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Name: Jeremy, Sarah, Myles & Damon Cochran
Location: Carl Junction, MO, United States

Damon Conner Cochran was born on Nov 16, 2006 in St. Louis, MO. He has a congenital heart defect called Hypoplastic Left Heart Syndrome. Damon has undergone 2 of the 3 surgeries he will need to repair his heart, the first on Nov 20th, 2006 and the second on April 13th, 2007. This site was created to keep our family and friends updated on Damon's condition. We also want to glorify God for all he has done for Damon so far and will continue to do. God bless all of you who check this site; we love you so much and thank you for your prayers and support. Jeremy, Sarah, Myles, and Damon Cochran

Aug 31, 2006

 

A Long Day

Our day started at 7am in rush hour traffic on our way to Sarah's 8 o'clock appointment. We got to the hospital and we were just overwhelmed with how big this hospital campus was. It was close to seven blocks of nothing but hospitals. We got to her first appointment, which was her ultrasound and we were both pretty calm. The tech which performed the ultrasound did confirm that the baby was a boy and that he weighed in at a booming 1lb 14 ounces. She said that she could tell that Damon had an abnormality with his heart, but that is nothing that we hadn't heard before.
After that appointment we went to Saint Louis Bread Co and had bagels and coffee before her next appointment started. We then headed back to the Center for Advanced Medicine. Her appointment was supposed to be at 11am, but we didn't get in to see the OBGYN until about 12:15. This doctor never examined Sarah, just basically went over her medical history and answered some questions that had been on Sarah's mind.
We then headed to our final and I feel Sarah's most important appointment of the day, the fetal echo. At this appointment we visited with several people and they were all great to talk to. The tech that performed the fetal echo said that she did see the hypoplastic left heart that we had seen in the first echo. It was funny though, everytime that she tried to get a different angle of the heart Damon would move so she couldn't see it. At one point Damon had his feet above his head so she couldn't see. Then she made Sarah get up and walk around for a little while hoping that Damon would switch positions, which he did. She got all of the pictures that she needed and that is when we thought we were heading home. Notice I said thought we were going home. We then met with the cardiologist who talked about what she saw in the pictures of the echo and discussed what our treatment options were. Which are the group of three surgeries or a transplant.
After talking with the cardiologist we talk with a doctor from the NICU. She was very helpful in answering all our question and helping us deal with our concerns. She then took us for a tour of the NICU. This is the only time all day that Sarah and I both almost lost it. What we both had heard and read about was now right in front of our very eyes. Newborn babies with hoses and wires all over them, hooked up to venilators and i.v.'s. I couldn't help but wonder how we are going to make it through this journey. It was and still is hard to think about all of those babies laying there helpless. Everytime I think about it, it brings tears to my eyes to think in a couple of months that is where Damon will be.
After leaving the NICU, we had a quick tour of the PICU and then we race down to the cafeteria to eat our lunch. At that time it was 4:30 and we were starving, but not really in the mood to eat. We managed to eat our food and made our way out of the hospital campus. We got back on I-44 and headed home. Much like our day started, it ended in STL rush hour traffic. I couldn't help but wonder how many long days we had ahead of us, yet in the back of my mind I knew the answer I was just too afraid to listen.

Aug 29, 2006

 

On Our Way

We are about to leave for our first trip to St Louis. We will be having an ultrasound at 8 or 8:30 am on Wednesday, an appt w/ the prenatal specialist (perinatologist) at 11:00am and a fetal echo at 1:00pm.

Depending on how worn out we are on Wednesday night, we might post the info we found out then, otherwise it will be on Thursday sometime. More to come...

p.s. Jeremy and I have both had dreams since the last ultrasound that this baby is really a girl. Wouldn't that be crazy!?!?! Unlikely, but possible I guess.

Aug 28, 2006

 

Outside In

Jeremy and Myles both got to feel Damon moving this last week. It was so cool. I have been feeling him for several weeks now, but his kicks are just getting strong enough to be felt from the outside in. It was funny when Myles felt him. I was lying on his bed and Damon was squirming around and I told Myles to put his hand on my belly. He said "No, I will put my foot." So he put his foot on my belly and Damon kicked twice really hard. I laughed and asked if he felt it and Myles just cracked up. Too cute!

Last night I was in Myles' room putting him to bed and I told him to give me a hug and kiss and he asked if he could give Damon one. I said of course. He has this thing where he thinks if he is gonna talk to Damon, my belly has to be exposed, meaning I have to pull up my shirt and pull the waist of my pants (which goes up to my neck practically) down under my belly. Myles was talking into my belly button and he looked at me and said "I see him! And I see he's momma!" I said "Myles, I'm his momma." Myles says, "No, I see his momma in there." I tried to explain it, but I don't know if it got thru....

Talk to you all soon!

Aug 24, 2006

 

Reality


We are about to go on an endevour that I thought that we'd never have to go on. On Wednesday morning we will go to St. Louis to start Damon's journey into this world. We will see many experts that will help to educate us and help us cope with Damon's condition. I can honestly say that I am scared to death of reality. It is so much different talking about his condition with family and friends and then going to talk to doctors. At least with the doctors in Joplin. They have given us no reason for hope that he will get better naturally without a heart transplant. I want the doctors to comfort us and help us cope with Damon's condition and help us face reality, whatever that may be.

