In Lagos, a Homegrown Ballet Academy Leaps Into the Spotlight

Anthony Mmesoma Madu, left, with fellow students from the Leap of Dance Academy, in Ajangbadi, Ojo.Stephen Tayo for The New York Times
Anthony Mmesoma Madu, left, with fellow students from the Leap of Dance Academy, in Ajangbadi, Ojo.Stephen Tayo for The New York Times
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In Lagos, a Homegrown Ballet Academy Leaps Into the Spotlight

Anthony Mmesoma Madu, left, with fellow students from the Leap of Dance Academy, in Ajangbadi, Ojo.Stephen Tayo for The New York Times
Anthony Mmesoma Madu, left, with fellow students from the Leap of Dance Academy, in Ajangbadi, Ojo.Stephen Tayo for The New York Times

In June, a minute-long video featuring a young ballet student dancing in the rain began circulating on the internet. As the rain falls, forming puddles between the uneven slabs of concrete on which he dances, Anthony Mmesoma Madu, 11, turns pirouette after pirouette.

Though the conditions for such dancing are all wrong — dangerous, even — he twirls on, flying barefoot into an arabesque and landing it. He indulges the camera with a smile, but only for a moment, before assuming a look of fierce determination, lifting his eyes toward the sky, his lithe arms and graceful fingers following closely along.

The wide reach of the video — it has been seen more than 20 million times on social media platforms — has turned a spotlight on the unlikely story of a ballet school in a poor suburb of Lagos, Nigeria: the Leap of Dance Academy.

Founded in 2017, the academy has transformed the lives of its students, affording them a place to dance and to dream. And in the last few months, it has inspired influential people in ballet to lend a hand. Seemingly overnight, a world of opportunity has opened up: for the students, scholarships and invitations to attend prestigious schools and companies overseas; and for the school, sizable donations, which will allow for building a proper space, outfitted with a real dance floor.

For now, the Leap of Dance Academy is housed at the home of its founder, Daniel Owoseni Ajala, in Ajangbadi, Ojo, on the western outskirts of Lagos. Every day after school, Mr. Ajala’s 12 students walk to his apartment, where he pushes aside his furniture and spreads a thin vinyl sheet over the concrete floor for class, throwing open the doors and windows to let in the light.

AAgainst swaths of candy-colored chiffon — intended to make the humble setting a little more festive — students move through their lessons in small groups, leaning against a short, stationary ballet barre and craning their necks to watch Mr. Ajala, or an overseas instructor on Zoom, give corrections.

Much of this is filmed and posted to the school’s Instagram feed, where the students’ joy is evident in each video, their movements precise and praiseworthy — as the comments, hearts and trembling star emojis left by their fans attest.

In the early days of Leap of Dance, many Ajangbadi families were suspicious of ballet. The form’s strict, regimented movements were very different from the more fluid African dances they knew well — as were the skimpy costumes and painful-looking shoes, which, they soon learned, could leave feet cracked, calloused and bruised.

“In the beginning, people kept saying, ‘What are they doing?!’” Mr. Ajala said. “I had to convince them that ballet wasn’t a bad or indecent dance, but actually something that requires a lot of discipline that would have positive effects on the lives of their children outside the classroom. I always say, it’s not only about the dance itself — it’s about the value of dance education.”

When Mr. Ajala, 29, founded Leap of Dance three years ago, he was a self-taught recreational dancer with a dream: to open a ballet school for students who were serious about learning the art form and possibly pursuing it professionally one day. “I wanted, more than anything, to give that opportunity to those younger than myself so they wouldn’t miss their chance like I did,” he said, in a recent Zoom call. “It was too bad that I was as old as I was when I realized I wanted to dance.”

As a child, Mr. Ajala became obsessed with ballet after watching “Save the Last Dance,” the 2001 movie about a lapsed ballet dancer (Julia Stiles) who moves to the South Side of Chicago after her mother dies; she falls in love with a classmate (Sean Patrick Thomas) who shares her passion for dance and helps nurse her dormant dream of becoming a ballerina back to life.

Though he found the love story formulaic and glib, Mr. Ajala said he was captivated by the movement he saw onscreen and, perhaps even more, by the discipline and sacrifice that was evidently required to master it. Ballet appealed to him for another reason, too: It wasn’t widely taught or practiced in Nigeria. “I wanted to be different,” he said. “I loved that ballet is not common here. When you talk about dance in Nigeria, it’s like hitting one-way traffic: Everybody does the same thing, and they all end up in the same place.”

He taught himself what he could by watching lessons and professional companies on YouTube; he also signed up for a few crash courses in ballet at a local dance center. When it came time for college, he studied business administration at Lagos State University at the request of his parents, intending to pursue dance on the side. But after taking his final exams, he decided his calling lay elsewhere: in dance. “I had to explain to my friends and family that sometimes white-collar jobs are not the picture they paint themselves to be,” he said. “They lack heart.”

