How do I know if I have Chronic Fatigue Syndrome / M.E.?
What signs or symptoms may make you suspect you may have Chronic Fatigue Syndrome / M.E.. People who have experience in Chronic Fatigue Syndrome / M.E. offer advice of what things may make you suspicious and which doctor you should go to to receive treatment
Post exertional malaise, poor, unrefreshing sleep, swollen glands, fatigue of unknown cause, all of a sudden onset with a viral flu-like infection beforehand.
Post exertion/exercise fatigue/malaise that takes days weeks or months to recover from (this seems to be the one factor we all have in common at the outset of ME/CFS).
Posted Sep 7, 2017 by 2560
It took 20 months of many doctors and mis diagnoses before I was finally diagnosed by an experienced cardiologist at a women's center.
If your life has been completely changed suddenly, if you sleep constantly or not at all, if someone asks you how you are and you wonder whether the pain you now feel is going to be gone by the time you answer and another one took its place... and in any case you know you are not just 'tired'... or if you had the flu and it lingers on without stopping... have all other diseases eliminated, go to an ME-CFS clinic to be seen by a real specialist to be sure. I would not skimp on this step.
Neurological and immune issues that are new and scary
a really long course of flu or mono that leaves you less able afterwards
the inability to stay in an upright position without edema
pallor
red crescents on tonsils
dropping things, unrestful sleep at night
migraines
a Dx of Fibro
strange and frequent infections
lack of former stamina
[this is all different in pediatric ME]
Go to your GP and keep a symptom diary between visits
ask for a referral to a neurologist and and immunologist
If you can't do the same you did yesterday, if you bothered by noises, certain smells, headaches, blurred vision, not able to think, memory problems, it is necessary to pass by the doctor.
If I have a persistent fatigue that keeps me from doing a normal life I already have which you suspect of suffering from CFS / me.
Are attached to cognitive disorders and memory.
Sleep disorders repeated.
All for more than 6 months.
...and many other symptoms more.
I consulted two neurologos, and a family physician.
The SPECT was the exam more relevant.
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Mine is a story of gradual onset MECFS. I was in my late twenties when my life began to 'not make sense'. This was in 1976.
I had always been active in sports and was fully engaged in being a wife and mother of two young preschool children. M...
Mold Warriors by Dr Ritchie Shoemaker
Gateway Press 2005
Chapt. 23
Mold at Ground Zero for CFS
The history of Chronic Fatigue Syndrome (CFS) begins in Incline Village, Nevada in 1985. In the medical history of CFS, each of the concepts applies-...
I wish that more MDs thought more carefully about CVID, PANS/PANDAS and EDS/MCAS. If I had been diagnosed and treated earlier in life with Igs (instead of being called a hypochondriac and shuffled off to conventional psychiatry), I may not have end...
I was your typical average teenage girl always out running around. always out scaring my parents because yet again i was doing something crazy like climbing a really high tree, or riding my bike to close to the duck pond, or going fishing and forgeti...
Hi all
Here is my story....
I started having problems with my knees when I was about 11yrs old, docs just thought it was growing pains and all they did was give me antiinflammatories. As I approached my mid teens I started sleeping in class althoug...
any supplement/homepathic med for adrenal fatigue insomnia (sudden awakening at night after 3-4 hours of sleep and then inability to fall asleep again)?
LBL did study of CO2 in air on thought and finds quite surprisingly, thought gets much worse if CO2 in outside air of 400ppmv, goes up from exhaled breath at 40,000 ppm, to raise room ambient to 1000ppmv or greater.
Free reference: http://...