I remember one night at work the day before we got the second ultrasound for Damon. We had no idea that anything was even wrong with him. I prayed to God to send our family a blessing. I believe that prayer was answered the very next day when we got the news that he had HLHS. Believe me when we found out we were devestated and sad, but after realizing what I had prayed I truly believe that Damon is the blessing sent from God. We don't know what the final outcome will be, but already his life is blessing us. Prayers have been prayed by people all acrossed the U.S. and even in other countries I have learned. I call that a blessing. Although my family and I are scared of reality, we find comfort in the support and prayers of friends, family and total strangers praying for a blessing.

Aug 21, 2006

 

Big Brother Myles

Just wanted to give you all a perspective that maybe we haven't let you all in on. In all of the shock of Damon's illness, I think what has been lost is the love of his older brother, Myles. Ever since he has found out that his new brother's name is Damon he has been so excited. Talking to him everyday, exciting to feel him move, and even trying to share his food with Damon are all things that Myles has done to show his excitement. I know that Sarah and I have learned so much from Myles in the three plus years that he has been alive and I know that through Damon's experience that we continue to learn from Myles' love and kindness.

We have tried to explain to Myles about Damon's heart, but all he understands is that he is sick and the doctors will give him medicine to make him all better. Through all the visits to the hospital, I know that Myles will begin to understand the severity of Damon's condition, but I know there is one thing that will not change and that is the love that Myles has for his little brother.

Aug 17, 2006

 

STL

I got a call from the admissions office at the hospital in St Louis today to set up my first appointment there. It will be on Aug 30th. I'll have 3 appointments that day, the first will be at 8am in the Center for Advanced Medicine and that will be for the ultrasound. The second will be at 11am and that will be with the perinatologist (prenatal specialist), and the third will be at St Louis Children's Hospital in the heart station for a fetal echo.

Since the first appointment is so early in the morning we will be going to STL on Tuesday right after I get off work and spending the night, then driving back Wed after the last appointment.

It was weird to get that phone call. It confirms the reality of all of this.

Aug 16, 2006

 

Dr's Appointment

We had a dr's appt today with our regular dr, who is actually a midwife. Didn't really find out too much. I have to go back there on the 31st to have my routine glucose test which will tell if I have gestational diabetes. They faxed all of my medical records to the hospital in St Louis, which is where we have decided to deliver the baby. I was told that soon after they receive my records in STL they will be calling us to set up an appt up there.

We also talked to the office manager at OBGYN, which is where I have my regular appts. They adjusted our bill since we won't be delivering here. Our midwife told them to charge me for my very first prenatal visit, the ultrasound, and any labs I have done, but to waive the fees for all other visits. She said the regular visits are like $98 a piece. So after ins kicks in, we should end up owing less than $100. That is a huge relief to us, and God's hand was at work in that, we know.

When we go to STL the first time, Jeremy is going to be able to go with me, but at the next appt, he may have a different job (hopefully) and not be available to go, so I'll be in search of a traveling buddy. Anybody interested?

The PayPal link is up and running, so if you want to make a donation to the account set up for Damon you are now able to do that from this site. I think there is a small charge for doing so, but if you live out of area, it would be the equivalent to paying for a stamp.

Talk to everyone soon.

Aug 13, 2006

 

Links

Hello everyone! We wanted to explain a little about the links on the right side of the page. The first one (I think it's the first one anyway) is a link to a website created by parents of children with HLHS. It is a great site for information. There are FAQ, and advise on what questions to ask the dr's, hospital, etc. Check that one out for sure. There is also a link to a hospital for more medical information about HSHS.

The links to Ronald McDonald House and Children's Miracle Network are there because we feel that we will be utilizing these two charities quite a bit through out this ordeal. Jeremy, Myles and I already volunteer at RMH, so that one if near and dear to our hearts anyway.

Soon there will be a link to Paypal. If you wish, you can go there and make donations to an account that has been set up for us. The money will be used for travel expenses, and other things we need while we are away from home and also to help whomever should be taking care of Myles during that time.

On the left side, there is a link to view our profile. We have written a short paragraph about ourselves so check that out if you want.

Right now it's hard to come up with very much to say b/c I haven't had a dr's appointment since the one where we found out. But I have one on Wednesday, so I'll for sure post then. Talk to you later.

Aug 11, 2006

 

What is up w/ Insurance?

This is my first attempt to update/post anything to this site, or any site, so I'm really just checking to see if I can do it right.

I've been calling some many people trying to figure out what hospital we can go to for delivery/treatment. The insurance company, the hospital, the company that handles out of area claims, and a dozen other places. I get so confused! If anyone out there is an insurance guru let me know!

Talk to you all soon! :~) Sarah

Aug 9, 2006

 

Giving Never Tasted So Sweet!

On Thursday, August 10th you will have the opportunity to change lives and make miracles happen.

It's Miracle Treat Day at participating Dairy Queen® locations.
Proceeds from every Blizzard® treat purchased will be donated to your local
Children's Miracle Network Hospital.

So bring your friends and family to a participating DQ® on August 10th,
for Miracle Treat Day, because giving never tasted so sweet!

Read more on Dairy Queen's Miracle Treat Day.