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The legal battles of many Colombians to obtain medicines for their treatments are reflected in the complaint that he recently made public Luly bossa. In her Twitter account, the Barranquilla actress stated that a court ruling denied him access to a “vital medicine available to us” for the treatment of his son Angelo.
“It is not the first time, and it sure is not the last, but nor of covers this stays like that. If God is with me, who is against me? #teamoAngelo ”, Bossa wrote in his publication that he accompanies with a video in which he is seen crying.
It is not the first time, and surely it is not the last, but neither covers it this way. If God is with me, who is against me? #teamoAngelo pic.twitter.com/I7jCmsZmBu
– Luly Bossa (@LulyBossaTheOne) December 11, 2020
Part of his treatment and Angelo’s life is shared by the actress on her social networks. These videos show the progress that the 17-year-old has been making and her dedication as a mother.
Angelo Bossa was diagnosed with Duchenne Muscular Dystrophy (DMD). This is a hereditary disorder characterized by progressive muscle weakness that generally occurs in boys. Most people with muscular dystrophy have Duchenne syndrome. As noted by specialists, symptoms include frequent falls, difficulty getting up or running, large calves, and learning disabilities. Although science has yet to find a cure, physical therapy and medications, such as corticosteroids, can control symptoms and improve quality of life.
Luly Bossa’s claim on Twitter became a trend in Colombia. Many of his followers expressed their support to be able to get the vital medicine that his son urgently needs today.
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