Becks Helping Hands

Becks Helping Hands Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from Becks Helping Hands, Atlanta, GA.

World Duchenne Awareness DayFor my son, Beck, who keeps fighting with so much strength and love. And for AJ, his best fr...
09/07/2025

World Duchenne Awareness Day

For my son, Beck, who keeps fighting with so much strength and love. And for AJ, his best friend—the one who made him laugh the most, his partner in mischief, and his brother in every way that mattered. 💔

Duchenne is cruel, but their bond was something beautiful that this disease could never take away.

For Beck, for AJ, and for every individual affected by Duchenne—those here and those we now carry in memory—you are loved, you are remembered, and you will ALWAYS matter ❤️💔🖤

This doesn’t need a caption or explanation.
09/03/2025

This doesn’t need a caption or explanation.

Education is key ⬇️
09/02/2025

Education is key ⬇️

HAD to share this one!
08/20/2025

HAD to share this one!

Parenting a Child with Special Needs Is Nothing Like Welcome to Holland

If you’re a parent of a child with disabilities, chances are someone has handed you Emily Kingsley’s poem Welcome to Holland. It gets passed around like some universal balm, as if those words can soften the blow of a diagnosis or wrap up our entire reality in a metaphor about tulips and windmills.

But let me be clear: parenting a child with special needs is nothing like Holland.

It’s not a vacation. It’s not a scenic detour. It’s not “different, but still beautiful.” That poem is a fairytale that might make outsiders feel better about our reality—but for those of us living this life every single day, it falls painfully short.

It’s Not a Missed Flight—It’s a Free Fall

Welcome to Holland wants you to believe this journey is like expecting Italy and winding up in Holland instead. But when I got my child’s diagnosis, it didn’t feel like a detour to a neighboring country.

It felt like being shoved out of an airplane without a parachute. You hit the ground hard. The impact knocks the air out of you. You’re shattered, bleeding in ways no one else can see. But you don’t die—you get back up, because your child needs you to.
This isn’t a “change of plans.” This is survival.

It’s Not a Sightseeing Tour—It’s a Battlefield

The poem paints this picture of simply adjusting expectations and learning to enjoy new scenery. But this life is not strolling through museums—it’s combat.

Every day is a fight:
Fighting for insurance approvals.
Fighting for services that are constantly cut.
Fighting school systems that see your child as a budget line, not a human being.
Fighting exhaustion while never having the option to tap out.
You don’t return from battle with souvenirs. You come back with scars.

The Loneliness Is Real

Kingsley suggests that if you just open your eyes, you’ll find Holland has its own community of travelers. The reality? Most of us are walking this road alone.

Friends fade. Invitations stop. Family doesn’t always get it. Society moves forward, and you’re left behind—living a life most can’t fathom. Yes, there are others in the trenches too, but the day-to-day weight of this journey is often isolating beyond words.

There are no tulips here. There’s silence, there’s distance, and there’s the ache of watching life move on without you.

The Poem Minimizes the Grief

What I resent most about Welcome to Holland is how it diminishes the grief to something as simple as missing out on Italy.

This isn’t about canceled gondola rides. It’s about mourning the life I thought my child would have. It’s about the milestones that may never come, the uncertainty of the future, and the brutal truth that love doesn’t erase suffering.

The grief doesn’t vanish—it evolves. It comes in waves, weaving itself into joy, pride, resilience, and heartbreak so tightly they’re inseparable.
But don’t tell me this is a “different kind of beautiful.” That minimizes the cost of what we carry.

Why Welcome to Holland Is Dangerous
The reason so many professionals love handing this poem out is because it comforts them. It gives them a tidy way to explain away our grief and reality without having to sit in the discomfort of it.

It suggests we’re all on some kind of accidental holiday—just not the one we signed up for. But we’re not tourists. We’re warriors. Survivors. Parents who have been drafted into a life we never chose, with no exit strategy.

Welcome to Holland doesn’t honor that reality. It sugarcoats it.

The Real Story
Parenting a child with special needs is relentless. It’s terrifying. It’s exhausting. It’s isolating. It’s also filled with a love so deep and consuming it often feels impossible to put into words.

But it is not Holland.
It’s waking up in a land with no map, no compass, no guidebook—where you build the roads yourself, where storms come without warning, and where every small victory feels monumental because of what it took to get there.
It’s not tulips and windmills. It’s scars, grit, grief, and resilience. It’s the kind of strength you don’t know you have until it’s the only option left.

So don’t hand us pretty metaphors. Don’t reduce this life to a postcard. Don’t try to sell us on Holland.
Give us resources. Give us understanding. Give us people who are brave enough to walk beside us in the trenches.

Because this isn’t Holland. It’s something much harder, much deeper, and much more real. And the truth is—we deserve for it to be seen that way.

“We’re not tourists here—we’re warriors.” Stacy Warden — Noah’s Miracle

Available on Amazon: https://www.amazon.com/dp/B0FP9YB4V2?ref_=pe_93986420_774957520

Copyright & Creative Commons Notice
This essay is © [Stacy Warden], [2005]. All rights reserved. It is licensed under a [Creative Commons License, e.g., CC BY-NC-ND 4.0]. You are welcome to read, share, and distribute this work non-commercially, provided you give appropriate credit, do not alter the content, and do not use it for commercial purposes. Any other use, reproduction, or distribution requires prior written permission from the author.

