This is a horrible picture! But we had a great birthday party for the boy! Despite the rain we still had fun inside playing the wii. It was very funny to watch my 85 year old grandparents learn how to bowl! We also had a very lovely dinner just the two of us.
I finally got the call today! We are all set for this week. Amber will be admitted on Wednesday afternoon and she will have her surgery at some point on Thursday. There are still some concerns from the anesthesiologist so hopefully things get worked out. I really don't have any information about how they will be doing the surgery. She will be in for a minimum of 4 days. Depending on how things are going I may or may not be updating.
Please be praying for us. We still have a few things to get set/altogether before we will be ready to go.
Monday, June 14, 2010
Friday, June 11, 2010
Flash Back Friday, "21 Years"
So it's not a traditional "Flashback Friday". I really don't seem to do as well with these as my "Wordless Wednesdays". Technically it's also not a "Flashback" till Monday and I wasn't around when it happened but I think it's worth a look back.
21 years ago (pretend it's Monday) in a little Pennsylvania town an adorable baby boy was born! Well the town is not so little, but he was adorable.
I'm very thankful for his parents. For the time and energy they put into raising him and making him the wonderful man, husband and father he is today! I could not ask for more!
I don't have much for new news on Amber. I did get to talk to the surgeon and one of his schedulers. We're just waiting for a bed to open up in the PICU so we can go ahead to schedule it for this coming Thursday.
As you can see I'm changing things around a bit. I might be adding/trying out some new things to keep you more updated when I'm not able to get to my computer! Hope you all have a great weekend!
21 years ago (pretend it's Monday) in a little Pennsylvania town an adorable baby boy was born! Well the town is not so little, but he was adorable.
I'm very thankful for his parents. For the time and energy they put into raising him and making him the wonderful man, husband and father he is today! I could not ask for more!
It's been my honor to celebrate his last 3 birthdays with him and I'm looking forward to celebrating many more!
We've celebrated with his parents already but since it's such a big birthday we'll continue celebrating for a wile. Tomorrow we'll have some of my family over. On Monday the actual day the two of us will do something fun!I don't have much for new news on Amber. I did get to talk to the surgeon and one of his schedulers. We're just waiting for a bed to open up in the PICU so we can go ahead to schedule it for this coming Thursday.
As you can see I'm changing things around a bit. I might be adding/trying out some new things to keep you more updated when I'm not able to get to my computer! Hope you all have a great weekend!
HAPPY BIRTHDAY BABE!
Thursday, June 10, 2010
The Waiting Game
We've been waiting and waiting to hear from Amber's surgeon. Today I finally shot an e-mail off to him. Thankfully he replied right away. Apparently his right hand lady has been out all week who is in charge of call backs and that's why we haven't heard from him. He said that he will call tomorrow! He also said that his "anesthesia folk" have some concerns going forward with the operation so soon after her being sick. Getting this news right after her evening routine of choking through her bed time bottle and screaming her head off as she becomes un-constipated I'm really not thrilled with waiting any longer. However I would like to have my little Amber forever so I guess if waiting is best then I'll wait.
In other good news: Amber is down to 1/4th of a liter of oxygen during the day and doing fine! Her heart rate is a little higher but she doesn't seem to be struggling. At night she is still on a 1/2 of a liter. I e-mailed with her pulmonary specialist about it and he said it's good. He thinks that maybe in a few weeks and after she's gained some weight she'll do better. I'm not really sure what the weight has to do with it but at that point she'll go in for another oxygen challenge.

