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The season is loud, the lists are long, and somehow butter still ends up on the floor. We invited you into our real world—coffee cups, thrift-store treasures, delivery drama—and then opened the door to the moment that changed our year: a hopeful cardiology checkup for our son. After months of charts and worry, his heart is functioning like a typical kid’s, the inflammation is gone, and we were able to drop two medications. The relief rang through our family like a bell. That kind of news reshapes everything, from how we plan the next appointment to how we savor an ordinary Tuesday.

Between the hospital hallways and holiday lights, we’re building our little brand brick by brick. We talk candidly about marathon vendor events, four-hour merch setups, and the tag-team rhythm that keeps us afloat—one of us in the weeds of product pages, the other swimming in labels and boxes. Black Friday stretched us, but meeting people who wear our work filled us back up. Along the way, we laugh about our bowl obsession and the thrift finds that spark joy because tiny delights matter when life feels heavy.

Parenting brought new terrain this year: a ten-year-old’s friend drama, big feelings over tiny texts, and the art of cooling off before we say too much. That’s where faith steadies the ship. Morning prayer, Scripture in a quiet kitchen, and naming seasonal depression out loud helps us trade panic for presence. We talk vitamin D, staying on meds, and resisting isolation, because mental health deserves the same care we give to holiday plans. If you’re juggling deliveries, deadlines, and small hearts under your roof, pull up a chair. We’re choosing peace over perfection, tiny rituals over big promises, and a home that heals the people in it.

If this episode brought you comfort or a smile, tap follow, share it with a friend who needs a lift, and leave a quick review to help more folks find our little corner of hope.

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Sara
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A recycled Christmas joke reel hit 1.9 million views, a tiny gravy ladle became a microphone, and a small-town restaurant watched guests drive in from three states after a single video. That’s the kind of year we just had—unexpected, joy-filled, and fueled by a community that shows up for laughter and for lunch.

We rewind our biggest moments with fresh eyes: the Cajun 911 operator skits that turned everyday mishaps into holiday “emergencies,” the gumbo reels that sparked spicy debates and taught us a thing or two about cleaning cast iron, and the boudin king cake that made us abandon calorie counting for pure happiness. We also share how our feature of Alain Manger in Crowley, Louisiana, translated into real foot traffic and why shining a light on local spots matters. Food, humor, and heart are our north stars, and this year proved that authentic Cajun stories travel far.

Beyond the camera roll, we talk about a women’s coffee in St. Amant that reminded us stories are enough. Moms asked how to juggle work, family, and creative life, and we answered honestly: it’s messy, it’s minute by minute, and that’s okay. We also revisit travel highlights from New York—sun bonnets, comfy shoes, and zero side-eyes—and our stubborn love for a holiday parody called “Home By Yourself” that still deserves its viral moment. Through it all, the podcast remains our porch swing, a place where long-form conversation builds deeper ties than any quick clip can.

Pour a cup and spend time with us as we celebrate the wins, laugh at the flops, and map out what to revive next. If our stories made you smile, share this episode with a friend, subscribe wherever you listen, and leave a review—then tell us your favorite Cajun Mamas moment of the year. Your picks might shape what we bring back next.

https://cajunmamas.com/

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Sara
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Koa
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A routine string of toddler troubles—ear infections, poor sleep, constipation—hid a rare diagnosis that would change everything. When Lydia tested positive for Sanfilippo syndrome (MPS III), her mom, Morgan, refused to accept “go home and love her” as the final word. You’ll hear how a nurse-mom turned her grief into a plan, translating complex genetics into a clear mission: fund access to gene therapy before regression begins around age four, when speech and skills start to fade.

We walk through the essentials in plain language: how missing enzymes let heparan sulfate build up in the brain, why clinical trials fill fast, and what a breakthrough designation really means for speed and access. Then we dig into the real bottleneck—the multi-million-dollar manufacturing cost that stands between children and treatment while the FDA review progresses. Morgan shares how three TikToks with zero followers exploded into millions of views, national coverage, and a focused giving strategy: if the crowd sends $16, a six-million-dollar mountain turns into steps we can all climb.

This is a story about faith, evidence, and community doing what bureaucracy can’t do fast enough. You’ll hear the Godwinks that kept Morgan moving, the Cajun community throwing benefit after benefit, and the coalition of families raising funds for roughly fifteen kids, not just one. The goal is urgent and specific: keep Lydia’s bright three-year-old mind safe long enough to receive a therapy that could change her trajectory. If rare disease, gene therapy, and real-world impact matter to you, this conversation offers a blueprint for action—and a reminder that small gifts can become big medicine.

Help us spread the word, share the $16 idea, and if you’re able, give to Lydia’s fund. Subscribe for more human stories at the edge of science, leave a review to boost the signal, and tell a friend who cares about turning hope into outcomes.

Go Fund Me Link HERE

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YouTube:
https://www.youtube.com/@CajunMamas

Sara
https://www.facebook.com/lllippylady
https://www.instagram.com/lllippylady/#
https://www.tiktok.com/@lllippylady

Koa
https://www.facebook.com/kgmelancon
https://www.tiktok.com/@koa.melancon
https://www.instagram.com/k_melancon/