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13692 results for "disease management"
University of Queensland researchers have developed a breakthrough drug that could transform Motor Neurone Disease from a terminal diagnosis into a manageable chronic condition within five years. The discovery unlocks a previously untargetable immune receptor that plays a key role in neurodegenerative diseases.
More than 14% of Americans have chronic kidney disease and don't know it, but simple blood and urine tests can catch the condition before it causes serious damage. Doctors say early detection and lifestyle changes can slow or stop this silent disease that affects every organ in the body.
A groundbreaking treatment for Huntington's disease just cleared a major hurdle, bringing hope to 240,000 Americans affected by this devastating condition. The experimental therapy could become the first disease-modifying treatment for a disorder that has had none.
Researchers at UConn have patented a breakthrough treatment that could reverse fatty liver disease, a condition affecting billions worldwide with almost no current cure options. The innovative approach targets the root cause of the disease rather than just managing symptoms.
A groundbreaking treatment for myotonic dystrophy type 1 reduced toxic proteins by 40% and improved muscle function in patients who've never had disease-modifying options. The New England Journal of Medicine just published results that could lead to the first approved therapy for this progressive, often fatal disease.
Researchers discovered how to disguise healthy mitochondria so they can slip into diseased cells undetected, extending the lives of mice with a fatal genetic disorder. The breakthrough could one day help children born with rare mitochondrial diseases.
A new treatment for a rare kidney disease just passed a major test, bringing hope to 330,000 patients in the U.S. and Europe. Vertex's drug successfully reduced a key disease marker by half in late-stage trials.
Pearl Jam's Eddie Vedder and Canadian director Matt Finlin created a documentary following the race to cure epidermolysis bullosa, a devastating skin disease affecting children worldwide. The Netflix film captures breakthrough research that could unlock treatments for thousands of rare diseases.
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.
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.
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.
Heart disease deaths fell by 25,000 between 2022 and 2023, reversing pandemic-era increases. The decline shows that prevention strategies are working, and experts say simple daily habits could save even more lives.
A drug already used for diabetic kidney disease just proved it can help the other half of kidney patients too, slowing disease progression by 23%. For 674 million people living with chronic kidney disease, this could mean more time before their kidneys fail.
Dancing with the Stars judge Carrie Ann Inaba is opening up about her decade-long journey with Sjogren's disease, an autoimmune condition affecting four million Americans. After a recent medical emergency, she's helping others recognize symptoms and find community.
Scientists created an AI tool that tracks how diseases spread in places like cruise ships and care homes, helping stop outbreaks before they spiral. The system can predict who will get sick next and suggest exactly when to clean surfaces or isolate patients.
The FDA has accepted a groundbreaking treatment for Alexander disease for priority review, offering hope to families battling a rare neurological condition that has no approved therapies. If approved by September, zilganersen would become the first medicine ever available for this devastating illness.
The FDA reversed course on a groundbreaking gene therapy for Huntington's disease, bringing new hope to thousands of families. The treatment from biotech company UniQure can now move forward toward U.S. approval.
A groundbreaking gene therapy called AMT-130 has slowed Huntington's disease progression by 75% in clinical trials, offering hope to families who've waited 154 years for effective treatment. The one-time treatment could preserve patients' ability to walk, speak, and connect with loved ones for years longer.
University of Edinburgh researchers discovered how immune cells trigger debilitating scar tissue in Crohn's disease patients, opening the door for treatments that could prevent the condition's most challenging complication. The breakthrough could help millions avoid surgery and transform lives.
Two people with a devastating autoimmune disease have been symptom-free for over 15 years after a groundbreaking stem cell transplant. The therapy replaced their immune systems and allowed them to reclaim their lives without medication.
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