He was given 6 months to live, made a wish list, and died at 24: today his mother is fulfilling the pending dreams
A mother is honoring her late son’s wish list after he was diagnosed with a terminal condition and passed away at just 24 years old.
Arthur Case: MP accuses man of creating fake PIX key to divert donations for treatment of child with rare disease
A man has been charged in São Paulo for creating a fake PIX key to steal donations intended for a child's medical treatment.
Scammer creates similar PIX keys to divert donations intended for the treatment of a 6-year-old child
A family in Sorocaba, Brazil, fell victim to a scam diverting donations meant for their son's costly treatment for Duchenne Muscular Dystrophy.
Young man with a rare disease passes in Law at UFPR and fights for the inclusion of people with disabilities: 'Fighting for myself and for others too'
Charleston Júnior, a 21-year-old diagnosed with Duchenne Muscular Dystrophy, has been accepted into Law School at the Federal University of Paraná and is determined to advocate for the rights of people with disabilities.
Getter Meresmaa's debut performance presents the story of a young person with special needs
Getter Meresmaa's debut performance "See You Again, Simon!" focuses on the life of a teenager named Simon with Duchenne muscular dystrophy, based on a true story by New Zealand author David Hill.
Sudanese family struggles to treat their son suffering from a rare genetic disease
The article highlights the struggles of a Sudanese family to obtain gene therapy for their son Imad, who is affected by Duchenne muscular dystrophy, a severe rare genetic disorder in children.