upworthy

Community

Community

Tim Tebow's Night to Shine event celebrated over 100,000 people with special needs

"Lord willing, we won’t stop until every person with special needs knows their worth," Tebow tells Upworthy.

The Tebow Group

Tim Tebow poses with Night to Shine attendee in Thailand.

The red carpets were rolled out around the world last Friday, February 7th, for a very special celebration of over 100,000 people with special needs at the Tim Tebow Foundation's 11th Annual Night to Shine event. Former NFL quarterback Tim Tebow founded Night to Shine in 2015 to center on celebrating, honoring and valuing people with special needs.

Held on one night, always the Friday before Valentine's Day, his Tim Tebow Foundation partners with local churches, providing support and resources to host a cost-free prom honoring individuals living with disability in their local communities. Anyone ages 14 and older is welcome to attend, where attendees enjoy a fun-packed evening that includes: a red carpet with paparazzi, hair and makeup stations, shoeshines, limousine rides, karaoke, gifts, a catered dinner, a Sensory Room, a Respite Room for parents and caregivers, and loads of dancing.

At its founding, Night to Shine was held solely in the United States at 44 different locations. Now in its eleventh year, Night to Shine has grown to 821 host churches in all 50 states—and has continued to expand internationally. This year, 62 countries worldwide hosted Night to Shine celebrations. Tebow celebrated this year's Night to Shine in Thailand and Vietnam, while his wife Together with his wife, Demi-Leigh Tebow, celebrated in her home country of South Africa.

“It was so awesome seeing Night to Shine in new countries this year—and to have the honor of celebrating in Vietnam for the first time!" Tebow tells Upworthy.

red carpet, tim tebow, night to shineRed carpet at Tim Tebow Foundation's Night to Shine.Jensen Sutta

Night to Shine's international presence expanded to several new countries for the 2025 celebration, including:

"What an unforgettable night at Night to Shine in Cape Town!" Demi-Leigh Tebow tells Upworthy. "This event means so much to me for so many reasons. Some of you may know that my little sister, Franje, was born with special needs, and learning about Night to Shine back in 2018 was actually how I met Tim!"

Currently expecting the couple's first child, Demi-Leigh Tebow will be a mom at next year's celebration—something she's eagerly awaiting.

"Since then, I’ve been incredibly blessed to meet countless Kings and Queens from all over the world—each one so valuable and deeply loved by God. But getting to celebrate this night in my home country was incredibly special. My heart is so full and I’m already looking forward to doing it all again next year!” she says.

demi leigh tebow, tim tebow, night to shineDemi -Leigh Tebow at Night to Shine 2024 in South Africa.The Tebow Group

After a night full of partying, Night to Shine concludes with a 'crowning' of the Kings and Queens with crowns and tiaras to signify a declaration of worth and love. "We crown every Night to Shine honored guest the King or Queen because that's how God sees them," Tebow wrote in an Instagram video montage of this year's crowning's.

In another post, he added, "For many, it's the first they've ever felt truly celebrated, especially by someone outside their family. But that's exactly why Night to Shine exists--to remind them that they are God's beloved royalty, seen and cherished by Him every single day."

Tebow's goal is to have Night to Shine in every country. Next year, Night to Shine will be held on Feb. 13, 2026. If you are interest in hosting a Night to Shine event in 2026, you can find more information here.

"Lord willing, we won’t stop until every person with special needs knows their worth—until the abandoned are embraced, the forgotten are celebrated, the overlooked are seen, and all people experience the radical love of Jesus," Tebow tells Upworthy.

Joy

They thought their son lived an isolated life. But when he died, friends showed up in droves.

Mats Steen's parents were shocked to learn their severely disabled son had lived a rich, independent life they knew nothing about.

Mats Steen lived a secret life that his family only discovered after he died.

Mats Steen was only 25 years old when he passed away, his body succumbing to the genetic disease that had slowly taken his mobility since childhood. He'd lived in a wheelchair since his early teens, and by his 20s, his physical abilities had deteriorated to the point of only being able to move his fingers. He could push buttons and use a mouse, and he spent nearly all of his waking hours playing video games in his parents' basement.

His family loved him and cared for him through it all, giving him as much of a normal life as they could. But they also lamented everything they knew he'd missed out on. "Our deepest sorrow lay in the fact that he would never experience friendships, love, or to make a difference in people's lives," Mats' father shares.

Mats left behind the password to a blog he kept. Not knowing if anyone would actually read it, his parents published the news of Mats' passing in a blog post, adding their email address in case anyone wanted to reach out.

