Full form of MEDIA:
MEDIA: myalgic encephalomyelitis Defense Intelligence Agency Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a disabling and complex illness. Complete similar symptoms of covid19 one can search it’s symptoms. People with ME/CFS are often not able to do their usual activities. At times, ME/CFS may confine them to bed. People with ME/CFS have overwhelming fatigue that is not improved by rest. ME/CFS may get worse after any activity, whether it’s physical or mental. This symptom is known as post-exertional malaise (PEM). Other symptoms can include problems with sleep, thinking and concentrating, pain, and dizziness. People with ME/CFS may not look ill. People with chronic fatigue syndrome want to be taken seriously and to receive personalised, empathetic care Chronic fatigue syndrome (CFS) is a complex, long-term condition that dramatically limits people’s activities. It is also known as myalgic encephalomyelitis (ME). People with CFS/ME are exhausted for no reason; rest does not help and it can take days or weeks to recover from any activity. Some describe ‘brain fog’ and problems with memory, concentration and speech. Doctors can find it challenging to care for people with this condition. There is no specific test for diagnosing CFS/ME and no ‘gold standard’ effective therapy. Many potential treatments are hotly debated by doctors and patients. A new study explored patients’ views on the care they would like to receive. Researchers pooled data from 47 studies on patients’ experiences of CFS/ME and their relationships with healthcare professionals. They found that people with CFS/ME wanted a personalised approach, and for doctors to provide a sense of safety to allow them to work through complex issues. But they often felt invisible and dismissed by doctors. The findings suggest doctors should take time to listen to the views of their patients (even if they disagree with them) and work together to find treatments that minimise the impact of the condition on the person’s daily life. The researchers say that training could help doctors build successful relationships with people with CFS/ME. What’s the issue? CFS/ME is characterised by debilitating fatigue; people may be unable to leave the house, or to get out of bed. It may take them days or weeks to recover from any activity. They are not refreshed by sleep and may have cognitive difficulties with memory or concentration; they may be confused, have slurred speech or problems finding words. This complex condition lasts at least four months and often much longer.Because of this media what we see in our daily life are serious cause of this pandemic and so called viral infection.Nothing is going good in everyones life after 2019 when pandemic hit for first time.What i sugguest you all is that dont watch tv,mobile phone more these tools have become attack source to individual which makes us brainwashed totally. Don’t trust media they are lier their information is released only after bigheaded people let them to publish to people. we dont know whats inside the box they only show whats outside the box.Instead reaserch your self try google deeper and deeper collect the information and find your own conclusion that is best for you to decide whats wrong and what is right.We are wasting our valuable time in watching and listening noonses news and media information.