Sammy Basso, who was known as the longest living survivor of the rare genetic disease progeria, passed away at the age of 28, as confirmed by the Italian Progeria Association. Progeria, also known as Hutchinson-Gilford syndrome (HGPS), is a condition that causes individuals to age rapidly, resulting in a shorter life span and decreased quality of life. Typically, those with progeria have a life expectancy of only 13.5 years without proper treatment.
This rare disease affects approximately one in every eight million people born, with a global incidence of about one in every 20 million individuals. Sammy Basso, born in 1995 in Schio, a town in the northern Italian region of Veneto, was diagnosed with progeria at the young age of two. In 2005, Sammy and his parents took the initiative to establish the Italian Progeria Association, aiming to raise awareness and support for those affected by this condition.
Sammy gained recognition through the National Geographic documentary titled “Sammy’s Journey,” which followed his travels along Route 66 in the United States from Chicago to Los Angeles, accompanied by his parents and close friend, Riccardo. This journey allowed Sammy to share his story and shed light on the challenges faced by individuals living with progeria.
The Italian Progeria Association expressed their sorrow over Sammy’s passing on their Instagram page, referring to him as their “light” and “guide.” Sammy’s contribution to the progeria community and his positive outlook on life have left a lasting impact on those who knew him.
Although there are only 130 documented cases of classic progeria worldwide, with four cases identified in Italy, the actual number of individuals affected may be higher. The Italian Progeria Association estimates that there could be up to 350 cases globally, as some cases, especially in developing countries, may go undetected or unreported.
Sammy Basso’s legacy as a progeria survivor and advocate for the condition will continue to inspire others to raise awareness and support research efforts aimed at finding effective treatments for this rare genetic disease. His story serves as a reminder of the resilience and strength demonstrated by individuals facing unique challenges, leaving a lasting impact on those who had the privilege of knowing him.