Much to their surprise, messages began pouring in from around the world—not just with condolences, but with heartfelt stories from people who called Mats their friend.

The Steens soon discovered that their son had lived a much fuller life than they'd ever imagined—one that included all the things they always wished for him.

As his online life was revealed, the family learned that Mats began his days with a routine 30-minute sprint through the forest. He frequented cafes and pubs, chatting with strangers and flirting with women. He sat by campfires having heart-to-heart conversations. He made friends and enemies. He fought heroic battles. He supported people in times of need. He gave advice that people took. He experienced his first kiss.

And he did it all as "Ibelin," his handsome, muscular avatar in the online game World of Warcraft.

- YouTubewww.youtube.com

Mats' life is showcased in the documentary, "The Remarkable Life of Ibelin," in which his parents share the story of how they discovered their son's group of friends they didn't know he had.

People who've never played an open world roleplay game like World of Warcraft may wonder how real community can be built through it, but Mats' story proves it's possible. The friends he made through the game have shared the real influence he'd had on their real lives, from helping them with problems they were facing to empowering them to make positive changes in their relationships.

Though he never met them face-to-face, Mats' online friends say he made a significant impact on them.

A young woman Ibelin had connected with as a teenager—the one with whom he'd shared that first virtual kiss—shared that her parents had taken away her computer when they feared gaming was interfering with her studies. When she logged on at a local library, Mats gave her a letter he had written to give to her parents, encouraging them to talk with her about her gaming hobby and to work out a solution together that didn't require her to give it up completely. She printed it and gave it to them. Miraculously, it worked.

Another woman had been having a hard time connecting with her autistic son as a young adult. When she talked with Ibelin about her struggles, he suggested that she and her son start gaming together and connect in that way first. Eventually, that connection via the virtual world led to warmer in-person interactions between them—and a life-changing shift in their relationship.

"I don't think he was aware of the impact that he had done to a lot of people," the mother shared.

Mats interacted with the same online friends as Ibelin for years, going through the kinds of ups and downs all real friendships experience. He kept his physical condition a secret until close to the end of his life, when he finally opened up to another player who convinced him to share his reality with the others. Some traveled from other countries to attend his funeral, with one of them speaking on the group's behalf and a few of them serving as pallbearers. Those who knew Ibelin also held a memorial in-game at his virtual gravesite—a tradition that has spread beyond just his own guild.

Typically, we think of someone escaping the real world and spending hours a day playing video games as unhealthy, but for Mats, it was a lifeline. As Ibelin, Mats was able to have a level of independence and a rich social life that simply wasn't possible for him in the offline world—an uniquely modern phenomenon that technology and human creativity have made possible.

Mats' impact on his online community was real, and 10 years after his passing his impact is spreading even further.

Duchenne muscular dystrophy, the genetic disease that Mats lived with and ultimately died from, affects 300,000 boys worldwide. It only affects males and it has no cure. But CureDuchenne, a global nonprofit dedicated to funding and finding a cure, has partnered with Blizzard and World of Warcraft in Mats' honor. From now until January 7, 2025, World of Warcraft players can purchase a limited-edition pet fox named Reven ("fox" in Norwegian). The Reven Pack, which includes a transmog backpack and Reven’s Comfy Carrier, costs $20, with 100% of the purchase price being donated to CureDuchenne.

The Reven Pack on World of Warcraft—100% of purchase cost goes to the CureDuchenne foundation.World of Warcraft/CureDuchenne

“Mats Steen lived a life in World of Warcraft that he couldn’t in the real world as he fought Duchenne muscular dystrophy alongside his incredible family, who I’m proud to have met and fallen in love with,”said Holly Longdale, executive producer of World of Warcraft. “Working with CureDuchenne for our Charity Pet Program, in honor of Mats’ memory, allows us to harness the power of our phenomenal global community to bring meaningful impact to so many lives.”

You can learn more about Mats' story in the award-winning documentary, "The Remarkable Life of Ibelin," on Netflix and learn more about the CureDuchenne fundraising initiative with World of Warcraft here.


This article originally appeared last year.

"Dee" the delivery guy stoked to get some Doritos.

Sometimes the smallest gesture can change someone’s day for the better, especially when that act of kindness lets them know their work is appreciated. During the pandemic, delivery drivers have done a fantastic job keeping people healthy, so Toni Hillison Barnett told KKCO News 11 that she and her husband started a tradition of leaving snacks for their drivers on the front porch around 2020.

The Barnetts, who live in Louisville, Kentucky, can see the drivers' reactions by recording them on their doorbell cameras. “I live for reactions like this to our snack cart! Thx to all of the delivery drivers out there! We appreciate you!” Toni wrote on an Instagram post.

