Calm the Soul, 7577 Park Avenue, Apata Ibadan (2025)

04/12/2025

Harry’s journey has been one of incredible challenges and resilience. My name is Charlotte, and I’m Harry’s mum. He was born with pulmonary atresia, a severe heart condition, and from day one, our world was turned upside down. After being airlifted to another hospital, Harry underwent multiple surgeries, including open heart surgery, to save his life.

Despite his battles, Harry’s strength and determination have amazed us. He quickly recovered, regained his playful self, and continues to thrive. However, his journey isn’t over, as we still face challenges ahead with his heart. But through it all, Harry remains our miracle.

His story is one of love, perseverance, and hope. We are forever grateful for the support of his doctors and for every precious moment with him.

📌 Full story in the comments 👇

04/12/2025

When Manon was born, everything seemed perfect. She was healthy and full of life, but within hours, we noticed signs that something wasn’t right. Despite reassurances from doctors, her condition worsened—she was grunting, struggling to feed, and became lethargic. By day four, her feet were cold, and she wasn’t feeding properly. Trusting my instincts, I rushed her to the hospital, where doctors discovered she had a critical heart condition: coarctation of the aorta.

Manon’s condition was urgent, and she was immediately placed on life support. After a tense surgery to repair the defect, we were relieved to hear it had been successful. The following days were a rollercoaster of emotions, but Manon’s strength amazed us as she slowly recovered.

This experience opened my eyes to the importance of early detection of congenital heart defects. If Manon’s condition had been identified earlier, her treatment would have been easier. I’m incredibly grateful for organizations like Tiny Tickers, which raise awareness and train sonographers to detect heart conditions in newborns. Manon is now thriving, but we’ll never forget the journey that brought us here.

📌 Full story in the comments 👇

04/12/2025

In December 2021, Louise and Ollie’s excitement over expecting their third child turned to fear when a 20-week scan revealed their baby had transposition of the great arteries (TGA), a life-threatening heart defect. Despite the grim news, surgery offered hope.

When Sebastian was born, he surprised everyone by breathing on his own, but his oxygen levels quickly dropped. After successful surgery and weeks in the NICU, he was able to go home just in time for Christmas.

Now two years old, Sebastian is thriving with a healthy heart and reaching all his milestones. His story is one of resilience, hope, and the power of early diagnosis.

📌 Full story in the comments.

04/12/2025

At just 20 days old, Cooper’s parents noticed something alarming when their baby monitor signaled dangerously low oxygen levels. Panicked, they rushed to the hospital, where Cooper’s condition rapidly worsened. He was transferred to a specialist hospital and diagnosed with Total Anomalous Pulmonary Venous Connection (TAPVC), a rare congenital heart defect. Without immediate intervention, Cooper’s chances were slim.

Cooper underwent life-saving surgery that day, and his recovery began. Despite the terrifying start, Cooper, now 21 months old, is thriving, full of energy and joy. His parents are forever grateful for the early detection provided by the oxygen monitor, which played a crucial role in saving his life.

Cooper’s story highlights the importance of early detection, the role of medical technology, and the strength of the human spirit. His journey is a reminder that with the right tools and care, miracles are possible.

📌 Full story in the comments 👇

04/12/2025

Today has been tough for a mother caring for her two young sons. Baby Hunter, battling pain, finds comfort only in his mother’s arms, while his treatment options are limited by his age. Meanwhile, Toby, struggling with epilepsy, saw his medical team today, bringing hope with new plans for his treatment.

Despite the challenges, this mother’s love never wavers. With support from family and friends, they continue to fight. Please keep baby Hunter in your prayers for relief from his pain, and send hope for Toby's ongoing journey.

📌 Full story in the comments 👇

03/12/2025

Four years ago, Alex Dean, born 14 weeks premature, faced incredible challenges, from surgeries to heart issues. Weighing just 2 pounds, 3 ounces, Alex fought for her life through multiple procedures, including one for an aortic valve blockage and Retinopathy of Prematurity.

Now, at 10, Alex is thriving—playing volleyball, basketball, and softball, and even hitting her first inside-the-park home run. Despite facing loss and hardship, Alex lives with gratitude and determination, inspiring everyone around her.

