We are constantly being reminded of Isaac Newton’s famous quote, “If I have seen further, it is by standing on the shoulders of giants.” Eleven such giants were recruited as volunteers from Gallaudet University (then Gallaudet College) in Washington, D.C. in 1958. Their task was to help researchers understand the effects of weightlessness on Deaf people who didn’t experience motion sickness.

Deemed the Gallaudet Eleven, they helped pave the way for hundreds of space flights, including the most recent Artemis II. Ranging in age from 25 to 48 years, the eleven men included Harold Domich, Robert Greenmun, Barron Gulak, Raymond Harper, Jerald Jordan, Harry Larson, David Myers, Donald Peterson, Raymond Piper, Alvin Steele, and John Zakutney. Each and every one of them selflessly gave their time and their bodies to what would become monstrous breakthroughs in astrophysics.

Houston had a problem

Actor and Deaf activist, Nyle DiMarco, recently took to social media to share the historical tidbit, lest people forget. In an Instagram reel, he wrote,

“Everyone’s talking about Artemis II. The first humans to travel to the moon in 50 years. Historic mission. But nobody’s talking about the Deaf men who made it possible.

In the late 1950s, NASA had a problem. They needed to understand what weightlessness does to the human body. But every test subject kept getting violently motion sick.

So they came to Gallaudet.

Eleven Deaf men. Most of them had lost their hearing to spinal meningitis as children, which also damaged their vestibular system. Their inner ears couldn’t be overwhelmed. They were immune to motion sickness.

NASA put them in centrifuges. Zero-gravity flights. A rotating room for twelve straight days. One experiment on a ferry in choppy Nova Scotia waters. The researchers got so seasick they had to cancel it. The Gallaudet Eleven? They were playing cards.

Their bodies gave NASA the data it needed to send humans into space.

No Gallaudet Eleven — no Mercury. No Mercury — no Apollo. No Apollo — no Artemis II.

Sixty years later, four astronauts just flew 252,000 miles from Earth and came home safely. They stood on the shoulders of eleven Deaf men most people have never heard of. Now you know! #nasa #gallaudet11 #artemisii @nasa”

The post has already received nearly 400,000 likes and over 6,000 comments. One Instagrammer writes, “Diversity in all its forms is what makes us great. And all of us working together is what helps us advance as a civilization! Thank you for sharing this and bringing visibility to this piece of history, and thank you Gallaudet 11 for your contribution.”

The official NASA website shared some of the tests in which the brave volunteers took part. “One test saw four subjects spend 12 straight days inside a 20-foot slow rotation room, which remained in a constant motion of ten revolutions per minute.”

Then, of course, there were the zero-g flights. “In another scenario, subjects participated in a series of zero-g flights in the notorious ‘Vomit Comet’ aircraft to understand connections between body orientation and gravitational cues.”

They even took the volunteers to Nova Scotia to test big waves. “Another experiment, conducted in a ferry off the coast of Nova Scotia, tested the subjects’ reactions to the choppy seas. While the test subjects played cards and enjoyed one another’s company, the researchers themselves were so overcome with seasickness that the experiment had to be canceled. The Gallaudet test subjects reported no adverse physical effects and, in fact, enjoyed the experience.”

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“We were young and adventurous”

The test subjects themselves shared their experiences. Barron Gulak reminisced, “In retrospect, yes, it was scary…but at the same time we were young and adventurous.”

On DiMarco’s identical Facebook post, Harry Larson’s child, “Moose” Larson, shared a photo and wrote, “They were recently recognized with a cool plaque at Gallaudet! My dad is one of them and, funny enough, never really talked about it.” A commenter responded, “I’ve worked with your dad a lot on this project during the museum exhibition several years ago. He’s been so wonderful, always willing to come to events. I’m so glad he’s sharing his story now.”

Ifrah Mansour is no stranger to conflict.

A Somali refugee and current resident of Minneapolis, the multimedia artist and activist draws on her lived experiences to create work that explores trauma, displacement, and resilience. But like so many of the guests on Freedom to Thrive, an award-winning podcast produced by the National Immigration Law Center (NILC), Mansour doesn’t want to focus only on trauma; she also wants to celebrate the unexpected beauty she’s found during difficult experiences.

“One of the beautiful things about tragedies is that it activates hearts, and courageous people are born,” she says. For example, Mansour has noticed more Minnesotans than ever are reaching out to help the vulnerable, after the anti-immigrant crackdowns carried out by the Department of Homeland Security. “They are bringing food, they’re bringing extra clothes, they’re walking with people, and it’s just really beautiful.”

Hector Flores, co-founder of the Las Cafeteras and host of Freedom to Thrive, agrees with her. A child of immigrants himself, he has also seen how hope and hardship often live side by side.

