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Gen Zer Films Himself Every Day—Then Uncovers a Shocking Truth

Gen Zer Films Himself Every Day—Then Uncovers a Shocking Truth

Newsweek22-06-2025
Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources.
Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content.
A teenager has shared how he noticed the first symptom that led to his cancer diagnosis—by watching his own videos back.
Felipe, 19, from Georgia, had recently moved to college in Oregon when he decided to take part in a viral health craze on TikTok. The Coconut Cult trend involves people documenting their daily intake of probiotic yogurt on TikTok and Instagram. But what he noticed watching back his videos wasn't digestive benefits—it was a lump forming in his neck.
"I took the daily videos after seeing the craze with Coconut Cult and wanted to see any results from its daily intake," Felipe told Newsweek. "I noticed something was wrong after the left side of my neck appeared swollen; I saw it was curvy on the video, and then that's when I felt the bump."
Pictures from the TikTok video that prompted Felipe to visit the emergency room.
Pictures from the TikTok video that prompted Felipe to visit the emergency room.
@felipedkl2/TikTok
Concerned, Felipe sought medical attention, initially receiving a suspected diagnosis of bacterial infections like strep throat or mononucleosis. But doctors recommended a biopsy to be sure.
"The ER had initially told me they suspected bacterial infections like strep throat or mononucleosis," Felipe said. "They immediately recommended a biopsy to see what's causing them to be inflamed."
When that result came back, it wasn't what anyone was expecting—Felipe was diagnosed with Hodgkin's lymphoma, a type of cancer.
What Is Hodgkin's Lymphoma?
"Lymphoma is a cancer of the lymph glands, and if the lymph glands contain specific characteristic cells, they fall under the category of Hodgkin's lymphoma," Dr. Siddhartha Ganguly, section chief of hematology at Houston Methodist and an academic professor for Weill Cornell Medical College, told Newsweek. "It is relatively rare. There are only about 8,000 to 8,500 new cases across the country a year."
Thankfully, when caught quickly, it is very treatable. "If we catch Hodgkin's lymphoma in the early stage of the disease, then the cure rate reaches as high as 95 percent to 98 percent in young Hodgkin's patients," Ganguly said.
Felipe, who didn't share his surname, posted the video that prompted him to get checked out on TikTok where it now has over 722,000 views.
Ganguly said the symptoms of Hodgkin's lymphoma you should look out for: "If somebody has enlargement of a gland, whether they have symptoms of unintentional weight loss, night sweats or fever, and the gland is present for more than seven to 10 days, see your primary care physician," he said.
"They may prescribe an antibiotic to make sure it's not an infection. If it is still there after that antibiotic, make an appointment to see a hematologist who deals with lymphoma. The only way to make a diagnosis is through a biopsy."
For Felipe, the next steps include a PET scan and chemotherapy sessions with the lymphoma medical team. He has continued to share parts of his journey on TikTok and remains positive, and is thankful for the support from viewers.
"I feel better now that I have an answer. I'm taking things day by day," he said.
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Boy, 4, With Cancer Deported by ICE Despite Being US Citizen, Lawsuit Says
Boy, 4, With Cancer Deported by ICE Despite Being US Citizen, Lawsuit Says

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Boy, 4, With Cancer Deported by ICE Despite Being US Citizen, Lawsuit Says

Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. A federal lawsuit filed in Louisiana alleges that U.S. Immigration and Customs Enforcement (ICE) deported a 4-year-old U.S. citizen boy with stage IV kidney cancer, along with his mother and sibling, to Honduras in April 2025. The complaint contends that the deportation occurred without adequate notice, legal counsel, or arrangements for the child's ongoing medical care. Why It Matters Immigration authorities have been under heightened scrutiny amid allegations of misconduct, with the agency at the center of the national debate over immigration policy. 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Woman Desperate for Diagnosis for Years—Then Notices Ear Looks Different
Woman Desperate for Diagnosis for Years—Then Notices Ear Looks Different

