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30 results for "disease treatment"
Ozempic and similar medications may heal arthritis, liver disease, and more by resetting the immune system, not just through weight loss. Scientists are discovering these drugs work throughout the body to reduce harmful inflammation while keeping infection-fighting power strong.
A four-year-old Australian boy has become the first child in the country to receive a revolutionary gene therapy for Epidermolysis Bullosa, a devastating condition that causes skin to blister at the slightest touch. The treatment is helping his body produce the critical protein his skin has been missing since birth.
Researchers created a new system that targets healthy mitochondria to damaged cells, offering hope for treating diseases like optic nerve damage and heart failure. In tests, transplanted mitochondria helped dying neurons survive.
A breakthrough treatment for ulcerative colitis brought 40% of patients into remission after just 12 weeks, offering fresh hope for millions living with inflammatory bowel disease. Spyre Therapeutics' experimental drug succeeded in its first major trial, setting up competition with pharmaceutical giants to deliver better digestive disease treatments.
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After nearly three decades of living with multiple sclerosis, Ann Romney has overcome debilitating symptoms through alternative therapies and now champions research that could stop MS progression within five years.
A secret FDA-approved drug called "compound X" helped mice with Parkinson's symptoms walk and balance normally by clearing toxic brain proteins. Human trials could start within a year, offering hope for 10 million people worldwide living with the disease.
Scientists discovered that keratin 16 acts as a natural "brake" on skin inflammation, explaining why mutations cause painful conditions like psoriasis and eczema. This breakthrough could lead to targeted treatments for millions suffering from inflammatory skin diseases.
Jeff Vierstra lost his mother and two sisters to a deadly genetic disease, but an experimental treatment may be preventing him from developing ALS for the first time in his family's history. After three years of spinal infusions targeting his mutated gene, the 41-year-old shows no signs of the disease.
Researchers in Denmark just launched a breakthrough project to stop Parkinson's disease by blocking toxic proteins from spreading in the brain. With $4 million in funding, they aim to have treatment candidates ready for testing in just three years.
Adults with Fabry disease in the European Union can now receive treatment once a month instead of every two weeks, giving patients and families more time to live beyond managing their condition. The new dosing schedule for Elfabrio could ease the lifelong treatment burden for thousands.
The FDA just approved Denali Therapeutics' new medicine for Hunter syndrome, bringing fresh hope to families affected by this rare genetic disease. The approval comes as a welcome surprise after the agency recently toughened its standards for rare disease treatments.
After a difficult year, biotech company Sarepta Therapeutics is bouncing back with early clinical trial results showing two new muscular dystrophy treatments appear safe and effective. The promising data offers hope for patients with rare muscle-wasting diseases who desperately need new treatment options.
Researchers in Edinburgh engineered bacteria to transform waste plastic bottles into L-DOPA, a critical Parkinson's disease treatment. This breakthrough could revolutionize sustainable medicine while tackling plastic pollution.
Scientists just figured out how a crucial vitamin-powered molecule reaches the tiny energy factories inside every cell in your body. The breakthrough could help doctors better treat brain diseases and metabolic disorders.
For the first time, a gene therapy has shown dramatic results in slowing Huntington's disease, offering hope to 8,000 UK families who've had no treatment options until now. Patients receiving the higher dose experienced 75% less disease progression over three years.
Children across Europe with a painful swallowing disorder finally have a medicine made just for them. The EU just approved Jorveza oral suspension, ending years of kids taking adult medications not designed for their bodies.
Microsoft scientists have found a way to combine quantum computing with artificial intelligence to dramatically speed up the discovery of new medicines, batteries, and materials. This breakthrough could help solve problems from climate change to disease treatment in a fraction of the time it takes today.
Morocco just launched a Precision Medicine Hub that will help thousands of patients with rare diseases get faster diagnoses and coordinated care. The new national center brings together advanced genetic testing, specialist teams, and patient support under one roof.
A heart condition once called a death sentence now has multiple FDA-approved treatments that are keeping patients alive and out of hospitals. Cardiac amyloidosis patients are being diagnosed earlier and living longer thanks to breakthrough medications approved in the past year.
Japanese researchers discovered that immune cells can selectively extract DNA from dying cells through a completely new process called nucleocytosis. This breakthrough could lead to better treatments for autoimmune diseases, infections, and cancer within the next decade.
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