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How is Chronic Fatigue Syndrome / M.E. diagnosed?

See how Chronic Fatigue Syndrome / M.E. is diagnosed. Which specialists are essential to meet, what tests are needed and other useful information for the diagnosis of Chronic Fatigue Syndrome / M.E.

Chronic Fatigue Syndrome / M.E. diagnosis

How is Chronic Fatigue Syndrome / M.E. diagnosed?


Chronic Fatigue Syndrome (CFS), also known as Myalgic Encephalomyelitis (M.E.), is a complex and debilitating condition characterized by extreme fatigue that cannot be explained by any underlying medical condition. Diagnosing CFS/M.E. can be challenging as there are no specific tests or markers for the condition. Instead, healthcare professionals rely on a combination of medical history, physical examination, and exclusion of other possible causes to make a diagnosis.



Medical History


The first step in diagnosing CFS/M.E. involves a detailed medical history assessment. The healthcare provider will ask about the patient's symptoms, their duration, and any factors that may have triggered or worsened the fatigue. It is important for the patient to provide a comprehensive account of their symptoms, including the severity and impact on daily life activities.



Physical Examination


After reviewing the medical history, a physical examination is conducted to rule out other potential causes of fatigue. The healthcare provider will assess various body systems, including cardiovascular, respiratory, and neurological systems, to identify any abnormalities or signs of other illnesses. While physical examination findings may not directly confirm CFS/M.E., they help exclude other conditions that may present with similar symptoms.



Diagnostic Criteria


Diagnostic criteria are used to establish a diagnosis of CFS/M.E. The most widely accepted criteria are the Fukuda criteria and the Canadian Consensus Criteria (CCC). These criteria require the presence of severe fatigue lasting for at least six months, along with specific accompanying symptoms such as impaired memory or concentration, unrefreshing sleep, muscle pain, joint pain, headaches, and post-exertional malaise.



Fukuda criteria:



  • Severe fatigue lasting at least six months

  • Exclusion of other medical or psychiatric conditions that could explain the fatigue

  • Presence of at least four accompanying symptoms, including impaired memory or concentration, unrefreshing sleep, muscle pain, joint pain, headaches, tender lymph nodes, and post-exertional malaise



Canadian Consensus Criteria (CCC):



  • Severe fatigue lasting at least six months

  • Exclusion of other medical or psychiatric conditions that could explain the fatigue

  • Presence of at least eight accompanying symptoms, including impaired memory or concentration, unrefreshing sleep, muscle pain, joint pain, headaches, tender lymph nodes, post-exertional malaise, and others



Exclusion of Other Conditions


Since there are no specific tests for CFS/M.E., it is crucial to exclude other medical conditions that could explain the symptoms. The healthcare provider will order a series of tests to rule out alternative diagnoses. These may include blood tests, imaging studies, and other specialized investigations depending on the patient's specific symptoms and medical history. The purpose of these tests is to identify any underlying conditions that may mimic or contribute to the fatigue experienced by the patient.



Collaborative Approach


Diagnosing CFS/M.E. often requires a collaborative approach involving multiple healthcare professionals. Due to the complexity of the condition, patients may be referred to specialists such as rheumatologists, neurologists, or infectious disease specialists to ensure a comprehensive evaluation. This multidisciplinary approach helps to rule out other potential causes and increases the accuracy of the diagnosis.



Longitudinal Assessment


It is important to note that diagnosing CFS/M.E. is not a one-time event. The condition is often diagnosed based on a longitudinal assessment of symptoms and their impact on the patient's daily life. Healthcare providers may request follow-up visits to monitor the persistence and progression of symptoms over time, ensuring that the diagnosis remains appropriate.



In conclusion, diagnosing Chronic Fatigue Syndrome / M.E. relies on a thorough medical history assessment, physical examination, exclusion of other conditions, and adherence to specific diagnostic criteria. While there are no definitive tests for CFS/M.E., healthcare professionals use a combination of these approaches to make an accurate diagnosis and provide appropriate management strategies for patients.


Diseasemaps
29 answers
We had to go eliminate MS and other neuroimmune issues like Lupus then research it ourselves and educate my wife's primary care physician who learned enough to diagnose her.

Posted Apr 17, 2019 by MEAction of CO
Blind Luck and perhaps a doctor that will listen

Posted Dec 20, 2019 by ME International
Currently by exclusion of other conditions and exhibiting a set of symptoms for more than 6 months.

Posted Feb 21, 2017 by Catherine 1002
By elimination

Posted May 4, 2017 by Ben 1079
I was diagnosed by my family physician assistant after all my test kept coming back normal but doctor could tell I was not ok at all.
I think having a medical professional that has known you for years & that genuinely cares about you is what is needed for a diagnosis, the level of degree they have doesn't matter if doctor doesn't believe CFS is anything more than a person being "lazy & crazy."

Posted May 12, 2017 by missylob 1056
Diagnosi di esclusione. Tipizzazione linfocitaria.
Matching the criteria (Canadian, Fukuda)

Posted Aug 27, 2017 by Emy 2050
Pretty much when they run out of options to test you for.

Posted Aug 30, 2017 by Jaime 800
There isn't a test for ME yet, it's diagnosed by eliminating everything else that it might be, and by using a questionnaire that looks at a range of symptoms. The key symptoms are post exertional malaise, fatigue for no particular reason and lasting for at least 6 months.

