Friday, September 13, 2013

Playing ball and various advertisements.

I have started to feel like the mother of a special needs child. I bought a calendar to keep track of all his up coming appointments, all the super secret phone numbers and emails of doctors, his b.m.s, water intake and calories. Woo, it is a lot. I have been gathering documents, sending notes to the different doctors offices, filling out intake forms and faxing things left and right (thanks to my employer :))

We had hoped that when we put Simon under general anesthesia for his dental surgery we would also be having his cloudy eye fixed. However, that eye doctor says that he won't do his surgery at the same time as the dental surgery because of a risk of infection. :( We still haven't seen him yet, perhaps he will have a change of heart when we see him next week and will want to help us???? Or perhaps he could explain his point of view (WITHOUT SAYING LIABILITY, which is a word that is driving me NUTS lately, it is a cultural problem, that is all I am going to say on that today) and I will understand and I won't want to combine the surgery any more?....perhaps.

Today we went to have Simon's hearing checked. Well, they couldn't really do anything because there was a layer of dark ear wax in the way, completely in the way, in BOTH ears. So we thought, well, perhaps someone could come to the dental surgery remove the wax and then do the hearing test while he is under. Then we were told that no one will do that for us because the audiologist or the ENTs aren't allowed in that O.R. (bummer) I plan on calling on Monday to see if they could just check his hearing while he is still asleep in recovery? (somehow I am doubting they will help us with that but I figure it is worth asking)

I got home and thought, why should we go to a specialists to get wax removed? I googled it and started getting some of that wax out myself. I was pretty excited when it started exiting his right ear...however, I have gotten no movement out of the left. You can pray for that. If we can get it all cleared out, we could go and get it tested again, successfully and then we wouldn't have to worry about getting his hearing checked while he is asleep.

We did have a wonderful conversation with the doctor who was trying to check Simon's ears today. She used to work at Boy's Town in Omaha and was briefly involved in the international adoption clinic up there. (it has since closed, the closest one to us is in Minnesota) She is pretty sure they would do all our surgeries for us at once. But that would mean starting all over really, so we would have to do an intake up there with the ENT/audiologist, a dentist and a ophthalmologist... and then get the surgery scheduled. That would surely mean pushing the dental surgery out much further than it's scheduled date of Oct 2nd. So we will have to pray about that....because it sounds like starting over....which would be a bummer. It would also require a lot of driving to Omaha, which could get stressful when both of us are working. Right now we have been able to get appointments during Ishmael's naps and get monitor sitters, that sort of thing isn't going to work if we have appointments in Omaha.

So on Monday of this week we had a meeting at the local school about getting services for Simon. we are getting that ball rolling, but I don't really know how fast we will let it go. As we sat there with the vice principal, the speech therapist, Occupational therapist and the school phsycologist the subject came up of a swallow study. This was not the first time that this has been brought up. Simon eats slowly, he holds food in his mouth and feeding him is a chore. The OT told us that getting a swallow study will be the first thing that anyone asks us to do before they will want to help us....its a liability thing. Anyway, the fact that we haven't gotten him a swallow study and that he COULD be a silent aspirator, really got into my head and freaked me out. Then last night Simon started coughing, and he coughed all today. I am sure that it is just a cold.....but I am a little stressed. So please pray for our hearts in this...and that the Lord would lead us in what to do.
(on a lighter note, he started sniffling yesterday and I was able to introduce Simon to the nosefrida...I sucked that snot right out of his nose. If you don't have one, you should really get one. They sell them locally at circle ME, the cloth diaper store where I have worked in the past! It would be great for you to buy one going into winter! For my friends not in Lincoln, you should order one online, they are very handy to have. Simon laughed a lot after he got used to it)

Another tool I had to purchase was a very small set of nail clippers. Simon's nails are growing very quickly and they are very thick and sharp. He scratches his face up if I don't keep them cut nice and short. I have to cut them every other day! Which I figure is a good sign that he is getting some good nutrition absorbed in him!

