Thursday, November 10, 2011

Fun, Craziness and Life

So, it's been a while since I have posted on here. As most of you know we have been quite busy with Olivia with Doctors visits, checkups etc. We have seen everyone from Hematology to GI to Cardiologists and Liver specialists. It has been crazy to say the least. But amongst all this craziness we have had some great times too!! In fact, the last couple of weeks have been amazing!


To start it off we did the American Heart Association Heart Walk starting at Turner Field and was a 5k on Sat. October 29, 2011 It was awesome and COLD!! :) I had two of my sweet friends from work Chrissy and Britanie who joined my family to support Olivia and walk with us on this special day! Here are a few pics from that day.....






The following weekend we went to be a part of a Make A Wish event that we were invited to at the GSU game. We had tons of fun and Olivia loved meeting the cheerleaders and coming out onto the field at halftime and seeing what goes on behind the scenes of a college football game! Cooper loved seeing the big football players and I think that he wanted to go play too!










On Tuesday Novemeber 8, 2011 we went to Dave N' Busters to meet some of the Atlanta Falcons and go Bowling. This was another Make A Wish event that we were invited to and it was AWESOME!!! Olivia meet a new best friend named Michael Palmer #81 Tight End. He was great!! Olivia had him spinning around and clucking like a chicken while he was bowling. He made her laugh and smile that would last a lifetime!!





 

Friday, July 29, 2011

Read This: It Could Save a LIfe.

Kristine Brite McCormick contacted me to tell the story of her beautiful daughter Cora and how a seemingly healthy newborn could be battling something life-threatening. Cora passed, but what was learned can save others. Here it is, in Kristine's own words.

Cora's Story: Screening Newborns for Heart Defects

A screening so simple it's called the fifth vital sign might have saved my daughter's life. Something so simple it's like getting your temperature or blood pressure taken stood between my daughter's life and death. I'm determined to make sure that doesn't happen again.

My pregnancy with Cora was normal and uneventful. I had no problems during labor and delivered a beautiful 8-pound, 10-ounce little girl on November 30, 2009. She scored nines on both her Apgar tests. I took her home with a clean bill of health.

One early morning, I nursed her. Everything was going great. As a new mom, I looked down almost constantly while she nursed. I looked up for a brief second to tell my husband something. I looked back down. Cora wasn't breathing. Cora was pale. Her face was covered in blood. I jumped up. We raced to the hospital. It was too late. At just five days old, Cora was dead.

Two days later, the coroner called and told me Cora died from a congenital heart defect. It was the first time I'd ever heard those words. When I asked my OB about it, she said it was rare.
I later found out CHD is not rare. It affects one in 100 babies according to the March of Dimes. I was devastated to learn Cora wasn't alone; CHD is one of the leading causes of deaths in infants, killing more babies than SIDS or accidents. A few weeks after her death, I learned that only half of all babies are diagnosed before birth. I learned that other babies are dying from late diagnosis, or suffering from delays and brain damage.

When I found out that a simple tool already found in every newborn nursery that costs less than a diaper change could have saved her life, I wasn't angry. I was determined to prevent other babies from suffering.
Pulse oximetry measures the oxygen saturation of a patient's blood. Almost all of us have had one at some point. For adults, it's a clip with a small light that goes on the end of your finger, and in newborns it looks like a Band-Aid.

Pulse ox doesn't find every CHD. There's no foolproof test for heart defects. But it helps. It's easy. It's cheap. It's not harmful to baby or mother. In fact, it's best when baby is calm, so the baby potentially never has to leave her mother's arms during the screening.

I'm not a fan of medical interventions. Had I learned something more invasive or painful caught some CHDs, I would have thought twice before becoming an advocate. But this is a no-brainer. It's so simple yet life-saving.

I'm proud to report, my home state of Indiana was the first to pass pulse oximetry screening for CHD legislation. I'm so proud of Cora, and what we've accomplished here. There's a national movement. Protocols are being developed. It's been recommended and studied. Two other states — New Jersey and Maryland — have pulse ox-related laws. Tennessee, Pennsylvania, and New York have bills.
Some hospitals already do this. If you deliver at a hospital that does the screening and your baby's saturation levels are low, the screening will most likely be repeated, and if the numbers are still low, an echo will be ordered.

I hope that never happens to anyone reading this. I honestly hope pulse ox doesn't catch any CHDs because I wish congenital heart disease didn't exist.

However, with mixed emotions, I realize that many mothers will first be alerted to their child's heart defect because of pulse oximetry screening. I'm sad that they have to enter the world of CHD. I'm glad they won't find out like I did, from the coroner.

Soon every baby in the nation will be screened with pulse ox. It's just a matter of time now, and now you know it's important. It affects real people. Sadly, Cora could have been your baby because most types of heart defects are not genetic but linked to random events.

What happened to Cora doesn't have to happen again.

If you'd like more information about pulse oximetry screening and how you can help, visit my website, pulseoxadvocacy.com. To read more about Cora, visit corasstoryblog.com.

Kristine Brite McCormick lives in Indianapolis with her husband, Ben, and two badly behaved dogs, Reggie and Lucy. Cora is her only child. She's an advocate and activist. Other projects include Operation Healing Hearts, helping children in Iraq with heart defects, and work with several other charities.

Friday, July 1, 2011

Camp Braveheart 2011`

Here are some more photos from Camp Braveheart 2011. Olivia made some great friends while she was there and had an awesome time but was ready to come home when we picked her up! I was ready for her to be home too....















