Thursday, February 16, 2012

Logan :: Child with Spina Bifida

Logan was born on October 17th, 2008. He weighed 6 lbs, 5 ounces and was 18 inches long! Logan was born with Spina Bifida: Myelomeningocele, Congenital Hydrocephalus, Chiari II Malformation. He has Asthma, GERD/Reflux and Hydronephrosis of the left kidney. Logan's SB level is at an L5/S1 (Lumbar 5/Sacral 1)...

On the day that Logan was born, my water had broke and I went into labor two & 1/2 weeks before my scheduled csection date, which was on November 4th! We lived almost 3 hours from the hospital that Logan was born at. We drove the 3 hours there. By the time we arrived to the hospital, I had been in labor almost 16 hours and the contractions hurt so much due to back labor.

I remember my husband being able to come into the room after they had laid me down and got me all secured and about 20 minutes later, I vaguely remember hearing the words, "And, we have a baby boy!" I remember waiting in agony for what seemed like forever to hear his little cry. When I finally heard it, tears streamed down my face and I passed out! They brought my husband over to where they brought Logan and let him see Logan's open lesion and then they carefully wrapped his opening and sent him on up to the NICU...

As I was in my room, I later learned that Logan had aspirated meconium and had to receive an NCPAP due to not being able to breathe, once he arrived up to the NICU. Logan went into surgery the next day to have his lesion closed up and after a day or two, I was finally allowed to go up to the NICU to see my precious, momma's boy!! The moment I saw him, lying there on his stomach- unable to move broke my heart but at the same time, I cried tears of joy. He was here and he was alive... (Not many people know this but before Logan was born, we almost lost him due to the Hydrocephalus growing too rapidly in his brain towards the end of my pregnancy.)

Logan spent the next 24 days in the NICU. He had his shunt placed in at one week old and was on & off oxygen.

Logan was released from the hospital on November 9th!! He came home in tow with oxygen and an apnea monitor. We would spend the next 3 months with many sleepness nights for fear that the apnea monitor wouldn't alert us if something went wrong! Logan would quit breathing while he was asleep, so there were nights where I was terrified to even sleep at all... In January 2009, Logan was officially weaned off oxygen!

Logan has had a total of 8 surgeries so far since birth... When he was about 5 months old, I had noticed that he was still breathing really rapidly. It just wasn't normal. So, I trusted my instinct and took him to our family doctor. We were referred to a Pulmonologist. It was then, that it was discovered that Logan had a paralyzed Diaphragm on his right side and would need surgery to have it fixed.


Later that year, Logan was hospitalized with Pneumonia for the first time about a month before his 1st birthday... And, then in February of 2010, he was hospitalized again for Pneumonia and it was then, that his Asthma was discovered.


Logan is now 3 years old and is a complete joy & light in our life!! He is sitting up, he is pushing himself up onto his hand and knees, commando crawls all over the place, rolls everywhere & is now working on his latest milestone: pushing himself up to a sitting position!! If I had known and was able to envision what life would be like as his mother, now almost 3 years later- I would not have been so scared or worried about what he would/would not do or if he'd even thrive or questioned the thought of a wheelchair, braces, catheters, meds or his needed therapies.

Logan is happy & healthy and lights up any room with his silly, little grin!! He doesn't talk, stand or even walk yet but none of that matters or is even an important factor. If I could do it all over again, I would not change a thing!

My blog: Growing from the Obstacles



Thank you for sharing Logan's story Tiffany! We still need more stories, click here to share yours!

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