And so the Leap of Dance Academy was born, its name a nod to the leap of faith Mr. Ajala took in leaving more secure job prospects behind. Turning again to online platforms, he joined an international dance teacher network on Facebook. He posted a note explaining that he was starting a ballet school in Nigeria that would provide free instruction and asked if anyone had used or unwanted dance kits they could send him, since many families in Ajangbadi wouldn’t be able to afford costumes. Soon, he was put in touch with someone from Traveling Tutus, a nonprofit organization in Florida that donates gently used dance wear to students around the world.

The New York Times



What Is ALS, the Disease That Killed Actor Eric Dane?

US actor Eric Dane speaks about his ALS diagnosis during a news conference to discuss health insurance at the Department of Health and Human Services Headquarters in Washington, DC, on June 23, 2025. (AFP)
US actor Eric Dane speaks about his ALS diagnosis during a news conference to discuss health insurance at the Department of Health and Human Services Headquarters in Washington, DC, on June 23, 2025. (AFP)
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What Is ALS, the Disease That Killed Actor Eric Dane?

US actor Eric Dane speaks about his ALS diagnosis during a news conference to discuss health insurance at the Department of Health and Human Services Headquarters in Washington, DC, on June 23, 2025. (AFP)
US actor Eric Dane speaks about his ALS diagnosis during a news conference to discuss health insurance at the Department of Health and Human Services Headquarters in Washington, DC, on June 23, 2025. (AFP)

Eric Dane, known for his roles on "Grey’s Anatomy" and "Euphoria," died this week from amyotrophic lateral sclerosis at age 53.

The fatal nervous system disease, also known as Lou Gehrig’s disease, killed Dane less than a year after he announced his diagnosis.

According to the Centers for Disease Control and Prevention, ALS is rare. In 2022, there were nearly 33,000 estimated cases, say researchers, who project that cases will rise to more than 36,000 by 2030.

The disease is slightly more common in men than in women and tends to strike in midlife, between the ages of 40 and 60.

Here’s what to know.

What is ALS? It affects nerve cells in the brain and spinal cord, causing loss of muscle control and getting worse over time.

ALS causes nerve cells in the upper and lower parts of the body to stop working and die. Nerves no longer trigger specific muscles, eventually leading to paralysis. People with ALS may develop problems with mobility, speaking, swallowing and breathing.

The exact cause of the disease is unknown, and Mayo Clinic experts said a small number of cases are inherited.

It’s called Lou Gehrig’s disease after the Hall of Fame New York Yankees player. Gehrig was diagnosed with ALS in 1939 on his 36th birthday, died in 1941 and was the face of ALS for decades.

What are some signs of ALS? Experts say the first symptoms are often subtle. The disease may begin with muscle twitching and weakness in an arm or leg.

Over time, muscles stop acting and reacting correctly, said experts at University of California San Francisco Health. People may lose strength and coordination in their arms and legs; feet and ankles may become weak; and muscles in the arms, shoulders and tongue may cramp or twitch. Swallowing and speaking may become difficult and fatigue may set in.

The ability to think, see, hear, smell, taste and touch are usually not affected, UCSF experts said.

Eventually, muscles used for breathing may become paralyzed. Patients may be unable to swallow and inhale food or saliva. Most people with ALS die of respiratory failure.

How is ALS diagnosed and treated? The disease is difficult to diagnose because there’s no test or procedure to confirm it. Generally, doctors will perform a physical exam, lab tests and imaging of the brain and spinal cord.

A doctor may interpret certain things as signs of ALS, including an unusual flexing of the toes, diminished fine motor coordination, painful muscle cramps, twitching and spasticity, a type of stiffness causing jerky movements.

There’s no known cure for ALS, but the drug riluzole has been approved for treatment. According to the Mayo Clinic, it may extend survival in the early stages of the disease or extend the time until a breathing tube is needed.

Another much-debated drug, Relyvrio, was pulled from the US market by Amylyx Pharmaceuticals in 2024. Its development had been financed, in part, by the ALS Association, the major beneficiary of the 2014 " ice bucket challenge " viral phenomenon.

Other medications are sometimes prescribed to help control symptoms.

Choking is common as ALS progresses, so patients may need feeding tubes. People may also use braces, wheelchairs, speech synthesizers or computer-based communication systems.

After the onset of the disease, experts say patients may survive from two years to a decade. Most people live from two to five years after symptoms develop, and about a fifth live more than five years after they are diagnosed.


