Melissa and I have been fighting the last couple of days with swaddling. She isn't wanting her arms tide down, so today I gave in an let her take a nap with her arms out and it worked! I don't know if I want to try it tonight.
This is all I wanted!
Our first outing together
Monday, July 30, 2007
Today was the first time that Melissa and I got out of the apartment by ourselves! Since I was just released from my doctor on Friday, I had to try getting out on my own with Melissa. We didn't go to far, just to Babies R' Us! She was so good, it made feel good about getting out with her.
One of the first
Thursday, July 26, 2007
Great Stride Walk for Cystic Fibrosis
Dear Family and Friends,
Paul and I are getting ready for the Great Stride Walk for Cystic Fibrosis and we need your help. If you would like to walk with our team and/or make a donation please go to the following website.
http://www.cff.org/Great_Strides/TraciLiberto
Please pass this onto your family and friends!
Thanks,
Paul, Traci and Melissa
More Visitors
My cousins on the Liberto side came to see me this past weekend! I wish I could play with them, but soon I will.
Sydney, Aunt Jackie, Me, Jordan and Conner
Melissa's 1 Month Pictures
Saturday, July 21, 2007
We took Melissa to have her 1 month pictures taken today! She did really good considering how young she is. I just had to have these made, she isn't going to be this small much longer. As they say, you always have lots of pictures of your first child and then forget about the others.
Melissa's 1 month check up
Friday, July 20, 2007
Today Melissa had her 1 month check up and she is doing well. She is weighing in at 8lb 8oz and is 20 1/4 in long. She is also cooing (talking), reaching out for things! Her doctor is very impressed with how she is growing. He didn't see anything wrong with her! She is also sleeping very well at night and taking good naps!
Melissa did get another Hepatitis B vaccine this time. Next month she gets 4 shots!
My Friend Kaelyn
Wednesday, July 18, 2007
Kaelyn came to see me in the hospital
Visitors
Since the day I was born, I have had a lot of visitors come see me! My mom and dad tell me I'm very popular. My mom can't post all the pictures of my visitors, but here a few to share. We will post more later on!
My great Aunt Cherry and Great Uncle Sherwood.
Melissa is 4 weeks old (1 month)
Sunday, July 15, 2007
On my way to church! I love my carseat!
Ok mom stop taking pictures I want to go to sleep!
I love playing on my playmat
Friday, July 13, 2007
Update on Traci
Thursday, July 12, 2007
Melissa is 3 weeks old!
Sunday, July 8, 2007
Today Melissa turned 3 weeks old! She is doing great! We have started her on medicine for her Cystic Fibrous (CF). She is weighing around 6lb 10oz and is 19in long.
Update on Melissa
At the beginning of the pregnancy with Melissa, I was tested for Cystic Fibrosis (CF). The test came back that I was a carrier. Paul also had to be tested as well. His test came back that he was a carrier. What this meant for us was that Melissa had a 25% chance that she would be born with CF or a 75% chance she would be a carrier or not have it at all.
You maybe asking the question what is CF? I will get to that.
We where sent to a genetic specialist to talk about CF. This is where we got all the good sonogram pictures of Melissa. Dr. Albert was looking for CF in Melissa's lungs and digestive system. He never saw anything, but that didn't mean it wasn't there. The only way we would know if Melissa had CF was to do a DNA test. We could have had a test done during the pregnancy, but there was a risk of loosing Melissa. Paul and I said we would wait until she was born to have her tested.
So here we are today. Melissa does have CF. We met with a team of specialist at Children's Hospital of Dallas today 7/5/07 and learned so much about CF. We do have our hands full, but with God seeing us through this and the support from our family and friends, we will be fine.
Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that
a.. clogs the lungs and leads to life-threatening lung infections; and
b.. obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food. In the 1950s, few children with cystic fibrosis lived to attend elementary school.
Today, advances in research and medical treatments have further enhanced and extended life for children and adults with CF. Many people with the disease can now expect to live into their 30s, 40s and beyond.
We ask that you go the Cystic Fibrosis Foundation website. http://www.cff.org/ This website is the only one you need to read. There is a lot of false information out there on the Internet.
Also we will be calling on you to help us with the Great Stride walk in September. This helps raise money for the CF Foundation. Thanks for your prayers.
Love,
Paul, Traci and Melissa
Happy 4th of July
Wednesday, July 4, 2007
Paul, Melissa and Grammie Liberto
Melissa is 2 weeks old
Sunday, July 1, 2007
We can't believe Melissa is already 2 weeks old today. Melissa is doing great, she is sleeping very well for a newborn. She is gaining weight and is very happy! As you can see in the pictures she loves her hands! Melissa is such a joy in our life!
Melissa 1 week old
Melissa 2 weeks old