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Baby Aiden’s life began with a serious challenge. 💔During a routine 6-month ultrasound, doctors discovered a large tumor...
10/05/2026

Baby Aiden’s life began with a serious challenge. 💔During a routine 6-month ultrasound, doctors discovered a large tumor growing on his neck — rapidly expanding across his face, chest, and airway.🏥
At 36.5 weeks, doctors made a critical decision to deliver him early to prevent life-threatening complications. ✨In a carefully coordinated procedure, they secured his breathing before cutting the umbilical cord.
Just days after birth, Aiden’s condition worsened as internal bleeding caused the tumor to grow, putting pressure on his airway. Doctors acted quickly — performing a high-risk, 4-hour surgery to remove the 1.1 kg tumor. 🙏

Hi world 👋 Meet Ollyver — one eye, full of life. Born with Amniotic Band Syndrome, Ollyver faced pain from his very firs...
09/05/2026

Hi world 👋 Meet Ollyver — one eye, full of life.
Born with Amniotic Band Syndrome, Ollyver faced pain from his very first moments. 🌈Doctors quickly stepped in to manage his discomfort, and early treatment — including a procedure to remove a painful skin flap — helped him become calmer and more comfortable.💔
There are still tough days, especially with sensitivity around his eye, and more surgeries lie ahead. But step by step, he’s getting stronger.

A 35-year-old mum went to the hospital thinking she had the flu — but within hours, she was rushed into an emergency C-s...
09/05/2026

A 35-year-old mum went to the hospital thinking she had the flu — but within hours, she was rushed into an emergency C-section at 27 weeks pregnant.💔👨‍👦
Her baby boy, Beau, entered the world small but full of life — a tiny fighter from his very first breath. 👶💙
Not long after his birth, his mother faced a sudden and serious medical crisis. A severe infection progressed rapidly, leading to toxic shock and causing her body to shut down. 🏥💔 She spent 10 days in a coma, underwent multiple critical surgeries, and battled through overwhelming complications with incredible strength. 🌈✨

Born at just 27 weeks, baby Carter weighed only 640 grams — tiny, fragile, and fighting for every breath from the very s...
09/05/2026

Born at just 27 weeks, baby Carter weighed only 640 grams — tiny, fragile, and fighting for every breath from the very start. She was rushed to the NICU, where she faced collapsed lungs, emergency treatment, and multiple setbacks that kept her on oxygen support for weeks.✨
There were times filled with fear and uncertainty, but little Carter never gave up. 💪💛 Step by step, she kept pushing forward — transitioning from intensive breathing support to a place of growing stability and strength. 🌈

Today, she weighs 3.3 kg and is reaching milestones that once felt so far away. Every small victory is a powerful reminder of her resilience. ✨ While she still needs ongoing care, her journey so far has been truly inspiring.

A story of courage, hope, and the quiet strength of a tiny fighter. 🕊️💫

Born with a severe spinal condition that left his body permanently bent forward, Jiang Yanchen became known as “the fold...
09/05/2026

Born with a severe spinal condition that left his body permanently bent forward, Jiang Yanchen became known as “the folded boy.” Doctors once believed he might never stand upright again.❤️‍🩹
For 19 years, even simple things like walking, breathing, or sitting caused constant pain. But Jiang refused to give up.🥺After enduring four complex surgeries and a long, painful recovery, he finally stood straight for the first time in his life. 💪
Despite everything he faced, Jiang continued studying at university and never stopped chasing his dreams. ✨His journey has inspired millions, proving that determination and courage can overcome even the hardest battles.🙏

A pregnant couple survived a terrifying house 𝚏𝚒𝚛𝚎 just weeks before welcoming their first child. 💔🔥 Rachel Standfest es...
08/05/2026

A pregnant couple survived a terrifying house 𝚏𝚒𝚛𝚎 just weeks before welcoming their first child. 💔🔥
Rachel Standfest escaped by jumping from a second-floor window, while her husband Travis ran through flames to get out. Both were seriously injured and rushed to the hospital.
Doctors performed an emergency C-section to ensure their baby girl’s safety — and soon after, they finally got to meet their daughter, Brynlee Rose. 👶✨
Despite losing their home and belongings, the family is now together, recovering, and holding onto gratitude after everything they’ve been through. ❤️🏥

