Bahian Jeane Passos was 34 years old and spoke to more than 44,000 followers about beauty, fashion and home
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The influencer became known for sharing her hair transformation with her followers and specialized in fashion and beauty content.
Photo: Reproduction/ Instagram
The fashion influencer Jeane Passos He died at the age of 34 after being hospitalized due to complications from sickle cell anemia. According to the newspaper Correio, the information was confirmed by the influencer’s team this Thursday the 16th.
Yesterday, Jeane’s Instagram profile was used for a statement explaining that Jeane could not use her cell phone and was asked for prayers.
“With this message, out of respect for my followers and partners, I would like to inform you that Jeane is in the hospital due to complications from sickle cell anemia. At the moment she cannot access her cell phone. “I ask for prayers for her so that God can restore her life,” the note said.
The influencer became known for sharing her hair transformation with her followers and specialized in fashion and beauty content.
The influencer’s wake and burial took place this Thursday, the 16th, at the Bosque da Paz Cemetery. Earth has contacted the influencer’s team but has not yet received a response.
Sickle cell anemia
According to the Ministry of Health, sickle cell disease (SCD) is a genetic and hereditary disease characterized by a mutation in the gene that produces hemoglobin (HbA), resulting in a mutated hemoglobin called S (HbS), which is inherited in a recessive manner.
In people with SCD, the red blood cells (red blood cells), which are round under appropriate conditions, take the shape of a “crescent” or “crescent” (hence the name “sickle cell anemia”). This shape change occurs in situations of physical exertion, stress, cold, trauma, dehydration and infections, among others. In this format, the red blood cells do not provide the body with enough oxygen because they have difficulty passing through the blood vessels, resulting in poor blood circulation throughout almost the entire body.
The clinical manifestations of sickle cell anemia can therefore affect almost all organs and systems, starting in the first year and lasting throughout life. The most important include, among others: pain attacks, jaundice, anemia, infections, handfoot syndrome, splenic sequestration crisis, stroke, priaprism, acute chest syndrome, aplastic crisis, ulcerations, osteonecrosis, renal and ocular complications, including late complications iron overload resulting from transfusions.
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