Dream Machine Foundation

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Dream Machine Foundation Non-profit using social media for social impact! Follow us to see our videos ❤️

🎉 HAPPY BIRTHDAY MATTHEWWWW!!! 🎉Today we’re celebrating someone who has never been afraid to dream big and keep pushing ...
10/12/2026

🎉 HAPPY BIRTHDAY MATTHEWWWW!!! 🎉

Today we’re celebrating someone who has never been afraid to dream big and keep pushing forward.

Matthew has faced more challenges than most people ever will, including cerebral palsy and 16+ surgeries, but he continues to show up, train, chase his goals, and REFUSES to let limitations decide what his future looks like. From working toward his dream of walking independently to building his own clothing brand, he’s constantly proving that NOTHING can stop him!!! 🥹💪

Matthew, we hope 28 brings you even more reasons to celebrate and plenty of moments that remind you just how far you’ve already come.

Help us wish Matthew a very happy birthday!!! 🥳 Matthew Caleb Fernandez

Happy 14th Birthday, Xavier!!!! 🥳From the little boy who dreamed of becoming a boxer to the fighter you’re becoming toda...
10/06/2026

Happy 14th Birthday, Xavier!!!! 🥳

From the little boy who dreamed of becoming a boxer to the fighter you’re becoming today, we’ve loved watching your story unfold. 🥊

We are so grateful we could help your dream of meeting Jake Paul come true when you were younger, and we hope you know just how many people are cheering you on and believing in you every step of the way!!!

Xavier, keep chasing those dreams and never forget how special you are. We can’t wait to see where 14 takes you!!! 🧡

Help us wish this incredible young man a very HAPPY 14TH BIRTHDAY!!! 🎂🥳 Xavier 🥊 10

Meet Kooper 🏈Kooper was born with a congenital heart defect, but that hasn’t stopped him from being part of the team. 🥺 ...
09/29/2026

Meet Kooper 🏈
Kooper was born with a congenital heart defect, but that hasn’t stopped him from being part of the team. 🥺 You can find him serving as the water boy and cheering on his brother and teammates from the sidelines. 🥹💛

When we met Kooper, we learned that one of his biggest dreams was to attend an Alabama football game. So for his birthday, we decided to make that dream come true! 🏈

We surprised Kooper and his family with a game of hangman, slowly revealing exactly what his birthday surprise was. His teammates were watching the entire time, getting SO excited as Kooper started to realize what was happening 🥹

Seeing the smile on Kooper’s face and watching his teammates rally alongside him melted our hearts, and we’re so grateful we could help make his dream come true!!! ✨

09/25/2026

Two years ago, Kara was dancing through a chapter she never asked for. ❤️‍🩹

And now, two years later… she’s still dancing. But this time, she’s happy, healthy, and cancer-FREE!!!! 🥹 We are SO proud of you, Kara, and how you continue to choose joy throughout any circumstance! We could all take some notes from you. 🫶✨ Kara

“I could spend September telling you how brave these children are.I could show you bald heads and hospital rooms. I coul...
09/22/2026

“I could spend September telling you how brave these children are.

I could show you bald heads and hospital rooms. I could tell you about chemotherapy, radiation, surgeries, transfusions and nights spent watching monitors beside a hospital bed.

But there’s another part of childhood cancer that doesn’t fit neatly into an awareness post.

Survival can come with a price.

When Jake finished treatment for Ewing sarcoma, I thought we had made it to the other side. We celebrated every clear scan. Every year farther away from cancer felt like another layer of fear being lifted.

And then, almost five years later, cancer came back into our lives in an entirely different form.
Therapy-related leukemia.

There are words a mother should never have to learn once, much less twice.

So when I advocate for childhood cancer research, I’m not only asking researchers to save our children.

I’m asking them to find ways to save them without sacrificing their futures.

I want children to survive cancer and grow into adults who are healthy enough to live the lives we fought so desperately to give them.

That is what more than survival means to me.

And that is why I will keep talking about childhood cancer long after September ends.

