The influencer gained popularity thanks to his good mood despite profound physical suffering
Epidermolysis bullosa (EB) is hereditary, rare, incurable and non-contagious. A genetic change causes severe blistering and sores on the skin, with pain comparable to second- and third-degree burns. The fingers end up “wrapped” limiting the wearer’s independence.
Looking like a child, Dai, 31, has made videos in which he describes the difficulties of living with such fragile skin and the fight against prejudice. Vain, she received countless compliments for her elegance.
Even with his arms and legs bandaged and with wounds on his body, including his face, he performed TikTok dances and comedic tendencies. Her activity seemed to make her happier.
Last year Daiane was being treated for leg cancer, according to the NGO Jardim das Borboletas, which provides care for people with rare skin diseases.
The fragile and charismatic influencer has become an example of resilience. The video app brought fame and provided friendships. The announcement of his death on his profile generated a wave of laments and tributes.

@daicruzoficial #epidermolisibollosa #jequiébahiabrasil #tic toc #dance ♬ original sound – Dai Cruz Oficial
Source: Terra

I am Amanda Gans, a motivated and ambitious professional in the news writing industry. With over five years of experience in this field, I have developed an eye for detail and an ability to craft stories that captivate readers. I currently write for Gossipify, where I specialize in beauty & celebrities news. My passion lies with exploring the world of beauty through writing, interviewing experts and developing articles that are both informative and entertaining.
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