As per a new study, people who suffer from chronic fatigue syndrome feel low and weak to face the world and researchers are batting for more work on their condition.

“There's no defined pathology of the illness which means that biomedical research is paramount because without finding out the actual mechanism of the illness, then it's very hard to then introduce a treatment,” she said.
Victims also say that the illnesses are often misunderstood and even more difficult to diagnose. May 12 is International Awareness Day for Chronic Immunological and Neurological Diseases.
It is estimated that chronic fatigue syndrome, also known as myalgic encephalomyelitis (ME), afflicts over 200,000 Australians.
Bob Townsend, president of ACT ME/Chronic Fatigue Syndrome Society, said victims could often feel isolated but for them a “normal” life is possible if they understand the problems and know when to stop from going overboard in order to prevent the problem from worsening.
Source-Medindia