Posted Sep 5, 2017 by Shirley 2050
It is a process of elimination really. Doctors need to run a whole range of tests to rule out other things such as cancer (my doctor first thought I had lymphoma) and it can be a lengthy process.

Posted Sep 8, 2017 by Sam 1400
A rheumatologist diagnosed Fibromyalgia in 2015, but I was not responding to meds so GP did the immune panel of blood tests and mine came back with off the charts reactivated Epstein Barr Virus. Since doctors are NOT taught about using anti-virals (they generally just leave viruses alone) by the time I had done the research AND fought for long term high dose anti-viral (Valtrex) EBV was entrenched and so was ME/CFS. It took only 4 years from initial, extraordinary fatigue after any exertion/exercise (a common early symptom) to being completely housebound & bedridden. Still fighting for SSDI and living off shrinking retirement funds. #SillySheets is a fundraiser I organized with a friend (12 years fighting ME/CFS) to benefit www.omf.ngo research. US government funding is essentially $5 per patient.

Posted Sep 8, 2017 by 2560
Process of elimination and presence of particular symptoms.

Although a few scientists are very close to a specific diagnostic test.

Posted Sep 10, 2017 by Sharon 1500
By elimination of other illness
Its usually after 6 months contant post viral illness u can be diagnosed
But these days its getting more compicated with pych doctors interferring

Posted Jan 17, 2018 by Annette 2500
If a patient gets their diagnosis from a doctor who is not a CFS-ME specialist, they should go to a specialist and get a confirmation through the latest diagnosis techniques. There are those who have been misdiagnosed because a doctor who assumes this is just overwork fatigue gives out the diagnosis to those who do not have the disease. I was diagnosed via T-cell testing, as well as fitting the criteria. I do not know how others are being diagnosed to date. I do know that the usual medical tests that have been done over and over for so many of us, are completely useless in diagnosing this disease. They usually come back normal and we are said to be 'fine' for which we are expected to leave happy. I have seen the list of those tests but cannot list it right now.

Posted Mar 2, 2018 by Beti 2700
Non-refreshing sleep for a period of months.
Tenderness or pain at specific anatomical points.
Exhaustion after simple tasks.
Breathlessness that does not result from hard work or exercise.
Weakness

Posted Aug 9, 2018 by cathy 2500
it takes years and multiple MDs to get an ME Dx
many exhaustive tests and humiliating appointments
but once Dx'd
ME patients need ME specialists
and Neurologists and Immunologists
all who are well versed in ME
and we have few to none

Posted Apr 6, 2019 by Fadra 2550
IOM or ICC criteria
PEM, OI, sleep, pain, cognitive problems

Posted Aug 3, 2019 by Jessica 1200
Go see a clinical ecologist to better understand the chemical origin of your disease. Acupuncturists and Chinese medicine practitioners can also help you--community acupuncture is most affordable.

Posted Dec 12, 2019 by Joanna 6200
If you can find a doctor that will listen, I would give them the IC primer and then tell them your conditions that bother you. They might be able to help with many conditons that can be treated. ME does not have a cure.

Posted Dec 21, 2019 by Pam 3550
It’s very hard. They have to rule out all other possibilities, and even then they don’t want to diagnose you.

Posted Jan 17, 2021 by Emmy 2250
Translated from spanish Improve translation
It is diagnosed by ruling out other neurological diseases.

Posted Feb 24, 2017 by Anabel Albornoz Molinari 1076
Translated from french Improve translation
By a process of elimination. This is a very long and nerve-wracking. Every new test there is hope and answers and fear of diagnosis. Finally, to say that there is not much to do except trial and error

Posted Mar 9, 2017 by Edith 1050
Translated from spanish Improve translation
There is No evidence. Is diagnosed with the medical history

Posted Mar 10, 2017 by Yabisa 700
Translated from spanish Improve translation
There are several key things that we suffer all, some criteria and then rule out other diseases

Posted May 12, 2017 by Marisa 1000
Translated from spanish Improve translation
Depends on the doctor. ideally, q would have a multidisciplinary team... But there is.. If q, there are two internists expeetas in the areas of Madrid and Barcelona.. The dra Quintana (Ana M Quintana 180 eu first consultation and 105 following) in Madrid ybBarcelona. The dra Ceacero in Madrid.. caring for asisa, dkv, sanitas... And tb private.. I don't remember the price.. But 100 euros approx. Send you super analysis .stress test, holter, test, sleep, etc to rule out q these diseases are due to problems of endocrine or heart.. And from there.. Decidrn... Are many tests and is not the best thing for the fatigue, or physical or mental.. But when you ask for a disability or. Work adaptation are useful or if there is a wrongful dismissal

Posted May 25, 2017 by Cristina 601
Translated from spanish Improve translation
by ruling out other diseases similar

Posted May 25, 2017 by Yolanda Valledor 600
Translated from spanish Improve translation
Ruling out other pathologies

Posted Sep 11, 2017 by Eduardo Casasnovas 2950
Translated from spanish Improve translation
The good professional will find out all of your patient and analyzes check-ups of blood and urine . Next to the proof of esfuersi.

Posted Sep 11, 2017 by Haydee de bielik 5120
Translated from spanish Improve translation
It is diagnosed by your symptoms described above, and always when they persist for more than 6 months.
In addition, you see changes in a test called SPECT of the BRAIN that demonstrates a hipoperfusion brain in certain areas.

Posted Oct 19, 2017 by Heidrun Kroner 2000

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