Chronic Fatigue Syndrome A Roadmap For Testing And Treatment

Chronic Fatigue Syndrome A Roadmap For Testing And Treatment

Chronic Fatigue Syndrome
A Roadmap For Testing And Treatment

Chronic fatigue syndrome (CFS), also called myalgic encephalomyelitis (ME), is a neurological condition characterized by cognitive dysfunction, mood disorders, fatigue, post-exertional malaise, and many more symptoms.

The following guidelines are an aid to determining: (1) whether you have chronic fatigue syndrome, and if so: (2) which laboratory tests should be performed to identify the infections and other causal factors that underpin your ME/CFS, and: (3) what treatments you can follow to address these infections and causal factors, and treat the symptoms that arise from them.

Chronic Fatigue Syndrome Diagnosis
There are currently no laboratory tests or biomarkers that can be singularly used to diagnose ME/CFS, so diagnosis is performed on symptoms alone. ME/CFS manifests a whole array of clinical symptoms,1 2 both physical and mental, which typically include the following:


Persistent fatigue not due to ongoing exertion, and not really relieved by rest. The fatigue is of a new onset, and and greatly reduces activity levels, compared to before the onset. Cognitive dysfunction (brain fog): short-term and working memory deficits, problems recalling words or names, disorientation, loss of focus and awareness. Mood disorders which may include: depression, anxiety, panic attacks, irritability, mood swings. Post-exertional malaise: symptoms profoundly worsen after physical and/or mental exercise, leaving an individual very incapacitated for several days, or even weeks, after exertion.
Headaches of a type not previously experienced. Tinnitus, dizziness, balance problems, fainting, irregular heartbeat. Abdominal pain, irritable bowel, diarrhea. Unrefreshing sleep. Chronic sore throat or recurring sore throat (often from the virus that initiated the ME/CFS condition), chronic cough, chest pain, dry mouth, dry eyes, blurred vision. Sensitivities to light, noise and chaotic or busy environments. Sensitivity to heat and/or cold. Increased allergies or sensitivities to foods, alcohol, odors, chemicals or medications. Muscle aches or weakness, tingling sensations. Enlarged or painful lymph nodes in neck and armpits. Joint pain moving from one joint to another without swelling or redness.

For the formal diagnostic rules of ME/CFS, see the:

Canadian Consensus ME/CFS DefinitionCDC 1994 CFS Criteria.

Ruling Out Other Conditions

The inherent problem with diagnosing ME/CFS by its symptoms is that many of the same symptoms manifest in other diseases and conditions such as: Lyme disease, hypothyroidism, celiac disease, lupus, anemia, hepatitis B or C, and many others. Thus if you have symptoms resembling chronic fatigue syndrome, you and your doctor first need to rule out diseases and conditions with very similar symptoms before a diagnosis of ME/CFS can be given with reasonable certainty.


Condition Tests and Results Interpretation
Lyme disease
Lyme disease is caused by a chronic infection with certain species of Borrelia bacteria, these bacteria being contracted through the bite of infected Ixodes ticks. Bites from Borrelia-infected ticks often (but not always) cause a characteristic erythema migrans rash. Early symptoms of Lyme disease include: fever, headache, fatigue and depression.
Borrelia culture. This is a more reliable test for the Borrelia bacteria that cause Lyme disease. It is available at Advanced Laboratory Services.Borrelia IgM and IgG antibodies. Dr A Martin Lerner uses Western blot and ELISA to test for Borrelia burgdorferi IgM and IgG antibodies.1More info on testing for Lyme disease: Lyme TestingLyme and ME/CFS differences in symptoms: Lyme often causes pain and swelling in the large joints, most often the knees; by contrast in ME/CFS there can be pain in the joints, but this occurs without swelling. Facial palsy can occur in Lyme, but this does not occur in ME/CFS. These symptoms can thus help distinguish Lyme disease from ME/CFS.
Hypothyroidism Hypothyroidism occurs when your thyroid gland does not produced enough of the thyroid hormone thyroxine. The symptoms of hypothyroidism are quite similar to those of ME/CFS. Hypothyroidism is diagnosed by a blood test which measures the levels of various thyroid hormones.
Celiac disease
Celiac disease is an autoimmune reaction triggered by gluten, causing damage to the small intestine and nutrient malabsorption. Celiac disease symptoms vary widely between patients. 

Transglutaminase antibody blood test and an upper endoscopy with biopsy of the duodenum are used to diagnose celiac disease. Since celiac symptoms greatly improve after removing ALL gluten from the diet, if you feel much better going gluten-free, it hints you might have celiac disease (though gluten-sensitive people without celiac disease will also feel better going gluten-free).
Systemic lupus erythematosus Most people with systemic lupus erythematosus (SLE) will have a positiveantinuclear antibody test (ANA), but ANA is usually negative in ME/CFS patients. Thus the ANA test is a useful tool to help distinguish SLE from ME/CFS. Around up to 50% of SLE patients exhibit a red butterfly rash on the face, which is not found in ME/CFS.
Anemia Anemia is a decrease in the number of red blood cells, or a decrease in the amount of of hemoglobin in those cells, either of which results in a reduced ability of the blood to carry oxygen. The symptoms of anemia are similar to those of ME/CFS. Anemia can be diagnosed by a full blood count.
Hepatitis B or C virus infection Chronic hepatitis B and hepatitis C viral infections can produce symptoms that resemble those of ME/CFS. Hepatitis B virus can be caught from unprotected sex, including anal and oral sex, and also from sharing needles to inject street drugs. Hepatitis C virus is most commonly caught by sharing of needles to inject street drugs, and is sometimes caught from unprotected sex. Your doctor or a sexual health clinic can provide testing for hepatitis B and hepatitis C virus infections.

More comprehensive lists of diseases that have similar symptoms to ME/CFS:
Chronic Fatigue Syndrome Diagnosis
Chronic Fatigue Syndrome: Evaluation and Treatment
CFS can be caused by chronic infection
Diseases similar to ME/CFS

Causes and Treatments of ME/CFS
Once you have ruled out common diseases with similar symptoms, and have settled on a diagnosis of ME/CFS, then next stage is to try to identify the underlying infections and other factors that may be causing or contributing to your ME/CFS. This is best performed with the help of a doctor specializing in chronic fatigue syndrome laboratory testing and treatment.

There are many laboratory tests that people with ME/CFS might choose to take. In this roadmap to ME/CFS testing and treatment, the tests suggested are grouped into various rounds, with the most important tests placed in the earlier rounds. After each round of testing, depending on the test results, advice on an appropriate course of action for treatment is given.

Tests for causal factors that have a corresponding treatment or cure are prioritized, since the main goal of this roadmap is to guide people with ME/CFS to treatments that may improve or cure their condition. Tests that provide insight into your circumstances of health, but having done so, do not lead to corresponding treatments, are deferred to later.

The suggested treatment plans are those generally employed by leading chronic fatigue syndrome doctors and researchers in the field. There are no hard and fast rules for chronic fatigue syndrome treatment, and you may wish to follow different courses of action to those given here. These guidelines are an ongoing project which aims to be reasonably comprehensive; but they are not an exhaustive chart of ME/CFS treatments.