Recommend Federal Newborn Screening for Critical CHD

Dear Heart Friends, before you turn off your computer before the holiday weekend, please take a moment and send HHS Sec. Kathleen Sebelius your support for national newborn CHD screening. I hope you all have a wonderful and safe 4th of July!! Thank you!

Recommend Federal Newborn Screening for Critical CHD

Tuesday, June 21, 2011

Pulse Ox in the Paper! June 21, 2011

Published Tuesday, June 21, 2011 in Close-Up
Olivia Harvey of Newnan, who will enter the third grade this fall, is in good health now despite being born with three heart defects. 
Olivia Harvey of Newnan, who will enter the third grade this fall, is in good health now despite being born with three heart defects.

Harvey raising awareness about pulse ox screenings

The Times-Herald

Melissa Harvey of Newnan hopes that Georgia will join the states of Maryland and New Jersey in requiring pulse oximetry (pulse ox) screenings for newborns.
Harvey's daughter, Olivia, was born with three congenital heart defects -- coarctation of the aorta, pulmonary stenosis and mitral stenosis -- all conditions that will impact her for life.
Pulse ox screenings, which take just seconds, can be a valuable tool in detecting heart and lung problems in infants. In Harvey's case, it was an alert nurse who noticed that Olivia wasn't breathing properly while breastfeeding.

"What we're hoping to do here in Georgia is to get the same thing passed," said Harvey, who is president of the "It's My Heart" chapter in Atlanta. It's My Heart works to support parents of children with congenital heart defects.
Harvey says that other states have pending legislation regarding pulse ox screening, and others have pilot programs in place.
Dr. Matt Oster, a pediatric cardiologist at Children's Health Care of Atlanta, explains that pulse ox is used to "measure the degree of oxygen saturation" in the red blood cells.
"It should be close to 100 percent," said Dr. Oster about the measurement.
According to Oster, there are two reasons for a low reading. The first is a lung infection or problem, and the second is a heart defect preventing the blood from reaching the lungs for oxygenation.
Oster said that many children with heart defects exhibit no symptoms and appear healthy at first. "Then they go home," he said. Having this simple screening can help "avoid kids getting into trouble."
The pulse ox test is non-invasive, and involves equipment hospitals have readily available.
The U.S. Health and Human Services (HHS) Secretary's Committee on Heritable Disorders in Newborns and Children recently recommended screening of newborns for Critical Congenital Heart Disease (CCHD) using pulse ox.

Oster said he would definitely support any proposed legislation to mandate pulse oximetry and says it would place Georgia "ahead of the curve."
"It's not expensive at all," noted Harvey. The screening meter is placed on the infant's foot with a reading available in two seconds.
According to the Children's Heart Foundation, approximately 4,000 babies do not live to see their first birthdays due to congenital heart defects annually. Nearly twice the number of children die from congenital heart defects in the United States each year as from all forms of childhood cancers combined.
For more information on the pulse ox campaign, go to http://pulseoxadvocacy.com or e-mail Harvey at Melissa.harvey@itsmyheart.org

Harvey has already contacted a state representative who is researching the issue in detail.
In Georgia, it is required by law for newborns to undergo a blood test screening for a number of genetic and metabolic disorders. Hearing tests are also conducted routinely for most babies born in Georgia.
At six months of age, Olivia Harvey began receiving care at the Children's Healthcare of Atlanta (CHOA) Sibley Heart Center. In June 2003, she underwent a cardiac catherization to treat the coarctation, or narrowing, of her aorta and pulmonary stenosis, a condition in which a narrowed pulmonary value restricts blood flow to the lungs. Her heart did not respond to the procedure, and she remained in the Children's Michael P. Fisher Cardiac Intensive Care Unit (CICU) while waiting for open-heart surgery.
A week later, Olivia underwent a successful surgery to remove her pulmonary valve and repair the coarctation of her aorta. She remained in the hospital for two-weeks to recover. She continues to receive routine check-ups to monitor her mitral stenosis and evaluate the need for a pulmonary valve replacement surgery.

Melissa Harvey said that she feels fortunate to have had the expertise of CHOA so close to home. "It was very scary," she said. "They were my support system."
To support other families who undergoing similar experiences, Melissa co-chairs Heart Friends, a group composed primarily of families who have children treated at the Children's Sibley Heart Center.
For Olivia Harvey, early detection was key in her longterm health, and that's why her mother is taking up the pulse oximetry campaign. "So many babies are dying," she said.

Sunday, June 19, 2011

Trip to Ga Aquarium with the McGough's! June 18, 2011

On Saturday we got to make a special trip to the Ga Aquarium to meet the McGough family! We had a blast and Olivia and Cooper made some great friends for life! They met Brooklyn and Mason and had so much fun looking a touching all of the sea life. Our favorite was the Dolphin show. Olivia and Brooklyn are both going to Camp Braveheart this week and can't wait!


















Camp Braveheart Starts! June 19, 2011

Today we took Olivia and dropped her off at Camp Braveheart in Rutledge, GA at Camp Twin Lakes. She was SO excited. Camp Braveheart is a camp here in Atlanta that kids with CHD can go and be with other kids just like them!  I already miss her and cannot wait until Friday! Here are some pics:





Olivia trying out her bed for camp!


Olivia, Brooklyn, and Georgia!




Best buds!








Silly girls!


Having fun!




Almost everyone is here!


Cabin #7




Alsion, Brooklyn, Olivia and me!


Cooper and Mason.


Olivia and Cooper.


Headed out...we said our goodbyes!








Jason playing with the younger kids in the gym...imagine that?!? Lol.