Actor Brad Pitt revealed in a recent interview that he suffers from prosopagnosia, a rare neurological disorder also known as “facial blindness.”
Dani Blum describes the disorder’s signs, causes, and remedies in an article for the New York Times.
Borna Bonakdarpour, a behavioral neurologist at Northwestern Medicine, claims that face blindness—not color blindness or general vision impairment—is the main symptom of prosopagnosia.
The National Institute of Neurological Disorders and Stroke states that there is no connection between the illness and memory loss, vision problems, or learning impairments.
Blum continues, “It is not the same as forgetting or occasionally having trouble finding the correct word.
The severity of prosopagnosia will differ from person to person.
For instance, some people might have problems identifying a familiar face, such as that of a close friend or relative, while others might have trouble identifying their own reflection.
Additionally, some people might not be able to distinguish between faces and objects.
Notably, some data indicates that individuals with prosopagnosia may have chronic anxiety or depression due to the loneliness and fear that are frequently associated with the illness.
Blum notes that some people avoid contact with family members and other loved ones out of concern that they won’t be able to properly recognize or acknowledge them.
“Navigating basic social relationships with prosopagnosia can become difficult,” she says.
Pitt admitted that he has trouble recognizing people’s faces for years in a recent interview with GQ, despite never having gotten a formal prosopagnosia diagnosis.
In fact, Pitt claimed in a 2013 interview with Esquire that his difficulty recognizing people’s appearances was so great that it frequently made him want to isolate himself.
He explained, “That’s why I stay at home.
What is the condition’s cause?
People who are diagnosed with prosopagnosia often fall into one of two categories: either they are born with it or they acquire it.
However, estimations reveal that as many as one in every 50 people may struggle with some lifetime form of the disorder, and experts hypothesize that it may run in families.
According to Blum, research “suggests that congenital, or lifelong, prosopagnosia is less prevalent.”
According to Andrey Stojic, director of general neurology at the Cleveland Clinic, children born with the illness “don’t seem to have any visible structural abnormality” in the brain.
Notably, doctors don’t fully understand what causes congenital prosopagnosia because there aren’t any obvious brain lesions in persons who have it.
In contrast, people who develop prosopagnosia later in life may have brain abnormalities brought on by a trauma or head injury.
According to Bonakdarpour, individuals can also develop prosopagnosia while dealing with Alzheimer’s illness or following a stroke.
What therapies are available for prosopagnosia?
Prosopagnosia is now untreatable, according to Bonakdarpour. The problem can be treated, though.
People who have the syndrome frequently attempt to distinguish between people by focusing on physical characteristics like hair color, gait, or voice.
This kind 8-year-old paid off his friend’s school lunch debt after he was denied food
Cayden Taipalus, eight years old, is here to restore your confidence in humanity, so do not lose hope if you feel that it has been lost.
This young man decided to take matters into his own hands after noticing that one of his buddies was not receiving a warm breakfast at school.
Specifically, Cayden witnessed his friend receiving a sandwich rather than a hot dinner at Challenger Elementary in Howell, Michigan, one day because there weren’t enough money in his lunch account. His heart was broken, and he felt compelled to change things.
After getting home, Cayden immediately told his mother what he had seen and that it had made him feel a little depressed. His mother, Amber Melke-Peters, concurred that action was necessary to stop incidents like that from happening in the future, so together they devised the concept of creating a fundraising website named “Pay It Forward: No Kid Goes Hungry.”
Cayden asked for donations to cover his friends’ lunch debts from neighbors, relatives, and friends. His endeavor, nevertheless, went beyond financial gain because many were inspired by his narrative as it spread.
In an effort to generate money on his own, he even launched a recycling drive. He then addressed the school’s lunch staff and asked that the money be transferred to the accounts of students who were having financial issues.
More than $41,000 has been raised since Cayden launched his effort, allowing him to feed many underprivileged pupils.
Cayden’s ultimate goal is to ensure that no child misses a school day without a hot meal.
“I am so very proud of my son,” his mother declared in an interview with ABC News. His understanding of this notion at the age of eight is quite remarkable, in my opinion. His heart is made of gold.
What started as a stirring feeling in Cayden’s gut turned into an initiative that might guarantee that many kids have hot lunches.
Many people appreciated him and were motivated to support his initiative.
We think this is a fantastic initiative you choose to work on, and we contributed to it. I’m hoping that your idea has received a nomination for the Make a Difference initiative. Someone wrote, “Cayden, you have really made a difference. You have done an amazing job of helping a lot of kids.” You wouldn’t imagine that children would go hungry in a land of plenty, but in actuality, for a lot of youngsters, the food they consume at school can be their only meal of the day. It breaks my heart. As they say, it takes a village to raise a child, and by doing this, we can contribute to the upbringing of a few children while preserving their dignity.
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