Our Heart Hero....Noah
On Saturday, September 12th, we attended the 2nd annual
Heart Walk for Intermountain Healing Hearts
It was a grueling 1 mile walk, which took us
22:57 to do. Can you believe that?
We may have tip toed the thing we went so slow.
Well, making a good time was not our goal,
showing up to support a wonderful cause with
people we love was our only purpose!
MISSION ACCOMPLISHED!!
After about 50 steps, there was a rest stop and snack station. Sheeew, I didn't think we would make it, but we did!! We learned that the snacks weren't suppose to be eaten until AFTER the walk.....silly us! Oh well, we didn't take anymore after the race, so I guess we can be forgiven.
You can do it!!
and taking off to be crazy little monkeys!
Noah and Tyler like to take it easy
Jason pushing a stroller with a McDonalds cup.
Gabe finally caught up to those crazy monkeys!
our NOAH!!
He took off to play with some friends he had met
at the heart camp last month.
We were minus Carrie because she had a church activity.
I guess when the lord calls......you must obey.
We were missing my Uncle Mike and Nikki, because they slept in.
My Mom had a client meeting she could not get out of,
and I plain ol' forgot to tell my dad.
Ooooops!!
They did register though, so donations were made in their names.
Gabe is so proud of this little guy
Me and my little man
Gabe and I are so proud to be their parents.
We are so lucky to have each one of them.
Finally, a picture with all of us!
The purpose of the Heart walk was not only to raise money and awareness to a great cause, but to honor the heart angels that earned their wings through a courage battle with CHD.
It was very touching to see the beautiful posters
the families had put together to honor their child.
There is so much love and support in this group, each and every family
is amazing to have gone through the struggles that having a child with CHD brings.
Gabe and I have so many mixed feelings when it comes to this.
We were introduced to Intermountain Healing Hearts by a member that did not even know us, but stumbled across my blog one day.
I feel like it had to have happened for a reason.
Gabe and I can look at all these other families who have children effected by this, and realize we are not alone. It would have been so helpful to have when Noah was little, when hope was all we had to hold onto. We never knew anyone in our situation, so we never knew what to expect from another parents point of view. Now we have an amazing 10 years old boy that can serve as an example of what the future can hold to others....something we never had.
It is truly nothing short of an honor to belong to this organization, and we hope to be more involved in spreading awareness to this cause that will continue to be a part of our lives.
It is truly nothing short of an honor to belong to this organization, and we hope to be more involved in spreading awareness to this cause that will continue to be a part of our lives.
There was a beautiful ceremony at the end, where we had a moment of silence for the fallen angels, as well as others that are fighting in the hospital. We listened to musician Paul Cardell, who is an adult with CHD, in fact, shares Noah's exact heart condition,
whom received a heart transplant the Thursday before.
It was beyond touching as I stood their watching these parents who had lost a child release a butterfly in their honor. It was amazing to watch them fly up in the air, where they all kind of grouped together, then took off out of sight.
It was a moment I was honored to have witnessed.
If you look closely, you can see the butterflies.
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