🎗️ Our children deserve cures that don’t create another battle.”
- Jake K

It’s time for a dreamer update, highlighting AJ!!! 🧡“Hi Niamh!! Hope you’re doing amazing! AJ is doing really well! He’s...
09/18/2026

It’s time for a dreamer update, highlighting AJ!!! 🧡

“Hi Niamh!! Hope you’re doing amazing! AJ is doing really well! He’s growing like crazy! This past weekend, his travel basketball team won their end of season tournament in Pismo, and he made the allstar baseball team. He finished 3rd grade with high honors and is so happy to be on summer break! He works so hard at everything he does! Super proud of him. He continues to advocate for pediatric cancer and share his story to help others. He is working with our local children’s miracle network to bring awareness and raise funds for our hospital where he was treated. He tells his story and is such an amazing advocate for being only 9 years old.
He had his scans about 2 weeks ago. His abdominal ultrasound came back amazing! And his chest xray came back with some shadowing, so we have to have that done again at the end of next week. I’ll keep you updated on that 💛
Thanks so much for checking in on him! That means the world to us!“
- AJ’s mom

AJ is kicking cancers butt and we are so excited to hear not only about how he’s excelling in sports and school, but how he’s continuing to advocate for the kiddos who are fighting through the same thing that he fought through. We are beyond proud of you AJ!! 🥹✨

Do you guys remember Miss Dia??? 🥹💛We met Miss Dia in 2023, when we found out she was facing living in a homeless shelte...
09/16/2026

Do you guys remember Miss Dia??? 🥹💛

We met Miss Dia in 2023, when we found out she was facing living in a homeless shelter after the fire in Calabassas, losing her mom 6 months later, and her son being diagnosed with autism. She was strong willed through the hardest battles and knew she wanted to get into UCLA and graduate for her son!!! We worked with Kidoodletv to send her $10,000 and help her through her tough chapter she was in. ❤️‍🩹

Now, in 2026, Miss Dia has GRADUATED from UCLA!!!! She has worked SO hard, her hard work has paid off, and we are beyond proud of her!!!!! We know she is going to excel in this next chapter of life, and we know her son is so proud of her. 🥹🥳

Everyone congratulate Miss Dia below!! 💛 Dia James

September: We Go GOLD ✨🎗️💛September is Childhood Cancer Awareness Month, a time to honor every child who has faced cance...
09/10/2026

September: We Go GOLD ✨🎗️💛

September is Childhood Cancer Awareness Month, a time to honor every child who has faced cancer, every family whose world changed overnight, every child we have lost, and every survivor who continues to carry the impact of cancer long after treatment ends.

Approximately 1 in 264 children in the U.S. will be diagnosed with cancer before age 20. While survival rates have improved tremendously, surviving cancer doesn’t always mean the journey is over. Many survivors face lifelong follow-up care, late effects, health complications, and uncertainties caused by both their disease and treatment.

But survivorship doesn’t mean forgetting.

It doesn’t mean cancer didn’t happen.

And it doesn’t mean there are no more appointments, scans, labs, questions, or worries.

So this September, we go GOLD for the children still fighting, the children we have lost, and the survivors who continue living with the impact of cancer long after treatment ends.

💛 For more research.

💛 For better treatments.

💛 For fewer lifelong side effects.

💛 For answers to rare diseases.

💛 For every child fighting.
💛

We go GOLD. For every child. Always. 💛🎗️
Caption: Cheyenne Martinez

Sweet Raylee is asking for our help & support as she walks the Santa Monica “Walk for Your Liver” this Saturday!!!!! 💚Ra...
09/08/2026

Sweet Raylee is asking for our help & support as she walks the Santa Monica “Walk for Your Liver” this Saturday!!!!! 💚

Raylee was only 4 years old when she battled liver failure and received a life saving transplant 🥹🙏🏼 Raylee is a warrior and a miracle and she is proud to support the Liver health Foundation in raising awareness on liver transplantation 🙌🏼💚 The Liver Health Foundation (LHF) is a California-based nonprofit organization dedicated to supporting the local liver community.

If you’re in LA and free on Saturday, miss Raylee would love for you to join her on the walk! If you’re out of state, it would mean the world if you could help spread the word or donate if you’re able. Anything truly makes a difference 💚 The link is in our bio! Raylee Jo

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5856 Adams Boulevard
Culver City, CA
90232

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