Jaber Q is a 14-year-old child diagnosed with Limb-Girdle Muscular Dystrophy ‎‎(LGMD), a genetic condition that causes progressive muscle weakness. He had been ‎experiencing physical decline for some time, but the underlying cause remained ‎unclear. We managed to interfere early in his case hopping to bring him remedy ‎wrapped with light and began following up on his case, aiming to understand how best ‎to support him.

Our team coordinated and funded the necessary medical tests—including a muscle ‎biopsy, chest CT scan, and heart echocardiogram—which ultimately led to a ‎confirmed diagnosis. Jaber was also found to have a congenital diaphragmatic hernia, ‎which cannot be operated on due to his fragile health.‎

Following the diagnosis, we proposed a ‎treatment plan focused on slowing disease progression and improving Jaber’s quality ‎of life through physical therapy, a customized wheelchair, and nutritional supplements.‎

Misk took on the full financial responsibility for Jaber’s case—not out of obligation, but out of belief; belief in dignity, in standing by those who need us, and in doing ‎what we can to ease the weight of suffering.