Snowstorm Paralyzes Vienna Airport

People wait at a tram stop after heavy snowfalls in Vienna, Austria, February 20, 2026. REUTERS/Elisabeth Mandl
People wait at a tram stop after heavy snowfalls in Vienna, Austria, February 20, 2026. REUTERS/Elisabeth Mandl
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Snowstorm Paralyzes Vienna Airport

People wait at a tram stop after heavy snowfalls in Vienna, Austria, February 20, 2026. REUTERS/Elisabeth Mandl
People wait at a tram stop after heavy snowfalls in Vienna, Austria, February 20, 2026. REUTERS/Elisabeth Mandl

Massive snowstorms caused power outages and transport chaos in Austria on Friday, forcing the Vienna airport to temporarily halt all flights.

Flights departing from the capital, a major European hub, were cancelled or delayed, and more than 230 arrivals were similarly disrupted or rerouted.

"Passengers whose flights have been delayed are asked not to come to the airport," the facility said in a statement.

The area received 20 centimeters (nearly eight inches) of snow, national news agency APA reported.

The main highway south of Vienna was closed for several hours, and other sections of highway were temporarily inaccessible because of snowdrift, stranded lorries or poor visibility, said the national automobile association, OAMTC.

According to AFP, electric companies reported power outages in several regions in the south and east, including Styria, where 30,000 homes lost electricity.

The weather was forecast to improve from around midday, but the risk of avalanches remained high.


NASA Delivers Harsh Assessment of Botched Boeing Starliner Test Flight

NASA duo Butch Wilmore and Suni Williams were stuck on the ISS for nine months. Handout / NASA TV/AFP/File
NASA duo Butch Wilmore and Suni Williams were stuck on the ISS for nine months. Handout / NASA TV/AFP/File
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NASA Delivers Harsh Assessment of Botched Boeing Starliner Test Flight

NASA duo Butch Wilmore and Suni Williams were stuck on the ISS for nine months. Handout / NASA TV/AFP/File
NASA duo Butch Wilmore and Suni Williams were stuck on the ISS for nine months. Handout / NASA TV/AFP/File

NASA on Thursday blamed what it called engineering vulnerabilities in Boeing's Starliner spacecraft along with internal agency mistakes in a sharply critical report assessing a botched mission that left two astronauts stranded in space.

The US space agency labeled the 2024 test flight of the Starliner capsule a "Type A" mishap -- the same classification as the deadly Challenger and Columbia shuttle disasters -- a category that reflects the "potential for a significant mishap," it said.

The failures left a pair of NASA astronauts stranded aboard the International Space Station for nine months in a mission that captured global attention and became a political flashpoint.

"Starliner has design and engineering deficiencies that must be corrected, but the most troubling failure revealed by this investigation is not hardware. It's decision-making and leadership," said NASA administrator Jared Isaacman in a briefing.

"If left unchecked," he said, this mismanagement "could create a culture incompatible with human spaceflight."

The top space official said the investigation found that a concern for the reputation of Boeing's Starliner clouded an earlier internal probe into the incident.

"Programmatic advocacy exceeded reasonable bounds and place the mission, the crew and America's space program at risk in ways that were not fully understood at the time," Isaacman said.

He said Starliner currently "is less reliable for crew survival than other crewed vehicles" and that "NASA will not fly another crew on Starliner until technical causes are understood and corrected" and a problematic propulsion system is fixed.

But the administrator insisted that "NASA will continue to work with Boeing, as we do all of our partners that are undertaking test flights."

In a statement, Boeing said it has "made substantial progress on corrective actions for technical challenges we encountered and driven significant cultural changes across the team that directly align with the findings in the report."

- 'We failed them' -

Isaacman also had harsh words for internal conduct at NASA.

"We managed the contract. We accepted the vehicle, we launched the crew to space. We made decisions from docking through post-mission actions," he told journalists.

"A considerable portion of the responsibility and accountability rests here."

In June 2024 Butch Wilmore and Suni Williams embarked on what was meant to be an eight-to-14-day mission. But this turned into nine months after propulsion problems emerged in orbit and the Starliner spacecraft was deemed unfit to fly them back.

The ex-Navy pilots were reassigned to the NASA-SpaceX Crew-9 mission. A Dragon spacecraft flew to the ISS that September with a team of two, rather than the usual four, to make room for the stranded pair.

The duo, both now retired, were finally able to arrive home safely in March 2025.

"They have so much grace, and they're so competent, the two of them, and we failed them," NASA associate administrator Amit Kshatriya told Thursday's briefing.

"The agency failed them."

Kshatriya said the details of the report were "hard to hear" but that "transparency" was the only path forward.

"This is not about pointing fingers," he said. "It's about making sure that we are holding each other accountable."

Both Boeing and SpaceX were commissioned to handle missions to the ISS more than a decade ago.