Lifestyle

BROKEN HEARTS

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2d ago

Jun 28, 2024 / 553 Views

LOVED Saoírse Ruane, who was on The Late Late Toy Show, died of cancer when she was only 12.

The brave girl from Galway, whose appearance on the Toy Show won hearts across the country, died on Tuesday, her family said this morning.

Saoírse was diagnosed with cancer in November 2019 after complaining of an injured ankle. In 2020, her leg was cut off because an Osteosarcoma tumor in her tibia was found to be cancerous and likely to kill her.

When Saoírse joined Ryan Tubridy on the Late Late Toy Show in 2020, her story became well known.

The Galway girl’s fight against a rare form of bone cancer amazed everyone with how strong and tough she was.

The death of Saoírse has broken the hearts of her parents, Roseanna and Ollie, and her little sister Farrah-Rose.

They told everyone about their terrible loss by saying, “After a long brave and dignified battle, our hearts are shattered to tell you that our beautiful little Saoírse took her last breath in our arms on Tuesday.”

“Thank you to all of our wonderful fans for thinking about Saoírse and us over the past few weeks.

“Today, we also think of you because we know how much the country loved Saoírse and how she changed the lives of so many people.”

“Cancer, you took her away from us. You also took away our dreams and the life we had.” Things will never be the same!

Please give us some space as we go on our last and final trip with our beautiful girl. “Farrah Rose and MaMMA Dadda.”

President Michael D. Higgins and stars from all over show business have paid tribute to the beloved girl. Her story was told on The Toy Show the first year they started their huge charity campaign.

through her battle, Saoírse’s family gave a “devastating” Health update in November of last year, saying that her cancer had spread.

After a recurring tumor was found in her left lung earlier in 2023, they said it was a “huge shock” to them that the cancer had spread to her other lung.

It was Saoírse’s “biggest battle to date” because she had to go through more chemotherapy.

In April, Roseanna said, “Little did they know that their world was about to fall apart again.”
“To say we’re devastated just doesn’t cover it,” she said. It’s not fair that she’s been to war so many times and fought so hard.

Saoírse had already had a few dreams come true, like going to Old Trafford to see Manchester United play and going on her dream vacation to Disneyland.
When people heard that Saoírse had died, they sent her a lot of tributes.
The office of President Michael D. Higgins said, “President Higgins has sent his deepest condolences to the family of Saoírse Ruane from Kiltullagh, Co. Galway, after her death at the age of 12.” Everyone was moved by Saoírse’s strength and kindness.
Tanaiste Micheal Martin also said, “Very saddened by the death of Saoírse Ruane.”
“I will always remember meeting Saoirse and her mother Roseanna in Croke Park and seeing her beautiful smile and love for GAA.”
“The Toy Show Appeal is an amazing thing she left behind.” We’re very sorry for her family and friends’ loss.
Tubs’ tears
After Saoirse’s appearance on The Toy Show, Ryan Tubridy, who used to host Late Late, became friends with her family. He said that the “world is a poorer place” without her.

According to him, hearing the news of his dear young friend Saoírse Ruane’s death made him feel the saddest thoughts possible.
“As soon as we met, we became friends.” People all over the country fell in love with her, and because of her, a charity was founded. Through this, she helped make the lives of thousands of Irish children better and more hopeful.
“A child who is selfless, humble, kind, hopeful, and thoughtful.” She was everything our country should and could be, and her death will make a lot of us think about things.
“My condolences and all the love I can muster go out to Roseanna, Ollie, and Farrah Rose. They are a beautiful family whose whole world has been turned upside down by this tragedy.”
“Thank them for letting us all know about their amazing Saorse.”
“The world is a poorer place without Saoírse but I do hope that twinkle in her eye shines on and on.”
The legacy of Saoírse
Roz Purcell, a radio host on RTE 2FM, said, “No one will forget Saoírse; she left a huge mark and mark on Ireland.”
“In 12 years, she did so much.” May she rest in peace. Think about all of her family and friends who will miss her a lot.
Patrick O’Mahony, the captain of Ireland’s rugby team, said, “I’m very sorry to read this.” She was an inspiration.
Rosana, I’m so sorry, said Kathryn Thomas of RTE. Your lovely daughter made our lives so much better.
“A small part of what she brought into your life.” That smile is great. Thinking about all of you. “Take it easy, little angel.”

Today FM It was DJ Declan Pierce who wrote, “My beautiful friend. It breaks my heart so much.
“The best thing about my job is getting to know Saoírse through the radio show. From the bottom of my heart, I love you all the time.
Singer RuthAnne wrote on her blog, “Heartbroken. She was truly unique, and her bravery knew no bounds.”
“I am so thankful that I met her and had the chance to sing with her. What an honor!”
“That is something I will always treasure and hold close to my heart. Lots of love and light to everyone.”
Saoirse’s funeral will be held at St. Peter and Paul’s Church, Kiltullagh, on Sunday at 1.45 p.m.
It also said, “Saoírse will rest at home on Friday, March 8, from 2 p.m. to 8 p.m.”
“From the Bullaun Church parking lot (H62 YH66), a bus service will leave. Please follow the stewards’ instructions and only use the bus service to get to the event.”

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