Thursday, October 30, 2008
Watermelon is back!
It is really interesting the way the palate heals, if you look in there it changes from day to day... one day there is a sort of skin looking stuff on the sides and then next there are "trenches" and the next there is some green looking stuff. Melissa said she does not want to look anymore. Emma was really good with the Dr. and opened her mouth for him and did not seem to have any apprehension about the day at all. If I was in her shoes the moment I saw the hospital complex I would begin to try and get away... speaking of which, Emma showed me a new talent last night. I was taking her to "night night" and she was so displeased with this proposed action she twisted in such a quick interesting way that I almost dropped her. We are used to her being sorta wobbly but this was a very deliberate twister type of action that took me by surprise.
Both Melissa and I could not help but laugh (under our hand) but we looked at each other and were pretty amused by this creativity and strength. She is strong and each day seems to be getting stronger and more comfortable in our family. Melissa also said yesterday that we really needed Emma, our family was getting boring and she has spiced things up. That is the understatement of the year!
I am in Houston today doing some work and we will be traveling to Florida in a couple days for work and to see family and friends. We thank God for the good report from the doctors and thanks to each of you for your support of our baby Emma and our family.
Monday, October 27, 2008
It's a small world after all
Okay, back to Emma... she is doing great and has not stuck her hands in her mouth at all. Everything seems to be healing fine and her breath is beginning to not smell like an open sewer. No offense Emma if you are reading this in 2020, it was not your fault, we have heard different theories. Could be general anesthesia "coming out of system" or could be the anti-biotics. Dr told us it was because there was food particles inside her mouth that was making the smell. Whatever it was we hope it will soon be something we can laugh about.
I have got a busy week this week, have to travel to Houston on Thursday and we will be heading to Florida this coming weekend for work. Emma will get to see our friends and family in Tallahassee and we are all looking forward to it.
Both Emma and Lily are at art class right now and I am taking lunch break to update blog since I noticed it has been about a week. Don't have pictures to post right now but should have some good ones over next couple weeks.
One interesting thing to note, I am using Google Analytics on the blog now and it shows where people are visiting from etc. and found that a family in Sweden is linked to our site so I left a comment for them and she quickly replied. They are adopting a little girl from the same orphanage as Emma and she also has a cleft lip/palate. How cool is that? What is even cooler is my step mother was adopted, her parents were from Sweden and her step mother is living in Sweden now with family.
It's a small world after all!
Monday, October 20, 2008
Doing okay
Before surgery Emma really handled things well and enjoyed the last moments of being able to suck on her hand. The hospital had great play areas for Emma to play in prior to surgery... then afterwards she was ready to play again. We were home day after surgery by noon. Rough few days but honestly she handled it all with such grace. She takes her medicine with little fussing, wears her no-no's when necessary with a little more fussing. Enjoyed visit from her cousins this weekend and is basically back at it 100%. The only thing slowing her down is not being able to eat normal food yet. Still on liquid diet, but again... she is handling it so well. When I get some sleep I will update with more details since it is pretty cute how she eats.
Friday, October 17, 2008
Back home
It was a tough day because Emma was just miserable. Overall she is recovering very well and continues to impress us with how she handles things.
At the hospital she was doing so well in the morning that we got released earlier than expected. There were hours of the day where Emma simply could not be happy or comfortable no matter what. We did our best and everyone loved on her and played with her. She is eating well, watered down yogurt and her protein shakes are favorites. We know the next two weeks will be challenging when it comes to food but whole family is being helpful. Trying not to have the old foods she enjoyed within sight and nobody is eating in front of her.
Lily is being very good with her sister, she would do things with her arms and hands and Emma would copy every move. Emma went to bed around 8 and our biggest concern of her sucking on her hand was completely unfounded. Emma has not once stuck anything in her mouth and out of habit a couple times when we thought she was getting ready to insert hand she caught herself and put her hand down.
So, day after surgery and she really is doing amazing, home and in her own bed fast asleep.
Her tone and voice does sound different now, pretty cool!
Long night but Emma is great
Melissa stayed in bed with Emma and I was on little pull out couch. Basically little to no sleep and things got bad somewhere around 4:30 and we got a little radio flyer and went for a walk. Emma did not want to end the walk for hours. We just went around and around. She is going to the bathroom perfectly, drinking perfectly and right now is sitting in the radio flyer with shoes on ready to go home. Food is on way up so hopefully that will give her something to do and pass time until dr gets here and starts release process.
She is really doing amazing and the way she talks is definitely different. She repeated "I love you" really well and said "no" really well every time we tried to go back in room and stop our long walk. Mom and Dad were a sight I am sure.
She just pulled her little hospital band off her leg. Every time she gets a little bit more of the hospital off her body she seems happier. The iv is the last thing she demands to be removed.... Hopefully soon.
