Benefit for Kinley Ray McCombs
Donation protected
Kinley Ray McCombs was born on March 4, 2019. She was born with a cleft palate and recessed chin and was diagnosed with Pierre Robin Syndrome. She spent her first couple of weeks in the NICU at St. Luke's.
She's now in the NICU at Primary Children's Hospital in Salt Lake City. Along with what she's already been diagnosed with, she has a deviated right nostril and Laryngomalacia which is the softening of the tissues of the voice box above the vocal cords. The laryngeal structure is malformed and floppy, causing the tissues to fall over the airway opening and partially block it. She is also on high flow oxygen because her carbon dioxide is too high in her blood which means she isn’t breathing through the O2 she is taking in.
As of today, April 4, she has the rhinovirus. For them to determine what surgery she will need, she needs a CT scan. To do the CT scan they will have to sedate her a little because she cannot move during it and they cannot sedate her until she is getting over the virus. Once they do the CT, they can determine the best course of action and schedule surgery.
Kinley has a long road ahead of her, but she's a fighter! Not to mention dearly loved by her parents, sister, grandparents, aunts, uncles and friends of the family. Please consider donating to help pay for expenses not covered by insurance. There will be many out of town trips and time off from work for Cody and Ashlynn. Your prayers are also much appreciated!
She's now in the NICU at Primary Children's Hospital in Salt Lake City. Along with what she's already been diagnosed with, she has a deviated right nostril and Laryngomalacia which is the softening of the tissues of the voice box above the vocal cords. The laryngeal structure is malformed and floppy, causing the tissues to fall over the airway opening and partially block it. She is also on high flow oxygen because her carbon dioxide is too high in her blood which means she isn’t breathing through the O2 she is taking in.
As of today, April 4, she has the rhinovirus. For them to determine what surgery she will need, she needs a CT scan. To do the CT scan they will have to sedate her a little because she cannot move during it and they cannot sedate her until she is getting over the virus. Once they do the CT, they can determine the best course of action and schedule surgery.
Kinley has a long road ahead of her, but she's a fighter! Not to mention dearly loved by her parents, sister, grandparents, aunts, uncles and friends of the family. Please consider donating to help pay for expenses not covered by insurance. There will be many out of town trips and time off from work for Cody and Ashlynn. Your prayers are also much appreciated!
Organizer and beneficiary
Andrea McCombs Andrus
Organizer
Twin Falls, ID
Ashlynn McCombs
Beneficiary