Research indicates that treatment-resistant ME/CFS of unproven etiology generally appears to be associated with viruses from the enterovirus genus (specifically: coxsackievirus B and echovirus) and/or to viruses from the herpes family (specifically: human herpes six virus, cytomegalovirus, Epstein-Barr virus). More treatable or curable forms of ME/CFS may be caused by parvovirus B19, Chlamydia pneumoniae, as well as other microbes. Non-microbial causes or contributory factors to ME/CFS include: mold toxin exposure and pesticide exposure. The first round of testing detailed below suggests you consider or get tested for all these microbes and causal factors.

Notes on Pathogen Testing
Most ME/CFS-associated microbes are very commonly found in the general population: Epstein-Barr virus, for example, is found in 95% of adults. Microbes found in the body are generally acquired from infections earlier in life, but once the immune system has them under control, these infections become largely inactive and dormant; so microbes from past infections normally exist in the body in a latent state (though these pathogens can reactivate and become more active if there is weakness in the immune system).

When a test is performed for a microbe, we want to know not only whether you have it in your body, but more importantly, whether it is active or not. In chronic infections, the level of activity of a microbe can be gauged to a certain extent by the amount of IgG antibodies your body produces in response to that microbe. High levels of IgG antibodies tend to suggest an active chronic infection.

Note that the activity of some microbes, notably enteroviruses, cannot be so accurately determined by antibody tests, due to the fact that these microbes can also live inside human cells, as an intracellular infection. The immune system does not readily make antibodies to microbes living inside human cells, so you may have a significant intracellular enterovirus infection, but show relatively low antibody levels when you take a test. Other means of pathogen testing may be employed in these situations. Alternative methods of testing for the presence of pathogens in the body include: PCR (polymerase chain reaction) and viral culture. Viral culture is usually the “gold standard” by which other viral detection methods are judged.

Empirical testing. While it is always better to test for pathogens or health conditions before using treatments, because some tests are expensive, not available in all countries, or might not always be reliable or sensitive enough to detect certain pathogens, you may choose to bypass the test and go straight to treatment. This is known as empirical testing: using a treatment itself as a test for a pathogen or health condition. Empirical testing makes the assumption that if you get better on the treatment, you may well have the pathogen or the health condition that the treatment targets.

1st Round Tests
The first set of ME/CFS causal factors to consider and/or test for is shown in the table below. The various microbial (and other) causal factors are listed in the left hand column, and recommended tests for these causal factors (plus some basic guidance on interpreting the test result) are given in the right hand column of the table. 


Causal Factor Tests and Results Interpretation
Epstein-Barr virus (EBV)
There is a high 95% prevalence of Epstein-Barr virus in the adult population, so most people will have this virus in their system, but usually in a latent inactive state. However, if you have an active EBV infection, it is possible this may be contributing to or causing your ME/CFS symptoms. New evidence indicates that some subtypes of ME/CFS may be due to partial reactivation of Epstein-Barr virus.1 2
Epstein-Barr virus antibodies. A blood test showing an EBV VCA IgG antibody titer of 1:1280 or more suggests an active infection.1 Dr A Martin Lerner says that a positive diagnosis of Epstein-Barr virus infection requires a positive EBV early antigen (EA) diffuse test, and/or a positive EBV IgM viral capsid antibodies (VCA) test.1Epstein-Barr virus PCR.Lymphocyte subset panel. If this test shows elevated CD8 T-cells, this can indicate an ongoing viral infection with EBV or cytomegalovirus, which both raise CD8 T-cells.1
Human herpes virus six (HHV-6)
HHV-6 is found in over 90% of adults, usually in a latent inactive state. If you have an active HHV-6 infection, this may be contributing to or causing your symptoms, as active HHV-6 is linked to ME/CFS.1 2 There are two main variants of HHV-6: variant A and variant B, often denoted as HHV-6A and HHV-6B. Tests for HHV-6 do not usually distinguish between the two variants. 
Most individuals that test positive for HHV-6 will have the more benign HHV-6B variant; but just under 3% will have the more nasty HHV-6A variant. It is this HHV-6A variant which is more strongly linked to ME/CFS.1 So a positive test for HHV-6A may be quite significant if this virus is active.Dr Kazuhiro Kondo has a theory that partial reactivation of HHV-6 may cause ME/CFS, as well as depression and bipolar disorder.1
HHV-6 antibodies. A blood test showing an HHV-6 IgG antibody titer of 1:320 or more suggests an active infection. Dr Jose Montoya believes that IgG antibody levels are a better guide to the HHV-6 activity in the central nervous system than viral culture from the blood.1 Nested PCR for HHV-6A. Regular tests do not distinguish between the these two variants of HHV-6, so if you tested positive for HHV-6, you could have either (or both). However, nested PCR tests can specifically determine if you have HHV-6A.HHV-6 PCR.Further info:

Cytomegalovirus (CMV)
Cytomegalovirus is found in 50% of adults, usually in a latent inactive state. If you have an active CMV infection, this may be contributing to or causing your ME/CFS symptoms.
Cytomegalovirus IgG antibodies. Dr A Martin Lerner says that a diagnosis of cytomegalovirus infection is made by examining the CMV IgG antibody titer. (Lerner says the IgM titer for CMV is inaccurate and insensitive.) The higher the CMV IgG titer, the greater the viral load.1 Cytomegalovirus PCR.
Coxsackievirus B and echovirus
There are six coxsackievirus B types and thirty-two different echoviruses. All are part of the enterovirus genus. Coxsackievirus B is found in 55% of adults, according to a study in Scotland.1 
If you have an active coxsackievirus B or echovirus infection, this may be contributing to or causing your ME/CFS symptoms.1 2 3 4Part of the difficulty in treating a chronic enterovirus infection is that this virus can exist in two distinct forms in the body: the regular enterovirus, and the non-cytopathic enterovirus. The infection begins with a regular enterovirus, but then some of these viruses convert into non-cytopathic enteroviruses within the body. Non-cytopathic enteroviruses reside within human cells, and are hard to detect. Dr John Chia thinks non-cytopathic enteroviruses may be a causal factor in ME/CFS.1 2 3
Coxsackievirus B and echovirus antibodies. Only one testing lab has an enterovirus antibody test sufficiently sensitive to detect the low-level “smoldering” chronic enterovirus infections of ME/CFS: ARUP Lab, in Utah. These test are:coxsackievirus B antibodiesechovirus antibodies. Titers of 1:320 and higher are good indicators of an active infection. ARUP tests can be ordered directly, or ordered through Labcorp. Stomach biopsy (immunohistochemistry). This test, which requires a sample of stomach tissue obtained by an endoscope, is the most reliable for detecting a chronic enteroviral infection. Dr Chia’s lab can process the stomach tissue sample.PCR testing is not sensitive for chronic enteroviral infections, as these viruses disappear from the blood after the acute phase of the infection is over (the acute phase of an enterovirus infection is a short window that starts just after initial exposure, and last for around 10 days).Complement fixation test (CFT) is useless for testing enteroviral activity in chronic infections. The CFT is only of value within the acute phase (first 10 days) of an enterovirus infection.Non-cytopathic enterovirus testing. There are no commercially available tests for non-cytopathic enteroviruses, which reside within human cells.Further info:


