As you probably know, we are planning on having a balloon release to wrap up the day's events for "Art for the Heart." Originally, I had my blinders on and was just thinking of Maverick... Ask any parent who has lost a child what is most important to them and they'll tell you - it's that their child is not forgotten. Then I started thinking... The stories of so many others have touched my heart this year. So many others heard the earth-shattering words, "Your baby has a heart defect." So many others had their babies
whisked away shortly after birth to a world of alarms, wires, and tubes. A world so different than the dreams we had for them. Dreams of snuggling them on our shoulders, smelling that wonderful baby smell and feeling their breath on our necks as they drifted off to sleep. So many others had to hand their children off with a last kiss and, "I love you," not knowing what the outcome of such a risky surgery would be. So many others prayed and prayed and prayed as they waited to hear the next update from the operating room. So many others watched, helplessly, as their precious child fought for each minute, each hour, each day - just wishing we could take their place. So many others held the tiny bodies of their little ones as they took their last breath here on this earth. So many others planned funerals and picked out tiny caskets and cemetery lots. So many others hurt, and miss, and cry. For all these other parents, in memory of all our fighters, we will have a balloon release. I have ordered one hundred red, heart-shaped balloons to release. If you have a
CHD angel, and would like their name attached to one of our balloons, please post their name, birth date, and angel date to this post. If you are able, we would love to have your support for our fundraiser for the
Children's Heart Foundation, however, there is no donation required. I will be adding a button to the side of our blog if you are interested in donating. It's quick and easy and no amount is too small. Together, we can have an impact on the cruel and awful reality of congenital heart defects.
3 comments:
Juli - just a quick note to tell you how proud I am of you. You are truly a blessing! By the way, I love the new look for the blog page and I can't wait until February 13th! Hope we go way, way above the goal you have set! Remember folks, your donations are tax deductible! Love you, Teresa
Juli,
We had planned on making it out to the event tomorrow, but my little guy had to have surgery, so we won't be able to make it. Our thoughts and prayers will be with you and your family. You are such and inspiration for all of the familys touched by CHD. I'm sure Maverick is so proud of his mommy!
Love,
Jaime
Dear Juli -
We will be lifting you and your family up in prayer tomorrow as you face this difficult day. God Speed, Little Man!
Love,
Jaime
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