Thursday, September 3, 2009
Jillian Has Been Banded
Wednesday, September 2, 2009
It Could Happen To Anyone...Right?
Anyhoo, I left Jared with the girls at about 7:45 and he was going to get them in bed and asleep. I left for my errands and was home by 9:00. He did a great job, both girls were fast asleep. One little lady was in her crib in her room, the other was in the pack-n-play in the guest room. We have found that naps and night time go a LOT easier if they are put in separate rooms to fall asleep. After both girls are asleep at night, I move the baby in the guest room to her crib. They don't wake each other up once they are asleep, but they have a hard time going to sleep with someone in the room. Especially if that someone else has the giggles.
So, I go to check the babies, making sure they are definitely asleep before I think about moving the one to her crib. Jared says that Jillian is in her bed and Jenna is in the guest room. Sure enough, Jilly is in her bed and asleep. So I go to move Jenna, grab her up, get her in her bed and I look down at her face and clothes and it isn't Jenna! I look again, trying not to wake the baby up too much and sure enough Jillian was in the pack-n-play, with Jenna's Lovie and pacifier. So I go and take a second peak at who I thought was Jillian in Jillian's bed and I am doing everything I can not to bust out laughing and wake up the babies. Jenna is in Jillian's bed with Jillian's Lovie and pacifier!!
Ha-Ha!! So I get them situated (I didn't move them to the right beds, I am not that insane!
I want them to stay asleep.) and go back in to our room. I ask Jared which baby he had put where....just in case I heard him wrong, and he says Jenna was in the guest room and Jillian was in her crib. So I ask him if maybe he was wrong and you should have seen the look on his face when I told him that the girls had been goofed! Priceless!! Then he said..."Hey, it could happen to anyone!" I don't think his excuse made him feel better though, he was still trying to sort out the mix up this morning.
So, the moral of the story is....if it can happen to the Daddy, it can happen to you. For all those who still don't know who is who (YOU KNOW WHO YOU ARE!!) you can rest easy; if we don't know which kid is which, we can hardly expect you to know. :)
More to Come (with updates on how it went with Jillian's band this afternoon),
Jess
Wednesday, August 26, 2009
Little Lambs
Jillian
Jenna
Friday, August 14, 2009
Lots & Lots to Say
Jenna and Jilly's bobos say it all. :)
I can't believe they keep them on but they do. Of course once they figured the sunglasses block that terribly, icky sun, they were more inclined to keep them on.
So I'll give you a heads up now....the next few weeks and months are going to be really busy for us. The ball has finally started rolling in regards to Jillian's cranial band (helmet). You might remember that we went to visit Cranial Technologies several weeks ago and they deemed Jillian a good candidate for treatment. We found out later that day Cranial Technologies wasn't part of our network of providers with our insurance company (not surprising). So we went to visit Hanger Prosthetics & Orthotics a few weeks ago. I didn't like this company as much. The Cranial Technologies' therapists were far more professional and the office was more advanced technology wise. Not to say that both offices weren't extremely helpful and courteous, because they were, but I just felt far more at ease with the first company. Plus, everything I have read about them on the Internet makes Cranial Technologies sound like a great place that gets the treatment done right the first time. They make sure the bands fit exactly perfect so that you get the best results.
But, since Hanger was in our network we had resigned ourselves to use them...or at least until our insurance company denied Jillian's treatment. Also not surprising. They denied our treatment request because Jillian's asymmetry was 3/10ths of a centimeter off. They require the measurements of her flat spot to be at least 1 cm different on one side than the other and Jilly's measurements were .7cm. OMG!!! What good is having insurance I ask? We won't go there though...Dad! :) Tee Hee.
But, the positional different of Jillian's ears is a big deal for us. We have noticed that her sunglasses don't stay on like Jenna's because one of Jillian's ears is so much farther forward on her face than her other. That makes me worried later on if she has to have glasses (which is highly likely since I am officially legally blind with out corrective vision and she was a preemie which puts her and Jenna at risk for vision problems, especially since they were assisted with their breathing for a little while--something about the CPAP and the blowing of oxygen that puts them at risk for ROP, which is why we see an eye specialist for the 2nd time in November, for preventative and detection reasons) we won't be able to get the glasses to fit properly--which is something the therapist at Cranial Technologies warned us about in regards to non-treatment of her plagiocephaly (medical term for flat spot).
The bummer is that the treatment is very expensive with no insurance at a whopping $3,600 for the consultation, measurement session, making of the band, fitting session and all therapists sessions thereafter to track her progression (sessions are every one to two weeks). But, we are blessed with wonderful families and some of our family (I am not sure they would want me to publish their names on my blog) have generously given us the money so that we could not only treat Jillian's plagiocephaly, but also use the company we felt more comfortable with, Cranial Technologies. I know they felt, as did we, that it was medically necessary for Jillian to receive treatment now so that later we wouldn't have to worry about non-treatments risks like vision problems, chronic ear infections, sinus infections, TMJ or lock jaw, etc. Not to mention the cosmetic shape of Jillian's head being something Jillian might be embarassed about later in life. We are blessed by family and we love them more than we can express.
So all that to say, Jillian goes in next week to get her head measured with the DSI equipment (digital 3-D cameras that measure her head to within fractions of a millimeter). Then on September 2nd we go and get Jilly's band fitted. From then on she will wear the band for exactly 23 hours a day (we take it off for one hour to clean the band and her head every day). We will go to our follow up appointments for once a week in the beginning and then probably every 10-14 days thereafter. She will most likely wear the band for between 8 and 12 weeks depending on how fast her head grows. It will be a commitment for sure but I think it will be well worth it.
In the meantime... I have been trying to decide how to decorate her band. We are provided with a sterile, white band. However, the outside material can be decorated. I thought about doing it myself but I don't have the time. Luckily, on one of the Plagio Support Group chat forums I saw some entries about Bling Your Band, which is a band design company owned by a mom whose daughter went through treatment. I have been working with Coree, the owner, on coming up with a design for Jilly's band. I think I am going to leave it as a surprise but I encourage you to check out her blog and see the designs she has come up with for other kiddos. I do know that Jillian's band will be cutest by far! :)
Pretty much the reason why parents decorate the band is the comments received from the public. Most people don't know what the band is for and I think they are made uncomfortable by it. Before I knew about all of this I am ashamed to say I thought it was because the child was mentally challenged or something. Maybe they needed extra protection on their head? I had no idea. I never asked or commented but I remember some people whispering. A lot of the parents on the chat forum said they would receive rude comments about their child. Decorating the band keeps the treatment less sterile and instead of being something people are apprehensive about, it might just be a conversation starter instead.
I know that Jared and I will have to deal with comments, stares, whispers, etc.--even naysayers within our own circle of friends and family who would like to tell us how it was when they were kids or were raising their own kids 20, 30 50 years ago and this is all silly and unnecessary. I am trying to prepare now for those comments so they may not be as hurtful later. I just know that what we are doing for Jillian is right for her and as a parent I am responsible for following through with what is best.
More to Come...
Jessica
Thursday, August 6, 2009
A Soothing Effect