Parvovirus B19
Parvovirus B19 is found in 50% of adults, usually in a latent inactive state. If you have an active parvovirus B19 infection, this may be contributing to or causing your symptoms.1 2
Parvovirus B19 antibodies. A blood test showing a parvovirus IgG antibody titer of 1:?? or more suggests an active infection.
Chlamydia pneumoniae
Chlamydia pneumoniae is an intracellular bacterium (one that lives inside human cells) which is found in a latent state in 74% of the adult population, according to a study conducted in Israel. About 10% of this population had a persistent active infection with this bacterium.1 
Further info:

Chlamydia pneumoniae
Mold toxin exposure
Mold can synthesize toxic substances (mycotoxins) that can damage the central nervous system, intestines, kidneys. These toxins have been linked to the triggering of ME/CFS. 1 2
Mold growth can be visible, or it may be hidden behind walls and domestic appliances. People can become ill from hidden mold growths without knowing the cause (though a moldy, musty smell in the environment provides a warning to the possible presence of mold). Usually several species of mold can be found in a mold infestation. Mold species that have very potent mycotoxins include: Stachybotrys, Memnoniella and Acremonium. These three species depend on damp cellulose material (wood, paper, cotton) for nutrition, and thus typically thrive in water damaged-buildings that contain plenty of wood, wallpaper, etc.
Pesticide exposure
Chronic exposure to significant amounts of organophosphate or pyrethroid pesticides can cause ME/CFS-like illnesses, or act as a co-factor in precipitating ME/CFS. 1      
Further info: PAN
Sources of pesticide exposure include garden sprays used by you or your neighbor, which can be tracked into the house on shoes. Agricultural exposure may occur in rural areas through crop spraying. Pyrethroids are found in pet flea control products. Pesticide residues on foodstuffs are generally very minimal, and are not of concern.1 Organophosphate pesticides are detoxified from the body by an enzyme called paraoxonase; differences in the paraoxonase gene can increase an individual’s susceptibility to organophosphates.1 2

1st Round Treatments
In the light of the results of the first round of tests:

Epstein-Barr virus infection. If your tests indicate you have a chronic Epstein-Barr virus infection and no other infections, it is quite possible that your symptoms are in fact a case of chronic Epstein-Barr virus syndrome (chronic mononucleosis syndrome), which closely resembles ME/CFS. Dr. A. Martin Lerner suggests that chronic Epstein-Barr can be considered a subtype of ME/CFS. Chronic Epstein-Barr infection often clears itself up within 6 months or less, and you should then achieve remission from your symptoms. Antivirals such asvalacyclovir (Valtrex) can hasten the healing process.1 Nexavir (formerly Kutapressin) may have some in vitro activity against Epstein-Barr virus.1
Herpesvirus infection. If your tests indicate you have an active infection with one or more of the three herpesviruses: HHV-6, cytomegalovirus and Epstein-Barr virus, then Dr. A. Martin Lerner has recently shown that an anti-herpesvirus treatment comprising the antiviral drugs valacyclovir (Valtrex) and/or valganciclovir(Valcyte) can return ME/CFS patients to a near-normal to normal life, provided you have no active co-infections with pathogens other than these three herpesviruses. Those who experience side effects from valacyclovir can substitute with famciclovir (Famvir), an antiviral which is usually much better tolerated. Unfortunately, if you have active co-infections with pathogens other than these three herpesviruses, this antiviral treatment on its own has proved ineffectual, according to Dr Lerner. However, it is possible (though not proven) that this anti-herpesvirus treatment, when combined with treatments for the other pathogens, may get results.1The antimalarial drug artesunate has efficacy against cytomegalovirus, and against HHV-6.1 2 Nexavir(formerly Kutapressin) displays potent in vitro activity against HHV-6.1 2 The HIV drug raltegravir may be effective against the whole family of herpesviruses.1
Enterovirus infection. If your tests indicate you have active an infection with one or more enteroviruses of the coxsackievirus B or echovirus species, then Dr John Chia has found that around 25% of people will noticeably improve with a herbal treatment named oxymatrine (although Dr Chia suggests that patients with autoimmune tendencies should not take oxymatrine).1 More info: Dr Chia: OxymatrineOxymatrine, Autoimmunity, ME/CFS and FM.Dr Chia has also used interferon therapy for CFS patients with enterovirus infections; many patients went into full remission after this therapy, but unfortunately tended to relapse within around six months, so this is not a permanent cure, but perhaps an encouraging result.1 More info: Chia’s Interferon Therapy.
Parvovirus B19 infection. If your tests indicate you have high parvovirus B19 antibodies and nothing else, then intravenous immunoglobulin treatment may fully cure you.1
Chlamydia pneumoniae infection. If you have Chlamydia pneumoniae and no other infections, then antibiotic treatment with azithromycin or rifampin may clear this bacterium, and may cure fully your ME/CFS. Chlamydia pneumoniae infection is an uncommon but treatable cause of chronic fatigue.1 More info: Cure from Chronic Fatigue Syndrome with Dr. Stratton’s original protocol.
Toxic mold. If you have been exposed to high amounts of toxic mold, ensure you prevent or minimise further exposure. If exposed in your home, carefully clean off the mold growths (wearing a face mask is advised), and reduce humidity by increasing ventilation, in order to inhibit mold regrowth.
Chronic organophosphate and/or pyrethroid pesticide exposure. If you have been chronically exposed to organophosphate or pyrethroid pesticides, ensure you prevent any further exposure. The amount of pesticides residues found in foodstuffs is very minimal, and not of concern.

Note: some cases of ME/CFS may be due to a combination of the above pathogenic infections (as well as other causal factors). In which case, conceivably, it may be possible to combine the above treatments in order to tackle the various individual infections.

Before undertaking any treatment, however, you should first become familiar with any risks of taking that treatment, and if unsure, you should run it by a good ME/CFS doctor first.

More info: Antivirals and Antibiotics for ME/CFS.

