Kasey Grant

Kasey Grant is a big warrior in a two year olds
body. Born at just 29 weeks gestation he spent 6  months in Cincinnati Children’s NICU fighting         against odds. Megan and Grant were told at her 10 week ultrasound appointment that he had an           abdominal wall birth defect called an Omphalocele that would require surgery after birth. With his
surprise premature entrance it threw a “wrench”
in plans and caused him to face more obstacles
than expected. Heart surgery, ventilators, a G tube, multiple surgeries, hearing loss, and the list goes
on. Kasey is a walking testament of Gods Grace.
Unfortunately kids born with the birth defect
Kasey had are super susceptible to bowel
blockages. He is in and out of the hospital quite
frequently dealing with these issues among his
others. Tuesday afternoon the 18th things
declined quickly for Kasey when he arrived at the ER for what Megan and Grant assumed was the
start of another standard blockage. He ended up
having a serious type that required emergency
surgery called a closed loop obstruction. Following surgery the doctors transferred him off the
surgery floor and into the ICU for decreased
oxygen levels, pain control, and other medical
needs.

Among all of this Grant and Megan, less than 3
weeks ago welcomed their second baby boy into
the world. Megan is currently on maternity leave
and there is now an influx of medical bills. If you
can find it your heart to donate, any amount is
appreciated to help with any and all medical and
living expenses.