MITCHELL'S JOURNEY GUEST ON PODCAST
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A Mitchell’s Journey reader-turned friend invited Chris to be a guest on her podcast. In this interview, you’ll hear his perspectives on Mitchell’s Journey, making sense of suffering, and the pursuit of meaning and purpose.

Chris Jones lives in Salt Lake City, Utah with his wife, Natalie and 3 living children. Their son, Mitchell Jones passed away from heart failure in 2013. He had Duchenne Muscular Dystrophy, a catastrophic muscle wasting disease that is fatal.

MITCHELL'S GRANDPUPPIES

When Mitch passed away, he left behind his puppy, Marlie, who at the time wasn’t much older than the furry kids in this video. Since then, Marie has become a tender mercy to our family in more ways than we can describe.

Last December, Marlie had puppies. In this video are 3 of her surviving pups and the father. Mitch would have loved this video. When he was young, he always did his homework quickly so he could watch a TV series called, Too Cute, which highlighted young animals who were trying to find their way in a big new world.

Mitch loved those videos because he identified with youth - and he loved anything that caused him to feel good on the inside. Natalie and I found this video and we looked at each other and said, almost simultaneously, “Mitch would have loved this.”

Mitch taught me to never waste a chance to smile. This video has me smiling so much, my face hurts.

If you’re into following cute animals, the little brown puppy was adopted by a family in Texas, who has been a friend to Mitchell’s Journey for years. His account is here: www.instagram.com/oliverdee_mitchellslegacy/

GOING HOME (UPDATED)

I took these photos the night Mitchell was released from Primary Children's Hospital. The hospital wanted to keep working on him because, as an institution, that's what they do. But our cardiologists were compassionate and knew better. Their personal advice was to go home as quickly as possible and love this boy with all that we had because the end was coming, and there was nothing they could do to save him.

I'll never forget the look on sweet Mitchell's face when we told him we were going home. In his soft voice, tempered by shallow breaths, he said, "Dad, really? ... I get to go home?" Mitch was relieved and excited. My wife and I were overflowing with fear. We were not doctors; our medical experience was limited to Band-Aids and Neosporin. But within hours, we were given a crash course on how to run oxygen tanks, manage the device that would pump medicine into his heart 24 hours a day, flush his lines, manually administer other drugs through an IV, and more. We were overwhelmed with sorrow, new information, and the inevitable.

Doctors inserted a PICC line that ran from his arm directly into his heart (no small procedure). This line was connected to a little computer that would administer Milrinone, the drug that would keep our boy alive a few more weeks. Without it, he would have become very, very sick within hours. Without it, he would have died rather quickly and painfully.

At the moment this photo [on the left] was taken, I had asked Mitchell if he was excited to go home. His soft smile and loving eyes melted my heart. But inside, I was falling apart. Inside, I was stumbling over the rubble of dashed hopes and dreams. I was trying desperately to feel my way through ashes and darkness. All the while, I tried to contain my fear and emotions so as not to frighten him. I wanted him to be happy. I had to find a way to live in the moment and let tomorrow be.

After he was discharged, Natalie rolled him to the curb – he was so anxious to live his life free of hospital constraints, to reclaim the life he loved so much, to be a little boy again. He had a look of determination in his eyes – an appetite for living I seldom see in anyone. At the time, he didn't know this was a one-way trip. And that trip was the longest, most painful drive of my life.

Once loaded, before we even left the parking lot, Mitchell reminded us it was his week to lead Family Night (a tradition we have once a week to spend time together as a family). We were humbled by Mitchell's desire to contribute, but Family Night was the last thing on our mind. We told him he didn't need to worry about it, that we could do something different instead if he wanted. Mitchell had a tremendous sense of duty. Once he understood a rule or expectation, he lived it to the letter of the law. A more obedient soul I've never known. Mitchell felt it was his duty (a duty he loved) to serve his family.

Two days later, Mitchell would humbly teach a Family Night lesson that focused on love and service. I filmed his heart-felt, soft-spoken lesson. He had prepared some ideas to teach us and games to reinforce what he taught. It was an evening never to be forgotten. Our boy, hanging by a thread, struggling to breathe, put what little energy he had into teaching us about one of life's most important lessons. Perhaps one day, I'll post the video of his lesson to our family. At this moment, my frail son sat on the edge of his couch to share his ideas on love. I was mesmerized. As great as his lesson was, the most powerful lesson wasn't found in his words but in his humble and faithful actions. This little boy, broken and withering away, was magnanimous. I stood in his shadow ... in awe.

Seven years have passed, and not a day passes that I don't reflect on Mitchell's longing for home. Home was where he felt safest, where he could love and be loved. And despite his love for his physical home, a simple touch, a hug, a kiss on the forehead took him home, no matter where he was. Mitchell taught me home isn't a place; it's a condition of the heart.

For the first few years after his passing, my physical home felt profoundly empty without him. There was, and remains, an echo in my heart that will last a lifetime. I don't get to see Mitch when I come home anymore – and I never will for as long as I live on this earth. So, I choose to remember the tender lesson Mitch taught me; that home is not a place but a condition of the heart – and in that way, Mitch is home in my heart and soul. It's not the same, but it's all I've got, and that will have to do.

But alas, there is another home where he now resides. I cannot see it … and oh, how I wish I could. But I have felt it. And it is that home that I long to be.

NOTHING LASTS, BUT EVERYTHING’S FOREVER


Ever since my sweet wife was a little girl, she wanted to be a mother. It was her dream to have and raise children – and it has been my deepest honor to watch this good woman love, protect, and nurture our kids. It has been my greatest honor to be her partner in life, love, and parenting.

Lately, I’ve been stumbling into little breadcrumbs Mitch left behind, and these breadcrumbs have brought me a great deal of joy and gratitude for all that ever was. One example happened just a few weeks ago; Natalie and I moved Mitchell’s bed and discovered a laminated poem he wrote in school. Somehow, someway, this little paper slipped and drifted under his bed, far from view. And there it slept for 7 years, Natalie and I unaware of its tender existence.

This is what Mitchell wrote in honor of his mother:

THE BEST MOM EVER
Golden, shiny hair,
Eyes like the ocean,
Pretty, young,
Special to me.

Cooks juicy stroganoff,
Makes my comfortable bed,
Buys me cool presents on my birthday.

Rode the Dragon ride at Legoland,
Pushes me on the swings.
Tucks me in at night.

My mom is the best.

When Natalie and I read that, our hearts gushed with gratitude. We marveled over some of his word choices (“eyes like the ocean”) but more importantly, we melted over his heartfelt sentiments. Although we cried tears of loss and longing later that night, at that moment, we were captured by the sweet innocence of our son.

Mitch was right; he had the best mom ever, and his short life reminds me that while nothing lasts, everything that matters is forever.