Jude&Jojos

08/21/2026

Please share JJP. 🤍 Share us to your stories, your feed, your Facebook groups, TikTok... anywhere our next family might be waiting to find us.

This is how so many of these faces found their way here. One share. One tag. One person who thought, “I know a family who needs to see this.”

And somehow, little by little, they all became our Crew.

When the world gets too dim to remember how much good is still here, we look at them. And there it is... a reminder that there is still so much worth looking after.

Help us find the next one.

Hit repost, share, join our mission ⟳
Molly Clotfelter Katie Startt Kenzi Taylor Teya Joi April Harris Joshua L Maylee Hope Caronia Savannah Prosser ♡ (Lawson) Isela Ponce carrahartley Destiney Haynes Caley Lawrence Carly Durham Brittany Werner Mariela Estrada mrsstephanyramos Dart E Ramos Dani Higley Jordan Steele SLOAN.CISNEROS Christian Cisneros Kassidy Locke Ledford Dahlia Swanson Justine Fitzgerald Shawn Fitzgerald Kayla Wilson Martha Hoot and a Half Savannah Prosser ♡ (Lawson) Kimberly Scott Lacie Bowlware Tiffany Marie Galan Rivera Maggie Taylor Sunshine On A Ranney Day | Charity Ms. Wheelchair America Down Syndrome Assn. of Atlanta

08/20/2026

“The world has labeled Carter as having ‘special needs.’ But, looking at the world today, I wonder if we all might not be better off recognizing and emulating all he—and others like him—have to give—not just what they need.”

Those words belong to Carter’s mom. In fact, every word of his story does.

She wrote this feature herself, with a transparency about motherhood, disability, comparison, advocacy, joy, and the everyday in-between that caught me off guard.

Carter and his mom traveled all the way from Virginia to ATL just to stand in front of our lens and I don’t think either of us could have known just how much they would stay with me.

Because before I am the person behind JJP, I am a mom raising a child with disabilities too. And somewhere in her words… between the appointments, the milestones that take a little longer, cheering a little louder, the laundry that never makes it out of the dryer, and wondering if we’re getting any of this right… I felt deeply understood.

I expected to read Carter’s story.

I didn’t expect to see pieces of my own motherhood reflected back at me.

That is the gift of a mother telling her own story without polishing away the parts that make it real. And it’s why I’m so grateful she trusted us with hers.

Her words. His story. And our absolute honor to put a face to both.

His Name Is Carter.

Meet him in our bio.

www.judejojosphotography.com/jjpcrew/carter

08/16/2026

We want you to look at his back. This scar has been with Elliott since he was just seven hours old. Seven whole hours after entering the world, he was already undergoing major spinal surgery. By 18 months old, he had been through seven surgeries.

When we photographed Elliott many moons ago, we knew we wanted this portrait. Not because his scar defines him, but because it’s part of him, his mom, his family... and we believe this part deserves to be photographed, too.

We share a lot of smiles around here... a lot of milestones, personalities and really amazing moments. But sometimes what our Crew has been through isn’t something you can see when you first look at them.

Elliott was born with Spina Bifida, bilateral clubfoot and hydrocephalus. He has a VP shunt and uses the cutest wheelchair. And underneath his shirt is a reminder of just how early his story began. So tonight, we’re sharing this view.

Scars like Elliott’s belong in portraits, too. Bodies like Elliott’s deserve to be seen growing up, hanging on walls and taking up space in the world exactly as they are. We’re really proud to have Elliott in our portfolio.

Ready to join the Crew?

Whether you want to share your story with the world or want beautiful portraits that feel like home, there is a place for you here.

Book through the link in our bio or email [email protected]. We’d love to have you

08/14/2026

Sometimes we sit and think on how life can feel pretty dark. Even when we know there are so many people walking similar paths, it can still feel like our own light has been blown out and we have nothing left to give.

And then you meet someone like Peter.

