history: Have you ever heard of Chronic Fatigue Syndrome?
knowledge: Diagnosis is based on a person's symptoms.
response: Yes, since the diagnosis depends on the person's symptoms.
history: Have you ever heard of Chronic Fatigue Syndrome?
Yes, since the diagnosis depends on the person's symptoms.
There has been very little research until recently and it was often misdiagnosed as Fibromyalgia. Many doctors think its linked to the Epstein Barre virus which causes Mono. Do you know anyone with Mono or Chronic Fatigue Syndrome?
knowledge: Biological, genetic, infectious, and psychological mechanisms have been proposed, but the cause is not understood.
response: None actually but another thing about the syndrome is that the cause is not understood, even though there are proposals like biological mechanisms or psychological ones.
history: Have you ever heard of Chronic Fatigue Syndrome?
Yes, since the diagnosis depends on the person's symptoms.
There has been very little research until recently and it was often misdiagnosed as Fibromyalgia. Many doctors think its linked to the Epstein Barre virus which causes Mono. Do you know anyone with Mono or Chronic Fatigue Syndrome?
None actually but another thing about the syndrome is that the cause is not understood, even though there are proposals like biological mechanisms or psychological ones.
It is still being researched. I also had mono and it has led to me having CFS. It is now know as Myalgic Encephalomyalitis or ME. Have you heard of the #MillionsMissing movement?
knowledge: There is no cure, with treatment being symptomatic.
response: I have not, is it about how there is no cure for the syndrome and treatment is symptomatic?
history: Have you ever heard of Chronic Fatigue Syndrome?
Yes, since the diagnosis depends on the person's symptoms.
There has been very little research until recently and it was often misdiagnosed as Fibromyalgia. Many doctors think its linked to the Epstein Barre virus which causes Mono. Do you know anyone with Mono or Chronic Fatigue Syndrome?
None actually but another thing about the syndrome is that the cause is not understood, even though there are proposals like biological mechanisms or psychological ones.
It is still being researched. I also had mono and it has led to me having CFS. It is now know as Myalgic Encephalomyalitis or ME. Have you heard of the #MillionsMissing movement?
I have not, is it about how there is no cure for the syndrome and treatment is symptomatic?
No, it was a movement telling their stories with CFS and other invisible illnesses. I think they also complained how the US hasn't done anything about it but I'm unaware what.
knowledge: No medications or procedures have been approved in the United States.
response: It might be how the US has not approved of any medications or procedures.