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60 results for "cystic fibrosis"
Scientists have created a precise gene-editing tool that could offer permanent treatment for cystic fibrosis patients, potentially replacing daily medications that cost hundreds of thousands of dollars per year. The breakthrough could transform care for people living with this and other genetic diseases.
Scientists at the University of Trento developed the first gene therapy for 10% of cystic fibrosis patients who had no treatment options until now. The breakthrough could lead to a permanent cure instead of lifelong drug dependence.
Australian researchers developed an AI system that makes gene editing safer by protecting healthy genes during treatment. The breakthrough could transform how doctors treat genetic diseases like cystic fibrosis.
A Kansas community turned clay shooting into a fundraising powerhouse for cystic fibrosis research, celebrating nearly a quarter century of support. Scientists can now cure CF in the lab but need funding to perfect the delivery method.
A chance discovery involving frog eggs led to medications that transformed cystic fibrosis from a death sentence into a manageable condition. Dr. Mike Welsh just won biomedicine's highest honor for research that saved thousands of lives.
A breakthrough cystic fibrosis drug may also transform diabetes outcomes for 30% of Australian CF patients who develop the condition. New research will investigate whether Trikafta can prevent or slow cystic fibrosis-related diabetes.
A breakthrough drug combination is giving families living with cystic fibrosis real hope for healthier futures. German researchers just proved the treatment reduces dangerous inflammation for years, not just months.
A major European survey reveals what drives doctors to prescribe the life-changing cystic fibrosis drug Kaftrio to patients with stable lungs. The findings could help thousands more patients access treatment earlier.
Adults with cystic fibrosis-related diabetes needed significantly less insulin after one year on Kaftrio, offering hope for reduced treatment burden. The French study of 107 patients also found more stable blood sugar levels and dramatic improvements in lung function.
A 20-year-old bride went viral after dancing at her reception while doing her twice-daily cystic fibrosis treatment. Her joyful video has inspired millions and given hope to other CF patients.
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A pediatric pulmonologist in Cape Town is finding creative ways to give life-saving cystic fibrosis medication to children who can't afford it. Seven-year-old Jaylin hasn't been hospitalized once since starting treatment that costs $200,000 per year.
Children with chronic lung diseases can now get detailed scans that reveal how their lungs are working, not just what they look like, without any radiation exposure. A UK hospital is already using the breakthrough technology to catch early signs of cystic fibrosis that traditional tests miss.
A small town in Saskatchewan is rallying behind families affected by cystic fibrosis, with youth bakers and community volunteers kicking off a week of heartfelt fundraising. Their efforts are building connections that organizers say matter just as much as the dollars raised.
Japan has approved a groundbreaking new treatment for two deadly lung diseases, offering hope to thousands of patients who've had limited options for over ten years. The drug slows lung function decline and could transform how doctors treat these life-threatening conditions.
More than 500,000 Europeans living with deadly lung scarring diseases just got their first new treatment option in over a decade. The oral medication slows lung function decline and doesn't require the burdensome liver monitoring older treatments demand.
Researchers discovered how a protein called vitronectin triggers deadly lung scarring, opening the door to new treatments for a disease that currently has no cure. The breakthrough could help thousands living with pulmonary fibrosis breathe easier.
Researchers have discovered what causes devastating scar tissue in Crohn's disease patients, opening the door to treatments that could prevent scarring rather than just treating inflammation. For the first time, scientists can target the root cause of fibrosis that sends thousands to surgery each year.
An 80th birthday celebration in Northern Ireland became a powerful tribute to a late husband, raising over €1,200 for pulmonary fibrosis support. The donation will help provide respite care and resources for families battling the progressive lung disease.
A new genetic testing approach at Mayo Clinic is transforming how doctors diagnose and treat pulmonary fibrosis, changing treatment plans for more than half of patients studied. The breakthrough combines telomere measurement with DNA testing to uncover hidden disease causes.
Scientists are developing better treatments for idiopathic pulmonary fibrosis, a deadly lung disease that kills most patients within five years. Understanding the genetic and environmental causes is finally leading to hope for the 3 million people affected worldwide.
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