When Peter and his family walked into our studio, the entire room instantly felt lighter. His gumption for life is undeniable, and his ability to find joy, connection, and humor left me feeling ready to take on the days ahead.

Peter was adopted from Russia as a toddler. At just two years old, he suffered a stroke and was later diagnosed with Leigh’s disease, a rare neurological disorder that has progressively impacted his strength, mobility, and independence. After additional strokes, Peter now uses a wheelchair.

But he is SO much more than his disabilities.

He dreams of becoming a police officer, is 100% a mama’s boy, has the funniest relationship with his dad, and shares that wonderfully real... and sometimes fiesty, sibling bond with his sister. He communicates in every way he can, stands and sits with assistance, laughs, jokes, and has absolutely no fear of being himself.

Peter alone made this photoshoot feel like we were shooting a commercial. His personality filled the room, and he reminded us that disability may shape someone’s life, but it does not define who they are. Now, as Peter approaches his teenage years, his family is working to give him something every teenager deserves: independence.

Together with Sunshine On A Ranney Day | Charity , his family is building a wheelchair-accessible bathroom and a dream bedroom designed specifically for him, complete with the things he loves, including Star Wars and the dark side (my personal fav, as well).

This isn’t just about building a bathroom or remodeling a bedroom. It’s about giving Peter privacy. Giving him choices. Giving him the ability to do more of his everyday life on his own. Giving a young man a space where he can grow, have friends over, and simply be Peter.

Help us keep his light burning. Learn more about Peter’s project and how you can help through the link in our bio.

https://www.judejojosphotography.com/partners/sunshine-on-a-ranney-day

08/07/2026

When you get the chance to update headshots, and you just CANNOT wait to share them... Anyone remember Emelia??? The tiny baby with the biggest, most beautiful eyes who completely stole our hearts?

Well... that baby is a toddler now, and she’s still making waves with those same unforgettable eyes. Emelia’s JJP story actually happened when her mom was searching for someone to capture her very first headshots as she stepped into the talent world. Along the way, she happened upon us and TBH we fell head over heels.

Born with Down syndrome and an AV canal heart defect, Emelia has been showing the world from day one that a diagnosis is only one part of her story. And now look at her! Not only is she growing into the most confident little girl with the cutest dance moves, but she’s also making her mark in the modeling world. Emelia is signed with ZBD TALENT and recently made her debut as an OshKosh B'gosh kid!

From our JJP Crew baby to a little girl with a growing list of accomplishments, we couldn’t be more excited to watch where this journey takes her.

08/05/2026

This week is another hurdle, another procedure, and another reason we call him a Heart Warrior. **Before you read Dylan’s JJP Crew feature, would you take a moment to leave his family words of encouragement before Thursday’s procedure? ** We know our community, prayers, and strength will mean the world to his family.

Meet our little dude, Dylan.

This Thursday, Dylan will undergo another cardiac catheterization procedure as part of his ongoing journey with congenital heart disease. While this won’t be his first time facing the unknown, that doesn’t make it any easier for his little body or his sweet family who loves him so fiercely.

Three years ago, his parents were told he likely wouldn’t survive. They refused to let one opinion define his future and fought for another chance. Today, that same little boy is walking, talking, laughing, and bringing joy everywhere he goes (especially in our studio).

His story is one of faith, resilience, unwavering advocacy, and hope. It’s also a reminder that a diagnosis is never the end of a child’s story.

Welcome to the Crew, Dylan. We’re so honored to share your story.

🔗 Read his full story through the link in our bio.

https://www.judejojosphotography.com/jjpcrew/dylan

07/30/2026

WE NEED YOUR HELP 💙 Every week, we hear from families hoping to become part of Disability Photography & Advocacy | JJP™ . Parents searching for a place where their child will be loved instead of rushed. Adults who have never had professional portraits that truly reflect who they are. Families just wanting to feel seen.

At the same time, local organizations continue reaching out, asking us to partner alongside them in serving the individuals and families they care for. Together, we’re creating more than portraits; we’re creating connection, building community, and reminding people they are important.

