STORIES

The partnership between CHRISTUS Ochsner SWLA and the Children’s Miracle Network is – quite literally – a lifesaver for people across our region.

Children’s Miracle Network

CHRISTUS Ochsner Southwestern Louisiana Foundation represents the exclusive Children’s Miracle Network hospital in Southwest Louisiana. The Foundation raises CMN dollars to create local miracles by funding advanced pediatric equipment and wellness education programs for the health and well-being of Southwest Louisiana’s children. All local money raised for CMN stays in Southwest Louisiana.

Why

Your investment in the CHRISTUS Ochsner SWLA Foundation is an investment in a healthy future for Southwest Louisiana.

We envision a health care organization that is the first choice for patients in Southwest Louisiana and beyond; that provides opportunities to match generous donors with ideal programs; and that ensures every individual experiences God’s healing presence and love.

 

Testimonials

BELLA

Bella - Photo 2Bella’s parents had struggled with infertility, trying for about 3 years to get pregnant. When they finally did, they were extremely happy, but around 29 weeks of pregnancy, Bella’s mom developed preeclampsia.

The condition can be dangerous for mothers and the baby needed to be delivered in the next 48 hours. Bella arrived weighing just 2 lbs., 2 oz., and her parents were able to hold her for just a few minutes before she was whisked away to the NICU, where she would spend the next several weeks. Thankfully, Bella exceeded everyone’s expectations during her stay. Bella - Photo 3Even when she was diagnosed with a heart murmur, doctors assured her parents that it was common in premature babies, and that it should close on its own. After six grueling weeks, Bella was released, and a few more weeks after that, the hole in her heart closed. Bella is now three and has never experienced any serious health problems as a result of being born prematurely. In fact, she has not contracted any severe sicknesses at all. Bella is a strong and resilient little girl, and her parents are reminded every day that she is a true miracle.

LOGAN & MASON

We underwent several rounds of fertility treatments before successfully conceiving triplets. We lost one baby early in the pregnancy, but the other two did well until about 20 weeks. At that time, one of the babies’ amniotic sacs burst. I spent the next three and a half weeks at CHRISTUS Ochsner Lake Area Hospital in an effort to help the babies go past 24 weeks gestation.

On April 2, at 23 weeks 6 days gestation, Logan was born naturally. Mason was delivered by C-section. Both boys weighed less than a pound and a half.

Together, the boys have been treated for under-developed lungs (requiring breathing assistance), patent ductus arteriosus (a persistent opening between to major blood vessels leading from the heart), retinopathy of prematurity (a potentially blinding eye disorder), a hernia, choanal atresia (a congenital disorder that blocks the back of the nasal passage and leaves only one nostril open for breathing), and bronchopulmonary dysplasia.

Despite all these challenges, our favorite place is the NICU at CHRISTUS Ochsner Lake Area, and our favorite people are the nurses and doctors there. Their dedication and commitment made a truly life-saving difference for our boys, and we’re forever grateful for them.

Logan and Mason are now 7 years old, and they really are walking miracles! From the day they were born, they have been in more hospitals and doctors’ offices than many of us will ever see. They are happy and smart, and they love each other and their family. Our lives are so full, and we cannot imagine life without them.

DRAKE

When expecting my first child, I began to have severe upper abdominal pain. At 29 weeks and six days gestation, I was diagnosed with a severe form of pre-eclampsia known as HELLP Syndrome, and my doctor recommended an immediate C-section. My son, Drake, weighed just two pounds and 10 ounces. His lungs were not fully developed, so he had to be on what they call a Continuous Positive Airway Pressure machine – better known as a CPAP machine. He also need oxygen and to use a bilirubin light.

 

 

His struggles didn’t end there. Drake’s digestion troubles began after they removed his feeding tube. He regurgitated most of what he ate, which made him fussy, and we tried numerous reflux medications before finding one that lessened his pain. Drake spent 43 days in the NICU, and when he was about 6 months old, things started to calm down.

During that time, I was so impressed by the NICU. The nurses were confident in themselves and in the mothers. I had no idea how much equipment is necessary in this environment, and I’m grateful that our NICU had what we needed to treat my son. Drake is a true miracle, and he’s the strongest person I know!

AVERY

AveryAvery Rodriguez

Severed Umbilical Cord
Age 1 year, 8 months

Avery

Avery was born in an extraordinary birth experience that occurred on route to the Hospital.

With her umbilical cord severed in two places leaving her without oxygen, Avery’s doctors doubted she would ever be able to lead a normal life.

While lasting effects are still unknown, Avery has already surpassed her medical team’s expectations.

Our CMN efforts help to fund the highly specialized equipment needed to treat babies like Avery.

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