Monday, January 28, 2013
Faith Telling a Story
I wanted to get a video of Faith talking before her surgery. I think her speech will regress a little after her surgery since they are taking out her tonsils as well as growing her jaw. So much change will probably mean she has to relearn how to position her tongue and lips again.
I think she learned this story at school, but she made a few changes to if. I love her dramatic flare!
The words...
"I made a snowball, perfect as can be,
I thought it could sleep with me,
I made it a pillow and let it sleep with me,
But last night it ran away, but first it wet the bed!!! (argh!!)
Note from Faith's Teacher
I got the greatest note from Faith's teacher, Mrs. Frank, who we actually knew from 5-10 years ago as her son, Ryan Frank, and our Ryan played baseball together! Anyway, Faith has really been enjoying 1st grade with Mrs. Frank and she has been getting over her shyness from last year. With her upcoming surgery, Faith has been talking about it quite openly at school. Here' the note from Nancy...
Nancy
Robin,
Thanks for
checking in with Mike regarding your visit to explain Faith's surgery. Let me
know what day works for you to come in to visit with first grade. I think he
mentioned Thursday was a possibility. Let me know what works best for you and
we will make it work.
Yesterday Faith
was sitting with a small group of classmates and her surgery came up. She was
very chatty about it, which I thought was great. This morning a student asked a
question about her surgery and I said, "Well let's ask Faith if she would
like to answer your question with all of us." She immediately said,
"yes", which was great. So after our morning message this morning
Faith stood before her classmates and said she was going to Cincinnati for
surgery, that she would have bars on her face and that dad would be turning her
pins. She told them it was to help her jaw grow so she could get rid of her
trach and she would be able to eat more. She also mentioned knowing a friend
that already had the surgery. She said she needed to stay home for awhile
because she would be sore and tired. We talked about being able to Skype her
when she was up for it, as well as what we could do, say when, and if we see
Faith with her "bars" on her face.
It was wonderful
and Faith was a champ! Her classmates asked very appropriate questions and were
truly interested in what she was telling them. I think she did a great job
laying the groundwork for your visit. It was so spontaneous and natural.
Let me know what
works for you. It seemed like surgery was so far away last time we talked and
now it is just around the corner. I am doing my best to keep our room healthy.
We have had some coughs and runny noses the last few days. I will keep my
fingers crossed, and hope that it is not passed on to Faith.
Take care,
Pretty cool, isn't it? I'm planning on coming in to talk with the class this Thursday, but I almost feel like I don't need to as Faith is doing such a good job of it all by herself! I asked Christy Holton, another mom with a kiddo (Harlie) going through the same kind of surgeries about ideas for how to present this to the kids. She made a book for her daughter when she started Kindergarten so all the kids could get to know her and not just stare at her the first time they saw her. She sent me the link to the book (http://lifesinceharlie.blogspot.com/2011/10/harlies-book.html) which is so sweet. And she gave me some pointers about keeping everything really short so the kids could understand. So, with that advice I created a couple slides to share with the kids and send home with them when I come in on Thursday.
I will try to post a copy here.
Robin
Thursday, January 17, 2013
Upcoming Surgery - February 6th
We are moving forward again on this journey of Faith's to continue reconstruction of her jaw in hopes of getting her trach removed and letting her live a more typical life for a kid. We had her bone graft done in June and now it is time to use that new bone to grow some more bone and give her a bigger jaw. So we have a jaw distraction scheduled on February 6th, along with a tonsillectomy and adenoidectomy. Apparently her tonsils are "huge" and taking up too much space in her throat.
So, Faith and I will be flying out on Tuesday, 2/5, she will have surgery on 2/6 and stay in the hospital for 2 nights, and then we will be in the Ronald McDonald House for 3 nights and flying home on Monday, 2/11.
Faith will have the distraction pins as well as a halo device (called a Rigid Extraction Device or "RED Device") in place for about 6-7 weeks. We will turn the distraction pins every day for about a month and then I will take her back to Cincinnati for another surgery on March 8th for a chin advancement to build more of a chin for her. We are still waiting to see if that will be approved by our insurance as apparently it is usually done for cosmetic reasons although for Faith it is really for reconstructive purposes.
Following the chin advancement we will fly home again to let that heal along with letting the distracted jaw bone solidify before they take all the hardware off a couple weeks later (around the end of March). Right now we are tentatively planning to have a local Denver surgeon do the removal rather than flying back to Cincinnati a third time.
Our primary goal in the timing of this surgery was to not take away another summer for Faith and to make sure everything is done in time to go to her cousin Megan's wedding in April in Branson, MO. But, since we are doing it during the school year, it will mean she is going to be out of school for the whole time. We are working with her school to set up "homebound" education, but that only gives her a visiting teacher 2 times a week for a hour or two at a time. Hopefully she will be able to learn enough to "pass" 1st grade and continue on to 2nd grade (I'm pretty sure they will work with her and us to make that happen).
