Chłopiec chory na SMA 11

A superhero figure in a wheelchair in the bedroom of Lorenzo de Oliveira Balbino, 10, who has the rare genetic disorder spinal muscular atrophy (SMA),...

Suhellen Oliveira Da Silva, whose children both have the rare genetic disorder spinal muscular atrophy (SMA), holds 2-year-old Levi while a nurse tend...

A weekly scheduling marker board for Levi de Oliveira Balbino, 2, who received an infusion of Zolgensma, a cutting edge gene therapy for his spinal mu...

Suhellen Oliveira Da Silva, top, and a nurse with her sons Lorenzo, 10, and Levi, 2, who both have the rare genetic disorder spinal muscular atrophy (...

A drawer filled with medications and medical supplies for Lorenzo de Oliveira Balbino, 10, who has the rare genetic disorder spinal muscular atrophy (...

A fresh tank of oxygen is delivered for treatment of Lorenzo de Oliveira Balbino, 10, who has the rare genetic disorder spinal muscular atrophy (SMA),...

The home of Suhellen Oliveira Da Silva and her husband Azen Balbino, whose two sons have the rare genetic disorder spinal muscular atrophy (SMA), on t...

Brothers Lorenzo, 10, left, and Levi de Oliveira Balbino, who both have the rare genetic disorder spinal muscular atrophy (SMA), at their home on the...

Levi de Oliveira Balbino, 2, who received an infusion of Zolgensma, a cutting edge gene therapy for his spinal muscular atrophy (SMA) that can cost mo...

A nurse works with Levi de Oliveira Balbino, 2, who received an infusion of Zolgensma, a cutting edge gene therapy for his spinal muscular atrophy (SM...

Residence towers in a wealthy section of Recife, Brazil, June, 3, 2022. A wave of transformative but hugely expensive treatments is challenging the bu...