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6695 results for "rare tumor"
A young man bleeding internally from a rare stomach tumor walked out of a Gurugram hospital just three days after emergency robotic surgery saved his life. Advanced technology turned what could have been fatal into a quick recovery story.
After eight doctors suggested removing her uterus, Brittany Pope finally discovered the real cause of her pain: a rare tumor specialists could treat. Her persistence led to answers that preserved her dream of expanding her family.
A six-year-old boy in China can finally eat normally again after doctors successfully removed a rare, egg-sized tumor from his throat. The risky three-hour surgery ended six months of difficulty eating and breathing for little Xiaoliang.
A 60-year-old woman who kept losing consciousness finally got answers when doctors found a tiny tumor in her pancreas and removed it using robotic surgery. Her blood sugar levels normalized immediately after the procedure.
Researchers in Tokyo have discovered a gene that causes dangerous insulin tumors, opening the door to better treatments for patients who suffer life-threatening blood sugar crashes. The breakthrough could transform care for people with insulinomas, tumors that have puzzled doctors for decades.
St. Bernards Healthcare just became the only hospital in Northeast Arkansas offering a targeted therapy for rare digestive cancers. The treatment delivers precision radiation directly to tumors, giving patients as young as 12 a new option when traditional therapies fail.
A free artificial intelligence system can now match rare cancer patients with potential treatments in minutes, offering new hope for thousands whose tumors have few dedicated clinical trials. The open-source tool worked for all 260 sarcoma patients tested.
Children with a rare brain cancer now have a new treatment option after European regulators approved Ojemda, a targeted therapy that works once a week. In trials, more than half of young patients saw their tumors shrink.
A breakthrough medication for a rare hereditary condition that causes tumors throughout the body is now affordable for hundreds of Australians. Patients who lived surgery to surgery finally have hope for their futures.
Judy Overton spent years supporting her husband through cancer treatment, then sharing those caregiving experiences in a blog. Now she's sharing her own victory over a rare spinal tumor.
When Caitlin Koehler was diagnosed with an extremely rare ovarian cancer at 27, she trusted MD Anderson's expert team to create a personalized treatment plan. Now cancer-free after beating two recurrences, she's proof that specialized care makes all the difference for young adults facing rare diagnoses.
A hospital in Indonesia built a successful rare disease registry in just two years, offering hope for similar efforts in Malaysia. The achievement could help 45 million people across Southeast Asia living with rare conditions get better care. #
A national trial found that an existing cancer pill may slow aggressive brain tumors in patients who had run out of options. Nearly 60% of patients saw their tumors stop growing for at least six months.
England approved its first new brain tumor treatment in 18 years, offering hope to 300 patients living in fear of their tumors growing. For Sally Penny, the pill has already given her a year without side effects and precious time with her children.
After a decade of stagnation where only 5% of rare diseases had treatments, Europe is overhauling outdated regulations to bring hope to 30 million patients. New pathways are finally treating ultra-rare conditions differently than common illnesses.
Scientists in Austin are developing a one-of-one therapy for baby Everett Blomstrom, who has an ultra-rare genetic disease affecting fewer than 50 people worldwide. The experimental treatment could be ready in two years and represents a breakthrough in personalized medicine for rare conditions.
After years without hope, Susannah Rosen received a breakthrough treatment for a rare neurodegenerative disorder that was slowly killing her brain cells. A nonprofit foundation now provides the custom-made medicine free for life to patients with ultra-rare diseases.
A mother whose daughter was diagnosed with a rare genetic disorder created an AI platform that saves families 53 hours a week and accelerates treatment research by up to 50%. Citizen Health now helps over 8,000 patients across 350 rare diseases navigate care and connect with others facing the same challenges.
Japan just made a breakthrough that could end its dependence on imported rare earth minerals. The nation successfully collected rare earth mud from 6,000 meters below the Pacific Ocean near a remote island.
Patients in England with low-grade brain tumors can now access a groundbreaking pill that slows disease and cuts seizures by 64%. It's the first new brain tumor treatment approved in the UK in two decades.
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