Faith that Shines

January 18, 2012 in Faith that Shines

Time for a look at faith that encourages us. Aaron Shust. His wife Sarah. A public Christian music couple. You might know his work.

In 2010 Aaron and Sarah discovered that their son Nicky, then two, had a rare disease called Eosinophilic Esophagitis, a painful disease that would not allow Nicky to take in nutrients. He was hooked to feeding tubes for months. 


The first days of the diagnosis were especially trying. Read this excerpt from Aaron’s blog in 2010: 

Wednesday 12/1: Sarah takes Nicky back to Children’s Hospital after reported discomfort.

Thursday 12/2: Nicky receives his 8th feeding tube, his 3rd GJ (a replacement) and my mom calls and tells me that my 90-year-old Grandma has until Monday to live, if that.

Friday 12/3: Nicky is discharged first thing in the morning and cleared to travel with us to Georgia to say our goodbyes to Grandma. We leave home at 1:40pm and arrive at 12:40 in the morning on…

Saturday 12/4: Nicky turns 2. Grandma hangs on and bounces between lucidity and living in the past. She’s bedridden, can hardly see, hear or move but is still the same, sweet, little lady we all love. Many hymns sung and “Jesus, There’s Just Something About That Name” sung countless times. Her obvious favorite.

Sunday 12/5: More time with Grandma. Nicky gets a fever. Steelers win.

Monday 12/6: Nicky’s fever won’t diminish with Tylenol, hovers around 102. We say our tearful goodbyes to a lady about to move into a pimp mansion and have dinner with her Savior and her God, then we hop into the car suddenly at 9:41PM and begin to drive back to Pittsburgh, checking Nicky’s temp ever hour. If he hits 103.5 and Tylenol doesn’t lower it, we have to stop at nearest ER.

Tuesday 12/7: at 2am maybe, Nicky hits 103.5. Tylenol works and we keep driving. My angel wife, Sarah, stays awake to help me stay awake (along with the prayers of friends and 5 hour energy drinks. blah) I drop off Sarah and Nicky at Children’s hospital at 10am, drop of Daniel at friends at 11 and go home to go to sleep. Wake up 4:30pm. Call Sarah for update: Nicky has severe Pneumonia, they can’t stabilize him enough to move him out of the ER and into his room. Heart rate is too high, BP is too low. Fever is still at 104.

My day has been much better than Job’s worst, but I’ll still say it. “The Lord gives and the Lord takes away. Blessed be the Name of the Lord.”
Miracously, after a few months of not knowing if little Nicky would survive, the Eosiniphilic Esophagitis, a life-long disease, disappeared. Doctors could not explain why. 
On January 13, 2012, the Shusts welcomed a third baby boy into the world. A new son, with a new series complications. But the shining story is not complications with the baby’s health. Read Aaron’s blog and watch his faith shine. It will encourage you. Read January 14 first. 

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{ 3 comments… read them below or add one }

Julie January 18, 2012 at 8:11 pm

Loved this post as it really puts life in perspective – God’s perspective.

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Laura January 18, 2012 at 8:57 pm

It inspired me too, Julie. I suspect God will allow the Shusts to minister to many people.

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Alene January 19, 2012 at 2:58 pm

Beautiful! Just beautiful.

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