Isn't she a cutie!
This is just one of many beautiful pictures her PA grandparents took!
Wednesday, June 9, 2010
Monday, June 7, 2010
What Happened On Friday
I'm sure you're all dying to know what happened at our appointments on Friday. I'm so sorry to keep you waiting but all the information has liquefied my brain, and then our PA parents were visiting and there was just no time to update....and on and on with my sad excuses :)
I'll start at the very beginning because it's a very good place to start.
Endocrinology: Found in the orthopedic department in case you were wondering. They had nothing new to tell us. They had not looked at any x-rays. They do not want to see us again until DECEMBER......hmmm sounds like some other endo dude I know. Anyways, since by the naked eye Amber's skeleton is only "messed up" on the top half they were not so excited. They did get blood work to check her vitamin D levels and said if anything interesting comes back from the blood work or the genetic testing then they'll see us sooner. Oh and they'd like us to see their orthopedic surgeon for a consult on her chest, maybe some other parts.
Pulmonary: Was a much better visit than I had expected. This is what liquefied my brain. All of Amber's breathing problems are due to her hernia and odd chest shape because of this prolonged use of oxygen is actually a bad thing. She will become dependent on the oxygen and will not take deep the breaths that are needed to help develop her lungs. So he wants to start weaning her off of the oxygen. If she is weaned off of the oxygen, due to her anatomical problems she will not get enough oxygen to help her overall development. So really its a lose lose situation. The first step is to get her hernia fixed. Then she'll have to go in for an Infant Pulmonary Function Test, this will tell them how well her lungs actually work. I'm not really ready to think about that test yet so I'll explain it when she's closer to having it done. Depending on the outcome of that test and some other blood tests they did we'll begin to discuss option to better Amber's breathing. They did do an oxygen challenge while we were in there, meaning they tried her on a lower level of oxygen every 20 minutes until she was on room air. She did a lot better than we had all expected so he told us to try her on a lower level of oxygen all weekend. It didn't really work because at home it's muggy and she still having a lot of breathing difficulties when she is in her car seat and eating. I'll be calling them tomorrow to discuss how she did, possibly the blood test results and see where we're going in the mean time. Oh she will also have a sleep and probably a swallow study after the hernia operation as well. I'm sure I'm missing other things but I'll remember and explain it better when things are happening.
Nutritionist: This was a surprise. The pulmonary specialist is also a neonatologist so he's very into the over all development of Amber and wanted us to meet with his nutritionist. They also pushed for us to see her because she has not gained a very good amount (for her) the last couple of visits. She was very nice. She still wants me to nurse as much as possible and add some formula to any bottles I pump. She also gave me "recipes" to get extra calories into the one formula bottle Amber gets and her cereal, fruits and vegetables. It makes feeding a little more stressful right now and it will definitely take some time for Amber and I to get used to. We'll see the nutritionist again in July. I'm not sure how I feel about this I don't think her bones or her muscles really need the extra weight.
Hernia: I finally got my call! It was rather awkward because I was in the same building as the surgeon and it probably would have been easier to just talk in person as I was trying to check out of pulmonary at the same time (thankfully my mom was with me!). He finally got the x-rays and agrees that her hernia definitely needs to be fixed and is the reason she is still having difficulties without the oxygen. He needs to go over her x-rays with his radiologist, discuss things with his anesthesiologist and should be calling me tomorrow to schedule either a consult or a surgery date. Amber needs to be over her respiratory infection for 2 weeks before they will do the surgery so they probably won't do it for another week or so. I'm really fine with this news. I think having the surgery now will really benefit her. When they mentioned the surgery before she did not have any complications from the hernia so I was really wary of the whole ordeal. I'm really hoping that once this is fixed she will be able to breath better, not be constipated, eat better and sleep better, so just improve things over all!
And then we finally ate and went home!
It was quite the day and we've been going non stop since!
But we had a very fun and lovely weekend, it was so nice to see our family again!
Now to bed!!
Thursday, June 3, 2010
Taste Of Summer
Amber's first taste of watermelon!
(please excuse our messy hair it's just one of those days)
She didn't seem to sure at first but, as soon as she got a taste of it she loved it!
We tried out her new mesh bag feeder.
It's a little too heavy for her but she can actually feed herself with just a little help.
Unfortunately I'm still having video issues so I don't have any happy pictures of her eating.
We're still adjusting to life on oxygen. We're working out the kinks with the company. There seems to be some lack of communication when it comes to orders so we've been waiting all week for new tanks. It looks like we'll have just enough for our trip tomorrow but I'm worried her big tank will run out tonight and we'll have to use the travel ones. They never told us but they deliver to our area on Monday, thankfully they're making an exception and coming out tomorrow.
Tomorrow (Friday) is our big trip to Boston. We'll meet with the new Endocrinologist. I'm actually excited to meet her. From what I've read about her she specializes and is really interested in the type of things that Amber has; skeletal dysplasia, rickets and other bone disorders. We'll also be meeting with a new Pulmonary Specialist. Hopefully they (not sure if its a he or a she) will be able to set us up with a sleep and swallow study and give us more insight into how long she will have to be on oxygen.
It's a stretch but I'm really hoping we'll be able to stop in and talk to the diaphragmatic hernia surgeon. We've been e-mailing back and forth and he wants to talk on the phone tomorrow (sounds like the recipe to a cute high school romance huh) but in all seriousness I'm worried because he still has not received the x-rays we sent out last week. Ugh hopefully he'll get them tomorrow.
Amber is looking forward to seeing her PA grandparents this weekend!! It's been far too long and it will be very nice to see them again! Amber would also like to say "Happy Birthday" to all her cousins who just turned one and will be turning one soon!
Wednesday, June 2, 2010
Subscribe to:
Posts (Atom)
Labels
Amber's Adventure
Amber's Birth Story
Amber's Birthday
And Baby Makes Three
Aspiration
Baby Boy
Baby Food
Car Seat Challenge
Cardiology
Cats
cooking mamma :)
Deployment
Diagnosis Search
Diaphragmatic Hernia
Early Intervention
Endocrinology
Eye Dr
Eye Dr.
Family Time
Flash Back Friday
G-tube
Gardening
Genetics
Glasses
Holidays
Hospital Stay
I-Cell
IUGR
Making of the Nursery
Milestones
Neurology
NSTAR Walk .
Nursing
Nutrition
Orthopedics
Oxygen
Pulmonary
Random Ramblings
She's Crafty
Sick Baby
Sleep Study
Splints
Surgery
The Amber Bump
Tummy Time
Ultrasound
Video
Walker
Wear Red Day
Weight
Wordless Wednesday

.jpg)


.jpg)