Broken and Content

Held

on
July 17, 2020

“Mama, I want to ask you something but I am scared.” Paisley’s sweet face looked up at me, craving my undivided attention. 

“Ok, let’s go out to the porch and talk.” I guided her out of the house quietly so no one would follow us out. We snuggled up under a blanket as the fall air was crisp and bright. 

“This is hard to saaaaay.” She squirmed beneath fear. “Uuuummmm…ok…”she took a deep breath, “When will Finley’s cerebral palsy go away?” 

My heart sank. Her always twinkling blue eyes peered into mine. I took her hand and pulled her closer. “Darling, Cerebral Palsy does not go away. There is no cure. There are…”

“So Finley will ALWAYS have CP?!” She interrupted with shock and hurt and confusion. 

Cerebral Palsy has been a norm for Paisley for as long as she can remember. Paisley was two years old when Finley was born and toddled through physical, occupational and speech therapies with Finley and I while the boys were at school, never once complaining about doing therapy again and again with me. She has fiercely loved her sister since the day she was born and CP and therapies and mama having to give Finley so much attention has never changed that. 

“Yes, sweet P. Unless God heals Finley, she will always have CP.” 

Big tears spilled down her freckled cheeks. “Well, why doesn’t he just heal her?” 

“I don’t know, darlin. I don’t know.” 

She cried and cried. I cried along with her. Our children have faced and grappled with questions and thoughts and fears that Matt and I are facing as adults. My heart hurts for them and I am confident that God will use this gift to grow a deep compassion for others through this pain. 

“Paisley, I think Finley is going to enjoy heaven the most out of our whole family.” 

She giggled through her tears, “yeah, she will be like, ‘look guys I can run!!!’” 

“That’s right. She will run and dance and jump and twirl…Paisley, we will continue to pray for God to heal Finley. He is able to do it. But, he may choose not too and we will never know why.” 

She was serious again, nodding and taking in my words.

“What we do know is that he is good and faithful and that he is taking such good care of our family.” 

“Thanks, Mama. I feel better.” 

I held her again, knowing that is what I have needed so much during this journey-just to be held, just to be close to the ones I love to be reminded that I am not alone and that God is good and faithful and that He is taking care of us. 

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2 Comments
  1. Reply

    Abi Rowe

    July 18, 2020

    Heather, your writings are teaching me so much of what it looks like to be content, and fiercely faithful in the midst of pain and confusion. Last Sunday, at church, I was sat a few rows behind your parents along with Jones, Mcray and Paisley. (apologies for any spelling mistakes). And, as I observed them, I saw such maturity and such grace in these young children of yours. And it wasn’t like I had much to observe, as they were just standing confidently and calmly with your M&D. It was like I was seeing through a spiritual lens. I can only imagine what it must be like to grow up with a sibling with a disability, but I can see that these kids of yours are strong and gracious, and unassuming and are already such an example of what it looks like to stand on the firm foundation of Jesus Christ as their rock. You and Matt are AMAZING parents!

    • Reply

      heathersweetman

      August 7, 2020

      Thank you, Abi! Thank you for your words of grace and encouragement. Love you and Kevin 💛

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