Adjunct Therapies for ME/CFS
As well as specific pathogen-targeted therapies, there are many adjunct or additional therapies that can be helpful in chronic fatigue syndrome. These include:

Immunomodulators. These are drugs and supplements that modulate the immune system. Many immunomodulators used in ME/CFS shift the immune response from the Th2 mode to the Th1 mode. There is evidence that ME/CFS patients are stuck in the Th2 mode, whereas they should really be in the Th1 mode; it is the Th1 mode immune response that fights viruses and intracellular bacteria.1 These Th2 to Th1 mode shifting immunomodulator drugs and supplements include: low-dose naltrexoneImunoviroxymatrine (probably),Nexavir (formerly Kutapressin), pine cone extractheparin, and transfer factor.1 2Note that Th2 to Th1 mode shifting immunomodulators can make you feel worse for the first few months, but benefits accrue after that initial period. Note also that Dr Paul Cheney believes immunomodulators lose their effect if you do not take regular breaks from them. Regular breaks means an on/off regimen, such as for example: taking them for 5 days, stop for 2 days; and taking them for 3 weeks, stop for 1 week.Other immunomodulators used in ME/CFS include: artesunate (often used by Dr Cheney; it inhibits the effects of TNF-alpha 1), azithromycin (an antibiotic that lessens ME/CFS symptoms 1), etanercept (inhibits the effects of TNF-alpha), Ampligen (a powerful but very expensive immunomodulator drug that modulates interferon and RNase L).Low-intensity exercises like walking, tai chi and yoga help shift towards the desirable Th1 mode, whereas higher intensity exercise and longer workout durations shift towards the undesirable Th2 mode.1
Low-dose naltrexone (LDN). A low-dose naltrexone regimen (3 to 4.5 mg daily, taken before bed) can help halt the progression of various autoimmune and neurodegenerative diseases, including multiple sclerosis, systemic lupus erythematosus, rheumatoid arthritis, Sjogren’s, Parkinson’s, Crohn’s. Many ME/CFS and fibromyalgia patients find LDN beneficial.1 LDN acts as an immunomodulator that stimulates the desired Th1 immune response, and LDN is believed to increase natural killer cell function (NK function is often low in ME/CFS patients). More info: LDN for ME/CFSLDN Overview.
Vitamin B12 injections or B12 sublingual tablets. Many ME/CFS patients find that high dose vitamin B12substantially reduces the cognitive dysfunction (brain fog) symptoms. The recommended forms of vitamin B12 are: methylcobalamin, adenosylcobalamin, and hydroxocobalamin. Injectable vitamin B12 doses are around 1000 mcg three times a week; sublingual doses are 5000 mcg taken daily. Improvements in symptoms usually appear after a few weeks of taking B12. Further reading: Rationale for using vitamin B12 in CFSMethylation, B12, Glutathione, Chelation.
Methylation protocol. Dr Richard van Konynenburg says that insufficient methylation is a factor behind ME/CFS, and recommends boosting methylation using supplement regimen based on the treatment program developed by Dr Amy Yasko for autism. The Health Diagnostics and Research Institute in New Jersey ( provide a test for methylation, as do the European Laboratory of Nutrients (see their “amino acids analysis”). More info: Glutathione and the Methylation CycleSimple Methylation Treatment Protocol for CFS.
Very low dose tricyclic antidepressants (TCA). Low doses (10 to 25 mg daily) of tricyclic antidepressants (TCA) such as amitriptyline or imipramine can be particularly helpful for ME/CFS. TCA antidepressants not only provide a mood-boosting for ME/CFS patients, they also are known to increase energy levels (though low doses are stipulated, as higher doses are usually found too stimulating for ME/CFS patients).1 2 TCAs can reduce vitamin B2 levels, so taking vitamin B2 with TCAs is beneficial, and may improve the effects of these antidepressants.1
Nexavir injections. The injectable drug Nexavir (formerly Kutapressin) is an antiviral, an anti-inflammatory and an immunomodulator that has demonstrated overall benefits for ME/CFS, and this drug is often employed by ME/CFS doctors, including Dr Cheney, Dr Enlander and Dr De Meirleir. Nexavir treatment protocols vary, but in one study, ME/CFS patients were given one subcutaneous 2 ml injection of Nexavir for the first 25 days of treatment; thereafter one injection every two days, for the next 50 days; and thereafter one injection three times a week for the next 105 days. This study reported a 42% remission rate in these patients at the end of this course of Nexavir treatment.1Dr De Meirleir reports that around 70% of his ME/CFS patients experience at least a 20 point increase on theKarnofsky scale as a consequence of taking Nexavir. Dr Enlander says that Nexavir helps about 30% of his ME/CFS patients. Nexavir is usually taken in conjunction with vitamin B12 injections.
Other drugs and supplementsAcetyl-L-carnitine improves mental fatigue in ME/CFS.1 L-carnitine helps ME/CFS.1 Omega 3 with omega 6 fatty acids (fish oil plus evening primrose oil) improve ME/CFS symptoms.1Magnesium (either applied transdermally on the skin, or given by injection) can be of benefit in ME/CFS.1DHEA improves pain, fatigue, anxiety, memory and sexual problems in ME/CFS patients.1 NADH helps ME/CFS.1Co-enzyme Q10 may increase energy in ME/CFS.1 Undenatured whey protein may help ME/CFS by boosting intracellular glutathione.1 Malic acid taken with magnesium can increase energy in ME/CFS and reduce pain in fibromyalgia.1 2

More info on various ME/CFS therapies:
ME/CFS Immune System Treatments at Phoenix Rising
Dr Jacob Teitelbaum’s 30 Top Tips for Treating CFS
Dr MyHill Fatigue Treatments
ME/CFS Medications Database

2nd Round Tests
This second round of tests and possible causal factors focuses on a few of the comorbid diseases and conditions that are frequently found in ME/CFS patients —€” in many cases, prior to the triggering factor that precipitated the ME/CFS condition (triggering factors such as an enteroviruses, herpesviruses, mold exposure, etc).

Comorbid conditions that are statistically more prevalent in ME/CFS or fibromyalgia patients (either prior to ME/CFS onset, or subsequent to onset) include: irritable bowel syndrome, small intestine bacterial overgrowth, interstitial cystitis and overactive bladder, chronic pelvic pain syndrome (prostatitis), endometriosis, Raynaud’s disease, multiple chemical sensitivity (increased allergies), temporomandibular joint disorder, myofascial pain syndrome, attention deficit hyperactivity disorder, eating disorders, Hashimoto’s thyroiditis, prolapsed mitral valve, and Sjogren’s syndrome (sicca syndrome).1

Some of these comorbid conditions likely play a causal role in the development of ME/CFS (though there is no direct proof of this; all we know at present is that these comorbid conditions are statistically more prevalent in ME/CFS patients).

