Ethiopian twins successfully separated after rare cranial surgery in Missouri

Twin infants born with a rare congenital condition requiring complex surgical intervention to enable independent development and quality of life.
They now have opportunities that would not have been possible without this intervention
The head surgeon reflecting on what separation means for the twins' futures, even as long-term outcomes remain uncertain.
Mark

So these are identical twins who were born joined at the head. That's the condition we're talking about?

Mimi

Yes. Hiyab and Wuhbto came into the world conjoined at the skull. It's extraordinarily rare—one in fifty to one hundred thousand births. And girls are affected much more often than boys.

Mark

And they came from Ethiopia to have the surgery?

Mimi

They traveled to the United States in March 2025, about a year before the operation. The surgery itself happened in February at a children's hospital in St. Louis. It took more than twenty-four hours.

Luke

Who paid for this? That's a major surgery on infants. That's not cheap.

Mimi

The reporting doesn't specify the financial details. But you can see the network involved—World Pediatrics, Ronald McDonald House of Charities, Ethiopian Airlines, hospitals in Missouri. It was clearly a coordinated effort across multiple organizations.

Mark

What can they do now that they couldn't before?

Mimi

Before separation, they couldn't sit upright independently. They couldn't eat on their own or speak or play with other children. Now they're working on all of those things. They're in rehabilitation, learning to sit, working toward standing and walking.

Luke

But we don't know what their long-term development will look like?

Mimi

That's right. The surgeon said it's too soon to know. What they do know is that the surgery opened possibilities that wouldn't have existed otherwise.

Mark

How long have they been recovering?

Mimi

More than six months now. They're at a pediatric bridge hospital in Missouri receiving intensive care and rehabilitation.

Luke

Why did the hospital wait six months to announce this publicly?

Mimi

The reporting doesn't say. But it suggests they wanted to see how the girls stabilized before speaking publicly about it.

Mark

So this is still an ongoing story.

Mimi

Very much so. The girls are two years old now. Their development will unfold over years. This is the beginning.

  • A surgery spanning more than twenty-four hours and drawing specialists across multiple institutions and continents was required just to give two toddlers the chance to sit up on their own.
  • The rarity of the condition — craniопагус twins, girls no less, arriving from Ethiopia to a Missouri hospital — meant every step of the process, from transport to operating room to recovery, carried compounded risk.
  • Six months of silence from the medical team signaled the genuine fragility of the outcome; the announcement itself was an act of caution, not celebration.
  • Now in rehabilitative care, the twins are achieving what had been structurally denied to them: sitting upright, eating independently, speaking, playing alongside other children as separate selves.
  • Long-term neurological development remains an open question, but the surgical team has reframed the horizon — the girls no longer face an impossible future, only an uncertain one.

In the long human struggle to give every child a chance at an independent life, two infant sisters from Ethiopia have crossed a threshold that medicine rarely reaches. Hiyab and Wuhbto, born joined at the skull — a condition so rare it touches perhaps one in a hundred thousand births — were separated in a twenty-four-hour surgery at a St. Louis children's hospital this past February. Six months on, the hospital has spoken carefully and with measured hope: the girls are alive, they are learning, and possibilities that were once structurally impossible are now simply uncertain. That shift, from impossible to uncertain, is the quiet measure of what was accomplished.

In February, surgeons in St. Louis completed one of medicine's most delicate undertakings: a twenty-four-hour operation to separate two infant sisters born joined at the skull. Hiyab and Wuhbto, identical twins from Ethiopia, had arrived in the United States in March 2025 as infants carrying a condition that occurs in roughly one of every fifty thousand to one hundred thousand live births — and when identical twins are born this way, girls are affected three times more often than boys. The surgery took place on February 24 and 25 at SSM Health Cardinal Glennon Children's Hospital, made possible through a web of organizations spanning two continents: World Pediatrics, Ranken Jordan Pediatric Bridge Hospital, a children's home in Ethiopia, Ronald McDonald House of Charities, and Ethiopian Airlines each played a part.

