Meet five-year-old Yunus Kidwai who’s affected by a uncommon dysfunction named Duchenne Muscular Dystrophy (DMD). His tender thoughts can’t fathom the severity of the uncommon genetic dysfunction the place he’s carrying out his muscle groups with every passing minute and making even getting off the bed a harrowing job for him.
Yunus was recognized with this illness in 2023 when his mother and father realised that he was not capable of carry out regular bodily duties. After intense therapy and prognosis on the PGI Lucknow, his case was referred to AIIMS New Delhi.
Talking to India At the moment TV, Yunus’s 39-year-old father, Fazal Kidwai, stated that his son is working out of time and his muscle groups are getting broken with every passing day.
A prescription-based gene remedy that consists of an injection is required to deal with the uncommon illness. However the price of treatment–over Rs 26 crore for a single shot– has posed an insurmountable job earlier than his mother and father.
Talking to India At the moment TV, Kulsum Aziz Kidwai, mom of Yunus, received emotional and stated that he’s the one youngster she has and can’t see him dropping his life with every passing day.
Interesting to individuals for mass funding, younger mother and father say that folks’s contributions, no matter measurement, is usually a lifeline for his or her youngsters’s therapy.
Each mother and father have additionally began a web-based marketing campaign to garner assist for his or her son. They’re working the marketing campaign by means of a social media deal with on Instagram and asking individuals to assist even with the smallest contribution to avoid wasting the lifetime of Yunus.