Causal Factor Tests and Results Interpretation
Intestinal dysbiosis
People with ME/CFS often have bacterial or fungal overgrowth in their intestines, and may also have some pathogenic microbial species present. These conditions may be contributing to your ME/CFS symptoms.
Full digestive stool analysis. A digestive stool analysis will determine whether you have bacterial or fungal overgrowth in your intestines, and will determine whether there are any pathogenic or potentially pathogenic microbes present (potentially pathogenic microbes are those that only cause problems if their populations in the gut become too large). More info on gut dysbiosis: Fermentation in the gut and CFS
Leaky gut (intestinal permeability)
Leaky gut is an intestinal dysfunction that can allow toxic contents of the small intestine to enter the bloodstream. Leaky gut arises from dysfunction of the tight junctions in the lining of the intestine.
Leaky gut test (lactulose/mannitol test). The lactulose/mannitol test can detect if you have a leaky gut. More info: Fixing Leaky Gut Helps ME/CFS.
Irritable bowel syndrome (IBS)
IBS symptoms may include: abdominal pain and bloating; bouts of diarrhoea and/or constipation. 
Irritable bowel syndrome is a very common comorbid condition in ME/CFS and fibromyalgia.1 2 One study found 92% of ME/CFS patients, and 77% of fibromyalgia patients had IBS in their lifetime (compared to 18% for healthy controls).1
IBS is generally diagnosed by its symptoms; there are no specific tests for IBS.
Small intestine bacterial overgrowth (SIBO) SIBO is a condition in which abnormally large numbers of bacteria grow in the small intestine. SIBO symptoms are very similar to those of IBS, and include nausea, bloating, vomiting, diarrhea, nutrient malabsorption (and thus malnutrition), and weight loss. SIBO is found in 84% of IBS patients, and some hypothesize that SIBO may be the cause of IBS in these cases.1SIBO is a common comorbid condition in ME/CFS and fibromyalgia.1 Hydrogen breath test. SIBO can be detected using a hydrogen breath test, which involves drinking some lactulose sugar, and measuring the hydrogen or methane gas produced by bacteria in the small intestine as they metabolize this sugar. (These gases enter the bloodstream and are expelled by the lungs, where they are detected in the breath). D-xylose test. Malabsorption due to SIBO can be detected by the D-xylose test, which involves drinking D-xylose, and measuring levels in the urine and blood; if there is no D-xylose is found in the urine and blood, it suggests that the small bowel is not absorbing properly.More info: Testing for SIBOLabs that offer hydrogen breath tests.
Interstitial cystitis (bladder pain syndrome) and overactive bladder
These two conditions involve an excessive urgency, and increase frequency, to urinate. Bladder pain is involved in interstitial cystitis.1Interstitial cystitis and overactive bladder are comorbid conditions in fibromyalgia and ME/CFS.1 2 3 Research on cats with interstitial cystitis shows that they may have mild primary adrenal insufficiency.1
Allergies or food intolerances
Allergy or food intolerances are commonly found in ME/CFS.1 2 Allergies or food intolerances, especially to gluten or dairy products, may exacerbate ME/CFS symptoms.

2nd Round Treatments
In the light of the results of the second round of tests:

Intestinal dysbiosis. If your digestive stool analysis test indicates bacterial overgrowth and/or the substantial presence of potentially pathogenic gut bacteria such as Aeromonas, Bacillus cereus, Campylobacter jejuni, Citrobacter, Clostridium difficile, pathogenic strains of Escherichia coli, Klebsiella, Morganella morganii, Proteus, Pseudomonas, Salmonella, Shigella, Staphylococcus aureus, Vibrio and Yersinia, then a course of antibiotics, and/or probiotics may help reduce these bacterial populations. Note that some people ME/CFS, typically those who have had this disease for a decade or more, may find their gut is too sensitive to take probiotics.
Irritable bowel syndrome. If you have been diagnosed with irritable bowel syndrome (IBS), note that IBS can be caused by the intestinal protozoan parasites Giardia lamblia, Blastocystis hominis and Dientamoeba fragilis, all of which are treatable. There is also evidence of bacterial infection in IBS (in that the antibiotic rifaximin can put IBS into remission for weeks).For Giardia lamblia, a single dose of antiprotozoal drug tinidazole is an effective treatment.1 For Blastocystis hominis and Dientamoeba fragilis treatment: see the triple drug cocktail (comprising secnidazole, diloxanide furoate and bactrim DS) at the Badbugs website. A two week course of rifaximin, a unique antibiotic which is not absorbed in the intestines (and so remains in the bowels), improves IBS symptoms for three months.1 Fecal transplant (bacteriotherapy) may be worth considering: it has a 58% response rate for treating ME/CFS patients with IBS.1
Small intestine bacterial overgrowth. If you have been diagnosed with small intestine bacterial overgrowth (SIBO), there are a number of treatment options, including: the antibiotics rifaximinneomycin andmetronidazole; an elemental diet (to starve the bacteria); and dietary treatments that reduce food sources for the bacteria. See: Treatments Strategy for SIBO. Once the the bacterial overgrowth in the small intestine is brought under control by theses treatments, it is then necessary to adopt a prevention strategy(such as an ongoing dietary treatment) to stop SIBO from reappearing. Without adopting a prevention strategy, recurrence of SIBO is common.
Leaky gut syndrome. If you find you have a leaky gut (intestinal hyperpermeability), this means that the potent endotoxins such as lipopolysaccharide (LPS) made by bacteria in your gut can escape into your bloodstream. LPS leaking into the bloodstream can create significant system-wide inflammation. LPS also reduces the antiviral Th1 immune response, making it harder for your body to fight off viruses.1 A leaky gut diet can help resolve leaky gut problems. Fixing leaky gut in ME/CFS can lead to clinical improvement in symptoms.1 Sometimes, complete remission from ME/CFS can be obtained by normalizing a leaky gut.1

3rd Round Tests
This third round of tests focuses on rarer microbial causes and contributory factors of ME/CFS.

Causal Factor Tests and Results Interpretation
Giardia lamblia
Giardia lamblia is a protozoan parasite that colonizes and replicates in the small intestine, causing giardiasis. Prior infection with Giardia lamblia predisposes to acquiring ME/CFS.1 2 3
Giardia lamblia antigen test.
Toxoplasma gondii
This intracellular protozoan parasite, which can be caught from undercooked meat and cat feces, can cause toxoplasmosis, a mild condition that usually clears up on its own. However, Toxoplasma gondii can sometimes cause or contribute to ME/CFS. Toxoplasma gondii does not spread from person to person. 
The prevalence of Toxoplasma gondii in humans varies from country to country. It is found in around 11% of people the US, 22% in the UK, and in around 88% in France.
Toxoplasma gondii antibodies.
Mycoplasma species bacteria
60% of ME/CFS patients are found to have blood infections with one or more of the following: Mycoplasma pneumoniae, Mycoplasma fermentans, Mycoplasma hominis and Mycoplasma penetrans. By contrast, such infections are detected in the blood of only 10% of healthy adults). ME/CFS patients infected with more than one mycoplasmal species generally had a longer history of illness, suggesting that they may have contracted additional mycoplasmal infections with time.1 2 
It has been speculated that Mycoplasma species may contribute to ME/CFS symptoms.
Mycoplasma pneumoniae IgM and IgG antibodies. Dr A Martin Lerner only considers a ME/CFS patient to have a persistent Mycoplasma pneumoniae infection unless the titer is 1:600 or more (Lerner uses LabCorp for testing).1 Mycoplasma PCR.
Coxiella burnetii
This rare bacterium causes a disease named Q fever, which has ME/CFS-like symptoms. Direct, person-to-person infection occurs rarely, if ever. It can be treated with antibiotics. The incubation period of Coxiella burnetii 2 to 3 weeks. 1    
Coxiella burnetii antibodies.
Brucella bacteria can cause ME/CFS-like symptoms. This bacterium can be treated with antibiotics. Brucella’s incubation period is 1 to 3 weeks.
Brucella antibodies.
If living in an endemic area, like Florida, infection with the HTLV virus is a remote possibility to explain a ME/CFS-like condition, though the symptoms of this virus take decades to appear (it has a very long incubation period).
HTLV I and II antibodies.
Ross River virus
This mosquito-borne virus is only found in parts of Australia (and some other countries). This virus has been associated with ME/CFS, though most infections of Ross River virus do not produce clinical symptoms and go unnoticed.
Ross River virus antibodies .
Herpes simplex virus 1 & 2 (HSV) 
HSV 1 is found in 58% and HSV 2 is found in 16% of the adult population. It has been suggested that HSV 1 & 2 may play a role in ME/CFS.1
HSV 1 & 2 antibodies. A blood test showing a HSV IgG antibody titer of 1:?? or more suggests an active infection.
Varicella zoster virus (VZV)
VZV is the virus which causes chickenpox. VZV may be linked to ME/CFS (it has been hypothesized that some cases of ME/CFS may be caused by the reactivation of VZV in peripheral nerve ganglia).1
VZV antibodies. A blood test showing a VZV IgG antibody titer of 1:?? or more suggests an active infection.