What the surgery has unlocked is best understood through what the girls could not do before it. They could not sit upright, eat independently, speak, or play alongside other children. They could not do the ordinary work of being a child. Now, receiving rehabilitative care at Ranken Jordan in Maryland Heights, Missouri, they are learning all of it — sitting, working toward standing, eating, speaking, socializing, playing with each other and with others.

The hospital waited more than six months before speaking publicly, a caution that reflects the genuine uncertainty surrounding surgery of this magnitude on infants. Dr. Joanna Kemp, the lead neurological surgeon, acknowledged at a Wednesday press conference that long-term development cannot yet be predicted with confidence. But she offered what is knowable: the surgery has opened possibilities that would otherwise have remained permanently closed. How the girls' brains will develop, what their capabilities will become, what lives they will lead — all of that remains unwritten. For now, the story is one of a door opening, and two girls beginning to learn what it means to walk through it separately.

In February, surgeons at a children's hospital in St. Louis completed one of medicine's most delicate undertakings: they separated two infant sisters who had been born joined at the skull. The operation on Hiyab and Wuhbto, identical twins from Ethiopia, consumed more than twenty-four hours and required a team of specialists working across multiple disciplines. Six months later, as the girls approached their second birthday, the hospital announced the surgery's success—not as a moment of triumph alone, but as the opening of a door that had been closed to them since birth.

The twins had traveled from Ethiopia to the United States in March 2025, about a year before their separation. They arrived as infants conjoined at the head, a condition so rare that it occurs in roughly one of every fifty thousand to one hundred thousand live births. When identical twins are born this way, girls are affected three times more often than boys. The surgery itself took place on February 24 and 25 at SSM Health Cardinal Glennon Children's Hospital. It was the kind of procedure that required not just surgical skill but coordination across institutions and continents—World Pediatrics, Ranken Jordan Pediatric Bridge Hospital, Lola Children's Home in Ethiopia, Ronald McDonald House of Charities, and Ethiopian Airlines all played roles in making it possible.

What matters now is what the girls can do. Before separation, certain things were simply impossible. They could not sit upright on their own. They could not eat independently or speak or play with other children. They could not do the ordinary work of being a child. Dr. Nick Holekamp, chief health transformation officer at Ranken Jordan, described the change in plain terms: the girls are now participating in therapies tailored to each of them individually. They are learning to sit upright. They are working toward standing and walking. They are eating and speaking and socializing. They are playing with each other and with other children. These are not small things.

The girls are currently receiving rehabilitative care at Ranken Jordan Pediatric Bridge Hospital in Maryland Heights, Missouri, where they have been since the surgery. Dr. Joanna Kemp, the head neurological surgeon at Cardinal Glennon, acknowledged at a press conference on Wednesday that it remains too early to predict their long-term development with certainty. But she framed what is knowable: the surgery has opened possibilities that would have remained closed. The girls now have a chance at independence, at the small and large milestones of growing up, that their condition would have denied them.

The announcement came more than six months after the operation, suggesting the hospital waited to speak publicly until the girls had begun to stabilize and show signs of recovery. That caution reflects the genuine uncertainty that surrounds any surgery of this magnitude on infants. Yet the fact of their survival, their movement toward independent function, and their ability to engage with the world as separate beings rather than as a single conjoined organism represents a significant medical achievement. What comes next—how their brains will develop, what their capabilities will be, what kind of lives they will lead—remains to be written. For now, the story is one of a door opening, and two girls learning to walk through it.

It is still too soon to know exactly what their long-term development will look like but what we do know is that they now have opportunities that would not have been possible without this intervention.
— Dr. Joanna Kemp, head neurological surgeon at SSM Health Cardinal Glennon Children's Hospital
They are now able to participate in individually-focused therapies, to do the activities of daily living they could not do while conjoined, such as simple things, like sitting upright, and they can eventually learn to stand and walk.
— Dr. Nick Holekamp, chief health transformation officer at Ranken Jordan Pediatric Bridge Hospital
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