Fur provides much-needed insulation from the cold, making it necessary for many animals.Besides, it makes them look different; there are some animals you would not even recognize when they are completely bald.
Rescuers have just brought in a more uncommon creature that resembles a hairless cat. Learn more about this unique species and her unlikely survival by reading on.
Hope for Wildlife, a nonprofit conservation organization in Nova Scotia, adopted the most bizarre animal last month. According to the Canadian Press, a couple in West Arichat discovered the animal in their property, suffering from the cold.
At first sight, the creature looks like a Sphynx cat, but it’s actually a completely hairless raccoon!
When their characteristic mask-like fur pattern is absent, raccoons are very hard to spot. This little creature is a northern raccoon, and it is completely bald due to severe alopecia.
The rescue said that while there have been cases of balding raccoons in the past, this one is unlike any other: “It’s just tufts of fur around the snout, ankles and feet.” Hope Swinimer, director of Hope for Wildlife, alerted the Canadian Press to the gravity of the issue.
The raccoon has been named Rufus in commemoration of the character from the Kim Possible cartoon who is a naked mole rat, even if it is a female.
The rescue said on Facebook that they are still trying to figure out why she is losing her hair, but they believe it could be an autoimmune disorder that is damaging her hair follicles. They found that her skin appeared healthy and ruled out parasites, fungal infections, and mange.
This precious little girl made her entrance into the world adorned with “polka dots”: Check out how stunning she is at the age of 8!
Rebecca Callaghan faced a challenging pregnancy in 2012 when doctors decided to induce labor early due to excess fluid around her baby.
It wasn’t until about an hour after Matilda was born that any issues were suspected. Initially, a large blue mark on her face and extending down her body was mistaken for a bruise. However, just 30 minutes later, doctors informed Rebecca and her husband that it was, in fact, a birthmark.
Two weeks postpartum, Matilda was diagnosed with Sturge-Weber syndrome, a rare neurological condition associated with skin abnormalities that can lead to paralysis, learning difficulties, and seizures.
Matilda’s health quickly deteriorated, necessitating her transfer to Alder Hey Children’s Hospital in Liverpool, England. The parents’ joy transformed into deep anxiety, as they feared they might lose their newborn. “We couldn’t travel with her because she was so sick. Watching her taken away, we were terrified we’d never see her again”, her father shared with the Daily Mail.
Adding to their worries, they discovered Matilda had two heart defects. Despite the grim prognosis, she displayed remarkable resilience, successfully undergoing surgery. She also began laser treatments to address her unusual birthmark, a process that could take up to 16 hours to fully fade.
“She receives treatments every two months. The laser leaves her skin red and covered in blisters, which eventually heal”, her father, Paul, explained in a 2016 interview. He recounted the misconceptions from others, stating: “People assume we’ve somehow harmed her”.
Although these treatments are painful, Matilda is a cheerful child. Sadly, many stare at her or make hurtful remarks, even asking if her parents had caused her birthmark by allowing her to burn herself. “They only see the surface and make judgments. I wish they could see beyond the mole to the beautiful person she is”, Paul lamented.
In addition to her birthmark, Matilda faces vision challenges and struggles to walk. Yet, with the help of specialized equipment, she has taken steps on her own.
Despite her struggles, Matilda remains upbeat and resilient. “She’s incredibly stubborn; she’ll do things her way or not at all!” her father noted, emphasizing that she always greets others with a smile. The family regularly confronts stares, insults, and teasing, but they remain proud of Matilda. “Despite everything, she’s thriving”, her father said.
Now nine years old, Matilda’s family recently shared an updated photo of her in her wheelchair in June 2019. They have set up a fundraising page to raise £5,000 for a new wheelchair, enabling Matilda to enjoy her favorite activity: spending time outdoors, away from crowds. “We want to help her continue doing what she loves”, the page states.
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