At just two years old, Edmund’s world shifted from toys to treatment after a devastating diagnosis of pineoblastoma, a r...
08/05/2026

At just two years old, Edmund’s world shifted from toys to treatment after a devastating diagnosis of pineoblastoma, a rare and aggressive brain condition. 💔
What began as subtle changes—slower movements, quiet struggles—quickly became a critical situation. His parents, Anna and Mark, watched helplessly as their once energetic toddler faced surgeries, chemotherapy, and complications no child should endure. 😢

When local options ran out, they made an impossible choice: travel abroad for experimental care, risking everything they had for one more chance. 🐾Savings disappeared, fear grew, but love never wavered.
His journey is still unfolding, filled with unknowns—but also with hope.❤️

A baby boy in England was born with a rare condition, Treacher Collins syndrome, causing severe facial differences and b...
08/05/2026

A baby boy in England was born with a rare condition, Treacher Collins syndrome, causing severe facial differences and breathing difficulties.💙
Loui, now 19 months old, needed urgent care right after birth and has since undergone multiple surgeries to help him breathe, eat, and hear. Despite everything, he’s growing into a happy, playful child who loves toys and laughter.✨
For his mum, Karly, the pain of those first moments has turned into unconditional love — she now sees only her son’s joy, personality, and bright spirit.🌈
But the journey isn’t over. Loui still faces more complex surgeries to improve his quality of life, and his family is raising funds to support the treatment he needs.🙏

A Rare Journey Shared by Two Brave Sisters💔Elis and Eloá Lima Carneiro are twin sisters from Brazil living with an extre...
07/05/2026

A Rare Journey Shared by Two Brave Sisters💔
Elis and Eloá Lima Carneiro are twin sisters from Brazil living with an extremely rare condition known as progeria — a disorder that causes the body to age much faster than usual. Their story is considered extraordinary because cases involving twins with the same condition are incredibly uncommon and have drawn attention from medical communities around the world. 🌍
Despite facing challenges from a very young age, the sisters continue to shine with their beautiful connection, joyful spirit, and remarkable strength. 💫 Their appearance may reflect the effects of their condition, but behind every smile is a story of love, resilience, and courage.🙏
Every day, Elis and Eloá continue to touch hearts simply by being themselves — proving that even the rarest journeys can leave the biggest impact. 🌈✨

Bruno Waszczuk was born with a rare congenital condition that left him without key leg bones, knees, and several fingers...
07/05/2026

Bruno Waszczuk was born with a rare congenital condition that left him without key leg bones, knees, and several fingers and toes — making it nearly impossible for him to walk.🦿

Doctors initially suggested amputation as the only option. But his parents refused to give up.💔

Determined to give Bruno a chance at life on his own legs, they sought help abroad and began an intense journey of advanced surgeries in the United States. 🌈Over the years, Bruno has undergone multiple complex procedures, including bone lengthening treatments that slowly reshape and strengthen his legs — a painful and demanding process.💫

Despite infections, setbacks, and countless hospital visits, Bruno continues to fight with incredible strength. Step by step, he has begun to stand, move, and build toward walking independently.🙏

Amalia was diagnosed in the womb with amniotic band syndrome, leading to multiple complications including cleft lip and ...
07/05/2026

Amalia was diagnosed in the womb with amniotic band syndrome, leading to multiple complications including cleft lip and palate, hearing issues, and one undeveloped eye. 💔
Born far too early at just 29 weeks, she weighed only 3 lbs 6 oz and spent her first 44 days fighting in intensive care. 💕👶🏥
Since that fragile beginning, her journey has been anything but easy—countless hospital visits, exhausting 8-hour trips to see specialists, and multiple surgeries along the way. Through it all, her mom, Missy, made the selfless decision to step away from work to care for her full-time, all while raising two children on her own. 💪❤️
A story of resilience, sacrifice, and a love that never gives up. ✨

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