@kpako_: Happy Sunday😳

KPAKO
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Friday 21 August 2026 05:39:28 GMT
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yeah_its_smuvee
SMUVEE’S SHOW :
Omor crazyyyy😂😂
2026-08-21 06:15:15
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everything_with_nene
Everything_with_Nene Intl :
😂😂😂
2026-08-21 09:10:24
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prettyriche
Pretty girl🧃🧃🤙 :
😂😂😂😂
2026-08-21 15:09:32
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clinton.063
CLINTON :
😳
2026-08-21 06:17:21
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user40207068567305
John ozioma :
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2026-08-21 06:00:07
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vicky21364
Vicky💕💦🧜‍♀️😇😍 baby🦋🥰🌺 :
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2026-08-21 08:19:38
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Denham Springs, Louisiana. It started during cross country practice. Double vision. A wave of lightheadedness on the second lap. Katie Tanton didn't think much of it at the time. Neither did anyone else. By November, the headaches wouldn't quit. Then, in January, her parents noticed something off with her eyes and rushed her straight to the emergency room. A scan found the answer nobody wanted. A mass on her brain stem. The diagnosis was DIPG, diffuse intrinsic pontine glioma, a rare and merciless cancer that grows directly into healthy tissue. It can't be cut out. On her 11th birthday, February 18th, Katie started radiation. Thirty rounds, five days a week, six weeks straight. She rang the bell on April 1st.
Denham Springs, Louisiana. It started during cross country practice. Double vision. A wave of lightheadedness on the second lap. Katie Tanton didn't think much of it at the time. Neither did anyone else. By November, the headaches wouldn't quit. Then, in January, her parents noticed something off with her eyes and rushed her straight to the emergency room. A scan found the answer nobody wanted. A mass on her brain stem. The diagnosis was DIPG, diffuse intrinsic pontine glioma, a rare and merciless cancer that grows directly into healthy tissue. It can't be cut out. On her 11th birthday, February 18th, Katie started radiation. Thirty rounds, five days a week, six weeks straight. She rang the bell on April 1st. "It was emotional because we know that she has a very long, hard journey ahead of her," her mother, Breann, said. In May, Katie was accepted into a clinical trial at Nationwide Children's Hospital in Columbus, Ohio, one of the only places offering a shot at something more than radiation alone. Getting there became its own fight. The Tantons were driving 2,000 miles round trip every month. Hotels, gas, food, rental cars, none of it covered, because Louisiana Medicaid doesn't pay for care received out of state. Eventually the math stopped working. The family packed up and left Denham Springs behind entirely, moving to Ohio to be near Katie's treatment full time. Then the money ran out anyway. For a week, the Tantons slept in tents at local campgrounds, holding onto whatever they had left for Katie's care instead of a roof over their own heads. Her most recent MRI delivered two truths at once. The tumor has shrunk. The shrinking has also triggered swelling and tissue death nearby, which is making some of Katie's symptoms worse, not better. "The brain doesn't know the difference between the tumor and the dead tumor," Breann explained. Then everything shifted again. Within hours of the family's story reaching a wider audience, a social media personality gave the Tantons $300,000 toward Katie's care. The family moved out of the tents and into a hotel, secured for the rest of the year. Katie has two younger sisters, one of whom lives with cystic fibrosis of her own. Both of Katie's parents remain out of work, entirely focused on keeping her alive. Her aunt, Annie Normand, has promised to shave her head the moment a fundraiser for the family hits $50,000. Through all of it, Katie is holding onto something simple. She still wants to see Disneyland. A family slept in tents to keep their daughter in treatment. One story, one gift, and a hotel room later, they're still fighting the same fight, just with a little more room to breathe. 🔗 in comments to read full story.

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