The influencer dies after hospitalization for sickle cell anemia

The influencer dies after hospitalization for sickle cell anemia


Bahian Jeane Passos was 34 years old and spoke about beauty, fashion and home to more than 44 thousand followers

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The fashion influencer Jeane Passos He died at the age of 34, after being hospitalized due to complications related to sickle cell anemia. According to the newspaper Mailthe information was confirmed by the influencer’s team this Thursday 16th.

Yesterday Jeane’s Instagram profile was used for a statement explaining that Jeane could not use her cell phone and for requests for prayers.

“With this message, out of respect for my followers and collaborators, I inform you that Jeane is hospitalized due to complications related to sickle cell anemia. At this moment she cannot access her cell phone. I ask for prayers for her, so that God restore her life”, reads the note.

The influencer has become famous for sharing her hair transition with her followers and specializes in fashion and beauty content.

The funeral wake and burial of the influencer took place this Thursday the 16th at the Bosque da Paz cemetery. Earth reached out to the influencer’s team, but has yet to receive a response.

Sickle cell anemia

According to the Ministry of Health, sickle cell anemia (sickle cell anemia) is a genetic and hereditary disease characterized by a mutation in the gene that produces hemoglobin (HbA), which gives rise to a mutant hemoglobin called S (HbS), transmitted recessive.

In people with sickle cell disease, the red blood cells (RBCs), which under appropriate conditions are round, take on the shape of a “half moon” or “sickle” (hence the name “sickle cell disease”). This change in shape occurs in situations of physical exertion, stress, cold, trauma, dehydration, infections, among others. In this form, red blood cells do not oxygenate the body satisfactorily because they have difficulty passing through blood vessels, causing poor circulation throughout almost the entire body.

The clinical manifestations of sickle cell anemia can therefore affect almost all organs and systems, manifesting themselves starting from the first year and lasting for life. The main ones include: pain attacks, jaundice, anemia, infections, hand-foot syndrome, splenic sequestration crisis, stroke, priaprism, acute chest syndrome, aplastic crisis, ulcerations, osteonecrosis, renal and ocular complications, among others, including complications late ones linked to iron overload secondary to transfusions.

Source: Terra

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