Days That End in ‘Why’: A Letter to My Parents

Days That End in ‘Why’: A Letter to My Parents

Dear Mom and Dad,

In the wake of FDA approval of Zolgensma, jubilant feelings soar like a kite, beyond the boundaries of wonderful to the highest altitude of hope.

Mom, we recently had lunch together and chatted about new SMA treatments and their incredible impact on SMA families. You mentioned how you wished there had been a treatment for me when I was a kid. I sensed sadness in your eyes. Dad, I’ve gathered your thoughts on the topic, too.

Trying to fall asleep last night, I thought about writing a letter to you both in a column. The bedroom was bathed in soft moonlight as I lay with five pillows supporting my body. Wide awake, my eyes darted around the room. I stared at the obscure silhouettes of the closet door, the vague outline of light fixtures. I began to think about my childhood and how I’d shape this letter.

My dim vision blurred with mounting tears along my eyelids. I felt the damp heat of sorrow streaming down my cheeks, along the edges of the mask that helps my nightly breathing. Other than thinking about how I needed to stop this crying nonsense and avoid waking Andy up to dry off my sopping-wet mask, here’s what encompassed my mind:

Mom, I thought about how you fought for what was best for me throughout my childhood. You chiseled away at the icy medical denials of mammoth insurance companies. You sat through drawn-out IEP meetings and educated the school system about how to meet my needs, even when you faced great opposition from administrators and teachers who didn’t understand. You tirelessly advocated for me and listened to my perspective.

When physicians coldly told you I wouldn’t live beyond my teenage years, you waved them along amid your tearfulness and sought supportive, knowledgeable healthcare providers. You never gave up. Sometimes, people labeled you as “the squeaky-wheel special needs parent,” and I remember you countering it by saying, “The squeaky wheel gets the oil.” They probably thought you flew around on a broomstick at night, but you didn’t care what they thought because they weren’t in your shoes. 

Dad, I owe all of my Super Nintendo skills to you, and I’d like to think our Mario Kart races helped forge my superb wheelchair-driving abilities. Whenever I was on the Pediatrics Unit, you’d reserve a television cart with Nintendo and wheel it into my hospital room, or I’d watch movies with you by my hospital bedside. You were a stoic rock who taught me to persevere through the worst bouts of pain, the agony of chagrin.

If I ventured to a place of asking “Why me?” you didn’t allow me to sing the blues for long. You showed me how to take life one day at a time, valuing the transformative power of humor and attitude. You viewed me as any other kid and treated me as such. You grounded me when I acted out, and you taught me the world wasn’t going to stop revolving or go easy on me because I have SMA. You always nudged me in the direction of independence, even if only a short distance would be gained.

As parents, you had to balance my sister’s needs along with mine. You navigated tough and maddening issues, and I want you to know your efforts aren’t lost on me. You valiantly traveled the road shared by many other SMA parents.

But I also want you to know that my life has been beautiful, and SMA is part of that. I don’t discount my triumphs over it. There was no treatment when I was a kid, and it’s been a hell of a ride. It’s made me who I am today. I can’t picture my life any differently because this is the only life I’ve ever known. I’ll never wish away a journey that has taught me strength and shown me the meaning of empowerment, compassion, and love.

Living with SMA has ignited my fiery spirit. The reason I cried when thinking about this letter is because I have heart. That’s from you. Heart and spirit intertwined, I’ve risen to the occasion and channeled my strengths — cupping my hands over my heart, capturing the words that flow from it, and extending my arms to the world.

People with disabilities often feel forgotten within our society, and you knew that I’d grow up to face such harshness within many different arenas. You prepared me to be a warrior against ignorance, unfairness, apathy, and ableism — things for which there’s still no cure.

I can’t imagine the breadth of emotion and worry you felt for me while I was growing up, but I hope you’ve seen beauty in everything that I’m capable of. 

All of my love and gratitude to you both.

***

Note: SMA News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of SMA News Today, or its parent company, BioNews Services, and are intended to spark discussion about issues pertaining to spinal muscular atrophy.

Katie is a Wisconsin girl at heart who strives to paint with her words, illustrating a soulful connection with nature and adaptive outdoor adventure. She was diagnosed with SMA shortly after crawling (but never walking) into toddlerhood. With a background in Human Development & Family Studies, she finds fulfillment in being an uplifting resource for others and encourages those with mobility challenges to chart their course, navigate the waters and embrace their distinctive beauty. When she’s not engaging in advocacy or writing, you’ll likely find her hiking an accessible trail, adoring a sunset, or eating a s’more somewhere. She has three companions who hold her heart – two of which travel by paws (the other has human feet). Follow her journey @wheelprintsalongthewildflowers on Instagram.
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Katie is a Wisconsin girl at heart who strives to paint with her words, illustrating a soulful connection with nature and adaptive outdoor adventure. She was diagnosed with SMA shortly after crawling (but never walking) into toddlerhood. With a background in Human Development & Family Studies, she finds fulfillment in being an uplifting resource for others and encourages those with mobility challenges to chart their course, navigate the waters and embrace their distinctive beauty. When she’s not engaging in advocacy or writing, you’ll likely find her hiking an accessible trail, adoring a sunset, or eating a s’more somewhere. She has three companions who hold her heart – two of which travel by paws (the other has human feet). Follow her journey @wheelprintsalongthewildflowers on Instagram.

2 comments

  1. Anne Raduechel says:

    Katie
    As I read each piece you write I think “this is the best one ever”. What a beautiful and heartfelt tribute to your parents. I certainly can relate to almost all of it, with the exception of ‘having to balance the needs of two children’. This is absolutely a beautiful tribute to your parents; who are both exceptional people and have raised you and your sister to be just as wonderful. Thank you for sharing your thoughts, so honestly written … as always.
    Anne

    • Katie Napiwocki says:

      Anne,
      Thank you so much for your kind and uplifting words – they are very meaningful to me. 🙂

      -Katie

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