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Home https://server7.kproxy.com/servlet/redirect.srv/sruj/smyrwpoii/p2/ Health https://server7.kproxy.com/servlet/redirect.srv/sruj/smyrwpoii/p2/ Baby born with a rare skin condition will remove the Batman-shaped patch

Baby born with a rare skin condition will remove the Batman-shaped patch



<p class = "canvas-atom canvas-text Mb (1.0em) Mb (0) – sm Mt (0.8em) – sm" type = "text" content = "6-month-old Florida born rarely skin condition will undergo a series of operations to remove a dark patch of the face resembling the symbol Batman . "data-reactid =" 16 "> a 6-month-old Florida girl born with a rare skin condition will undergo a series of operations to remove the dark patch of the face resembling the symbol Batman .

<p class = "canvas-atom canvas-text Mb (1.0em) Mb (0) – sm Mt (0.8em) ̵

1; sm" type = "text" content = "Luna Fenner's family will travel to Russia, to have the girl treated for congenital melanocytic nevus, Luna's mother, Carol Fener, & nbsp; Inside Edition Congenital melanocytic nevus is a skin condition characterized by "unusually dark" body, & nbsp; according to the US Department of Health and Human Services . People with the disease are at high risk of developing melanoma, according to the agency. "data-reactid =" 17 "> Family Luna Fenner's vote will travel to Russia to treat the girl for congenital melanocytic nevus, said Luna's mother, Carol Fenner, Inside Edition . Congenital melanocytic nevus is a skin condition characterized by an "unusually dark" patch on the body, according to the US Department of Health and Human Services. People with the disease are at high risk of developing melanoma, according to the department.

<p class = "canvas-atom canvas-text Mb (1.0em) Mb (0) – sm Mt (0.8em) – sm" type = "text" content = "" We will remove it, "says Carol ["Thiscanturnintocanceralsobecauseoftheharassmentandthethingsweexperiencewhenwegoout Inside Edition ." People say bad things about it. "" data-reactid = "18"> "We will remove it," says Carol Inside Edition . "This can turn into cancer, also because of the bullying and the things we go through when we go out. People who say bad things about it. "

Baby born with rare skin The status will remove the patch in Batman format

<p class = "canvas-atom canvas-text Mb (1.0em) Mb (0) – sm Mt (0.8em) – sm" type = "text" content = "Carol was" shocked "when she gave birth to Luna in March and saw a dark patch covering much of the girl's face, she & nbsp; told WPLG . She began looking for treatment options after as light in the US, they recommended Luna undergo several surgeries over the next four years. "data-reactid =" 30 "> Carol was" shocked "when she gave birth to the moon in March and saw the dark patches covering much of the girl's face, he said. she before WPLG. She began looking for treatment options after US doctors recommended that Luna undergo multiple surgeries over the next four years.

"We have seen many doctors. We went to Boston, Chicago and New York, trying to find a better result, "she told WPLG.

Soon a Russian doctor contacted his desperate mother: "He said, 'Come here. I can do something they don't do in the US. ""

<p class = "canvas-atom canvas-text Mb (1.0em) Mb (0) – sm Mt (0.8em) – sm" type = "text" content = " RELATED: This 6 a year-old boy has a disease so rare doctors say he is the first to receive it "data-reactid =" 33 "> RELATED: This 6-year-old boy has a disease so rare doctors they say that he is the first to receive it

<p class = "canvas-atom canvas-text Mb (1.0em) Mb (0) – sm Mt (0.8em) – sm" type = "text" content = "Russian surgeon Dr. Pavel Popov will perform up to eight operations in 18 months, & nbsp; according to SWNS . Carol and Luna will travel to Russia while the husband of Carol, Tiago Tavares, remains back in Florida, she said. "Data-reactid =" 34 "> Russian surgeon Dr. Pavel Popov will perform up to eight surgeries in 18 months, according to SWNS. Carol and Luna will travel to Russia while Carol's husband, Tiago Tavares, remains in Florida, she said.

"Everybody thinks I'm crazy to go to Russia, but I've done a lot of research and got advice from several doctors and I really think it's the best option for the moon right now," she told SWNS. "It will be a huge relief if it works for the moon. I don't want her to be harassed. People ask if it is contagious and say they really mean things. ”

<p class =" canvas-atom canvas-text Mb (1.0em) Mb (0) – sm Mt (0.8em) – sm "type =" text "content =" A & nbsp; Page GoFundMe, created & nbsp; in April to cover family travel, and Luna's medical expenses raised nearly $ 40,000. " data-reactid = "36"> A GoFundMe page created in April to cover family travel and Luna's medical expenses raised nearly $ 40,000.

<p class = "canvas-atom canvas-text Mb (1.0em) Mb (0) – sm Mt (0.8em) – sm" type = "text" content = "" Hi, I'm the Moon ", begins page written in terms of the moon. "I'm 4 months old. I was born with a rare disease that affects 1.5% of the world's population called congenital melanotic nevus. "" data-reactid = "37"> "Hi, I'm the moon," begins the page, which is written from the perspective of the moon. "I am 4 months old. I was born with a rare disease that affects 1.5% of the world's population called congenital melanotic nevus. "

" People like me with big moles get more than their fair share of looks, looks, whispers, and finger pointing, "the statement continues. "It's heartbreaking for my parents and can have a detrimental effect on me as I grow up. I need your help because I want to be a normal kid and have a normal life. “


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