Her family continues to celebrate her progress, hoping her health stays stable. To read more about Alex’s amazing journey, check out the full story in the comments below 👇.

03/12/2025

Ten-year-old Braxton Bragg’s life changed in an instant when he was attacked by three unprovoked dogs in his own backyard. The attack left him with severe injuries, requiring five surgeries and over 500 stitches. Despite the trauma, Braxton’s strength and resilience have been nothing short of inspiring.

Though his recovery journey is far from over, with more treatments and surgeries ahead, Braxton continues to fight. His family remains hopeful, cherishing every small victory along the way.

Please keep Braxton in your thoughts and prayers as he continues to heal.

📌 Full story in the comments below 👇

03/12/2025

On World Prematurity Day, I’m sharing the story of my son, Noah, who was born at just 25 weeks, weighing only 700 grams. From the moment he was born, his life was a battle, but Noah’s strength and resilience defied the odds. Despite being told to expect the worst, he fought fiercely in the NICU, growing stronger each day. After 130 days, we brought Noah home, but his journey didn’t end there. He faced multiple surgeries and continuous medical challenges, but his courage and ability to find joy in the smallest moments have been inspiring.

Noah’s development has been slower due to his early arrival, but every milestone—like holding his bottle or taking his first steps—is a victory. On this World Prematurity Day, we celebrate not only Noah but every preemie who continues to fight. We are forever grateful for the medical teams, family, and friends who’ve supported us. Noah’s journey is a testament to resilience, hope, and love.

Please join us in honoring all preemies by reading the full story in the comments below 👇.

03/12/2025

In the midst of Sky's ICU stay, I turned to my mom for support. After days of stress, Grandma stepped in to care for Sky while I took a much-needed break at home. When I returned, I was amazed to find Sky awake and alert, with Grandma by her side, offering the love and comfort only a grandparent can provide. Her presence made all the difference in Sky’s recovery, allowing me to recharge and be there for my other children.

Family, especially grandparents, has been a lifeline during this challenging time. Their love and support continue to uplift us, giving us strength as we move forward.

To every grandparent, thank you for the magic you bring into our lives. 💖

Read the full story in the comments 👇

03/12/2025

12-year-old Caden Ballard’s world changed when a TikTok experiment went horribly wrong, causing his shirt to catch fire. Despite his brother’s quick thinking in pulling the shirt off, Caden suffered severe burns. His mother, Christina, arrived to find him badly burned and rushed him to a burn unit for urgent care.

Though the road ahead is long, with surgeries and therapy, Caden’s resilience shines through. “He’s a fighter,” says Christina. With the unwavering support of his family, Caden is pushing through each challenge.

Caden’s journey is a powerful reminder of strength, love, and determination in the face of adversity.

📌 Full story in the comments.

02/12/2025

Mallory, born at 36 weeks and just 6lbs, has defied all odds since her early, uncertain start. Her first few weeks in the hospital were filled with fear, as she battled feeding, breathing, and temperature regulation challenges. But with the support of a dedicated medical team, Mallory quickly proved that she was a fighter.

Now, just a week away from turning 9 months old, Mallory is a thriving, joyful baby, hitting milestones that once felt out of reach. Her journey reminds us of the incredible strength in every preemie, and the unwavering love that carries them through.

On World Prematurity Day, we celebrate Mallory and all the tiny fighters who overcome the odds. Your strength is an inspiration.

📌 Full story in the comments 👇

02/12/2025

Born at just 29 weeks, Lena’s early days were filled with uncertainty. With months of critical care ahead, the Ronald McDonald House became a lifeline for her parents, Maggie and Jace, providing a place of support and comfort.

Despite Lena’s improving health, a new challenge emerged—she was diagnosed with liver cancer. But through it all, Maggie and Jace remained strong, finding strength in their love, family, and the community at the House.

Lena’s journey is far from over, but her family faces each challenge with hope, courage, and the support of those around them. This World Prematurity Day, let’s honor families like Lena’s and continue to support the organizations that help them fight.

📌 Full story in the comments 👇

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