The disease is progressive, meaning that symptoms worsen over time. Most people with Duchenne muscular dystrophy need to use a wheelchair from adolescence and their life expectancy is reduced.
Angelo and Luly’s fight
Since Ángelo was diagnosed at age 10, Luly Bossa became his main support and confidant. The actress not only provided her son with the necessary love and care, but she also became an important voice to make the disease visible and advocate for research into a cure.
Through her social networks and interviews, the actress shared with the world the happy and difficult moments of Angelo’s life. Her bravery and resilience inspired thousands of people who identified with his story.
Despite the difficulties, Ángelo filled the lives of the 60-year-old Barranquilla woman and everyone who knew him with joy, love and hope. His fighting spirit and his passion for music and art made him an example of improvement.
Angelo’s departure leaves an immense void, but his legacy of love and hope will continue to live on in the memories of all those who knew him and were moved by his story.
Did the illness that Luly Bossa’s son suffered have a cure?
Although there is no cure for Duchenne muscular dystrophy, there are advances in research that offer new hope for the future. It is important to support organizations working to find a cure and improve the quality of life of people living with this disease.
2024-03-09 17:03:48
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