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.”
A Man Who Was Called “The Tree Man” Was Able to Hold His Daughter Again After Many Surgeries
“The Tree Man” is a man whose life has been defined by a rare malformation in his hands. Once dubbed for his distinctive condition, he has undergone numerous surgeries, overcoming tremendous challenges on his journey. Now, with unwavering determination and the skilled hands of medical professionals, he has reclaimed a simple yet profound joy—holding his daughter once again.
Abul Bajandar has a rare condition called ’Tree Man’ Syndrome.
Abul Bajandar, a man hailing from Bangladesh, is afflicted with an extraordinary and rare condition known as ’Tree Man’ Syndrome. This hereditary condition, though non-contagious, is unfortunately incurable, and surgical interventions offer only temporary relief. Abul is not alone in his struggle, as there are others worldwide grappling with the challenges posed by this syndrome.
This syndrome manifests through the development of wart-like skin growths that bear a striking resemblance to tree bark. These growths, while initially small, have the potential to grow significantly in size, resulting in considerable disability for those affected.
He has it from a young age.
The onset of his condition began during adolescence, with small warts appearing on his body at the age of 13-14. Regrettably, as he advanced in age, the affliction rapidly escalated, affecting various parts of his body.
After 16 surgeries he was able to hold his daughter again.
After undergoing a series of 16 surgeries between 2016 and 2017 at Dhaka Medical College Hospital in Dhaka, Bangladesh, Abul Bajandar achieved a poignant milestone—he could once again hold his daughter. The surgical procedures aimed to remove the bark-like lesions from his hands and feet, offering a glimmer of hope in his battle against Tree Man Syndrome.
Bajandar shared the profound joy he experiences spending time with his daughters, emphasizing, “If I recover from this, I want to work again, to build a small business to help my daughters in her studies and to give them a good life.” These words reflect not only his determination to overcome the challenges posed by his rare condition but also his unwavering commitment to providing a better future for his family.
Throughout Abul Bajandar’s challenging journey with Tree Man Syndrome, he draws strength from the unwavering support of his wife and mother. In the face of the condition’s recurrence, their steadfast presence provides him with comfort and encouragement. Bajandar reflects on the transformative power of fatherhood, sharing, “When my daughter was born, she brought me the hope of life again. I didn’t want to leave her as an orphan. I felt like I must live for her.”
Abul Bajandar’s condition returned but he remains hopeful.
Despite facing the disheartening recurrence of his condition, Abul Bajandar maintains a resilient sense of hope. Doctors, initially uncertain about the possibility of the condition’s return, witnessed its reappearance. Undeterred, Bajandar expresses his unwavering optimism, declaring, “My only dream is to recover from this situation and live a healthy life.”
His poignant words reflect not only the personal challenges he endures but also a universal desire for health and well-being. Bajandar’s enduring hope shines through as he states, “All I can say is that I truly believe and hope that a cure exists for this disease.” In the face of adversity, his spirit remains unbroken, embodying the strength of individuals confronting rare and challenging medical conditions.
Another person born with a rare condition has defied societal norms and emerged as a symbol of extraordinary resilience. Meet the girl affectionately referred to as “Voldemort” due to being born without a nose.
Preview photo credit Tansh / Alamy Stock Photo, ZUMA Press, Inc. / Alamy Stock Photo
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