From “I just want to live” to “Yes, I will live”: Anas battles Duchenne muscular dystrophy with hope
Translated from English and summarized by DistantNews. Read the original for the full story.
At a glance
- Egyptian child Anas Mohamed Allam is receiving treatment for Duchenne muscular dystrophy at Al Jalila Children's Hospital.
- He received Elevidys, a one-time gene therapy costing Dhs10.6 million that introduces a functional version of the dystrophin gene into cells.
- The treatment aims to help his body produce dystrophin, a protein that strengthens muscles as the disease progressively reduces muscle function.
At Al Jalila Children's Hospital, the story of Anas Mohamed Allam is framed as a journey from fear toward hope. The Egyptian child is confronting Duchenne muscular dystrophy, while his parents remain beside him through treatment and the daily challenges of a disease that gradually weakens the muscles and reduces mobility.
Anas received Elevidys, one of the world's most expensive treatments, at a cost of Dhs10.6 million. The therapy is delivered in a single intravenous session and introduces a functional version of the dystrophin gene directly into the patient's cells.
Duchenne muscular dystrophy is a neuromuscular condition caused by a defect in the dystrophin protein. Elevidys is intended to help the body produce this crucial protein, which supports muscle strength. For Anas and his family, the treatment represents a medical intervention carried out against a steadily progressive illness, with his parents providing what the article describes as a foundation of courage and comfort.
Originally published by Gulf Today in English. Translated, summarized, and contextualized automatically by DistantNews, with a note on how the source frames the story. Not individually reviewed before publishing. How this works.