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Why do I blog?

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I'm nudged once again to rekindle this little blog.  It was created to serve as a public diary for those who call me Mom, Nana, or simply Cheryl.  Oh, how I wish there were blogs back in the day when my parents, grandparents and in-laws traveled their earthly journeys.   I know without a doubt had the technology been introduced to them in their younger days ~ they would have used it.  What joy it could have been to revisit their lives with technology ease. I've been pondering all of my life changes in recent months ... I'm so very thankful for God ~ My heavenly Father and Creator of ALL things including the beautiful universe, my loving family, and me.  I thank Him daily for loving me, guiding me, and His blessings and healing miracles in our family. I'm so very thankful for Jesus ~ My comforter and teacher.  He understands the difficulties and evils of this world.  He continues to teach me the power and legacy of unconditional love.   I melt into His

It's been a while ...

... I know, since I last posted.  A lot of life has happened since then. At the time of my last blog post in June 2016, our family was still deeply grieving the unexpected deaths, 31 days apart, of my father-in-law and my mother.  Sudden cardiac arrests for both of them resulted in them leaving us just weeks before the holidays.  They were active parents and grandparents one day, then gone the next day.  Taylor's miracle testimony, at least for me at that time, was the salve for my grief ~ helping me to "remember" God is Good. I found it difficult to continue writing about Taylor's miracle when others, outside of our family, were experiencing unanswered prayers.  Death was their heartbreaking result.  My faith and trust suddenly brewed-up more questions than answers.  One of which was ... how does God choose who He grants a miracle to when others deserving of one, die?  With this puzzling question, it was just too difficult for me to continue the testimony.

Songs in the Night

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Taylor's Miracle ~ Part Six

Completely drained, confused and not knowing what to do or where to go next, we walked through the O.R. double doors and decided to return to Taylor’s ICU room to await his arrival from recovery. That room was temporarily home now. We were informed by the nursing staff when we arrived at his room, however, that he would be held in recovery for quite a while. As we waited in the quiet, empty ICU room, Chris said, “One of us should probably try and get some sleep in that sleeping room the surgeon reserved for us tonight.” I nodded in agreement, but knew I couldn’t sleep. All I wanted was to be near Taylor. “How about you sleep first and I’ll stay with Taylor,” I said, knowing my suggestion would not convince my husband. As suspected, Chris replied, “No, you sleep first and I’ll stay with him.” Since neither of us wanted to be apart from Taylor, we decided to at least check-in at the reservation desk since the surgeon told us the suite would soon be closing reservations fo

Taylor's Miracle ~ Part Five

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It was Thursday, June 15, 2006 and we waited for Taylor’s turn in the operating room to install the dialysis catheter. There were no changes overnight for hopeful signs of kidney function. I methodically checked the urine bag that hung at the bottom of his ICU bed as we watched, waited, and prayed for the precious return of what we called “liquid gold”. But, as was the case all week long, there was only about a tablespoon or two of a pale liquid that the nurses assured us was not good urine. The blood counts continued to show extremely high and rising creatinine and BUN counts associated with kidney failure. It appeared more certain he would need the dialysis as the kidney’s were refusing to function. By mid-afternoon, the operating room alerted the ICU staff they were ready for Taylor. He was wheeled down the hall in his ICU bed by the surgical nurses in green scrubs. They paused at the double entry doors to the O.R. so his dad and I could give him a quick kiss goodbye. T

Taylor's Miracle ~ Part Four

The ambulance arrived at the emergency room doors of Riley Children’s Hospital at around 7:00 Monday evening, June 12 th , 2006.   Taylor was wheeled into a private emergency room and attached to monitors to record his vitals.   I was shocked to lay eyes on him again after the two hour drive from the transferring hospital. He was now extremely bloated.   His entire face was so swollen that he could hardly move his lips to speak.   His previously thin chest that clearly showed his sternum and every rib, was now so bloated that it looked like a barrel had been implanted inside his torso.   His hands and feet were so puffed I was afraid his fingers and toes might pop if it became any worse.   The hive blotches had also grown much larger over his face and body and now appeared to blend all together changing his pale skin to a deep reddish purple sea of welts.   If it wasn’t for his trademark curly, red hair he would be completely unrecognizable.  And then we waited. We waited for ho