20/05/2026
Huge news for ME/CFS, Long Covid and other post viral/immune event illnesses. Identification of an immune element to MECFS is game changing to early diagnosis and treatment of the condition.
Currently, the mechanism of the conditions is still unknown and some medical professionals still debate its existence. We know that many people develop chronic fatigue syndrome and other similar conditions after a viral infection or another traumatic immune event.
Chronic fatigue syndrome diagnosis currently involves ruling out other conditions and monitoring symptoms over time which can take years and leave people financially, physically and mentally crippled. With the identification of dysfunctional immune cells, it’s hopeful a test can be developed - like a blood test or something similar.
There’s also no definitive medical treatment regime at the moment as to treat the conditions with medication requires an understanding of the mechanism. Researchers and some doctors have trialled some prescription medications which seem to work for some people. However, without set medical guidelines, majority of sufferers are left just able to treat their symptoms through lifestyle modifications like mobility aids and activity modifications.
Ella Engel saw many specialists before she was diagnosed with myalgic encephalomyelitis/chronic fatigue syndrome. Her blood may help researchers understand the condition.