The need is growing, and our hearts are willing. But we can’t do it alone.

We’re looking for local businesses and community leaders who believe that success isn’t measured only by what we build, but by the lives we help impact along the way.

When you become a Jude&Jojos Photography Community Sponsor, you’re helping us serve more families, strengthen local partnerships, connect people with trusted resources, and ensure more individuals with disabilities and complex medical needs have the opportunity to feel seen, celebrated, and supported... because the reality is that for some of the individuals we photograph, these portraits become part of the legacy they leave behind.

If your business has a heart for serving our community, we’d love to invite you into this mission or advocate on our behalf!

Together, we can reach more families, support more organizations, and create a lasting impact that extends far beyond a photograph.

Learn more through the link in our bio:
https://www.judejojosphotography.com/sponsor

Or reach out to us directly at [email protected]. We’d love to start a conversation about how we can make an impact together.

07/21/2026

It’s funny... a few weeks ago, a trending YouTuber was spreading the idealism that a Down syndrome diagnosis would somehow diminish a family’s life, future, or overall measured happiness. Meanwhile, over here at JJP, our DM has been filling up with families from the Down syndrome community.

And TBH, I think we’d rather hear from them. We would MUCH rather hear from the parents raising these incredible kids, the siblings who grow up alongside them, the families who have been forever changed because of them.

Families like Kinlin’s.

As I read through his mom JJP questionnaire, I found a quote that I loved:

“We truly hit the jackpot.”

Before Kinlin was born, Dani lost her dad, and at the same time, her mom was battling stage IV ovarian cancer. Dani and her husband, , were raising twins, navigating unimaginable grief, and getting ready to welcome a new baby into the world when an unexpected Down syndrome diagnosis entered their story.

And yet, when Dani and her husband talk about Kinlin, they don’t focus on what was lost; they talk about what their family gained. A son who made his siblings kinder, who taught his family to slow down, and helped them find light in places they may have otherwise missed.

One of my top things Dani shared was this:

“People often see the diagnosis before they see the gift. We get the privilege of seeing the gift first.”

People can debate diagnoses all day long, but we’d rather introduce you to the people living them. Today, meet Kinlin. 🤍

His full Crew story is now live through the link in bio.
http://www.judejojosphotography.com/jjpcrew/kinlin

07/17/2026

Two (I thought It was three until I fact checked and realized how young he really was 😭) years old. Sometimes vulnerability when building something important with the people who are ready to do It with you, is incredibly important. This photo showed up in my memories this week, and whew... At the time, Jude was recovering from surgery to remove his tonsils and adenoids (after we were told this would “fix” It all). We didn’t know about the neurological birth defect, the autism, the epilepsy, the vision challenges, or all the pieces that would eventually help us understand who he is.

What we did know was that he was our Jude, who quite literally resembled George from Stuart Little. Looking back now, I wish I could go back and tell that version of us something important:

You’re doing the right thing, and one day you’ll live a much humbler life that you didn’t even know was there.

As JJP continues to grow, I’ve found myself reflecting a lot on where it all began. Every time a memory like this appears, it feels like a reminder of the gift we were given to serve through Jude’s journey. What once felt like uncertainty became passion and purpose, and what once felt like surviving each day became a foundation for growth.

This year feels like a season of planting seeds, and so many have already begun to grow. Each family we meet, story we tell, and portrait we create reminds us why we started in the first place.

It is the belief here that every person deserves to be seen. Every story you all share with us deserves to be told in the midst of all the celebrations or the battlefields. And every family deserves photographs that reflect the beauty, dignity, and value that have been there all along.

We are grateful for the foundation that brought us here, and we’re committed to continuing to nurture it as it grows into something even bigger than we imagined.

This is our why.

And we can’t wait for you to meet our next Crew member, coming soon. 🤍

xoxo,

Jude’s mom

07/16/2026