Find uplifting stories about heroes, innovations, and solutions
52 results for "disease research"
Billionaire Dan Gilbert is pouring $50 million yearly into rare disease research after losing his son Nick to neurofibromatosis. His foundation has already helped create the first FDA-approved treatments for the incurable genetic disorder.
Former British Prime Minister David Cameron, whose son died from a rare disease, is leading a major international effort in Cleveland to develop cures for conditions that have stumped scientists for decades. The partnership has already advanced 227 potential medicines and launched 47 companies.
A small Queensland community funded Australia's first TMS machine for motor neurone disease research, turning heartbreak into hope. Early detection could change everything for future patients.
Brown University scientists created a breakthrough worm model that could help find treatments for alternating hemiplegia of childhood, a rare disease causing paralysis in kids. The discovery offers hope to families who've waited years for effective therapies.
University of Pennsylvania researchers created a smarter way for AI to solve one of science's hardest math problems, using 1940s mathematical theory instead of more computing power. The breakthrough could help scientists understand how DNA works and improve disease research.
A breakthrough technique reveals hundreds of tiny "dark proteins" scientists never knew existed, opening new paths to understanding and treating heart disease. This global effort to map the body's hidden proteome is transforming how researchers approach human health.
Chemical engineering student Ashley Blake just earned one of America's most prestigious undergraduate honors for her work developing treatments that could help millions living with Alzheimer's and Parkinson's. The Goldwater Scholar is creating drug delivery systems that can break through the brain's natural barriers to deliver medicine where it's needed most.
Latus Bio just secured $42 million to advance treatments for two devastating genetic diseases, including Huntington's. The funding brings hope to families waiting for breakthroughs in conditions that currently have no cure.
A Nashville family transformed their annual Kentucky Derby party into a powerful fundraiser after their daughter was diagnosed with an incurable nerve disease. Last year alone, they raised $75,000 for research into Charcot-Marie-Tooth disease.
Scientists discovered chaotic laser light can organize itself into a precision beam that images the blood-brain barrier 25 times faster than current methods. The breakthrough could accelerate treatments for Alzheimer's, ALS, and other neurological diseases.
NYU is solving diseases faster by throwing out the old playbook: instead of keeping scientists in separate buildings, they're mixing engineers, doctors, and AI experts into teams focused on beating specific diseases. Early wins include a startup detecting airborne pathogens and "inverse vaccines" that could cure celiac disease and allergies.
Southern Italy just gained its biggest pediatric research hospital after Santobono Pausilipon joined the nation's elite network of scientific medical institutes. The milestone brings specialized childhood disease research and treatment to a region that's needed it for decades.
Former England rugby captain Lewis Moody is cycling 500 miles to deliver the ball for a major championship match, rallying his World Cup-winning teammates to raise money for motor neurone disease research just months after his own diagnosis.
Former England rugby captain Lewis Moody, diagnosed with MND last September, is leading a seven-day, 500-mile cycling challenge with his 2003 World Cup-winning teammates to raise funds for motor neurone disease research. The ride ends at Twickenham's final match in June, channeling the same fighting spirit that once defined his playing career into finding a cure.
After nearly dying five times from a mystery illness, Dr. David Fajgenbaum turned to artificial intelligence to save his own life—and now he's finding treatments for thousands of other forgotten patients. His AI system has already identified potential cures for over 60 rare diseases that drug companies won't touch.
Four leading European research institutes have joined forces to speed up treatments for Alzheimer's, Parkinson's, and other brain diseases affecting millions. The CURE-ND Alliance brings together over 2,500 scientists working to transform how we understand and treat neurodegenerative diseases.
The late Doddie Weir's foundation has surpassed £2 million in fundraising for motor neurone disease research, driven by a grueling 750-mile cycling challenge. His widow Kathy says the growing support proves his legacy is "driving real progress" toward a cure.
A mother is running the London Marathon to fund research for gene therapies that could save her daughter from kidney failure. Her eight-year-old was diagnosed with a rare, incurable form of nephrotic syndrome that currently has no treatment options.
Researchers at the University of Michigan have discovered what causes a rare condition that makes walking so painful patients crawl instead. An FDA-approved cream has already shown promise in early trials.
.png)
A Colorado scientist's breakthrough research is transforming treatment for children with a devastating rare disease, bringing relief after years of pain. Two patients are already showing remarkable improvement from a new therapy approach.
Showing 20 of 52