Flores comes from a family with mixed status and is highly aware of the challenges immigrants and refugees in his community face, and how they’re affected by people’s misconceptions. “People want to know about trauma all the time, but we’re more than just undocumented,” he says. “We’re artists, singers, creatives … there’s so much richness in the culture.”

At its core, Flores’ comment is exactly what the Freedom to Thrive podcast is all about: Celebrating immigrants as complex, dynamic individuals, and challenging the dominant narrative that too often reduces them to symbols of hardship.

Launched in 2024, Freedom to Thrive explores heritage, resilience, community, and the ways art and comedy can spark social change. Now in its second season, the podcast continues to feature conversations with immigrants, policymakers, artists, musicians, activists, and more. Recent guests have included comedian Mo Amer, Grammy Award-winning singer Lila Downs, and Pulitzer Prize-winning author Viet Thanh Nguyen.

Where the first season focused on individual stories of identity and belonging, Flores says his goal for season two, where he joins as host, is to “take it to the next level” — using storytelling to highlight “the fact that we’re more similar than different.”

One recent podcast episode drives this point home. In December, Flores interviewed Bryan Andrews, a rising country music star and rural Missouri native who frequently uses his platform to speak about issues affecting immigrant families. At the heart of his message and his songwriting, Andrews says, is the idea that small-town Americans and the rest of the country, including immigrants, have more in common than they realize.

“It doesn’t matter where you’re from,” Andrews says on the podcast. “We’re all trying to make a living and we’re tired of getting railroaded by corporate greed or by politicians who don’t care.”

Rural Americans, Andrews says, are often stereotyped as racist and misogynistic but “the overwhelming majority of people in my home town have love in their hearts.” Media stereotypes often amplify differences and divide, he says, but at the end of the day, “we’re all in this together.”

Flores, who was raised in a working-class immigrant neighborhood in East Los Angeles, had similar thoughts. He says he often sees its residents stereotyped as wealthy, consumerist, and status obsessed. “That exists, but that’s not my life, that’s not my community,” he says. Like small-town Americans, people in the city “just want to work hard and take care of their families. We all want the same thing.”

Although the podcast tackles some heavy issues, each episode’s ultimate focus is how personal and collective struggles can be healed through art, driving home a message of hope and resilience: 

Mansour’s episode about her experiences in Minnesota is just one of many examples. Flores asks her,

“What gives you hope for the people creating a home here?”

“The love I feel from other Minnesotans. It is trumping any hate we’re experiencing,” she replies.

CTA: Stream all episodes now on the Freedom to Thrive YouTube channel or the website, here. 

The podcast has been nominated for a Webby in the “Belonging & Inclusion” category. You can vote for it to win until Thursday, April 16!

This article is part of Upworthy’s “The Threads Between U.S.” series that highlights what we have in common thanks to the generous support from the Levis Strauss Foundation, whose grantmaking is committed to creating a culture of belonging. 

It’s a parent’s worst nightmare: Taking your child to the doctor and receiving a life-changing diagnosis. It only adds to the heartbreak when they find out there may be no effective treatment at all, and that all they can do is hope for the best.

Few diagnoses strike fear in the heart of parents and doctors more than a cancer called diffuse intrinsic pontine glioma, or DIPG. Primarily found in children, DIPG is a highly aggressive brain tumor that is uniformly fatal, with less than 10 percent of children surviving longer than two years after diagnosis. The tumors grow fast and on extremely vital areas like the spine and brain stem, making them exceptionally hard to remove. Though young patients have been treated with radiation, chemotherapy, and surgeries, no one had ever been cured of the fatal cancer.

But for the first time ever, a 13-year-old boy from Belgium named Lucas Jemeljanova has beaten the odds.

Diagnosed with DIPG at age six, Lucas’ doctor Jacques Grill told Lucas’ parents, Cedric and Olesja, that he was unlikely to live very long. Instead of giving up hope, Cedric and Olesja flew Lucas to France to participate in a clinical trial called BIOMEDE, which tested new potential drugs against DIPG.

Lucas was randomly assigned a medication called everolimus in the clinical trial, a chemotherapy drug that works by blocking a protein called mTOR. mTOR helps cancer cells divide and grow new blood vessels, while everolimus decreases blood supply to the tumor cells and stops cancer cells from reproducing. Everolimus, a tablet that’s taken once per day, has been approved in the UK and the US to treat cancers in the breast, kidneys, stomach, pancreas, and others—but until the BIOMEDE clinical trial, it had never before been used to treat DIPG.

Though doctors weren’t sure how Lucas would react to the medication, it quickly became clear that the results were........

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