I told you I would be posting all month about CHD… in an effort to become educated properly myself before sharing with you I have come across some amazing stories, and some terribly sad and scary ones. This poem I found at a website called ‘Kids with Heart” and I just had to share it with you! I love it!
Who are we?
Start counting… we’re roughly 8 out of every 1,000 people (or 1 out of every 125, if you want a number you can get your head around.) We represent both genders and we are all ages. A million of us are adults, and about 800,000 of us are children.
We’ve made it through surgeries, hospital stays, infections, Endocarditis (infection of the heart), pacemakers, and heaven know what else. We’ve given gallons of blood, one vial at a time. We’ve fought back against tremendous odds. We’ve been so sick that we’ve scared the world’s best doctors witless… and then amazed them even more when we’ve fought back.
We’ve celebrated our victories and we’ve mourned our losses. We know that most of those who came before us died, including 14 of the first 70 to have the Blalock-Taussig Shunt. We know that most of us shouldn’t even be here and so we live every moment as if it is our last – because it could be.
We’re Cardiac Kids and Heart Warriors. We have an amazing inner strength, but we are terribly fragile at the same time. We refer to our parents as Heart Dad and Heart Mom, and we use those titles as Badges of Honor. Why? Because they DESERVE them! They were the first ones to discover that a heart defect doesn’t just break one heart, it breaks three.
We work, we play, we pay our taxes and we live our lives. We’re in your community, in your church, in your school, in your office, and quite possibly in your home. We move a little slower, do some things a little differently, but we usually get along without causing a fuss.
We are people living with Congenital Heart Defects.
42 year old male with Tricuspid Atresia
3 thoughts on “Who are we?”
Hi! I enjoyed reading this… my name is Becca and I'm 26 years old with a baby boy who has tricuspid atresia. He is 3 1/2 months and has already had one open heart surgery at 11 days old and just had an angiogram 5 days ago to prepare for his next open heart. It is crazy how much our life has changed… we have four older kids and, now that we have Micah, it is sometimes hard to wrap our heads around what we have been through in the past summer. I've been writing a blog, myself, to help sort through all the emotions and share our story. Thank you for sharing this poem
I'm sorry! Wrote it wrong http://www.blessedmommyof.blogspot.com