Chłopiec chory na SMA

EN_01552308_0004
Chłopiec chory na SMA
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 (SMA), at their home on the outskirts of Recife, Brazil, June, 4, 2022. A wave of transformative but hugely expensive treatments is challenging the budgets of health coverage systems in both wealthy nations and some countries with far fewer resources. (Dado Galdieri/The New York Times)
Minimum price 100USD
2022-06-04
DADO GALDIERI/The New York Times Agency/East News
The New York Times Agency
DADO GALDIERI
15793692
8,14MB
42cm x 28cm przy 300dpi
10, 2, 2022, 4, A, AMERICA, AND, AT, ATROPHY, BOTH, BRAZIL, BUDGETS, BUT, CHALLENGING, COST, COUNTRIES, COVERAGE, DA, DADO, DISEASE, DISORDER, EXPENSIVE, FAR, FEWER, GALDIERI, GENETIC, GOVERNMENT, HAVE, HEALTH, HER, HOME, HUGELY, IN, IS, JUNE, LEVI, LORENZO, MEDICAL, MEDICATIONS, MUSCULAR, NATIONS, NEW, NURSE, OF, OLIVEIRA, ON, OUTSKIRTS, PRICE, RARE, RECIFE, RESOURCES, SILVA, SMA, SOME, SONS, SOUTH, SPINAL, suhellen, SYSTEMS, THE, THEIR, THERAPIES, TIMES, TOP, TRANSFORMATIVE, TREATMENTS, WAVE, WEALTHY, WHO, WITH, YORK,