In Northeast Ohio, there’s been talk lately about this unusual and intriguing critter that resembles a hybrid between a skunk and a squirrel.
The creature, called a “squnk,” has a squirrel’s body but a skunk’s dark black fur and white-tipped tail:
Recently, there have been multiple reports of sightings of this unusual creature in Ohio, and pictures of it have gone popular on social media. According to some theories, the “squnk” may indeed be a cross between the two species.
It turns out that this “squnk” is a black squirrel. Even without any skunk DNA, it’s still a really uncommon sight. According to Smithsonian Magazine, black squirrels are the offspring of coupling eastern gray and fox squirrels. The squirrel in question is actually an eastern gray squirrel that got a gene variation that gave it a darker pigmentation.
There is only one black squirrel for every 10,000 squirrels, making them extremely rare. They are able to stay warmer in the winter and in colder climates thanks to their darker coat, which gives them a thermal advantage over typical gray squirrels.
Since their release on campus in 1961, ten black squirrels have been an iconic feature of Kent State University, earning them the title of unofficial mascot.
Therefore, don’t worry if you see a “squnk” in Ohio; it’s only a black squirrel with some fur on its tail that resembles that of a skunk, and you won’t get sprayed.
What a remarkable creature, wow! Even while it may not be a squirrel-skunk hybrid, it is nevertheless a rare critter to find.
If you are an animal lover, please share this tale!
’’We Got Stares’’, Parents Choose to Remove Baby Girl’s Rare Birthmark to Avoid Rude Reactions
A happy mom recently told the story of how her little girl said goodbye to a birthmark on her forehead, even though they initially faced some criticism from doctors.
A very uncommon birthmark.
© viennarosebrookshaw / Instagram, © viennarosebrookshaw / Instagram, © viennarosebrookshaw / Instagram
Here’s the story of Celine Casey and her two-year-old daughter, Vienna Shaw. Vienna was born with a rare birthmark called congenital melanocytic nevus (CMN) on her forehead, which only occurs in one out of every 20,000 newborns.
When Celine learned about the birthmark, she felt worried and wondered if she had done something wrong during her pregnancy. She didn’t know what the birthmark would mean for Vienna but was determined to remove it so that her daughter could grow up without feeling different.
© viennarosebrookshaw / Instagram
Even though the birthmark didn’t affect Brookshaw’s physical health, Casey knew it could impact her daughter’s mental well-being as she grew older and interacted with other children who might be curious about her condition.
Celine shared that the family sometimes used to hide Vienna’s birthmark by covering her face when they went out. She said, “We went out daily with her and got a few stares.”
The surgery was challenging.
© viennarosebrookshaw / Instagram
When they sought help from the NHS, the family received disheartening feedback. Doctors couldn’t go ahead with the surgery to remove the birthmark, categorizing it as a cosmetic procedure.
However, the parents viewed it differently. They were genuinely worried about potential teasing from other kids, which could affect their daughter’s mental well-being at a young age. Casey was also concerned that if they didn’t remove the birthmark, her daughter might grow to resent her and her partner.
© viennarosebrookshaw / Instagram, © viennarosebrookshaw / Instagram, © viennarosebrookshaw / Instagram
The parents took matters into their own hands and privately raised the required funds. Through crowdfunding, they managed to gather $52,000 within 24 hours. However, due to increased hospital costs in 2020, they had to raise an additional $27,000. With a new funding request, they eventually reached their goal.
They encountered difficulties with doctors.
© viennarosebrookshaw / Instagram
Disagreements between the medical team and the parents have led to differing opinions. Vienna’s parents wanted the birthmark removed through surgery, but the surgeon refused to perform the procedure. The surgeon’s stance is rooted in the belief that the child should make the decision once she reaches an appropriate age.
After this controversy arose, Daniel Brookshaw, Vienna’s father, expressed his dissatisfaction with the doctor’s viewpoint. The doctor also consulted with a dermatologist who concurred with the surgeon, emphasizing that the birthmark doesn’t threaten Vienna’s health and is not cancerous.
The surgery was completed successfully.
© viennarosebrookshaw / Instagram
Vienna is now two years old, and her doctors have successfully removed her birthmark, leaving only a faint scar between her eyebrows. Casey regularly shares updates on Shaw’s scar and recovery process on her social media, and followers often comment on how beautiful her little girl looks.
Despite the birthmark being gone, Casey mentioned that they still have to travel between cities to check the healing of the scar and see if any additional procedures are needed beyond the three she has already undergone. Shaw is now enjoying the typical life of a two-year-old.
© viennarosebrookshaw / Instagram
This little girl’s case with her birthmark brings attention to the delicate balance between parental advocacy and a child’s autonomy in medical decisions. While her parents aimed to secure her social acceptance and well-being, medical professionals stressed the importance of respecting Vienna’s future autonomy over her own body.
This story serves as a reminder of the intricate ethical considerations that arise when navigating the boundaries of parental authority and individual autonomy, prompting broader reflections on the rights of minors in the medical realm.
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