3rd Round Treatments
In the light of the results of the third round of tests:

Giardia lamblia infection. If you tested positive for an Giardia lamblia infection, then either a week course ofmetronidazole, or a single dose of tinidazole or ornidazole is curative in 90% of cases.1
Mycoplasma infection. If you have a Mycoplasma infection, macrolide and tetracycline classes of antibiotics (such as azithromycin and doxycycline) are effective treatments. For healthy people, two or three weeks treatment is required; longer treatment is usually needed in chronic illness like ME/CFS.1Dr A Martin Lerner treats Mycoplasma pneumoniae infection in his ME/CFS patients with intravenous doxycycline 150 mg for six weeks, followed by oral doxycycline 100 to 150 mg twice daily or moxifloxacin400 mg once daily for three months.1
Varicella zoster virus infection. If you have an active infection with varicella zoster virus, then the supplement L-lysine (1000 mg twice daily) may be useful.
Herpes simplex virus infection. If you have an active infection with herpes simplex virus I or II, then the supplement L-lysine (1000 mg twice daily) may be useful.1

4th Round Tests
This fourth set includes rarer causes/contributory factors of ME/CFS.

Causal Factor Tests and Results Interpretation
Jaw bone infection
Cases of ME/CFS have occasionally been caused by bone infections (osteomyelitis) inside the jaw bone. Such infections can develop inside jaw bone cavitations (the hollow pockets in the jaw bone left after a tooth extraction). 
Further info:

I think I put the puzzle together

Jaw bone infections can be very hard to detect, as they often cause only very minimal local symptoms. Yet a local infection in the jaw bone can cause symptoms identical to ME/CFS.A simple test for jaw bone infection is applying pressure to jaw bone with a finger; if any area feels painful, this indicates a possible bone infection.Jaw bone infections will usually not show up on X-rays. However an MRI can detect jaw bone infections. Ultrasound and thermal imaging cameras can also be used to help detect a jaw bone infection. A handheld device called the Cavitat scanner can detect infections hidden within the jaw bone.Jaw bone infections come under the category of focal infections, which are defined as infections localized in a small region of the body. Focal infections within the tonsils may also lead to fatigue symptoms.Dr Graeme Munro-Hall and Dr Lilian Munro-Hall are UK dentists that specialize in testing for and treating jaw bone infections.
Sinusitis (sinus infection)
Sinusitis can cause chronic fatigue, and so conceivably sinus infections may worsen ME/CFS.1
Patients suffering chronic fatigue (but not proper ME/CFS) due to obstructive sinusitis have reported significant improvements in fatigue after undergoing sinus surgery. The improvements are likely to derive from the easing of sinus inflammation after surgery.Further info:

Lymph fluid obstruction/stagnation
Some patients with ME/CFS have improved, and some have even been cured, by massage that circulates lymph fluid. Thus lymphatic congestion and/or dysfunction in the thoracic duct which pumps the lymph fluid may be a factor in underpinning ME/CFS.
Further info:
Perrin Technique
Testing for lymph flow obstruction. Raymond Perrin, a osteopath who has developed lymph massage techniques to treat ME/CFS, found that his patients have a sore and tender spot just under the third rib on their left side. The presence of this soreness indicates a lymph flow stagnation. To test this spot in yourself, press your fingers into a point around 2 cm above and to the left of your left nipple; if there is soreness or tenderness at this point, this indicates to Perrin that there is a lymph flow blockage. Perrin theorizes that lymph stagnation prevents proper cerebrospinal fluid drainage, thus creating a toxic build-up in the central nervous system that underpins or contributes to ME/CFS.1
Physical trauma (eg: car accident)
Physical trauma such as a road accident or a fall can precipitate fibromyalgia and ME/CFS, particularly if a head or neck injury is sustained (such as whiplash or concussion). 
Further info:

Fibromyalgia and ME/CFS can appear immediately after an accident, or begin to develop over the subsequent months.The mechanisms that precipitate fibromyalgia and ME/CFS after a physical trauma producing anatomical damage or misalignment are not clear, but it is easy to hypothesize that causal factors may include anatomical misalignment restricting lymph flow from the head and through the neck; or anatomical misalignment pinching on the vagus nerve.1 2 Note that trauma to the spine can sometimes cause a syringomyelia to later form in the spinal cord, which may result in ME/CFS-like symptoms. Syringomyelia can be treated surgically.
Temporomandibular joint dysfunction (jaw misalignment) 
Temporomandibular joint dysfunction (TMJD) is an inflammation and misalignment of the temporomandibular joint (the joint which connects the jaw bone to the skull). TMJD can cause symptoms similar to fibromyalgia and ME/CFS.
More info:

Temporomandibular joint dysfunction can be diagnosed by dental professionals. One theory on how jaw misalignment precipitates fibromyalgia-like symptoms relates to a compound called substance P. Substance P is normally raised in fibromyalgia patients (but not in ME/CFS patients) and some believe it may play causal role in fibromyalgia. Now, higher levels of substance P are also found in TMJD patients. Substance P is released into the cerebrospinal fluid when the trigeminal nerve (which runs through the lower jaw) is stimulated. So substance P, originating from TMJD, offers a possible explanation of how TMJD might trigger fibromyalgia-like symptoms, and may explain how treating TMJD can lead to remission from fibromyalgia.
Silicone breast implant
Silicone used for breast and other implants, as well as silicone injections, can in rare cases cause an ME/CFS like illness, as well as autoimmune conditions. Silicone is known to affect the immune system (silicone is used as an immune stimulating adjuvant in vaccines for this reason).
More info on silicone illness here.
Hepatitis B vaccination
In very rare cases, ME/CFS is reportedly triggered by hepatitis B vaccination (and this is usually a rapid onset: that is, the symptoms of ME/CFS appearing almost immediately after the vaccination). 1   

4th Round Treatments
In the light of the results of the fourth round of tests:

Jaw bone infection. If you suspect you may have an focal infection within the jaw bone, you need seek help from a knowledgeable dentist, but these are hard to find. More info hereDr Graeme Munro-Hall and Dr Lilian Munro-Hall are UK dentists that specialize in testing for and treating jaw bone infections.
Lymph flow obstruction. If you think you may have a lymph flow obstruction, you may wish to try the Perrin Technique, which improves lymphatic and cerebrospinal fluid drainage using osteopathic massage and manipulation. Patients also follow a massage and exercise routine at home, involving spinal twists (Perrin twists) which manually activate the thoracic duct (the body’s main pump for lymph fluid).
Physical trauma. If you think your ME/CFS or fibromyalgia may be due to a physical trauma, such as a car accident that involved a head or neck injury, physical therapy spinal manipulation such as cranial osteopathy or chiropractic may perhaps yield benefits.
Temporomandibular joint dysfunction. If you have fibromyalgia-like symptoms, and you have been diagnosed with temporomandibular joint dysfunction (jaw misalignment), consider treating this, because it may help improve your fibromyalgia-like symptoms too.

