The Symptoms of Chronic Fatigue Syndrome
August 1, 2006 by laura
Filed under Diseases & Conditions
I have been thinking about how difficult it is to get a diagnosis of Fibromyalgia or Chronic Fatigue Syndrome. Basically doctors exhaust every other possible condition before giving the diagnosis of CFIDS. You have to be sick for at least 3 months but usually longer for a doctor to even consider a CFIDS diagnosis.
Here are the symptoms of Chronic Fatigue Syndrome, as reported on by the CFIDS Association of America.
incapacitating fatigue- experienced as profound exhaustion and extremely poor stamina
poor concentration and short term memory
flu like symptoms such as pain in the joints and muscles, unrefreshing sleep, tender lymph nodes, sore throat, and headache
a worsening of symptoms following physical or mental exertion occuring within 12-48 hrs of the exertion, and requiring an extended recovery period
word finding difficulities, comprehension inabilities, impairment of speech and/or reasoning
visual disturbances (blurring, sensitivity to light, eye pain)
psychological problems (depression, irritability, anxiety, panic attacks, personality changes, mood swings)
chills and night sweats, dizziness, shortness of breath, sensitivity to heat and cold, irregular heartbeat, irritable bowel, low grade fever, numbness, dry mouth
chest pains, rashes, ringing in the ears, allergies, sensitivies to noise/sound, chemical sensitivities, weight changes without change in diet, mental fogginess, muscle twitching, and seizures
If you suspect that you might be suffering from CFIDS, or any other auto-immune disorder (which also have symptoms like the ones listed above) go see your doctor immediately.















My dr. called fibromyalgia, a disease of exclusion, meaning that they diagnoisis you with everything else, and when they’ve ruled everything out, you either have fibro or cfs. So scientific. Yes that was sarcasm, or as I like to call it saracasm, thanks for the great article.
(Sara)kastic-great name by the way.
the exclusion thing is really frustrating isnt it. you wait and wait and wait…and when it isnt anything else, they kind of decide that its cfs or fm….it really is insane. since doctors can never be 100% sure on what you have, how is it that we expect everyone else to accept it. i still after living with this for 8 years, have people in my life who insist that this illness is all made up. and while i know that the head can play a large part in this illness…this illness is very real.
oh there i go ranting again….i cant seem to stop. i really need to control this pseudo anger thing that ive got going.
thanks for the comment….always appreciated