All About Carver

Carver was born 2 months premature on March 18, 2012. While in Mommy's belly, he was diagnosed with severe Schizencephaly (a very rare brain deformity) and Hydrocephaly (fluid pressure in the skull). He was born weighing 3 lbs 14 oz, and 16 inches long.

To define Schizencephaly: it is a developmental birth defect. It is characterized by abnormal slits or clefts in the cerebral hemispheres of the brain. People with clefts in both hemispheres commonly have developmental delays, delays in speech and language skills, seizures, and problems with brain-spinal cord communication. Individuals with clefts in only one hemisphere are often paralyzed on one side of the body, may have seizures, and may have average to near-average intelligence. Other signs and symptoms may include an abnormally small head (microcephaly), hydrocephalus, intellectual disability, partial or complete paralysis, or poor muscle tone (hypotonia). Treatment generally consists of physical therapy and drugs to prevent seizures. In cases that are complicated by hydrocephalus, a surgically implanted tube, called a shunt, is often used to divert fluid to another area of the body where it can be absorbed.

In Carver's case, there is no significant brain matter on the left side. This means that almost all of his frontal, parietal, and occipital lobes are missing on the left side of his brain. They have been replaced with cerebral spinal fluid. On the right side, there is a very thin layer of brain in the shape of an "O", which is filled with a large amount of spinal fluid. His cerebellum and lower brain (which regulates bodily functions such as heartbeat and breathing) are intact and functioning, although some reports have said it is hypoplastic (which means underdeveloped).

A few days after birth, Carver's head began to swell at a very fast pace. Because of the excessive fluid pressure, he underwent surgery to have a shunt (drain) placed in his head. It is basically a tube that runs under his skin from his skull down to his abdomen. It helps to drain the excess fluid and will most likely remain there for the rest of his life. A few weeks after his surgery, his incision site got a staph infection which put him in the hospital for another 2 weeks (and 2 additional operations).

Because of the nature of his diagnosis, Carver has seizures which have (thankfully) been helped with medication. It is very easy for him to become over-stimulated, which can create stress for him and in turn, cause seizures. He also has microcephaly (a small head due to lack of brain tissue growth) and a little trouble regulating his body temperature (because of his brain condition).

Despite these few downfalls, Carver is doing exceptional! Even though he has only a small amount of significant brain tissue, he passed his hearing and vision tests, he smiles and giggles, he coos and squeals, he can hold his head up and rolls over, and he can grasp objects with his hands. He is doing very well developmentally so far! He is truly a a miracle and has come to be our greatest teacher. Thank you for showing him support and love by following his journey with us!

This blog was created so that others can watch him grow and follow his journey with us. He is beyond miraculous and we want to share his story with the world! Contact us: carversjourney@gmail.com

Carver's Brain

Carver's Brain

Sunday, March 18, 2012

Carver Arrives!

At 12:56am Carver Bradley was born into this world. He and Mommy are doing great. Mom's water broke on its own at 31.5 weeks gestation. They were able to hold off labor for a few days, but we were a little rattled because they awoke us to the news that we needed an emergency c-section ASAP due to very low biophysical ultrasound scores (a 0 out of 8).

Despite that, Carver is already demonstrating himself to be very special. He came out breathing on his own, with good weight (3 lbs. 14 oz.), he is 16.5 inches long, and everything in the right place in good working condition. His apgar scores were a 9.9 out of 10!! He is being kept in NICU and will have an MRI on Monday. Cord Blood has been drawn and is already in flight to Arizona.

He is beautiful, has great color, and is impressing us all beyond belief. He has been moving his arms and legs around like crazy, and has all of his 10 lovely fingers and 10 lovely toes.

Thank you all for your support, warm thoughts and prayers. We are very grateful for Carver. He's our lucky charm!   :)

8 comments:

  1. Carver is a beautiful gift from God! What a special little guy that moves the hearts and spirits of many. Much love from his grateful nawnaw....

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  2. He is beautiful Lauren! Sending a lot of love your way.... <3 <3 <3

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  3. beautiful. Congratulations and lots of love

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  4. He's beautiful!

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  5. Im all teary eyed! This little guy has been in my thoughts and prayers so much, beautiful!

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  6. Amazing!I am so happy and so relieved for you!He looks perfect! :)

    FILM

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  7. Congratulations...and rejoicing with you and the family on your beautiful gift from God....

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  8. We had a great time this week but but nothing fills our hearts more with such such joy and happiness to know that this precious little fella is born and doing so well!! My God bless you and your child.
    Our love and prayers--Terri and Ramiro Ybarra

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