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7861 results for "chronic disease treatment"
Ghana's Parliament has approved $2.9 billion to help families afford treatment for cancer, kidney failure, and other chronic diseases. The Ghana Medical Trust Fund will reduce crushing medical costs that push vulnerable patients deeper into poverty.
Patients with a rare liver disease finally have relief from debilitating itching that robbed them of sleep and quality of life. The FDA just approved the first treatment specifically designed to ease this painful symptom that affected thousands.
Families fighting Huntington's disease celebrated a breakthrough this Valentine's Day as researchers announced the first treatment for the deadly brain condition. The discovery brings renewed hope to a community that has waited decades for medical progress.
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.
Scientists have discovered that a cancer treatment called CAR T-cell therapy can stop autoimmune diseases like lupus and multiple sclerosis without the dangerous side effects. Hundreds of patients are already experiencing remarkable recoveries, and the first treatments could be approved next year.
Nearly 2 million Africans die prematurely each year from hypertension and diabetes complications, but a new continental program is transforming how health systems respond. Africa CDC just launched SPARK-NCD, integrating chronic disease care into existing platforms to save lives across the continent.
A revolutionary therapy originally designed to fight blood cancer is helping people with severe lupus and other autoimmune diseases achieve remission. Early results show the treatment can reprogram the immune system instead of just suppressing it.
As chronic illnesses surge across Uganda, health experts are calling for physiotherapy to become a standard part of treatment, not an afterthought. The shift could help thousands regain mobility and independence while reducing long-term healthcare costs.
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.
A groundbreaking NHS study using data from 29 million people reveals how secure health monitoring can spot disease trends early and help fix care gaps. The research shows chronic kidney disease diagnoses jumped 35% above expected levels, likely due to better testing and new 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 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 California space company just partnered with a major pharmaceutical firm to manufacture impossible-to-make drugs in orbit. The collaboration could unlock breakthrough treatments for rare lung diseases by 2026.
A therapy that fights cancer is being adapted to treat lupus, MS, and other autoimmune diseases affecting nearly one in 10 Americans. Researchers at Roswell Park aim to replace lifelong medications with a single infusion.
A therapy originally designed to fight blood cancer is giving hope to people with severe autoimmune diseases who've run out of options. Early results show some patients are achieving years of remission after just one treatment.
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.
Two companies are teaming up to manufacture medicines in orbit, where zero gravity could create more effective treatments for people with rare lung diseases. The first missions launch in 2026, bridging decades of space research with real patient benefits.
The FDA just approved the first treatment for Menkes disease, a rare genetic disorder that has claimed countless young lives. Copper histidinate could help babies with this devastating condition finally have a fighting chance.
After decades of limited options, five new therapies have been approved for IgA nephropathy, a kidney disease that affects millions worldwide. Doctors say this is just the beginning of a treatment revolution.
Scientists at MIT built a tiny working liver model that could revolutionize how we find treatments for liver disease affecting over 100 million Americans. The breakthrough offers hope for discovering drugs that actually work for everyone.
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