Healing Journey, 201 East 33rd Street, Mymensingh (2026)

05/01/2026

Cherie hasn’t slept much since doctors said the words no parent is ever ready to hear: brain tumor.

Her son Corey is just 20 years old — kind, funny, full of dreams — when two seizures led to the discovery of a tumor on his brain. Doctors are hopeful it’s benign, but the only way to know for sure is surgery, now scheduled for January 13.

For Cherie, the waiting is unbearable. The fear. The helplessness. The reality that she can’t fix this for her child.

Corey is trying to stay strong, even cracking jokes, even holding onto hope — but everything about his future now feels paused. A young life suddenly focused on survival instead of plans.

All this family is asking for right now is prayer, strength, and support as they face the unknown together.

👇 Read the full story in the comments below.

04/01/2026

Today brought hope.

After days of waiting and prayer, doctors shared encouraging news — they plan to try removing the tubes from his neck on Monday. His breathing is improving, and that alone feels like a miracle.

Then, unexpectedly, while still deeply sedated, he opened his eyes and lifted his arm — something that wasn’t supposed to happen. Even the nurses were surprised. It was a quiet but powerful reminder of how strong he is.

Nothing is guaranteed, but today showed us he’s still fighting.

📌 Full update in the comments.

04/01/2026

Louis is a pediatric brain tumor survivor.
His childhood was shaped by surgeries, therapy, and hospital rooms instead of playgrounds.

Watching his son endure so much pain changed Sergio forever.
Even now, fear lingers — every scan, every follow-up brings the same quiet question: what if?

Families like theirs don’t just need treatment.
They need connection. Understanding. Community.

💛 Support reminds parents they are not alone — during treatment, in recovery, and long after.

📌 Full story in the comments.

04/01/2026

💔 Eight days ago, we welcomed our daughter — and she’s been fighting for her life ever since.

Liana was born with a serious heart defect and needs open-heart surgery before she can come home.
While she’s in the NICU, we’re facing an impossible choice: stay by her side or return to work just to pay bills.

Liana needs her parents with her — to be held, comforted, and loved during this critical time.
We’re asking for help so we don’t have to choose between our baby and survival.

🙏 Any support or prayers mean everything.
📌 Full story in the comments.

04/01/2026

Twelve-year-old Kuba has battled severe leg deformities caused by hypophosphatemic rickets. Despite twelve surgeries, his condition remains challenging, and he relies on crutches to move. Kuba dreams of walking independently, but the necessary surgeries and rehabilitation cost 315,462 PLN, a sum his family can't afford alone.

Kuba’s family is determined to help him live a pain-free life, but they need your support. Every donation, big or small, will bring him closer to his dream. Please help by clicking the link in the comments below. 👇

04/01/2026

Ola’s journey has been marked by unimaginable challenges since birth. Born with Apert syndrome, she faced severe brain and physical deformities, including fused fingers and toes, and a skull that didn’t allow her brain to grow. Despite the grim prognosis, Ola’s mother refused to accept defeat and sought life-changing surgeries. With support from generous donors, Ola underwent multiple surgeries, including one to separate her fingers and toes and another to reshape her skull, significantly improving her quality of life.

Now, at 9 years old, Ola is thriving—dancing, singing, and attending school. However, she still faces a critical challenge: her skull needs further surgery to allow for more brain growth. The necessary Le Fort III surgery will cost around 500,000 PLN, a sum that is beyond her family’s means.

With your support, Ola can receive this vital surgery and continue to live a fuller, healthier life. Every donation, no matter how small, will help give her a chance at a brighter future.

Please consider supporting Ola’s journey by donating or sharing her story. Your help can make all the difference. For more details, please click the link in the comments below. 👇

03/01/2026

Palinka, a 3-year-old girl, has faced unimaginable challenges since birth. Born prematurely, she was diagnosed with GMFCS cerebral palsy and spastic diplegia, requiring constant care and rehabilitation. Despite these struggles, Palinka remains joyful, curious, and determined to improve.

Her daily treatments include the NDT-Bobath method, massages, exercise, and botulinum toxin treatments. However, these therapies are costly, and Palinka needs medical aids like a standing frame, orthoses, and a wheelchair. With intensive rehabilitation, there is hope that Palinka could one day walk independently.

