Progeria Sammy Basso: A Story of Hope and Resilience

Who is Sammy Basso?

Sammy Basso was born in Italy in 1995 with a rare genetic condition called Hutchinson-Gilford progeria syndrome (HGPS). This condition causes rapid aging, leading to a shortened life expectancy. Despite his condition, Sammy has lived a full and inspiring life, becoming an advocate for others with HGPS and raising awareness of the condition.

What is Progeria?

Progeria is a rare genetic disorder that affects children. It is caused by a mutation in the LMNA gene, which is responsible for producing a protein called lamin A. Lamin A is essential for maintaining the structure of the cell nucleus. In children with progeria, the mutation in the LMNA gene leads to the production of a defective form of lamin A, which causes the cells to age prematurely.

Symptoms of progeria typically begin in the first few months of life. These symptoms include:

• Slow growth
• Wrinkled skin
• Hair loss
• Stiff joints
• Heart problems
• Stroke

Sammy's Story

Sammy was diagnosed with progeria at the age of two. Despite his diagnosis, Sammy has lived a full and active life. He has attended school, played sports, and traveled the world. He has also met with world leaders and spoken at conferences to raise awareness of progeria.

In 2014, Sammy founded the Sammy Basso Foundation, a nonprofit organization dedicated to supporting research into progeria and providing support to families affected by the condition. The foundation has raised millions of dollars for research and has helped to improve the lives of countless children with progeria.

Sammy's Legacy

Sammy Basso is an inspiration to everyone who has ever faced adversity. He is a reminder that anything is possible, even if you are facing a life-limiting condition. Sammy's story is a testament to the power of hope, resilience, and determination.