Testing Laboratories
Testing laboratories (pathology labs) where the tests recommended in this document can be obtained are listed below.


USA UK / Europe Canada
Australia New Zealand Ireland
MedLab Pathology

ME/CFS Doctors and Clinics
Some of the world’s leading ME/CFS doctors and clinics are listed in the table below. More info on ME/CFS doctors and clinics here: Co-Cure ME/CFS & Fibromyalgia Good Doctor ListPhoenix Rising Forum ME/CFS Doctors.

Dr John Chia (Torrance, California)      Article on Dr Chia
Dr Chia is an infectious disease specialist with special interest in enteroviruses (which include coxsackievirus B and echoviruses), and is the leading researcher in enterovirus-associated ME/CFS. 
Dr A Martin Lerner (Oakland, Michigan)      Article on Dr Lerner
Dr Lerner is a leading researcher in ME/CFS associated with herpesvirus and used antivirals to treat these infections. He also has particular interest in the cardiac problems and insufficiency often found in ME/CFS.Dr Jose Montoya (Stanford University, California) 
Dr Montoya is a leading researcher in ME/CFS associated with herpesvirus such as HHV-6, EBV, cytomegalovirus, and uses powerful antivirals to treat these herpesviruses where appropriate.Dr Daniel Peterson (Sierra Internal Medicine, Nevada)      Article on Dr Peterson
Dr Peterson is a very experienced ME/CFS doctor and researcher, and has a special interest in natural killer cell functioning in ME/CFS.Dr Paul Cheney (Asheville, North Carolina)      Article on Dr Cheney
Dr Cheney is an innovative doctor and researcher using leading edge medicine to treat ME/CFS.Dr Nancy Klimas (Miami, Florida)      Article on Dr Klimas
Dr Klimas is a ME/CFS doctor and researcher who runs a ME/CFS clinic. She has significant experience in using immune modulators for treating ME/CFS.

Dr Charles W. Lapp (Charlotte, North Carolina)      Article on Dr Lapp
Dr Lapp runs clinical trials for drugs for ME/CFS and fibromyalgia, and has been using ampligen for ME/CFS.

Dr Derek Enlander (New York) 
Dr Derek Enlander uses immune modulators for treating ME/CFS.

Dr Garth Nicolson (Huntington Beach, California) 
Dr Nicolson works with ME/CFS, autoimmune diseases, Gulf War illness, and the infectious causes of autism and neurodegenerative diseases.

Dr Daniel Dantini (Ormond Beach, Florida)      Article on Dr Dantini
Dr Dantini uses antivirals (famciclovir and valacyclovir) for herpesviruses in his treatment of ME/CFS where appropriate.

Dr Andreas M. Kogelnik (Mountain View, California) 
Dr Andreas M. Kogelnik is an infectious disease doctor, and an ME/CFS specialist and researcher.

UK / Europe
Dr Sarah Myhill (Powys, Wales, UK) 
Dr Myhill is GP with significant experience of CFS, and has a website from which various lab tests can be ordered and interpreted by Dr Myhill.Breakspear Medical Group (Hertfordshire, UK) 
Breakspear focuses on allergy and environmental illness. For ME/CFS treatment they use antivirals, gammaglobulins for parvovirus, and test and treat rickettsial and bacterial co-infections.Dr Kenny De Meirleir / Red Labs (Belgium) 
Dr Kenny De Meirleir is a ME/CFS doctor and researcher who runs a ME/CFS clinic in Brussels with a particular focus on the intestinal dysfunction and intestinal dysbiosis of this disease.
Australian ME/CFS Good Doctor List 

Sourcing Pharmaceutical Drugs
Good ME/CFS doctors who provide the appropriate drugs for ME/CFS patients are few and far between, and the average primary care doctor is often reluctant to prescribe drugs for off-label or experimental use in ME/CFS. Thus it may be necessary to buy the drugs you need directly from a reliable online pharmacy.

The law in most counties allows 3 months worth of prescription drugs for personal use to be imported from abroad (though these drugs of course cannot be controlled substances). Courtesy of this law, it is possible to easily and legally obtain drugs from online overseas pharmacies, usually without needing to provide a prescription. There are many online overseas pharmacies to choose from, but it is important to find a good one that is trustworthy and reliable. The following sources for reliable overseas pharmacies are very useful:

Updated lists of reliable overseas online pharmacies are maintained by the following website, in which each pharmacy is rated by user-feedback: 
Before you consider taking any pharmaceuticals, make sure you are fully informed about them, and check for any contraindications or drug interactions with other medications or supplements you are taking, via a website such as the:Drug interactions checker at
Sourcing Cheap Supplements

ME/CFS patients often take a range of supplements to help combat the myriad symptoms of this problematic disease. To save on costs, note that vitamin, herbal and amino acid supplements can be obtained at substantial discounts —€” around 80% to 90% less than the regular price —€” if you buy these supplements in bulk powder form, rather than tablet or capsule form. Supplements in powder form can taken by swallowing the powder with a little water. It may be an idea to buy a digital weighing scales to accurately measure the power dosage (digital scales can be obtained for as little as $10).

Some bulk powder supplement suppliers include:

USA UK Australia

Support Groups for People Suffering of Chronic Fatigue Syndrome and Fibromyalgia

Support Groups for People Suffering of Chronic Fatigue Syndrome and Fibromyalgia


People with FM and/or CFS/ME often feel alone with their disease and with the everyday struggles their medical condition brings to their lives. We all need to know we’re not alone in our pain and suffering. Often, the best medicine can be laughter shared between people like “us”, people with FM and/or CFS/ME.

The following groups meet online only. They offer help for people unable to leave home for an actual support group meeting. Many of these groups offer monthly newsletters, research, information, and forums for people with FM and/or CFS/ME. Groups can vary in size.

The groups below are listed in alphabetical order by group name.

