'There's nobody like him': Sammy Basso, longest survivor of rapid ageing disease, dies at 28 | CBC Radio - Action News
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As It Happens

'There's nobody like him': Sammy Basso, longest survivor of rapid ageing disease, dies at 28

Nobody expected Sammy Basso to live as long as he did, but his sudden death at the age 28 still came as a shock to those who knew and loved him.

Basso dedicated his short life to research and advocacy around the gene disorder called progeria

A man in a tuxedo and bowtie smiles and makes an Italian hand gesture. He's very short, with a large, bald head and glasses.
Sammy Basso, a scientist and advocate who was the longest known survivor of progeria, has died at the age of 28. (John Phillips/Getty Images/Business of Fashion)

Sammy Basso lived longer than anyone else with his disease, but his deathat the age 28 still came as a shock to those who knew and loved him.

"We all knew that Sammy had a terrible circumstance that was not going to allow him to live a full life. But he was so vibrant. He was so alive. He was so engaged," Dr. Francis Collins, Basso's friend and colleague, told As It Happens host Nil Kksal. "I was stunned."

Basso, a molecular biologist from Italy, died on Oct. 5. He was the longest knownsurvivor of progeria, a rare genetic disease that causes rapid aging. Many people who have it don't make it past their teens.

He dedicated hislife to studying and raising awareness aboutprogeriain the hopes that future generations would not have to go through what he did.

Those who knew him say he was not only committed to the cause, butalso funny and kind,a brilliant conversationalist, the life of a party, and someone who extolled the kind of joie-de-vivre that comes from knowing all too well that every second counts.

"I like my life as it is, because it's my life. I have my friends, my parents, my family. These are the most important things," he said in a 2016 interview with the Catholic publication Aleteia.

"Progeria is a small part of my life, because it only affects the body."

'Today our light, our guide, has gone out'

Born in 1995 in Schio, in the northern Italian region of Veneto, Basso was diagnosed with progeria at the age of two.

His friends say hepacked more life into his 28 years than most people everdo. He travelled the world, hobnobbing with celebrities and politicians, and even once meeting the Pope.

In 2005, when he was 10, he and his parents founded the Italian Progeria Association, a charity that supports research into progeria and supports families dealing with the disease.

"Today our light, our guide, has gone out. Thank you Sammy for making us part of this wonderful life," the association wrote on its Instagram page.

A group of people run on a track, carrying white balloons, and wearing in matching sky-blue shirts that read
Basso headed up a group called Sammy's Runners, which fundrasied for the Italian Progeria Association, a charity founded by his parents. (Sammy's Runners/Instagram )

Nicola Berti met Basso about fiveyears ago at a party, when Basso asked him to run a half-marathon forSammy's Runners, a run club that raises money for hischarity.

"I accepted, and from that moment, we became friends," Berti said.

Berti says he saw Bassoalmost every weekend, sometimes organising charity fundraisers, but often just hanging out. Basso, he says, quickly became the heart and soul of their group of friends.

"He was like glue," Berti said. "When Sammy sent us a message in our WhatsApp group saying, 'OK,tonight I can join you,' it was always like a party. It was always better. You could feel that Sammy was there, because he was like a magnet."

A post on X from the Progeria Research Foundation, featuring a black and white photo of a young man with a large head and wrinkled skin smiling brightly. Text on the photo reads:
Basso was an ambassador for the Progeria Research Foundation, which paid tribute to him on social media. (Progeria Research Foundation/X)

Basso could talk to anyone about anything, Berti says, andhad a knack for making people comfortable enough to open up about their feelings. Whenever there was a conflict in the friend group, he would step in and make peace.

He also had a way of inspiring people to do things they never imagined they could do. Berti remembers running his first marathon two years ago in Venice with Basso by his side.

"It was one of the most beautiful things I've ever [done].And I'm not talking about finishing a marathon, but the joy of sharing this event at the last kilometre, when we were all tired and we were literally suffering," he said, choking up.

"But seeing this beautiful soul in his cart, smiling and encouraging us to keep going on, it was something that I cannot describe."

Renowned for hissense of humour

Progeria, also known as Hutchinson-Gilford syndrome, is caused by a single gene mutation. There are only 130 recognized cases worldwide, of which four are in Italy.

It can cause a wide array of health issues, including pain, stunted growth, cardiovascular disease and joint problems, as well as a distinctive appearance that usually includes baldness, a large head, a pointed nose, and a lack of fat beneath the skin.

"He was one of those people who knew he looked unusual, and made that into something that he and everybody else could actually smile about instead of feeling uncomfortable," Collins said.

Four people sit around on chairs eating and talking.
Basso, right, in 2023 at the Boho Farmhouse in Chipping Norton, England, for a Business of Fashion event. (Samir Hussein/Getty Images/Business of Fashion)

The most famous example, he says, is when Basso was travelling along Route 66 from Chicago to Los Angeles in 2014,raising awareness about progeria and documenting his travels for his memoir, Il viaggio di Sammy (Sammy's Journey), and a National Geographic documentary of the same name.

"They stopped in Area 51, which is where there are these rumours, you know, about aliens have landed, and Sammy put on this remarkably alien looking pair of sunglasses and sat outside," Collins said with a chuckle. "And that, I'm sure, shook some tourists up."

Basso was renowned for his sense of humour, his friends say.

Berti and his friends have been collecting testimonies from Basso's loved ones to put in a book, and he says "the first thing that everyone can remember about him were his jokes, his smile and his love."

"If I close my eyes and I try to remember him, I can see him laughing, smiling, because he was like that," he said.

Researching his own disease

Basso worked on a research team alongside Collins, a renowned geneticist, with a mission to develop a gene-editing therapy to treat progeria.

The average life expectancy for people with progeria is 15, according to the Mayo Clinic, and 13.5 without treatment, according to the Italian Progeria Association.

One of the reasons Basso livedas long as he did, Collins says, is that he volunteered for the clinical trial of what would become the first approved drug for the disease.

"There are a few other progeria individuals now living into their 20s. That never used to happen before. But it's not good enough. We want something even better than that. And that's what he was helping us work on," Collins said.

He contributed so much and always in the most selfless, optimistic, fun-loving way.- Dr. Francis Collins

Basso, he says, "put himself into it, heart and soul."

"He set the agenda oftentimes. He was the guy who hounded everybody about action items," he said.

He did this, Collins said, despite knowing that whatever progress they made, it likely wouldn't save his own life. Science is slow, and his disease had already progressed so far.

Collins says they've had promising results with gene editing on mice with progeria in a lab setting.

"But that's a mouse. People are not the same," he said. "Working with Sammy and the rest of our small team, we were aiming towards and we will continue to aim towardsa human clinical trial of that approach in the next couple of years."

Collins was in Nigeria for a genomics conference, driving fromLagos to Ede, when he got the news that Basso had died. He'd been exchanging friendly emails with him just the day before.

"I confess I cried pretty hard. The other people in the car wondered what was going on," he said.

"I loved this young man. He was such a special guy. He contributed so much and always in the most selfless, optimistic, fun-loving way. There's nobody like him."

Interview with Francis Collins produced by Nishat Chowdhury

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