GOD with Us

GOD with Us Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from GOD with Us, News & Media Website, Hoa kỳ, Texas City, TX.

💔 SHE SHOULD BE SPENDING HER DAYS PLAYING, NOT FIGHTING CANCER.At just 8 years old, Dianne is facing osteosarcoma, a rar...
08/28/2026

💔 SHE SHOULD BE SPENDING HER DAYS PLAYING, NOT FIGHTING CANCER.

At just 8 years old, Dianne is facing osteosarcoma, a rare and serious bone cancer that has affected the area around her knee.

The pain has made everyday life incredibly difficult. Walking, standing, and even trying to rest can become a challenge. 🥺

Her doctors have advised continued treatment, but the cost of medical care continues to place tremendous pressure on her family. Through it all, they’re holding onto hope and praying for better days ahead. 🙏

📌 Full story in the comment 👇👇

# She Was Given Little Hope. Now She’s Preparing to Become a Nurse. 🥹🎓🩺Jacqueline Rodriguez was born in California with...
08/27/2026

# She Was Given Little Hope. Now She’s Preparing to Become a Nurse. 🥹🎓🩺

Jacqueline Rodriguez was born in California with a rare lymphatic malformation that caused significant growths on her cheeks and tongue. 💔

Her condition brought challenges that most people could never imagine, but Jacqueline refused to give up on the future she wanted.

Through years of difficulties, she continued to learn, grow, and push beyond the expectations placed on her.

Now, she is preparing to graduate from school and pursue the career she has dreamed about for years: becoming a nurse. 🎓🩺

Jacqueline’s journey shows just how far courage and determination can take someone. What once seemed like an uncertain future is now filled with possibility. 🌈✨

She has defied the odds in ways that continue to inspire those around her.

Read more in the comments 👇️

When Finlee June was born with Treacher Collins syndrome, her family knew they were facing an unexpected journey. The ra...
08/26/2026

When Finlee June was born with Treacher Collins syndrome, her family knew they were facing an unexpected journey. The rare condition affects facial development and brought many medical challenges during her early life. 💕

There were hospital visits, uncertain days, and moments filled with fear. But Finlee never stopped showing an incredible strength.

Even through the hardest times, her smile continued to shine and bring joy to the people who loved her.

Her journey reminds us that true beauty comes from within, and that courage can be found in the smallest smiles. ❤️

📌 Full story in the comment below 👇

**Doctors Feared the Worst 💔**The moment Ebrar Jaber was born, her family faced a devastating reality. 👶Ebrar had **ence...
08/25/2026

**Doctors Feared the Worst 💔**

The moment Ebrar Jaber was born, her family faced a devastating reality. 👶

Ebrar had **encephalocele**, a rare birth defect that occurs when part of the brain pushes through an opening in the skull. Her condition was so serious that doctors in Winnipeg warned her mother, Safaa, that Ebrar might not survive.

For her family, every moment became precious. What followed was a journey filled with fear, uncertainty, strength, and hope. ❤️

Read the full story in the comments 👇️

😳 Eight ultrasounds. Eight reassuring updates. And still, doctors couldn't see what was coming.Emily Carter and her husb...
08/24/2026

😳 Eight ultrasounds. Eight reassuring updates. And still, doctors couldn't see what was coming.

Emily Carter and her husband believed their pregnancy was progressing normally. Every scan gave them another reason to feel hopeful and excited about meeting their baby. 🤍

But the moment their son arrived, their world changed. Doctors discovered a cleft palate and a serious congenital heart condition that had not been identified before birth. 💔

Instead of simply bringing their newborn home, the family was suddenly facing specialists, procedures, and difficult decisions.

Doctors later explained that their little boy might need up to nine operations, including complex surgeries requiring highly specialized care. 🏥

And the journey would be much longer than surgery alone. He could require ongoing medical support and monitoring for years as he grows.

For parents who had been told everything looked normal during pregnancy, the diagnosis was devastating and completely unexpected.

