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Featured Posts Heartache and Hope

Rewind

Dear Jud Bud…

14 years without you. I miss you so much! You and your sister are my greatest joys and my longing for you never wanes.

The other day I was at a dinner party where someone was asked the question, “If you could return to any year of your life and relive it, what year would you choose?”

Though I wasn’t personally being asked the question, I had an answer that came to mind immediately. 

It’s just a small window to which I’d return. It’s not even a full year. There is a sliver of my life that was the highlight, Juddy. I didn’t know it at the time. But I know now that this tiny stint was a climax in my life and a season for which I long. 

I’d push rewind to the day Jessie was born, and I’d delightfully relive every moment until you began to stumble. It was my nine months of heaven where I got to live with both my kids in a life unadulterated by Krabbe disease and death.

It’s not that these months were easy, by any means… I was transitioning to being a mom of two kiddos. I was exhausted with all that comes with having an infant and a toddler, your sister and you being just 19 months apart. I was really struggling with breast feeding your sister. We were strapped financially. And I was longing for friends after having just moved to a new area. 

But those were my months to which I’d rewind and relive over and over and over again. Just ordinary days. But oh what a delight — having you and your sister together and our family whole! Those memories feel complete. 

Once Krabbe Leukodystrophy entered the picture, everything changed. And since losing you,  every breath has felt incomplete. Every family dinner, Every vacation. Every holiday. Every family picture. Every momentous occasion. Every. Thing. Incomplete.

I miss you so much, Judson!

Which begs the question of a fast forward button… my answer, again, comes to mind immediately.

This time it’s a massive window to which I’d fast forward. It’s infinite. The bulk of my existence, will, in fact, be the climax.

I’d push the fast forward button to eternity with Jesus — the time when your dad, Jessie, and I will all be reunited with you by our loving and gracious Father. I’ll experience every moment with sheer joy and delight. It will be true heaven, where your dad and I get to live with our Savior and both our kids in a life unadulterated by Krabbe disease and death.

Complete. Whole. Fully Alive.

But there is no rewind button. And there is no fast forward button. There is only this moment…

And I want to live this moment well — not only in light of my past with you, my precious son, but especially in light of my future to come, with God’s precious Son. 

Just a few more weary days, my beloved boy. Just a few more weary days.

Every ounce of my love,
Mama

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Our Latest News

Leukodystrophy Families in Texas

Leukodystrophy Texas

The Levasheff family had the privilege of visiting three leukodstryophy families in Texas this last weekend: the Brooks, Chappells, and Wallaces. Each of these families are incredibly inspiring and have important stories that need to be told. So we are grateful that two Texas-based media groups, Ethos Media and Baesel Media Group, offered their services pro bono so that we were able to record the stories and hearts of these families, especially related to faith and hope in suffering. We look forward to sharing them with the Judson’s Legacy community in the future.

Filming Texas 2a
Beth Brooks and her daughter, Eden, who has Metachromatic Leukodystrophy.

Beth Brooks decided, as a single mother, to adopt a special needs child from Ethopia. When Beth adopted Eden, it was understood that Eden’s delays were due to malnutrition. However, it was a short time later that Eden actually began to lose more abilities even though she was receiving all the sustenance she needed. Soon thereafter Eden was diagnosed with MLD, a terminal leukodstrophy.

Beth is an incredibly inspiring woman and mother who teaches us all about love, sacrifice, commitment, and hope. Judson’s Legacy loves Beth and Eden Brooks!

Chappell Filming Texas
Scotty Chappell and Lauren Green with their son Lucas who has Krabbe Disease.

Scotty and Lauren were young adults when they had Lucas and it was in infancy that Lucas was diagnosed with Krabbe Disease. But Scotty and Lauren have beautifully risen to the challenge of loving and caring for their terminally ill son and have found faith and hope in the midst of their struggles. We all have so much Love for Lucas!

Wallace Texas Filming
Mike and Jenna Wallace with their son Jackson who has Krabbe Disease.

Mike and Jenna Wallace were only married a short time when they were blessed with their beloved son Jackson. Life was all they hoped it to be until Jackson was diagnosed with Krabbe Disease at just six months old. Although their lives have required a yielding to all they imagined, Mike and Jenna unabashedly talk about the way God has been making Himself known to them throughout this journey and the hope they carry through Jesus that is far greater than any suffering they may endure.

Jackson is the epitome of preciousness and his life is touching so many, including all of us at Judson’s Legacy. You can learn more about Jackson at The Jackson Project.

We are grateful to those who support Judson’s Legacy, enabling us to take trips to come alongside other leukodystrophy families and help share their stories!

 

Categories
Heartache and Hope

Beauty in Brokenness

Katelynn 1

BEAUTY IN BROKENNESS

written in memory of
Katelynn Abner: October 31, 2008 ~ July 4, 2014

Her beauty
Mesmerizing and pure

Porcelain skin
Translucent and soft

Long golden hair
Silky and flowing

Eyes of blue
Enchanting and deep

Lengthy lashes
Graceful and fine

A button nose
Freckled and fair

Rosy cheeks
Round and radiant

Dainty hands
Feminine and fancy

Her precious frame
Delicate and lithe

She was incredibly beautiful…
In brokenness
Strong and courageous

Now she is beautifully perfect

 

Me Holding KatelynnWhen I would sit with Katelynn in my arms, I’d soak in her beauty; she was a gift to behold. It was not simply a physical allure, though she is a gorgeous girl, but she had such a peaceful, serene presence in the midst of her suffering. I studied every detail of her lovely face. I breathed her in, shared secrets with her, and felt her warmth.

I emphatically believe that one of the greatest gifts one can experience is to engage the life of a child whose presence on this earth thins the veil that separates us from heaven; they are truly special messengers.

Jessie BridesmaidWhen we were with Katelynn a few times these last couple months, my kisses lingered on her tender forehead a bit longer, fearing it may be the last time I’d behold her beauty. Indeed, it was goodbye. Katelynn lost her battle with Metachromatic Leukodsytrophy on the 4th of July. Our hearts are broken with the Abner family as they must now navigate life without their precious girl.

Thank you, Katelynn, for gracing our lives with your beauty while modeling strength and tenacity in brokenness. Until we meet again, sweet girl, until we meet again!

Katelynn and I asleep