We volunteered to do a story of our experiences for the NICU to hang on their wall of success stories to encourage parents during their babies stay. Even five years later I still cry when I look at pictures, read or write about our experiences with our kids. I love that it always reminds me how truly blessed we are to have these two special kids in our family. I know you have all heard the story, but I thought that I would share what I wrote as a reminder to all of you that miracles do still happen every day.
Taya at birth.
Taya at 5 years old.
Taya's story....
Our little miracle girl Taya was born at 26 weeks 4 days
gestation. She weighed 1 lb. 6oz. at birth and was 12 ¼ inches long. After a very quick peek at her, she was
whisked through the operating room window to the NICU doctors and nurses waiting
on the other side to help her. She needed a lot of help to get her
breathing. Taya spent 2 ½ months on and
off of the ventilator before she could finally move onto the CPAP and then
eventually on to a nasal cannula. Her
biggest struggle in the NICU was breathing on her own. Her right lung kept
collapsing each time she was extubated.
After numerous tries she was finally successful and strong enough to get
air into her lungs. After being on the vent for so long we worried about ROP.
She did have stage 1 ROP that corrected itself before she left the NICU and has
had no lasting effect. When it was time
to learn how to eat Taya again struggled with keeping her oxygen level up. She would desat almost every time she
ate. Sometimes it was discouraging
because it was a very slow process to get her up to a full feed in an
acceptable amount of time. It took a few
weeks and a specialized feeding plan but she caught on! After 96 days of the ups and downs of the
NICU life we were ecstatic to take her home with the help of portable oxygen
and a pulse-ox monitor! Taya thrived at
home and was able to go off of the oxygen completely within three weeks. When Taya was 18 months and still not walking
on her own we suspected something was wrong. Taya was diagnosed with Cerebral
Palsy by the time she was 2. Even though we expected some long term effects
from her premature birth, it was hard to hear the diagnosis. Not knowing what to expect we feared the
worst. Five years later we realize how
blessed we truly are. Taya is a fully functional, happy, smart, funny and
beautiful child. She has a strong will
and does not let her CP limit her. She
continues to amaze us every day with her determined and uplifting spirit. She
truly is our little miracle!
Garrett at birth.
Without miracles and modern day medicine the three of us would not be here today. I am so grateful for all of the blessings that Heavenly Father has given us.
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