I sit here and all I can think about is:
Cardiopulmonary bypass (CPB) is a technique that temporarily takes over the function of the heart and lungs during surgery, maintaining the circulation of blood and the oxygen content of the body. The CPB pump itself is often referred to as a Heart-Lung Machine or the Pump. Cardiopulmonary bypass pumps are operated by allied health professionals known as perfusionists in association with surgeons who connect the pump to the patient's body. CPB is a form of extracorporeal circulation.
Tomorrow we find out if we are going to proceed with surgery or if Maccoy's runny nose will set us back.. If its a go I have to hand my sweet baby over to a surgery team and let them cut him open and stop his heart... STOP HIS HEART......HURT HIM to make him better.... while I just sit and wait and wonder all the while my heart is breaking.. I am so scared... I cry, I scream, I hit the wall but I can't make this go away .. I have to pull it together for my kids I have to put on my big girl pants and a brave face kiss my sweet baby tell him everything is going to be fine, to be brave and strong and that I LOVE him soooo much and then leave him scared and alone and hope and pray he comes through all this with a mended heart..
3 comments:
Melissa, it's Tuesday morning and your making me cry!! :) I forgive you! :) And, I'm scared too for you...but I'm saying lots of prayers for you and I know in my heart that everything will be OK!!! ((hugs))
Thoughts and prayers coming your way.
Melissa,
Hang in there! Stay positive and take things one day at a time! **Deep Breathes**! My parents have been in your shoes Twice and once is scary enough! All you can do is trust in the doctors and pray! Technology has come along way since I had open heart surgery in the late 80's. You are not alone and Maccoy is a strong little boy, he is doing great now before his repair and that is a really good sign!
Sending you LOTS of **Heart Hugs**! Keeping Maccoy and you in my prayers!
With LOTS of Hope, Love, and Faith,
Lauren (22yr. old w/Tricuspid Atresia, HRHS...CHD Survivor)
Blog: www.laurensheart.blogspot.com
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