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Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. For a decade, Holli Barron went in and out of doctor's offices, desperate for answers to a growing list of mysterious symptoms—throat swelling, rashes, extreme fatigue, and more. Despite receiving multiple diagnoses over the years, no treatment brought relief, leaving her feeling as if she was locked in a battle she couldn't win. That changed recently when she developed a new and unusual symptom: red, hot ear cartilage. It led to the correct diagnosis—relapsing polychondritis—a rare condition that causes repeated episodes of swelling and inflammation in cartilage and other tissues throughout the body, affecting fewer than 5,000 people in the U.S. Barron shared her experience in a TikTok video (@therapyandthings) that has been viewed over 526,000 times. She wrote: "When you send your rheumatologist a photo of 1 new weird symptom and suddenly after YEARS of no diagnosis you're getting seen by two specialists." She added that she underwent multiple tests and two CT scans in just 48 hours. "Living with a rare autoimmune disease also takes an emotional toll," the South Carolina mom told Newsweek. "Going years without a diagnosis can be difficult," Barron added, stressing the importance of caring for the mind, body, and soul, while navigating chronic illness. Two screenshots from the viral video showing Holli Barron looking puzzled and shocked. Two screenshots from the viral video showing Holli Barron looking puzzled and shocked. TikTok/@therapyandthings Sharing Her Story Online The licensed mental-health counselor later posted another video featuring photos of her ears. She warned viewers not to panic if they experience redness, as it was just one of many symptoms she had. "Prior to the ear redness and pain," Barron said, "including inflammatory arthritis, Raynaud's Phenomenon, tinnitus, episodes of minor vertigo, extreme fatigue, sensation of throat swelling, pain on the bridge of my nose. "Following CT scans, it was determined that I also have calcifications in the cartilage of my trachea," she added. The cartilage of Barron's ear is red and the lobe is the usual color. The cartilage of Barron's ear is red and the lobe is the usual color. Holli Barron Understanding Relapsing Polychondritis The Genetic and Rare Diseases (GARD) Information Center says relapsing polychondritis (RP) can also affect the airways (trachea), rib cartilage, eyes, heart, blood vessels, skin, kidneys, and nervous system. Signs and symptoms vary widely between individuals, depending on the areas involved. The exact cause is unknown, though both genetic influences and unidentified factors are believed to play a role. RP often occurs alongside autoimmune disorders. "Autoimmune disease symptoms can tend to overlap," Barron said. "So I don't want to say I was 'misdiagnosed,' but it did take many years to land at this correct diagnosis. Some previous diagnoses I was told included seronegative rheumatoid arthritis, lupus-like illness, tendinitis, and inflammatory arthritis." Living with an autoimmune disease while juggling mom life, a Ph.D., and work can be "challenging," Barron said—especially during flare-ups. "The fatigue and pain can be debilitating at times, making everyday tasks more difficult to complete," she added. How Is Relapsing Polychondritis Treated? Since only around 5 percent of rare diseases have FDA-approved treatments, finding a health-care team that can effectively manage symptoms and overall well-being is critical. People with rare diseases often face delayed diagnoses, limited treatment options, and difficulty finding providers with the necessary expertise. Building a care team that understands the patient's needs can greatly improve quality of life. For now, Barron will continue taking hydroxychloroquine, a disease-modifying antirheumatic drug (DMARD) that can reduce the pain of arthritis and swelling and prevent joint damage. "I will also be adding an immunosuppressant medication called Enbrel to hopefully slow the progression of the disease," Barron said. Is there a health issue that's worrying you? Let us know via health@ We can ask experts for advice, and your story could be featured on Newsweek.

Opioids: Parasitic Worm Discovery Could Lead to Safer Painkillers
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Activation of the protein leads to rapid mobilization of immune cells, including gd T cells, monocytes and neutrophils, which induce inflammation. This inflammation, the researchers explained, plays a crucial role in host resistance to the larval entry into the skin. These findings highlight the importance of neurons that sense pain and itching in successful immune responses. "Identifying the molecules in S. mansoni that block TRPV1+ could inform preventive treatments for schistosomiasis. We envision a topical agent which activates TRPV1+ to prevent infection from contaminated water for individuals at risk of acquiring S. mansoni," said Herbert. In the study, mice were infected with S. mansoni and evaluated for their sensitivity to pain as well as the role of TRPV1+ in preventing infection. "S. mansoni infection significantly reduced thermal pain sensitivity evoked by TRPV1+ neurons. Consistently, isolated skin sensory neurons from infected mice had significantly reduced calcium influx and neuropeptide [chemical messenger] release in response to the TRPV1 agonist capsaicin [an irritant for humans and mammals] compared to neurons from naïve controls," the study authors wrote. "Using gain-and loss-of-function approaches to test whether TRPV1+ neurons initiate host-protective responses revealed that TRPV1+ neurons limit S. mansoni skin entry and migration into the pulmonary tract." The researchers are now planning to identify the nature of the secreted or surface-associated helminth molecules that are responsible for blocking TRPV1+ activity and specific gd T cell subsets that are responsible for immune responses. They also seek to further understand the neurons that helminths have evolved to suppress. Newsweek has reached out to the researchers for additional comment. Do you have a tip on a health story that Newsweek should be covering? Do you have a question about opioids? Let us know via health@ Reference Inclan-Rico, J. M., Stephenson, A., Napuri, C. M., Rossi, H. L., Hung, L.-Y., Pastore, C. F., Luo, W., & Herbert, D. R. (2025). TRPV1+ neurons promote cutaneous immunity against Schistosoma mansoni. The Journal of Immunology.

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