The grieving parents of a young girl have honored her memory through an incredible act of generosity by donating her organs. Aurora Masters, a five-year-old, tragically раssеd аwау on May 13, following a freak accident that resulted in her accidental strangulation on a disc swing just five days earlier. Her family made the heart-wrenching decision to turn off her life support after doctors confirmed she had suffered fatal brain damage.
Tom and Krystal Masters, Aurora’s parents, revealed that her organs were donated to Donor Alliance, an organization dedicated to organ and tissue donation for transplantation in Colorado and most of Wyoming. “We know that Aurora’s heart is beating somewhere,” said Krystal, with Tom adding that this knowledge “genuinely helps” them cope with their immense grief.
Aurora’s family described the donation as a final act of kindness from a little girl who always wanted to help and lead. “I am proud of my daughter,” Krystal told KUSA. “I was already proud, but she’s still giving.”
A GoFundMe campaign has raised over $30,000, showing the outpouring of love and support from family and friends. The family wrote, “Our sweet Aurora Rae has once again demonstrated her ninja quality of bravery, partnering with the Donor Alliance to complete her giving of gifts. She is demonstrating the qualities of a black belt.”
Little Girl’s Final Act Of Kindness Before Taking Her Life On The Playground
The grieving parents of a young girl have honored her memory through an incredible act of generosity by donating her organs. Aurora Masters, a five-year-old, tragically раssеd аwау on May 13, following a freak accident that resulted in her accidental strangulation on a disc swing just five days earlier. Her family made the heart-wrenching decision to turn off her life support after doctors confirmed she had suffered fatal brain damage.
Tom and Krystal Masters, Aurora’s parents, revealed that her organs were donated to Donor Alliance, an organization dedicated to organ and tissue donation for transplantation in Colorado and most of Wyoming. “We know that Aurora’s heart is beating somewhere,” said Krystal, with Tom adding that this knowledge “genuinely helps” them cope with their immense grief.
Aurora’s family described the donation as a final act of kindness from a little girl who always wanted to help and lead. “I am proud of my daughter,” Krystal told KUSA. “I was already proud, but she’s still giving.”
A GoFundMe campaign has raised over $30,000, showing the outpouring of love and support from family and friends. The family wrote, “Our sweet Aurora Rae has once again demonstrated her ninja quality of bravery, partnering with the Donor Alliance to complete her giving of gifts. She is demonstrating the qualities of a black belt.”
A service in Aurora’s honor will be held on Saturday, June 8, at a local church. “Our hearts are shattered, and we continue the journey to honor and celebrate her worldly gifts,” the family shаrеd.
Aurora, from Fort Collins, was playing in her family’s garden when the accident happened. She had moved her small plastic slide close to a disc swing and somehow got her neck caught in the ropes while sliding down. This tragic incident led to her brain being starved of oxygen. Doctors at the Children’s Hospital Colorado in Aurora delivered the devastating news that she would not survive.
In the face of this tragedy, the Masters family found solace in the support of their extended family, with 19 members traveling from Wyoming and Nebraska to be by Aurora’s bedside. “We do know the power of family,” said her aunt Kennedy.
Aurora was pronounced dеаd on May 13. The family has struggled to comprehend how the accident occurred, as it seemed to happen while she was innocently playing on her own outside. Her aunt Kennedy explained, “She pulled her little plastic slide over to where her swing was and somehow got caught up in the swing, and the swing strangled her.”
Tom Masters spoke about how Aurora had reinvigorated his life when she was born. “She came along when I was in a really bad mental health place,” he told the Denver Post. “It felt likе there was something almost magical about her. I’m hearing all these stories that she was likе that for everybody.” He added, “She literally just had fun and went around and brought her light with her and gave it away for free.”
Krystal hopes Aurora’s story will inspire other families to cherish every moment with their children. “I guess what I would say to parents is: Love your kid every minute, have a dance party, and just live life. Because you never know when it’s going away.”
“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.”
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.
Preview photo credit A True Story / Youtube
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