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ONE OF THE TWO HEARTS WASNโ€™T DEVELOPING NORMALLY ๐ŸฅบA routine 20-week scan suddenly changed their plans when Mary Ellen wa...
07/09/2026

ONE OF THE TWO HEARTS WASNโ€™T DEVELOPING NORMALLY ๐Ÿฅบ

A routine 20-week scan suddenly changed their plans when Mary Ellen was found to have several complex congenital heart conditions, along with a curved spine and only one kidney, while her twin sister, Kahleesi, was developing normally. ๐Ÿซถ

Just weeks after birth, Mary Ellenโ€™s condition took an unexpected turn, and she was rushed into emergency open-heart surgery. โค๏ธโ€๐Ÿฉน
๐Ÿ“Œ Full story in the comments.

DOCTORS GAVE BABY CASPIAN LESS THAN A 50% CHANCE โ€” BUT HIS STORY WASNโ€™T OVERBorn weighing just 1 pound, baby Caspian Ker...
07/09/2026

DOCTORS GAVE BABY CASPIAN LESS THAN A 50% CHANCE โ€” BUT HIS STORY WASNโ€™T OVER

Born weighing just 1 pound, baby Caspian Kerley began his life on a journey no one expected, spending 162 days in the NICU. Every hour brought a new challenge as his tiny, developing body worked to master what most newborns do naturally โ€” breathe, grow, and become strong enough for the next step. ๐Ÿฅ

For more than five months, his family stayed by his side as doctors worked tirelessly to help their little one grow stronger.๐Ÿ™
๐Ÿ“Œ Full story in the comments.

๐Ÿ’” No one expected baby Jonathanโ€™s first days to begin with such an unexpected journey.When he was born, his parents were...
07/09/2026

๐Ÿ’” No one expected baby Jonathanโ€™s first days to begin with such an unexpected journey.

When he was born, his parents were ๐—Œ๐—๐—ˆ๐–ผ๐—„๐–พ๐–ฝ to learn he had bilateral clubfoot, a condition affecting both feet that had gone unnoticed during pregnancy.

At just five weeks old, Jonathanโ€™s little journey took an unexpected turn, beginning with casts, procedures, and weekly hospital visits. ๐Ÿฅ Over the following months, he went through 13 casts and three tendon procedures, showing incredible strength with every step. ๐Ÿ‘ฃ
๐Ÿ“Œ Full story in the comments.

๐–ง๐–ค ๐–ช๐–ค๐–ฏ๐–ณ ๐–ก๐–ด๐–ฌ๐–ฏ๐–จ๐–ญ๐–ฆ ๐–จ๐–ญ๐–ณ๐–ฎ ๐–ณ๐–ง๐–จ๐–ญ๐–ฆ๐–ฒโ€”๐–ถ๐–ง๐– ๐–ณ ๐–ฃ๐–ฎ๐–ข๐–ณ๐–ฎ๐–ฑ๐–ฒ ๐–ฅ๐–ฎ๐–ด๐–ญ๐–ฃ ๐–จ๐–ญ๐–ฒ๐–จ๐–ฃ๐–ค ๐–ง๐–จ๐–ฒ ๐–ก๐–ฑ๐– ๐–จ๐–ญ๐Ÿง What began as an ordinary start to Benjamin Gutierrezโ€™s ...
06/09/2026

๐–ง๐–ค ๐–ช๐–ค๐–ฏ๐–ณ ๐–ก๐–ด๐–ฌ๐–ฏ๐–จ๐–ญ๐–ฆ ๐–จ๐–ญ๐–ณ๐–ฎ ๐–ณ๐–ง๐–จ๐–ญ๐–ฆ๐–ฒโ€”๐–ถ๐–ง๐– ๐–ณ ๐–ฃ๐–ฎ๐–ข๐–ณ๐–ฎ๐–ฑ๐–ฒ ๐–ฅ๐–ฎ๐–ด๐–ญ๐–ฃ ๐–จ๐–ญ๐–ฒ๐–จ๐–ฃ๐–ค ๐–ง๐–จ๐–ฒ ๐–ก๐–ฑ๐– ๐–จ๐–ญ๐Ÿง 
What began as an ordinary start to Benjamin Gutierrezโ€™s life soon became a mystery his parents couldnโ€™t ignore. As a baby, he began having unusual episodes, frequent seizures and his face turning red while he ate. He would also bump into things often and struggle to see where he was going.

An MRI finally revealed a large cavernous malformationโ€”an unusual cluster of blood vessels deep in his brain that required prompt medical attention. ๐Ÿ’”
๐Ÿ“Œ Full story in the comments.

๐Ÿ˜ข A SIMPLE PENCIL TURNED INTO A ๐–ญ๐–จ๐–ฆ๐–ง๐–ณ๐–ฌ๐– ๐–ฑ๐–ค...๐Ÿ’” A sweet little moment of joy took an unexpected turn for two-year-old Wren...
06/09/2026

๐Ÿ˜ข A SIMPLE PENCIL TURNED INTO A ๐–ญ๐–จ๐–ฆ๐–ง๐–ณ๐–ฌ๐– ๐–ฑ๐–ค...
๐Ÿ’” A sweet little moment of joy took an unexpected turn for two-year-old Wren Bowell. Like many toddlers, Wren loved coloring and drawing. One evening, she excitedly ran out of her room to show her parents the picture she had just finished.