We have been talking to Faith about the surgery and preparing her, Fred is very good at talking it up and making it just an expected event. She is so brave and asks questions about whether she will be able to eat with the halo device on. Luckily she met a little girl at the Ronald McDonal House last summer who was going through this same surgery and was wearing the RED device and she saw her eating with it on, so we know she can try to eat, although it will likely be messy, which it is now anyway!! She also asked me if she will be able to sleep with the device on, which is a good question since it will probably be pretty uncomfortable. I told her I think we will be able to use lots of pillows to help her find a comfortable position to sleep in.
I will be posting a "before" picture soon for us to have a baseline to see how much growth she gets from this distraction. I am very hopeful this surgery could be the one to get her trach out, but I think Fred is more cautious thinking she'll have it for many more years still. I should know better than to get my hopes up, but I just can't help it!!
Thanks for reading!
Robin
So, Faith and I will be flying out on Tuesday, 2/5, she will have surgery on 2/6 and stay in the hospital for 2 nights, and then we will be in the Ronald McDonald House for 3 nights and flying home on Monday, 2/11.
Faith will have the distraction pins as well as a halo device (called a Rigid Extraction Device or "RED Device") in place for about 6-7 weeks. We will turn the distraction pins every day for about a month and then I will take her back to Cincinnati for another surgery on March 8th for a chin advancement to build more of a chin for her. We are still waiting to see if that will be approved by our insurance as apparently it is usually done for cosmetic reasons although for Faith it is really for reconstructive purposes.
Following the chin advancement we will fly home again to let that heal along with letting the distracted jaw bone solidify before they take all the hardware off a couple weeks later (around the end of March). Right now we are tentatively planning to have a local Denver surgeon do the removal rather than flying back to Cincinnati a third time.
Our primary goal in the timing of this surgery was to not take away another summer for Faith and to make sure everything is done in time to go to her cousin Megan's wedding in April in Branson, MO. But, since we are doing it during the school year, it will mean she is going to be out of school for the whole time. We are working with her school to set up "homebound" education, but that only gives her a visiting teacher 2 times a week for a hour or two at a time. Hopefully she will be able to learn enough to "pass" 1st grade and continue on to 2nd grade (I'm pretty sure they will work with her and us to make that happen).
We have been talking to Faith about the surgery and preparing her, Fred is very good at talking it up and making it just an expected event. She is so brave and asks questions about whether she will be able to eat with the halo device on. Luckily she met a little girl at the Ronald McDonal House last summer who was going through this same surgery and was wearing the RED device and she saw her eating with it on, so we know she can try to eat, although it will likely be messy, which it is now anyway!! She also asked me if she will be able to sleep with the device on, which is a good question since it will probably be pretty uncomfortable. I told her I think we will be able to use lots of pillows to help her find a comfortable position to sleep in.
Here is Ellie and her brother John John,
and this is the RED device (which is purple, not red!)
I will be posting a "before" picture soon for us to have a baseline to see how much growth she gets from this distraction. I am very hopeful this surgery could be the one to get her trach out, but I think Fred is more cautious thinking she'll have it for many more years still. I should know better than to get my hopes up, but I just can't help it!!
Thanks for reading!
Robin
Wednesday, January 9, 2013
Birthday, Christmas and a New Year!!
Life keeps flying by! I keep meaning to post new pictures (when I remember to take any!) and let everyone know how well Faith has been doing, but then I get distracted by whatever is going on at the moment. I'm at Anthony's first basketball practice tonight, so seems like a good time to do some catching up!
Anthony celebrated his 9th birthday early in VA at Mimi and Papa's house and then on the 15th with about a dozen boys from school over for games, pizza, cake and a sleepover on Saturday, Dec 15th, and then one more time with the family on his real birthday on the 19th. It seemed like a never ending birthday! I hope he enjoyed it!!
Anthony with Faith and niece Carly!
He also won a great award at school right before Christmas for "living" the school's golden rules of respect, responsibility, and safety. He was so excited to win this!
Faith has had a great first semester in first grade. She is really learning a lot and has started to read on her own!! That's exciting as she was so hesitant in Kindergarten to take any risks!
Christmas was very nice, although Anthony woke with some kind of 24-hr bug and had to go back to bed in between presents. Santa brought lots of new toys including an Xbox for Anthony and a bike with a horn for Faith (ask me sometime about Santa's big mistake!) and we had Lauren, Carly, Ryan, Dana, Aaron, Karen and Bill over for a big brunch and more gifts. It was really nice to have such a full house!
On New Year's Dana and Aaron moved into the "new basement apartment"! It seems pretty good for them and they are getting ready for baby Hallie to arrive soon (2/22 is the due date). The baby shower is this weekend at Karen's house.
We are also getting ready for Faith's next round of jaw surgeries, on Feb 6th and March 8th in Cincinnati again. I'll post more soon with details.
Gotta run for now, my cell phone battery is about to run out!
Robin
Wednesday, October 31, 2012
Friday, October 5, 2012
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