Patients with chronic fatigue syndrome/myalgic encephalomyelitis (ME/CFS) have heightened innate immune responses to bacteria, viruses, and fungi. While these responses are essential to fight ...

Bethesda, MD — New research into the mechanisms underlying myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and long COVID is aimed at identifying potential approaches to treatment of ...

ME/CFS is a long-term condition that can affect different parts of the body, resulting in a wide range of debilitating symptoms.

The number of ME/CFS patients is expected to rise drastically due to long-term effects of the COVID-19 pandemic. Scientists have now identified possible biomarkers that could improve the diagnosis ...

People with long COVID, ME/CFS and other chronic conditions are taking up science to find symptom relief and inspire new directions for professional scientists.

On Monday, September 19, 2022, #MeAction Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and long COVID activists protested to address the crisis in the country with post-viral ...

“A quarter of ME/CFS patients are bed-bound or house-bound," said Beth Pollack, a research scientist at MIT studying ME/CFS and related illnesses. Up to 75% are too sick to work, she added.

Myalgic encephalomyelitis / chronic fatigue syndrome investigators are now including people with long-term post-COVID-19 symptoms in their studies, aiming to elucidate 'post-viral' pathophysiology.

There are almost two-thirds more people living with ME/CFS in England than previously thought, a study says. The new estimate suggests that approximately 404,000 people are affected by ME/CFS ...

'The Dragon's Den debacle shows we urgently need more research into ME/CFS' One writer, who has witnessed the ravages of the condition up close, makes the case By Lauren Clark Published: 31 ...

The National Institutes of Health has promised to put more money into research on an illness that many people feel has been dissed by the medical establishment.