Yet their son's story is also one of love, resilience, and a family determined to be there for him every step of the way. 💙

📌 Full story in the comment 👇👇👇

When baby Skylyn Victoria was sent home on hospice care, her family feared they were running out of time. She had alread...
08/22/2026

When baby Skylyn Victoria was sent home on hospice care, her family feared they were running out of time. She had already fought through a rare genetic condition, life-threatening blood clots, and a dangerous infection. Doctors believed there was little else they could do. Then, just weeks later, something extraordinary happened. Skylyn began growing stronger, and her condition improved so much that she no longer needed hospice care. Her incredible fight has touched thousands and proves that sometimes the most unexpected moments can bring the greatest hope. ❤️

📌 Full story in the comment 👇👇

Jade Gordon never realized she was carrying a baby. Then Noah Connell was born, and his family immediately found themsel...
08/20/2026

Jade Gordon never realized she was carrying a baby. Then Noah Connell was born, and his family immediately found themselves facing an unimaginable medical battle. 😳

Noah arrived with several uncommon congenital conditions that required urgent medical attention.

His jaw was underdeveloped, his neck was unusually small, and his airway was extremely fragile. He also had a cleft palate and was missing part of his spine. 💔

Because of his fragile airway, something as simple as swallowing saliva or drinking liquids could become life-threatening.

The happiness of welcoming a newborn quickly turned into fear as his family learned how serious his condition was.

Doctors had to carefully monitor Noah and work to manage the many challenges affecting his tiny body.

Through it all, his little body continued to fight, giving his family hope during an incredibly difficult time. ❤️

Noah’s beginning was heartbreaking, but his courage made his story one worth remembering.

**Full story in the comment👇👇👇**

💔 When baby Jamison was born, doctors feared he might not survive for long.He was diagnosed with harlequin ichthyosis, a...
08/20/2026

💔 When baby Jamison was born, doctors feared he might not survive for long.

He was diagnosed with harlequin ichthyosis, an extremely rare condition that caused severe, painful changes across almost his entire body. His damaged skin left him at serious risk of infection and other complications.

For his parents, every day became a fight to keep their son safe. They followed a treatment routine prescribed by his medical team, including twice-weekly baths using carefully diluted bleach.

Those baths were painful, but his father stayed by his side, holding Jamison close and helping him through every difficult moment. ❤️

There were times when the future seemed uncertain. Yet his parents continued believing that their son could overcome the odds.

Eventually, Jamison reached a milestone that once seemed almost impossible. For his family, it was more than a milestone—it was a reason to celebrate and keep believing. 🥺

This little boy has already shown incredible strength, and his story continues to inspire everyone who hears it.

Send a ❤️ to Jamison and his family.

📌 Full story in the comment 👇👇👇

The odds were stacked against Phillip Matthews from day one. Arriving in the world with a severe cleft lip, cleft palate...
08/19/2026

The odds were stacked against Phillip Matthews from day one. Arriving in the world with a severe cleft lip, cleft palate, and a brain condition, he fought through 25 grueling surgeries just to grow up. Recognizing that his survival was a privilege not available to every child globally, his parents turned their gratitude into a lifelong mission to help kids in need.
His journey mirrors the ancient question, “Who sinned that this man was born blind?”
Check out the full story in the comments! 👇👇👇

Only 2 years old, Dik Putri is already facing a devastating medical battle that has changed her life.She has been affect...
08/19/2026

Only 2 years old, Dik Putri is already facing a devastating medical battle that has changed her life.

She has been affected by an aggressive eye cancer that has spread beyond her eye and caused a large tumor to develop along the side of her face and neck.

The disease has taken away her vision, making the world around her much harder to experience.

Basic activities like eating and sitting upright have become exhausting challenges for the little girl.

Her doctors continue providing specialized care, working to manage the condition, slow its progression, and keep her as comfortable as possible.

Meanwhile, her mother, Nia, spends long hours doing laundry to help pay for her daughter's medical needs.

The growing costs of treatment, transportation, and travel have placed enormous pressure on the family, but Nia continues to stand beside her daughter.

Through every difficult moment, Dik Putri's family continues to hope for a chance to give her more comfort and brighter days ahead.

**Full story in the comment 👇👇👇**

Address

Hoa Kỳ
Texas City, TX
77099

Website

Alerts

Be the first to know and let us send you an email when GOD with Us posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Shortcuts

Share

Category