A woman with a terrifying genetic condition that causes blisters and oozing pain on her skin proudly shows her scars in a series of sexy photos to prove that she doesn’t stop accepting her natural beauty. I’m showing off to.
Fernanda Tanajura, an influencer from the Brazilian Libramento de Nossa Senora, was born with a rare condition called epidermolysis bullosa (EB). This genetic disorder is caused by the thinning and sensitivity of the skin due to the irregularities of collagen in the skin, which means that friction with the skin can cause blisters and pain.
Having lived in her lifetime, it is something Fernanda is accustomed to dealing with.
As a child, she couldn’t play in many outdoor areas because trees and shrubs could rub against her skin, but Fernanda wasn’t treated differently by other children. ..
Proud: A Brazilian woman born in a rare condition that causes blisters and pain on her skin proudly shows off her scars in sexy photos.
Overcoming Obstacles: Influencer Fernanda Tanajura in her twenties was born with a rare condition called epidermolysis bullosa. This thins the skin and makes it sensitive to rubbing.
Struggle: As a result of her EB, Frenanda remains covered with blisters and pain resulting from the slightest rubbing of her skin.
Fernanda needs to maintain a rigorous skin care regime that uses sunflower oil and body cream daily to moisturize the skin in order to control her condition. She also has to dress for any pain with bandages that change them daily.
Throwback: Fernanda was diagnosed with a childhood condition and since then she had to wear a bandage on her skin to protect it.
Fernanda’s hands are the most affected area, as the skin here encounters the most friction. This trauma and lack of movement caused muscle atrophy. This means that Fernanda’s hand muscles are wasted.
Nevertheless, Fernanda is unrestrained and can live independently regardless of her limited movements.
She was particularly proud to understand how to make up despite her condition.
Although not as painful as most people think, Fernanda regularly bandages her hands to protect her skin from further damage. She rarely experiences noticeable pain.
Fernanda has always been loved and supported by family and friends, but he also has followers online. Fernanda started posting on social media like any other teenager, but soon became the voice of people with epidermolysis bullosa.
Although rare, Fernanda encountered an online vandalism that criticized her appearance. However, the majority of her followers praise her self-confidence, and it is these people who motivate influencers.
She wants to continue to reach out to people with epidermolysis bullosa, who are often underestimated and unrecognized.
Side effects: Influencers say that the condition actually causes little pain, but it wastes the muscles of the hands.
Inspiration: Fernanda hopes to show off her condition with sexy photos to help give others with EB the confidence to accept their appearance.
Fighter: She’s proud that she doesn’t allow her condition to prevent her from accepting her life-and Fernanda puts on her own makeup despite the lack of mobility in her hands. I even learned to do
“I have had an EB ever since I was born,” Fernanda said. “It is considered rare and it has a major impact on my health and daily life.
“I need to maintain a daily skin care routine, change dressings, and may need medical monitoring if my condition worsens.
“Nevertheless, when I was a kid, I didn’t realize I was different. All my friends treated me normally.
“I had some restrictions. I couldn’t set foot in the forest or similar outdoor spaces because the vegetation could hurt me, but that’s what I take for that age. I had a very happy childhood.
“I developed atrophy with my own hands, but I can incredibly learn to adapt and do almost everything normally, including my makeup.
“EB is not as painful as people think. It rarely causes pain unless it is seriously injured. In my daily life, I live fairly normally.
“Even now, my friends and whole family support me. My condition never prevented me from connecting with people.
“I’m single now, but my EB hasn’t affected any of the relationships I’ve had. People look past it.”
Blooming Love: She says her condition has never affected her relationships and explains that most people can “see the past” with her EB.
Brave: Fernanda admits to receiving negative comments on social media posts, but argues that the trolls don’t let them feel confident.
Praise: “I received so many comments about my aggressiveness and people complement my appearance,” she said.
Fernanda started posting his photos on Instagram in 2014.
“Posting to Instagram was very natural to me, as I’m passionate about photography and never worried about what others think,” she said.
“I received so many comments about my positivity and people complement my appearance.
“It made me feel very welcome. There have been several verbal attacks that criticized my appearance and merciful me, but people are rarely negative.
“I don’t have to sympathize and I don’t want to please everyone, but respect is essential.
“I want to reach out to more people like me – to increase expression and bring something positive to people’s lives.
“I want to be a professional model someday. It’s a big dream for me and a great thing for EB’s expression.
“Living with EB is not always easy, but the sum of the positive experiences I have motivated me to believe that I have a greater purpose.”
Women in conditions that cause blisters and pain show them off with sexy pictures
Source link Women in conditions that cause blisters and pain show them off with sexy pictures