 Group Name  Description
Action for ME Support for ME patients in the UK.
AFFTER – (Advocates for Fibromyalgia Funding, Treatment, Education and Research)
A Non-Profit, 501(c)(3) Organization that is on a mission to help those with FMS and related illnesses: We participate in awareness activities; coordinate educational events and offer the educational literature to patients and general community; support the patient population with on-line groups and resources; and organize charitable events to raise funds for fibromyalgia research and
CFIDS Assoc. of America Working to conquer Chronic Fatigue and Immune Dysfunction Syndrome.
CFS/FM Online Support, Referrals, & Resources
Pat Gurnick, CLC (Psychotherapist, Healer, Empath, recovered from CFS/FM) is located in Boulder, Colorado. She offers free online support, referrals and resources. You can also email her for guidance.
Chronic Fatigue Syndrome Support Group
A community of patients, family members and friends dedicated to dealing with Chronic Fatigue Syndrome, together.
Chronic Pain Conditions
This group has been created for those who suffer from RSD-Reflex Sympathetic Dystrophy, Chronic Pain conditions, Fibromyalgia etc.
Chronic Pain Support Group A community of patients, family members and friends dedicated to dealing with Chronic Pain, together.
CNY Fibromyalgia Support Group
Support and discussion monthly. For those that have Fibromyalgia, CFS or Lupus, all welcomed. This group is not always serious but a fun group with great tips.
Daily Strength – Support Community People sharing their advice, treatment experiences, and support.
EDSAUS – Ehlers-Danlos Syndrome in Australia We are the primary Australian support and awareness group for people with Ehlers-Danlos Syndrome and their loved ones. Many people who have EDS are also diagnosed with FM, CFS or both. All information on EDSAUS is public.
The Environmental Illness Resource The Environmental Illness Resource is an information resource and interactive community site for people suffering from a range of chronic multi-system illnesses (e.g. ME/CFS/Fibro) which are poorly understood and for which there is currently very limited healthcare available.
 Fibromyalgia Support Group
A community of patients, family members and friends dedicated to dealing with Fibromyalgia, together.
Fibro Family United Support Group of NJ
My main goal is to create a support group in Somerset/Middlesex County, New Jersey. My mission is to support others that suffer from Fibro as much as I do. To offer understanding, guidance and support. To build a foundation for more people to become aware of Fibro! We are a Fibro Family and we are United! Together we will BEAT this dreadful illness!
Fibro Mates Support Group
A community of patients, family members and friends dedicated to dealing with Fibromyalgia in the Family, together.
Fibro Pals
Website includes Fibromyalgia support group finder for the UK, information on FMS, interesting and funny videos, details of groups, when and where they meet and a fibro forum, chat room and gallery for members of the groups who join.
Fibromyalgia and CFS
With over 2500 members, this group has an amazing amount of resources to help the newly diagnosed to understand what is happening to them. This is a non-religious, non-political, worldwide support group.
Fibromyalgia Coalition International
Group meets 1st & 3rd Saturday of each month alternating between speakers and Bonding and Sharing Hope meetings.
Fibromyalgia & Lumps Support Group
A community of patients, family members and friends dedicated to dealing with Fibromyalgia & Lumps, together.
Fibromyalgia Assoc. UK
We have over 100 local support groups and help lines throughout the UK, Ireland and the Channel Isles who are there to help you on a local basis.
 Fibro Splashes – For Those Who Live with Fibromyalgia
Fibro Splash is an email discussion group, in a Christian environment, where encouragement, tips, joys and sorrows are shared from one’s experience with fibromyalgia. We welcome you and are eager to get to know you.
Fibromyalgia Support Group
A community of patients, family members and friends dedicated to dealing with Fibromyalgia, together.
Fibromyalgia Support & Understanding
Providing a positive and informative support group to serve the community. Providing information on our disease with the latest news. I am available to the members 24/7 offering a shoulder to lean on when the times are bad; a hug to know that someone cares; a ear to listen when we just need to cry out our frustrations. Discounted services offered to our group members from a Yoga instructor, message therapist, and Chiropractor services.
Fibromyalgia Teens Support Group
A community of patients, family members and friends dedicated to dealing with Fibromyalgia Teens, together.
Friends Because We Have Fibro and/or CFS/ME!
Support group for those who have Fibromyalgia and/or Chronic Fatigue Syndrome. Great support and wonderful information!
Friends International
FMS-CFS Friends International is a friendly cyber-community for people with chronic pain, FMS, CFS, ME and/or back pain.
Friends With Fibromyalgia & CFS
Exchange of information such as remedies and techniques for coping with Fibromyalgia & CFS, or simply to talk about how your day is going or simply to ask your fellow fibromites for advice. My goal is to make this group a fun place to come where you will not be judged.
We launched our online support newsgroup, GUAIGROUP in September, 2002. Since then, more than 2000 people have signed on and received help and support from our community. The group was established to help those wishing to reverse their fibromyalgia using R. Paul St. Amand M.D.’s guaifenesin protocol…and friends and family are welcome to join, too.
healKick is a social network for young adult patients 40-&-under with neuro-immune illnesses such as: Myalgic Encephalomyelitis, Chronic Fatigue Syndrome, Chronic Lyme Disease, Fibromyalgia, Rheumatoid Arthritis, Lupus, Sarcoidosis, Reflex Sympathetic Dystrophy, Multiple Sclerosis, Multiple Chemical Sensitivity, Mold-Related Illness.
ME/CFS Forums
Part of the forum is concerned with research and news, and is open to reading by the public. The other part of the forum is for support and sharing and is available only to members. We have members from all over the world.
 Men with Fibro Online Support Group
A community of patients, family members and friends dedicated to dealing with Men with Fibro, together.
National Fibromyalgia Assoc.
The National Fibromyalgia Association organization’s mission is to develop and execute programs dedicated to improving the quality of life for people affected by fibromyalgia.
Open Arms
Fibromyalgia and C.F.S. Support site. We are a small group of People who all deal with the same illness, pain, fatigue, and misunderstanding.
Young Adult Patients with ME CFS, Chronic Lyme, Fibromyalgia etc The owner is a 27-yr young man with ME/CFS and chronic lyme for the last 5 years. He recently created an online group that aims to provide a medical and social support for 40-and-under young adult patients with neuro immune disease (ME, fibromyalgia, chronic lyme, atypical MS, MCS, and mold illness.)
ProHealth Inc. Fibromyalgia & Chronic Fatigue Syndrome news, information and support.
Reaching Out Supporting those suffering from Fibromyalgia & CFS/ME
STEPS Care for Carers This is a private chat group for Carers only. The Carers share ideas and post questions to get advice from other Carers. As administrator, Steps Care for Carers also posts any information that we feel will be useful to Carers from funding opportunities to respite and everything in between. Acceptance to the group is through request and verification of your caring role.
SOFA: South Okanagan FM-ME Association Non Profit Organization with Programs and Services for those with the FM-ME/CFS and their family, community, medical community.
Foggy’s “invisible illness” Support Group Dedicated to providing support, raising awareness and promoting positivity!!
The ME Assoc. Our ME Connect volunteers provide information and practical advice & support.
TMJ Worldwide An open forum where you can discuss any issues surrounding the Tempero Mandibular Joint (TMJ) and the related health issues. This page is a collection of personal journeys and thoughts and in no way has an ‘alignment’ towards any one particular type of treatment. TMJ Worldwide’s ‘voice’ is one of the ‘sufferer’ and their personal account and experiences, it does not reflect on TMJ Worldwide specifically.