Simon has also not been digesting very well yesterday and today. Although, on the bright side he is eating well. Please pray that we will know what to feed him to help his stomach digest better.
Please pray that all of our insurance stuff will go through and get resolved for August's bills. So far I have
Thanks everyone.
For other adoptive moms. Mealtrain is a great way to organize meals for the first month you are home. We had a wonderful soup brought to our home tonight and cookies. It was great. As I ease into laundry and eventually work I have LOVED not having to worry about cooking. I have been running to the store but only for a small amount of staples, fruit, yogurt and toilitires...and that has been a HUGE blessing. Google mealtrain, it is easy to use and free ( you don't need the fancy one!) My friends and family like knowing what they can do to help and I like having the food and company. They get to meet Simon, I get to eat great food....a WIN WIN.

Simon has been doing great with these appointments. I wear him in the baby carrier in all of them....it really relaxes him and the doctors and pretty much do whatever while he is on me. Most of them are very okay with that and so am I. We borrowed a Boba carrier from my friend Grace....it has worked wonderfully. I am VERY thankful we have it. If you are an adoptive mom, you should really at least give the carrier a try it is GREAT for attachment with you little one and it is really helping me with Simon in these appointments and anywhere really. I tried to go in the pharmacy without him in it yesterday and it was ridiculous. He doesn't hold still and attracts a lot more questions when he moving all around in my arms and I couldn't set him down anywhere....the baby carrier is where it is at. (Again, this can be purchased locally at circle ME!...shoot they will even mail you one will you are out of state :) )

That is all, I am tired and going to bed and I am turning into one big commercial :)

6 comments:

  1. So glad to see your sense of humor is intact, Anna! It will grow along with your heart and lighten the load! Love ya!

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    1. THANK YOU! I hope that it does!!!! Love you too!!

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  2. Wow! You are doing such a good job. I hear ya on the liability thing... "Look, can't I just sign a waiver and have you do what I want you to do?!"
    I have a question about baby carriers... Is there any concern with posture and bone development depending on the carrier you use? I love wrap style carriers, but I worry about support. Do you have any opinions on this?

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    1. What I hear most about baby carriers is how they effect the hips of the child. I have heard concerns raised about having the child face forward (away from your body) and their legs just dangling there for long periods. With Simon facing me, he is in more of a seated position, so his hips are at a good angle.

      As far as I know Simon doesn't have any hip troubles....we will be getting them checked more closely once he is closer to walking. My chiropractor, and boss, said that using the carrier I am using would help push his hips into place, if Simon was having that problem, so that is good. The boba also has little stirups for his feet, so that is a nice option.

      I like wraps too, but I am not as expeirenced with them. I will say that Simon doesn't "help" like a baby does in a carrier. Meaning, he is a little squiggly in the carrier, he pushes away from me at times, wants to move his arms in and out, ect. For that reason I found this carrier was easier and faster for me to use. (I didn't use a buckle carrier with Ishmael, my favorite was the maya ring sling!) I would research using a wrap with "taller" children. I don't know how tall your little one is, Simon is TALL for the carrier at 39 inches and he has more legs and arms then this things was intended for! :) But his weight is low enough to use it :(

      Thanks for the support! I can't wait until I can see photos of you with your girlie!!!

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  3. Hello! I am a Reece's Rainbow advocate and have been following your story for awhile. I wanted to say that my best friend is an audiologist at Boy's Town in Omaha. I told her about your situation, and she said, "We so SO MANY adopted kiddos here – our director has about 10 kids, 8 of them adopted from China. Boys Town is the best place, so I hope they are able to make it work!" If you are interested or choose to pursue, please feel free to contact me at jillharrison1@gmail.com. Blessings, Jill Harrison

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  4. If you'd like to email me at theclanton5@aol.com about your son's eye please feel free to. Our bio son and adopted daughter have Peter's Anomaly which is a cloudy cornea. Your eye doc may not really now about it. It's rare.... I can tell you more. Don't let anyone do anything until PA is ruled out! There are surgeries for PA!!!

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