UPDATE 2025:

From 2023-2024 we ran a campaign for a little deaf girl in Paraguay and her mother, and raised enough for preliminary testing to evaluate her fitness for a surgery. Things turned out differently than we anticipated–or hoped–but not necessarily in a bad way. Just a bittersweet one.
So here’s the story of strangers caring about each other…and a little girl who can’t hear her mother’s voice.
ORIGINAL POST:
Hey there! Jen here. Today, I want to talk to you about Debora.

It’s not mother’s day, but I’d love for you to email me and let me know what your mom sounds like. My mom’s voice is high and harsh, with a powerful operatic soprano when she sings. She’s worried it’s getting weak, and old, but I like softer edges. She’s not a hugger. With that strong tongue I’ve never doubted that she’d defend me to the death.
Debora’s never heard her mom’s voice. Cochlear implants are controversial in the deaf community, but in Debora’s case, she lives in Paraguay, where there is no sign language “community’ or “culture” for her to lose. She knows a few signs she does with her family, taught dutifully to her by therapists, but she can’t truly meaningfully communicate. At her current rate, she’ll never find independence. Community. Herself.
Earlier this year, while I was in Paraguay, a team of Americans came down to help some of the local pastors with their church, and to run a couple of health fairs with me. About a month later one of them texted me.
“Please, is there anything we can do for Debora?” he asked.
Gordon–a gruff-looking, no-nonsense ex-Navy vet–had teared up seeing Debora struggle to interact with her family. He found himself perseverating over everything she’s missing. And he asked me what we can do.
So I asked Debora’s mom for an official quote from the surgeon for how much a cochlear implant would cost, and Gordon asked some financial advisors how to make sure everything’s above-board. This week is the special week we’re taking the plunge. I really hope you’ll help me out. I’m COUNTING on you, my future hero team, to make a difference for this little girl.
You guys always come through, so I’m excited to see you plaster her poster EVERYWHERE! It’s linked in the updates section of that page.
And of course, as always, I have a little freebie for you, too. This one’s a hidden science fiction video I haven’t made public on my channel–this is probably the only time I’ll share it with this list, and after that, it’s probably patreon-only except for the special few who find it through an old email form. It’s a Neodymium-based video where you’re an insomniac on a Frelsi mission to Burbura.
Here’s that.
You’ll also find a new historical fiction video up on that same channel, if you prefer, for your bedtime story tonight.
Sleep tight, okay? And thanks for being a group I can rely on to make change.
-Jen
ORIGINAL CROWDFUNDING CAMPAIGN, DEC 6th 2023:
Debora Martin has never heard her mother’s voice, a bird song, or other children playing.
Because sign language isn’t widely used in her impoverished area, she has no possibility of meaningful communication with the outside world.
She waves people over to play with her–she loves playing “shop-keep”–but other children don’t know what she wants.
She has little to no chance of having her own job or living alone as an adult, and because she has other developmental disabilities and no contact with an extended deaf community, she may never have a family of her own.
But all that can change.
Debora’s physician has recommended a cochlear implant surgery, which is a small device in her brain that would give her the ability to hear. To begin catching up with other kids at school. To learn her mother’s name.
Unfortunately, the surgery would be $31,500, an impossible sum that would take a lifetime for a family like Debora’s to save–not to mention transitional therapy as she learns how to use her newfound hearing, which could cost another several thousand (and that’s without mentioning payment processing fees!).
That’s where we come in.
We’re US people of faith who met Debora and her family through joint ministry work in Paraguay. We’ve known and supported Debora’s extended family for years in wonderful ministries like Barrio Parque church and Project Paraguay, and when we watched Debora struggling, we were heartbroken. We’ve invited other folks on board to guarantee financial accountability, and we’re dedicated to providing you reports and receipts so it’s clear exactly what’s going on at all times. Debora needs our help, and we’re willing to do what it takes to make sure she gets it, securely and honorably.
In Paraguay, the indigenous language has two words for “we,” one “ore,” which means “just us not you”-we, and one “njande,” which means “all of us, you, too”-we.
When we say we, hopefully you’ll allow us to include you, too.
Will you be part of our “njande”?
With hope,
Gordon, Kean, Mike, and Jen – The Debora’s Ears Team,
and
Melissa, Lazaro, and Melanie – Debora’s family
Update 1:
THE COST BREAKDOWN: The official bill that’s keeping Debora from hearing

December 6th, 2023
We are budgeting for the surgery, plus additional transitional therapy to help her adjust to the dramatic change.
POSTER FOR YOU TO PRINT OUT AND SHARE!
December 6th, 2023
Here’s a full link to where you can download all the posters in PDF and PNG to share with people who care: https://icedrive.net/s/RDBf9y4uG2PG6FY3zTzXkvWz6GTQ
UPDATE 2:
Why I want to help Debora
February 13th, 2024
Why would someone from the US want to be part of the life of a little girl in Paraguay?
Watch here.
-Kean
FROM 2023-2025,strangers from all over the world contributed $1395 to Debora’s campaign. Debora’s mother took her to multiple other specialists, and we contacted the Cochlear Institute to try to help us make up the rest of the cost. During this time, additional testing was performed using funds people had sent.
LAST UPDATE:
A change in focus…
August 19th, 2025
Thank you everyone who helped give to Debora’s ears.
The money that you gave was put into in-depth pre-surgical testing for Debora. She was found at this time to not be a good candidate for a cochlear implant due to her autism, and given the advice of the physicians and some new developments in Debora’s personality, her mother would like to wait for two years until Debora has passed puberty before resuming investigation.
So we’re putting a hold on the fundraising. We’ve used most of the funds for pre-surgical testing, and the small amount left over after that will be given to a local organization that’s providing medications for free for the needy in Paraguay via the Project Paraguay medical fund.
Thank you again for helping us further this dream for this mother. This wasn’t the answer we wanted to hear, but for now, it was the right one. We’ll let you know in two years if things change–we’re still committed to supporting Debora.
<3
With love,
Jen
Becoming Hero Charities