 6 (or was it 7? I lost count) in the first year of his life, and then this summer we got a chance to meet with an outstanding ENT who is also a State Legislator for Utah. Our family probably paid for some of his campaign with our 4 surgeries in 3 days. Go Barlow! He was fantastic! I would have voted for him. For Logan, he took his adenoids out and put ear tubes in. Sounds like the Hokey Pokey song, huh? Logan became a different baby. He babbled, he learned to stand, he interacted more with people, he was on track to be normal. People always say, "It's okay to be different!" But they probably have "normal" children. (I know all kids are different. But it still stresses parents out when they are below the "mark." It's lame, but we do.)
| Do you see sweet Logan tugging at his ear? Poor guy. |
So we started with PT. Physical Therapy made me want to cry along with Logan. Someone told me that they call it PT for a reason. Pain and Torture! It was HARD for Logan and hard to watch him go through it, but I can attest that it was totally worth it. They would work with him for 30 minutes, then make me do the exercises for 15 minutes to make sure that I knew what I was doing when we went home and did it.
Logan hated me. No, I'm serious. We would work hard every morning and then throughout the day he would try to avoid me as much as possible. When we were shopping in Walmart he made me feel like I was a kidnapper because he would reach for anyone and everyone walking by and whine
So we fast forward a bit and his development started slowing down. We were waiting for funding for PT so we can continue this "fun" race. The exercises I have been doing became useless because he was finally crawling, but I didn't know how to help him with walking. He wouldn't even walk around furniture. I'm sure you have all played the waiting game. I tend to lose every time. I get cranky and dwell on it. Not so good for your overall well being.
Then BAM! He gets a MAJOR ear infection. Again. One tube is draining this yucky booger-like gunk, but he is pulling on both ears, so we go to the doctor here who can't see the tube in his left ear. Crap. No tube. He's not positive, so we go to an ENT to make sure. He gets his fancy shmancy microscope and looks into the ear and concurs that there is indeed no tube. Logan gets connected to a machine that can tell if he can hear out of his ear, and it flat lines. Just like a heart monitor. His ear is dead. Double crap.
Sooooo, we talk about going to London to reinsert another tube, but B leaves for DC for almost a month. Good timing huh? So another round of the waiting game. I get no sympathy from Logan. Ha ha mom. Now it's your turn to suffer! We go on yet another round of antibiotics and since this is his first time in Prague getting antibiotics, I tell the doctor the exact kind of antibiotics that work for him and even the dose. Mr Doctor is the kind of doctor that isn't really impressed with that kind of parent know how. He's more the type of "sit there and listen to my knowledgeable self and you may just nod in approval and bask in my smartiness and big words" kind of doctor. I'm sure we will get along GREAT... if I could only just keep my big yapper shut. Not a chance. Wish me luck for the next 3 years. I digress...
After 3 days on the antibiotics he is back to his "normal" self and then some. Within a week he is scooting around furniture. Within 2 weeks he is taking steps and saying words! He couldn't even say the sound of that word, let alone the actual word! If his life were a movie, there would be loud angelic music in the background singing, "Hallelujah! Hallelujah! Brothers and Sisters it is a miracle!"
The antibiotics have cleared his infection and has catapulted his development. I am convinced that his clogged ears are linked to his balance and speech. Okay, so it doesn't take a genius to make the connection, but I had to state the obvious so that obviously I don't get messages from my smarty pants friends and family who have noticed the obvious.
But we still have a tube missing. crap. In the mean time, my family is praying, B's family is praying, our family is praying, and friends are praying that it will all work out because if I fly to London with Logan, it would just be a tough situation all around. B trying to be a single working dad with 2 kids at home seemed impossible...
BUT, drum roll please I went in today for a followup appointment for Logan and GUESS WHAT??!!!? He has both tubes in his ears!!
Now I have a choice. I can lose faith in the Doc(s) and blame them for unnecessary worry, or I can gain greater faith in God. Come on. Why bring all that negativity around? I am going to thank my Heavenly Father and all those who have been praying for our family and that we don't have to do the Hokey Pokey again. Today was a great day and I am not even going to think about the HOW or WHY this happened and just be grateful that it did. Just for Logan, tonight say a little prayer thanking our Maker for this little miracle in our little life. Man we have it good. The End.








