On October 1, 1924, James Earl Carter Jr. was born in Plains, Georgia. James Earl Carter Sr., his father, was a prosperous businessman who made investments in farms. Carter was born in the Wise Sanitarium, where his mother, Bessie Lilian, was employed as a nurse.
Young Carter attended the local high school from 1937 to 1941. Motivated by his father’s World War I service in the U.S. Army Quartermaster Corps, he pursued his desire of serving in the armed forces and was accepted into the Naval Academy in 1943.
Carter wrote in the book What Makes a Marriage Last by Phil Donahue and Marlo Thomas that he felt an immediate connection with his wife, Rosalynn. In 1946, following Carter’s graduation from the Naval Academy, the youthful pair tied the knot. Carter gave his all to his family, which now consisted of his wife, four kids, and the family company, after leaving the Navy. He constructed a ranch-style home in Georgia in 1961 for his family; it is currently estimated to be worth $210,000. The Washington Post claims that Carter chose not to leverage his time in the White House into a financial advantage and instead returned to this house after leaving office. “I don’t see anything wrong with it, and I don’t hold it against other people,” he remarked. Simply put, I never really wanted to be wealthy. Carter had sold the peanut company and was deeply in debt, but he was able to maintain a comfortable standard of living because to his $217,000 pension.
According to data from the General Services Administration for the 2019 fiscal year, Carter spent $456,000 on expenses. This is much less than the budgets allotted for other former presidents, like George H. W. Bush, who spent $952,000, and even less than the $1 million that each of Barack Obama, Bill Clinton, and George W. Bush spent.
Furthermore, Carter has been seen often purchasing his clothing from the Dollar General store that is close by. Even when he does travel, he would rather take commercial aircraft over private ones. Following his term as president, Carter continued to teach Sunday school at a nearby Baptist church and at Emory University.
“People Only Know Me as a Freak,” The Wolf Man Struggles to Find a Job Outside the Circus
Jesús Aceves has hypertrichosis, which makes his hair grow abundantly over his face and back. Because of his condition, he’s also known as The Wolf Man. But he’s tired of this alias and wants to live a normal life.
Meet Jesús Aceves, a 55-year-old man born with a condition called hypertrichosis, which means he has abnormal hair growth over his body, especially his face. Although married with kids, Jesús isn’t fully happy with his living conditions. He says he and his family suffer discrimination. In an interview, one of his kids mentioned, “People call me names, and they even tell their kids not to be my friends.”
© Chuy, El hombre lobo / Chuy, The Wolf Man / Facebook
He worked in the circus all his life, traveling through several cities. But now, he’s tired of being seen as a freak. As a consequence of years on the road, he’s been known as The Wolf Man.
Back home and not in the circus anymore, he’s facing another challenge: finding a “normal” job. He needs to support his family since his wife works in temporary jobs.
After several failed job interviews, he agreed to try something he had always avoided: shave his face. He relied on his family barber to transform him, even creating eyebrows and lashes.
The experience was difficult since the face is an extremely sensitive body area, but both he and his wife believed that simply by shaving, he would be able to find a job.
Jesús did several interviews, and it’s confident that now he’ll find somewhere to work besides the circus. If this happens, he must shave his face every 2 days.
Although rare, some conditions aren’t impossible to have. Luckily, people find a way to overcome the difficulties a rare condition brings and strive in life. Hannah Tyre, for example, was born with osteogenesis imperfecta, meaning that her bones break very easily. But her love for makeup made her an internet influencer, reaching millions of followers. We hope that, by reaching the mainstream media, people with genetic diseases won’t suffer more discrimination.
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