Then, while running with a pencil in her hand, Wren stumbled. In an instant, the pencil entered near her eye and reached deep ๐—‚๐—‡๐—Œ๐—‚๐–ฝ๐–พ her head. โœ๏ธ๐Ÿ’”
๐Ÿ“Œ Full story in the comments.

๐Ÿ˜ณ โ€œ๐–จ๐–ณ ๐–ถ๐– ๐–ฒ ๐–  ๐–ฒ๐–ง๐–ฎ๐–ข๐–ชโ€: SHE MAY NEED MORE THAN 20 SURGERIES BEFORE STARTING SCHOOL.When Debb Stevens learned at her 25-week ...
05/09/2026

๐Ÿ˜ณ โ€œ๐–จ๐–ณ ๐–ถ๐– ๐–ฒ ๐–  ๐–ฒ๐–ง๐–ฎ๐–ข๐–ชโ€: SHE MAY NEED MORE THAN 20 SURGERIES BEFORE STARTING SCHOOL.

When Debb Stevens learned at her 25-week ultrasound that her baby had a rare genetic condition called Apert Syndrome, everything suddenly felt uncertain.๐ŸŒˆ

Apert syndrome is a spontaneous genetic mutation that affects around 1 in 65,000 babies and is characterized by skeletal differences.๐Ÿ’ž The condition means seven-month-old Daisyโ€™s skull, hands and bones in her feet developed differently.
๐Ÿ“Œ Full story in the comments.

THEY WENT IN FOR ONE FINAL CHECKUP... BUT LEFT WITH A HEARTBREAK THEY NEVER SAW COMING.๐Ÿ˜ญr years of dreaming of becoming ...
05/09/2026

THEY WENT IN FOR ONE FINAL CHECKUP... BUT LEFT WITH A HEARTBREAK THEY NEVER SAW COMING.๐Ÿ˜ญ

r years of dreaming of becoming parents and lovingly preparing for their baby boy, Ren, Tommy and his wife thought they were just days away from finally holding him. โค๏ธ

But during a routine appointment at nearly 36 weeks, doctors could no longer find Ren's heartbeat. Their long-awaited son arrived peacefully soon after, giving his parents a few precious hours to hold him close, say hello, and cherish every moment together. ๐Ÿ•Š๏ธ
๐Ÿ“Œ Full story in the comments.

๐Ÿ’” SHE SHOULD BE RUNNING AND PLAYING AT 8... BUT A RARE BONE CONDITION HAS CHANGED EVERYTHING.Instead of running, playing...
04/09/2026

๐Ÿ’” SHE SHOULD BE RUNNING AND PLAYING AT 8... BUT A RARE BONE CONDITION HAS CHANGED EVERYTHING.

Instead of running, playing, and enjoying school, young Dianne now spends her days managing osteosarcoma, a rare condition affecting the bone around her knee. Each step can be difficult, while even standing or taking a moment to rest can feel like a challenge. ๐Ÿฅบ

Doctors have recommended continued treatment, but the growing medical costs have placed a tremendous burden on her family. ๐Ÿ™
๐Ÿ“Œ Full story in the comments.

๐Ÿ’” DOCTORS DIDNโ€™T KNOW WHAT THE FUTURE HELD... BUT HER PARENTS CHOSE HOPE.At just four months into the pregnancy, one ult...
04/09/2026

๐Ÿ’” DOCTORS DIDNโ€™T KNOW WHAT THE FUTURE HELD... BUT HER PARENTS CHOSE HOPE.

At just four months into the pregnancy, one ultrasound changed everything. ๐Ÿ’” Doctors discovered that baby Helianny had Amniotic Band Syndrome, a rare condition causing significant differences affecting her face, skull, brain, hands, and feet. Some specialists were uncertain about what lay ahead and urged her parents to prepare for a challenging journey. ๐Ÿ•Š๏ธ

But her mother made one powerful decision: "We're giving our daughter every chance." โค๏ธ
๐Ÿ“Œ Full story in the comments.

SHE NEARLY LOST HER LIFE AT JUST 5 MONTHS OLD... AND LOST BOTH OF HER LEGS.๐ŸฆฟOne moment, little Amy Wolstenholme was a ha...
04/09/2026

SHE NEARLY LOST HER LIFE AT JUST 5 MONTHS OLD... AND LOST BOTH OF HER LEGS.๐Ÿฆฟ

One moment, little Amy Wolstenholme was a happy little girlโ€”the next, her familyโ€™s world was turned upside down. โค๏ธโ€๐Ÿฉน Amy developed meningococcal septicaemia, a serious infection linked to meningitis. Doctors worked tirelessly to help her through it, but the illness brought lasting challenges, leading to dozens of surgeries over the yearsโ€”including losing both legs. ๐Ÿ•Š๏ธ

With a prosthetic leg and walking frame, Amy did her best to keep moving forward, but getting around remained difficult, and joining her friends in games was something she often had to miss.
๐Ÿ“Œ Full story in the comments.

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