Matthew and Hannah just completed two weeks of swimming lessons. They had a lot of fun going with their friends each day. They both came away a lot more comfortable with the water.
Monday, June 28, 2010
Saturday, June 26, 2010
Friends.
Matthew and Casen have been friends since they were babies. They have such diverse personalities, some times they fight, and they really have different tastes; but in the end they are the best of friends. Now that summer is here, it has been spent swimming, riding bikes, and having sleep-overs. Such fun!
Friday, June 25, 2010
T-Ball
This was Hannah's first summer to play T-Ball. She came in with no real knowledge of the game. Sad to say, I didn't get her properly prepared. My poor girl didn't even know how to hold the bat or what running the bases meant.
She has come a long way. She plays every game with a HUGE smile. Most of the time she is playing in the dirt or wearing her glove on her head.
She has come a long way. She plays every game with a HUGE smile. Most of the time she is playing in the dirt or wearing her glove on her head.
Monday, June 21, 2010
Storm Damage
Todd was in Denver last week on a business trip. We had a pretty major storm move through while he was gone. We had several small limbs and one rather large limb come down in the 60+ mph wind. Along with the wind was a heavy downpour of rain. Needless to say, the basement wall has not been fixed yet so we ended up with water in the basement again.
I am proud to say that the kids and I picked up all the limbs and I even managed to cut the large limb up without injuring myself.
Todd came home from his long week away with no yard clean up awaiting him.
Friday, June 18, 2010
Dance Recital
Hannah had her dance recital earlier this month. This was a first for our whole family. It was so much fun to watch Hannah learn throughout the year. She has become very close to several of the girls in her dance class.
The recital was held at the Stiefel Theatre which was wonderful choice of locations. I do not believe that there was a bad seat in the house.
The recital was held at the Stiefel Theatre which was wonderful choice of locations. I do not believe that there was a bad seat in the house.
Saturday, June 12, 2010
Sold.
Tuesday, June 8, 2010
Riding the Rails.
Friday, June 4, 2010
Camp
Memorial Weekend
Thursday, June 3, 2010
Hannah.
Wednesday, June 2, 2010
Tuesday, June 1, 2010
Looking Back.
10 years ago was when our journey started with Mallory.
10 years ago in March, we had our defining moment. That fateful day in Salina. Mallory left by helicoptor for Children's Mercy for her first heart surgery. Definately not what we expected for our little girl. I'll never forget the look on the cardiologist face when he realized the severity of Mallory's heart defect and how sick she truly was.
10 years ago this September, Mallory had her open heart surgery. That was the longest 9 days. A temporary pacemaker, a collapsed lung, tube feedings. What more could a parent take?
10 years ago, at the suggestion of our cardiologist, Mallory was screened for genetic defects. I am thankful now for that, although at the time I thought he was crazy.
After seeing the struggles that many parents go through trying to find the answers for their children with special needs, I am so very thankful that we had our answer 10 years ago. Long before it was evident that there were going to be issues. Long before we were prepared. But early enough to start all the interventions that were needed.
We are headed to Mallory's annual appointment in Salina with cardiologist today. I still get anxious as we await the cardiologist's report. I still get a chill up my spine every time I walk into the hospital there. Knowing that the day is getting closer for Mallory to have a valve replacement. Praying for good news today!
10 years ago in March, we had our defining moment. That fateful day in Salina. Mallory left by helicoptor for Children's Mercy for her first heart surgery. Definately not what we expected for our little girl. I'll never forget the look on the cardiologist face when he realized the severity of Mallory's heart defect and how sick she truly was.
10 years ago this September, Mallory had her open heart surgery. That was the longest 9 days. A temporary pacemaker, a collapsed lung, tube feedings. What more could a parent take?
10 years ago, at the suggestion of our cardiologist, Mallory was screened for genetic defects. I am thankful now for that, although at the time I thought he was crazy.
After seeing the struggles that many parents go through trying to find the answers for their children with special needs, I am so very thankful that we had our answer 10 years ago. Long before it was evident that there were going to be issues. Long before we were prepared. But early enough to start all the interventions that were needed.
We are headed to Mallory's annual appointment in Salina with cardiologist today. I still get anxious as we await the cardiologist's report. I still get a chill up my spine every time I walk into the hospital there. Knowing that the day is getting closer for Mallory to have a valve replacement. Praying for good news today!
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