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.
Days before she died, a courageous young girl was brought down the aisle by her father to marry her school sweetheart
If you ask any parent in the world, they’ll probably tell you that they would do anything for their child. Our lives transform in the most profound ways the day we become parents. We acknowledge that we will take care of, treasure, and worry about the new life we have brought into the world for the remainder of our days here on Earth.
However, regrettably, there are some things that parents are powerless to stop. Each year, far too many children suffer from circumstances and illnesses that are completely beyond their control. Accidents and disease are as much a part of human life as happiness and celebration.
The day Alina and Aaron Edwards found out that their nine-year-old daughter, Emma, had been diagnosed with acute lymphoblastic leukaemia, altered their entire world. They were dealt a heartbreaking blow when physicians informed them after a few months that there was nothing more they could do to save Emma’s life, despite their obvious anguish and desperation to hold onto the hope that she could overcome cancer.
With the limited time they had left, Emma’s anguished parents resolved to do everything in their power to grant their daughter’s desires. Of course, it goes without saying that the great majority of kids would relish the opportunity to meet a famous hero in such a situation, maybe go to Disneyland or watch their idol compete on the pitch.
Emma, however, had completely different wishes. She requested permission to wed DJ, her ten-year-old boyfriend. After Sunday, I will have so much more to say and so many people to thank, but for now, my brain is simply not working properly, and I
Emma’s campaign quickly gained a lot of support from her neighbourhood. The group of supporters and volunteers took on the moniker “Emma’s Army” and decided to fulfil this young girl’s aspirations before it was too late. Emma’s family eventually received assistance in raising money from the Make-A-Wish Foundation. “Most kids want to go to Disneyland, but Emma wanted to get married, be a wife, and have three kids,” Emma’s mother Alina clarified.
Reports state that Emma and DJ had attempted to get married before their “wedding.” When they were eight years old, the two kids attempted to tie the knot in school, choosing their own groomsmen and bridesmaids from among their peers. Sadly for Emma and DJ, though, their teacher would not allow the wedding to take place, no matter how informal.
But this time, their second attempt at marriage had the support of many wonderful people who wanted Emma to have the day of her dreams, as well as the approval of their parents. In less than two days, we put it together, and everything was donated in the end. It came together so beautifully and was so wonderful, Alina disclosed.
When the big day finally arrived, it was recorded on tape featuring interviews with a few guests, including the DJ and the groom. She struck me as the most gorgeous person I have ever laid eyes on. I’ve adored her ever since,” DJ remarked. Alina, on the other hand, was gushing about her daughter’s charming young partner. She sent a tearful message on Facebook that said
Since third grade, DJ has been Emma’s “Boo bear.” I promise that watching these two adorable together will make your heart melt. Her heart leaps when DJ helps and shields her. She adores him. I also know that he adores her! He has supported her through all of her highs and lows, never letting her smile. DJ and his family will always remain connected.
Emma’s big day finally arrived on June 29 when she arrived at the location pushed by her parents in a wheelchair. For the event, she dressed elegantly in purple, and she grinned as her father led her down the aisle. After exchanging vows and rings, Emma and DJ finished the ceremony with a kiss from DJ to his bride.
Emma went back to her bed to recuperate after the wedding, but everyone could see how happy she was to have experienced her special day. After her battle, young Emma passed away a few weeks later on July 11, 2023.
Emma’s obituary stated: “On July 11, 2023, Emma Brooks Edwards passed away and was embraced by her closest loved ones as she entered paradise in the tender arms of her great-grandma Frannie Annie. Emma, then ten years old, fought leukaemia, dubbed “The imposter,” for sixteen months.
The Edwards family was completed with the birth of Emma, our little unicorn, on April 22, 2013, to devoted parents and three elder siblings. She cherished DIY projects, clever jokes, her loved ones, Jesus, and her brand-new “husband,” DJ. To everyone she encountered and to those who loved her, Emma was an inspiration. She was the most wonderful friend, cousin, aunt, “wife,” haha, sister, grandchild, and cousin. Her legacy is one of humour, fortitude, and unending love for everyone.
Emma, rest in peace. A young girl of such beauty, taken far too soon. Please join us in extending our condol
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