Sad news about Brad Pitt. The announcement was made by the great actor himself:

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.

НЕR НUSВАND USЕD ТО ВЕАТ НЕR FRЕQUЕNТLY, SО SНЕ ТООK НЕR СНILDRЕN АND RАN АWАY FRОM НОMЕ

They say that if life hands you lemons, make lemonade. We all know that this is easier said than done, yet nothing is truly impossible if we set our minds to something and put in a lot of effort to achieve it.

Cara Brookins ended up in a vioIent marriage. She left her husband, took her kids with her, and started over in a new house since she was a mother of five and understood she had to protect her kids from the toxic environment they were made to live in. How was it accomplished by her? by creating her own construction blueprints and viewing YouTube videos that demonstrated various building skiIIs, such as installing plumbing, running a gas line, laying a foundation, and erecting walls. It sounds amazing, doesn’t it?

Now that she’s thinking about it, she acknowledges that it has been impossible the entire time.

Cara, a computer programmer analyst, came up with the idea to build her family’s new home from the ground up because she couldn’t afford to buy a house big enough for all of her children at the time she started building it in 2007.

Cara described the feeling as being that “if anyone were in our situation, they would do this.” “I know it sounds crazy now, but no one else saw it likе this.”

She borrowed about $150,000 for construction and paid $20,000 for an acre of land.

Her children helped build their 3,500-square-foot home; the eldest was only two years old at the time and the youngest was seventeen.

Since there was no running water on the property, her 11-year-old daughter Jada had to use buckets to carry water from the neighbor’s pond. Her son Drew assisted her in creating the plans. After that, she combined it with concrete bags weighing eighty pounds to create the foundation mortar.

The children would visit the site and assist every day after school. This tenacious mother paid $25 per hour to a part-time firefighter with building experience to complete the most difficult tasks. He was “a step ahead of us in terms of knowledge,” she recalled.

The family finally moved into Inkwell Manor on March 31, 2009, which was named in honor of Cara’s aspiration to become a writer.

“We felt ashamed that the only option available to us was to construct our own shelter,” Cara remarked. “We weren’t particularly proud of it, but it ended up being the best thing I could have done for myself.”

“Anything is possible for you if I, a 110-pound computer programmer, can build a whole house,” she exclaimed.

She continued, stating, “Select one goal and stick to it. Choose a big project you’ve always wanted to do, start small, and take the others who also need to recover with you. That has a great deal of power.

This isn’t it one of the most amazing tales you’ve heard recently?

If this family’s tenacity inspires you as much as it does, please SHARE their amazing tale on Facebook with your loved ones!

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