Thursday, October 16, 2008
All tucked in
We were able to go back with Emma in recovery, the nurse was asian which was nice we think. Again, not like other recoveries we have been in, room was small and we were only ones in there.
She was still bleeding a little and some blood came out from nose and mouth.
we were only in there about ten minutes and then moved to room by 3:10 cst. Took a little while to get settled but things are going smooth so far.
Emma is drinking out of a cup and had oral tylenol with codeine. She has an iv for fluids and anti-biotics and is laying on me in bed mostly sleeping. The hospital also got a new cleaning lady :). Melissa and her lysol scrubbed our room from top to bottom. I warned her that they are going to keep moving us to new rooms to get free cleaning.
We brought some toys and our own little cd player with calm music Emma likes and the room is great. I just ordered some broth and since she is doing so good drinking we know she must be hungry, close to 24 hours since she ate.
Melissa did a great job packing, Emma has her own blankets, toys, cups etc.
We are told that the numbing medicine they use on her palate for surgery will wear off and this evening may be rough. The only pain meds she is getting is the tyl/cod every four hours so we shall see.
Thanks again to everyone for e-mails and comments of your support and encouragement. One thing for Andy and Amy --- please send us an e-mail, we don't have your email address (Melissa lost it!).
All done
Surgeon just came out and told us it went perfectly, we should be able to go back with her in about five mins.
He said she had plenty of tissue (sometimes a concern) and he is very confident about a two week recovery.
Worst part now may just be her not being able to suck on her fingers for comfort.
In surgery
Emma did better than Melissa so far (Emma got drugs and Melissa did not). She was almost asleep before going back and everything went smooth. While writing this the ENT surgeon came out, tubes are in... She had fluid behind both ears (explains the hard flight back to usa probably).
He told us Emma was pretty much asleep when they put her under general and was peaceful.
They are beginning palate surgery now and should take at least an hour.
Just as a side note, the way everything was handled today was really great. We played in a big playroom until they were about ready, then Emma had the "goofy juice" rolled to surgery. Emma sat in Melissa's lap on the bed as they rolled down. Love the way this is done compared to previous experiences with our boys having surgery. If you have a choice, I highly recommend a childrens hospital, wonder if they will take adults? :)
Wednesday, October 15, 2008
Long day
Finished all the appointments and Emma handled them all really well. Mom and Dad are in worse shape. Emma did her hearing exam and we had final meetings with ENT and craniofacial surgeons. Everything is in order and ready to go. We leave the house around 9 in the morning again and surgery is scheduled for 11:30 I think. We have to look at all the paperwork because right now it is a bit of a blur.
She should be in surgery for about an hour and then we get to spend the night with her in a private room. So far we are extremely impressed with the hospital and staff. I will write more tomorrow when we have more time.
She can't eat past midnight and only clear liquid until 9, will pick update from hospital. Last night with cleft palate!
Pre-op
We are all registered, Emma is doing great so far. She had pictures taken including with a mirror inside her mouth and right now we are finishing up with a lady that came in with a big doll dressed in the clothing Emma will wear tomorrow and we are just playing with all sorts of toys, stethoscope, little sticky wires, mask etc. etc. Not sure if they do this at every hospital but it is amazing. Emma has no apprehension being here. We seem to come here to play. Not like hospital visits we are used to. They also give her a little doctor set to take home and play with. Melissa was smart enough to get an extra one for Lily so they can play tonight and hopefully tomorrow will be peaceful as well.
She is doing great, we are about halfway through the day. Still have to get hearing test and appts with surgeons.
Doctor Doctor Doctor
Today we will get details of what time we report for surgery tomorrow morning. Yesterday Emma slept in a little late after not sleeping all that well the night before. Praying for peace during these next few days/weeks.
Tuesday, October 14, 2008
Blessing Shower
Monday, October 13, 2008
Thanks to our Texas friends
It was really amazing and incredibly generous of them. We have been so blessed by the friends that we have here in TX and in FL as well as family from around the country.
Here are some pictures from the weekend.
Thanks to the Heather, Denise, Martha, Susanna, Jene', Donna, Shelly, Julie, Kether, Elizabeth, Brenda, Jeana and Chelsea for making it like Christmas at our house.
There is a little movie of us all making lots of music, Emma loves it. We also took a little outing to department store and a new shopping area in Cedar Hill. It had little play areas and a big water fountain for the girls to play in. Battery died on the camera so sorry we missed those pics. We have role reversal going on, Lily wants to be in the stroller and Emma wants to push... the store clerks found it quite amusing.
Few more days until surgery, all is well and it was a really nice weekend. Thank you again family and friends for your support and practical demonstration of love to my wife and children. It means so much.
Friday, October 10, 2008
Preparing for Surgery
All of this is leading up to surgery next week, we can't help but be a little apprehensive, things are going so well with Emma and we don't want to lose any ground with her bonding and comfort with us.