Recently, one of the Barnetts’ delivery guys, a joyous fellow that we believe is known as Dee, went viral on TikTok because of his positive reaction to receiving some snacks during his deliveries. The snacks are tasty, no doubt. But it’s also wonderful to feel appreciated. After Toni posted the video, it received more than 100,000 views.

“Oh my God, you guys are the best, I gotta take a snapshot of this,” Dee can be heard saying in the video. “Oh, Capri Suns are my favorite. Yes!”

@toniraebarnett

Snacks for our delivery drivers. This reaction might be one of the best! #snackcart #fyp #ups #nestcam #christmas #delivery #foryou

“Seeing a grown man get so excited about Capri Sun is extra wholesome," abigailbaet wrote on the TikTok post.

A fellow delivery driver explained the reason why he probably appreciated the gift so much: "I'm a delivery driver and so far had one house to do this … it was the best. Half the time we don't have time for a break and work 10+ hours," Michelle Mumpower wrote.

Dee returned for another delivery and found more snacks waiting for him. The follow-up video received more than 400,000 views.

“Thank you! Oh yes, no way, we’re back again with the Capri Sun,” he continued. “I think this is where I went viral, isn’t it? You guys are awesome. Thank you. Doritos … Thank you, have a great day. Thank you for making me go viral.”

@toniraebarnett

Replying to @itskatiepatton Dee is back again and we had the @caprisun waiting! TY tiktok for making this awesome @ups driver go viral!! The world needs more of his energy & attitude! 🤍 #snackcart #ups #caprisun #wholesome #fyp #foryoupage #christmas

The driver may have found out that the video was popular after a friend told him she saw it on the platform. “That’s my friend Dee!!!! He’s the best,” Katie wrote.

“Oh I'm so glad you commented! I was hoping someone would claim him! What an awesome vibe he has!! Tell him I'll keep the @Caprisun stocked!” Toni responded.

According to NBC News 11, the family has been giving out snacks to delivery drivers for the past three years as a thank-you for all of the hard work they’ve done since the beginning of the pandemic.

It’s touching to see a kind gesture of appreciation be accepted with such glee. It’s also wonderful that the videos have been seen by so many people, because they’re a wonderful reminder for all of us to show our appreciation to the people that are the backbone of our communities. As the Barnetts have shown us, sometimes a small gesture can make a big difference. Oh yeah, and be sure to stock some Capri Suns while you’re at it, just in case Dee is working in your neighborhood.


This article originally appeared three years ago.

Photo by Katerina Holmes|Canva

Mom in tears after another parent calls about daughter's lunch

People say having children is like having your heart walk around outside of your body. You send them off to school, practices or playdates and hope that the world treats them kindly because when they hurt, you hurt. Inevitably there will be times when your child's feelings are hurt so you do your best to prepare for that day.

But what prepares you for when the child you love so much winds up accidentally healing your inner child. A mom on TikTok, who goes by Soogia posted a video explaining a phone call she received from a parent in her daughter's classroom. The mom called to inform Soogia that their kids had been sharing lunch with each other.

Soogia wasn't prepared for what came next. The classmate's mother informed her that her son loves the food Soogia's daughter brings to school and wanted to learn how to cook it too.

That may seem like a small thing to some, but the small gesture healed a little bit of Soogia's inner child. Growing up as a Korean kid in California, Soogia's experience was a bit different than what her children are now experiencing.

"I guess I just never thought that my kids would be the generation of kids that could go to school and not only just proudly eat, but share their food with other kids that were just so open and accepting to it," Soogia says through tears. "Knowing that they don't sit there eating their food, feeling ashamed and wishing that their fried rice was a bagel instead or something like that. And I know, it sounds so small and it sounds so stupid, but knowing their experience at school is so different from mine in such a positive way is just so hopeful."

Soogia's tearful video pulled on the heartstrings of her viewers who shared their thoughts in the comments.

"Soogia! It will never be small. Your culture is beautiful & the littles are seeing that every day. You've even taught me so much. I'm grateful for you," one person says.

"Beautiful! I can see your inner child healing in so many ways," another writes.

"Welp. Now I'm sobbing at the airport. This is beautiful," someone reveals.

"These Gen Alpha babies really are a different, kinder generation. I love them so much," one commenter gushes.

You can hear the entire story below. You may want to grab a tissue.

@soogia1

These kids, man. They’re really something else. #culturalappreciation #breakingbread #sharing #

This article originally appeared last year.