Her family, having left everything behind in search of a better life, is overwhelmed by the financial burden of her care. They need your help to continue her treatments and give her the chance at a more independent future.

Please consider donating or sharing Palinka’s story. Your support can make a life-changing difference for this brave little girl. For more details on how you can help, please click the link in the comments below. 👇

03/01/2026

Sara, just 6 years old, has faced unimaginable challenges since birth. Born prematurely with spina bifida and other complications, she has undergone numerous surgeries, from a life-saving operation shortly after birth to treatments for her clubfoot and spine. Despite her struggles, Sara has shown incredible resilience and continues to fight for a better life.

Currently, she needs a critical osteotomy surgery to straighten her legs, improving her mobility and giving her the chance to walk more freely. This surgery is costly—160,000 PLN, plus additional expenses for orthotics and travel. Without help, her dream of walking without assistance may not be realized.

Sara’s family is reaching out for your support to make her dream a reality. Your donation can help cover the surgery and necessary treatments.

For more information on how to help, please click the link in the comments below. 👇

03/01/2026

Krystian, a 17-year-old boy, has faced an unimaginable journey since birth, battling congenital insensitivity to pain with anhidrosis (C**A), a condition that leaves him unable to feel pain, resulting in frequent, unnoticed injuries. Over the years, he’s undergone multiple surgeries and faced constant health challenges. His recent triumph, taking his first steps after years in a wheelchair, has been a beacon of hope. However, his knee replacement is loose, requiring urgent surgery and rehabilitation in the U.S., costing around 800,000 PLN.

We are reaching out for help as the financial burden of Krystian’s care is overwhelming. Every donation and prayer brings us closer to providing him the life he deserves.

For more information on how you can help, click the link in the comments below. 👇

03/01/2026

Oliwier, a 13-year-old boy, has fought for his life from the moment he was born with Hypoplastic Left Heart Syndrome. Despite enduring 18 surgeries, a stroke, cerebral palsy, and other serious health complications, his strength and resilience continue to inspire. Oliwier’s biggest dream is to walk independently, but he faces more obstacles ahead, including a critical surgery to lengthen his Achilles tendon.

The cost of this surgery, rehabilitation, and necessary orthoses is 50,000 PLN, a financial burden his family can’t bear alone. His mother, Magda, has already sacrificed so much, but she needs help to give Oliwier the chance to live a life free from pain and limitations.

Please consider supporting Oliwier’s journey by donating or sharing his story. Every bit of help brings him closer to his dream of independence. For more information, please click the link in the comments below 👇

03/01/2026

My name is Mary, and I am the mother of a beautiful 9-month-old girl named Dafnie Jean. From the moment she was born, Dafnie has been a light in our lives—her laughter, her smile, and her endless love. But at just a few months old, Dafnie was diagnosed with serious health conditions that have turned our world upside down.

Dafnie was born with no a**s, requiring an emergency colostomy surgery. Despite the odds, she bounced back quickly, showing strength beyond her years. But just when we thought things were improving, a devastating new diagnosis came: congenital heart disease, including a Ventricular Septal Defect (VSD), a Large Patent Ductus Arteriosus (PDA), and Severe Pulmonary Hypertension. Her condition is critical, and without open-heart surgery, her future is uncertain.

The surgery costs SGD 22,500, a sum far beyond our ability to pay. We’ve already sold our home and car, and our savings are exhausted. Dafnie needs immediate surgery to survive, and we are turning to you for help.

Please support Dafnie’s surgery so she can live a life free from pain and struggle. Every contribution, no matter how small, brings us one step closer to saving her life.

To help, please click the link in the comments below 👇

02/01/2026

This Christmas Eve, as we reflect on our journey, we’re reminded of the joy in being together. Despite the challenges with Milo’s health, we chose to focus on what truly matters—family. We made memories, laughed, and embraced the present moment. Milo’s fight is far from over, but every day with him is a gift.

This year, more than ever, we cherish family over everything else. Every milestone, no matter how small, is a victory. We’ve been given a miracle we never expected, and we hold on to that with all our hearts.

For us, the greatest gift is the health and happiness of our children. Thank you to everyone who has supported us. Your kindness has been a constant source of strength.

Read the full story in the comments below 👇

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