Happy Friday 🙌🏼 It’s so hard to believe Beck is now a high schooler 🥹 FLORIDA families 🚨 This would obviously be for any...
08/08/2025

Happy Friday 🙌🏼 It’s so hard to believe Beck is now a high schooler 🥹

FLORIDA families 🚨 This would obviously be for any special need family who is in need. We can put you in touch with the family if you are in need of a stander. Family is located near Daytona Beach 😊 We hope to find someone who can use this!

Hi everyone! We hope your weekend is off to a great start!Beck is competing for Youth Athlete of the Year! It would mean...
08/02/2025

Hi everyone! We hope your weekend is off to a great start!

Beck is competing for Youth Athlete of the Year! It would mean so much to us if you would simply click the link below and vote for him! He’s in second place as of right now, we’d love to see him in first! You get one free vote a day so make sure to get on there and vote EVERY DAY!

You can scroll down and read about Beck and his “why.” Winning this would not only be huge for Beck, but it will also bring so much awareness not only towards Duchenne, but all disabilities as well as power soccer!

PLEASE VOTE. 💚💪🏼

Love you all and so thankful for each and every one of you!

Beck Is Defining The Odds Of Duchenne Muscular Dystrophy. He Currently Plays Wheelchair Power Soccer And Has Goals To Join The USA Team.

07/28/2025

July 21, 2025 Dear Duchenne Community,This evening, Sarepta has made the difficult decision to voluntarily and temporarily pause all U.S. shipments of ELEVIDYS effective at the end of the day tomorrow, including for ambulatory patients. This step will provide Sarepta with time to fully respond to an...

⭐️⭐️East Coast families! Please see the photo below and if you have any interest please let us know and we will get you ...
07/28/2025

⭐️⭐️East Coast families! Please see the photo below and if you have any interest please let us know and we will get you in touch with the owner!

THIS! ALL of this but we continue to fight each and every day 🖤💚
07/06/2025

THIS! ALL of this but we continue to fight each and every day 🖤💚

What Our Duchenne Sons Don’t Know…

They don’t know the calendar in our heads —
Booked months in advance with hospital appointments, equipment and educational reviews, and therapy sessions.

They don’t know the quiet hours we spend researching late into the night —
Reading clinical trials, new treatments, Facebook group threads, and medical papers — searching for hope.

They don’t see the coordination behind every outing —
The ramps, the accessibility checks, the backup plans — just so they can feel included, free, normal.

They don’t notice the way we stockpile medications, chase down prescriptions, call, email, chase again —
Because we never want them to go a single day without what they need.

They don’t realise the quiet grief we carry —
For the milestones that won’t look the same, the questions we can’t answer, the future we try not to fear.

They don’t know how we advocate in every space —
Fighting battles with quiet strength so they don’t have to —
With schools, doctors, systems, even family.

They don’t know the weight of our silence when they ask, “Will I be able to…?”
And we say “Of course, you can do anything your way” —
Because love can’t always be honest, but it can always be strong.

They don’t know the strength it takes to be soft,
The courage it takes to keep going,
And the love that fuels it all.

But one day, maybe they will.
And until then, we keep going —
Because we’re their mums.
And we would do it all again a thousand times over. 💙

We have no doubt that this chair will go on MANY amazing adventures with its new owner 🦼♿️We are SO grateful we were abl...
06/08/2025

We have no doubt that this chair will go on MANY amazing adventures with its new owner 🦼♿️

We are SO grateful we were able to gift this chair to a VERY special and deserving person in our community!

Of course we HAVE to share this handsome picture of José! We know his smile will definitely put a huge one on your face ...
06/04/2025

Of course we HAVE to share this handsome picture of José! We know his smile will definitely put a huge one on your face today too 😊

José is 11 years old and also lives with Duchenne Muscular Dystrophy. He finally received his cough assist 🎉👏🏼! His mother, María is such an amazing advocate for Duchenne. She is so patient and kind all while making sure José receives so much love and care for her son.

We are so thankful he finally has a cough assist which is crucial for those with Duchenne. We are so grateful we had a part in making this happen for his family. The more equipment we can donate, the more time you can spend with your loved ones. With a diagnosis like Duchenne, you have to stay prepared.

Keep smiling José! Continue to be brave, strong and fearless 💪🏼 YOU are an inspiration!

(Check out the special words from his mom below and what this means to his family 🫶🏼)

Meet Henry! Henry is 10 years old and lives with Duchenne Muscular Dystrophy. His super witty personality, love for anim...
05/30/2025

Meet Henry! Henry is 10 years old and lives with Duchenne Muscular Dystrophy. His super witty personality, love for animals and contagious smile are what stand out the most 😊

His parents are strong advocates in the Duchenne community and Henry lives his best life through many activities. His parents understand the importance to conserve energy when needed. We are so grateful that we were able to provide Henry with a pediatric manual chair so he could enjoy a trip to Texas with his family 🫶🏼💚

Check out this handsome young man below 😍

The first picture was taken at Morgan’s Wonderland in Texas!

We are so happy we were able to help this wonderful family along their journey.

Keep changing the world Henry 🫶🏼

Address

Atlanta, GA

Alerts

Be the first to know and let us send you an email when Becks Helping Hands posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to Becks Helping Hands:

Share

Share on Facebook Share on Twitter Share on LinkedIn
Share on Pinterest Share on Reddit Share via Email
Share on WhatsApp Share on Instagram Share on Telegram