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How M.E. was never associated with Fatigue.

Stonebird is delighted to post this important summary by Jerrold Spinhirne

The early description ME by E.D. Acheson in 1959, based on careful observation of 14 outbreaks of the disease, did not mention fatigue of any kind as a commonly observed or diagnostically useful symptom:

"All the outbreaks shared the following characteristics: (1) headache; (2) myalgia; (3) paresis [muscle weakness, partial paralysis]; (4) symptoms or signs other than paresis suggestive of damage to the brain, spinal cord or peripheral nerves; (5) mental symptoms; (6) low or absent fever in most cases; (7) no mortality. In addition, (1) a higher attack frequency in women; (2) a predominantly normal cerebrospinal fluid, and (3) relapses have occurred in almost all outbreaks. In eleven of the fourteen epidemics symptoms which suggest activity of the disease have persisted for months or years in a few cases, and in eight instances there was an apparent predilection for the nursing or medical professions. Lymphadenopathy was a feature in four outbreaks."

Neither does Melvin Ramsay's 1986 case definition of ME mention fatigue of any kind.

“A syndrome initiated by a virus infection, commonly in the form of a respiratory or gastrointestinal illness with significant headache, malaise and dizziness sometimes accompanied by lymphadenopathy or rash. Insidious or more dramatic onsets following neurological, cardiac or endocrine disability are also recognised. Characteristic features include:

(1) A multisystem disease, primarily neurological with variable involvement of liver, cardiac and skeletal muscle, lymphoid and endocrine organs.

(2) Neurological disturbance – an unpredictable state of central nervous system exhaustion following mental or physical exertion which may be delayed and require several days for recovery; an unique neuro-endocrine profile which differs from depression in that the hypothalamic/pituitary/adrenal response to stress is deficient; dysfunction of the autonomic and sensory nervous systems; cognitive problems.

(3) Musculo-skeletal dysfunction in a proportion of patients (related to sensory disturbance or to the late metabolic and auto immune effects of infection)

(4) A characteristically chronic relapsing course."

In the last paper published by Ramsay, and with Elizabeth Dowsett, in 1990, this was the ME case definition they used:

"We adopted the following clinical criteria for investigation of ME: a syndrome commonly initiated by respiratory and/or gastro-intestinal infection but an insidious or more dramatic onset following neurological, cardiac or endocrine disability occurs. The pathognomonic features are: a complaint of general or local muscular fatigue following minimal exertion with prolonged recovery time; neurological disturbance, especially of cognitive, autonomic and sensory functions; variable involvement of cardiac and other systems; a prolonged relapsing course."

The symptom of post-exertional muscle fatigue used here is very different from the symptom of perceived, non-post-exertional general fatigue, the subjective feeling of tiredness, used as the basis for making a CFS diagnosis.

Perhaps post-exertional muscle depletion or dysfunction would have been a better term to use than "muscle fatigue" to avoid confusion with subjective, perceived fatigue. Muscle fatigue can be objectively measured. Perceived, general fatigue can only be evaluated by psychometric questionnaires – an important distinction.

Dr. Elizabeth Dowsett said in an 1992 interview:

"One of the most striking features of ME is that the patient is not tired all the time! Extreme and sudden variability of energy levels both within and between episodes of illness differentiate this syndrome from other diseases associated with fatigue. One can only deplore the current fashion in the United States as well as the United Kingdom to redefine and rename a disability which has been clearly described in the literature for at least 100 years."

"There is nothing to be said in favour of the American acronym CFIDS (chronic fatigue immune deficiency syndrome) with its connotation of a primary immune dysfunction. The term 'chronic fatigue syndrome' recently adopted in this country also is nonspecific and non-descriptive because most of the definition is based on a vast number of exclusions (some of which, for example, endocrine disturbance, are actually found in ME)."

"'Post-viral fatigue syndrome', another British name, describes one essential feature (the association of the illness with viral infection) but gives the impression that the infection was antecedent rather than, as we now know, persistent. I prefer to use the more specific term 'myalgic encephalomyelitis' as it emphasizes the essential encephalitic component of the illness, the muscle pain, and the close clinical and epidemiological similarity to poliomyelitis."

An open letter to my wife, following David Bowie's death.

Dear Linda,

They are still marvelling at Bowie’s death; how well he looked in his sharp suit, what a masterpiece it was.

As you know, I agree. You may never be able to view it, but I have tried to convey to you what a profoundly shocking experience Bowie’s last video “Lazarus” is. It is difficult - being limited to so few words, that must be spoken quietly, softly, with as little body movement as possible.

Even then things are infinitely fragile. The wrong information, conveyed at the wrong moment, in the wrong tone, being far too much to take in and comprehend, is likely to throw you into excruciating, paralytic agony, ruin the day, the week or longer, cause hours of suffering torment.

Last night, late, the pain radiating from your slumped body was tangible. I didn’t need to look into your dark, sunken, seared eyes, to feel it as something malicious , alive, unspeakable, jagged, gut-tearing. “I can’t bear it anymore”, that soft cry, after twenty three years of non-stop physical torment, is impossibly hard to bear.

Bowie’s well dressed, sharp-suited , dancing, famous death, contrasts so much with your unknown struggle to get through each moment. You hear it mentioned how Severe ME compares to terminal Cancer. My love, we know how it is much, much worse.

I bet Bowie wasn’t left, as you are, with no medical expertise, intervention or input. What do you think, did they ever couch his suffering in terms of “fatigue”, as everyone does these days with your disease ?

I struggle, terribly, Linda, to live with the knowing that my decades of struggle and activism have done nothing to prevent your illness being taken over and finally buried.

We have both said it, there is no “ME” anymore only “CFS”. The Oxford Criteria are dead, long live the DePaul Questionnaires, of this fatigue-focused, fucked-up world. How many people with ME are going to be killed by investing in the likes of Rituximab ?

In 20 years I will be 80, will the world have come to its senses by then ? Can your body bear the hopeless wait my love ?

Lazarus was a street person, like you, Linda, he existed, somehow, on the far edge, on crumbs.

Likewise, any help, assistance or aids, we have managed to get for you has been done “on the side”, cast-off bath aids that badly hurt you, well-know clinicians who did immense harm, in their ignorance of Severe ME; you have still not recovered, all these years later and likely never will.

“How many people lie, instead of standing tall ?”, Bowie asks.

Your disease is soaked in lies, your life has been ruined by spin and deliberate cover-up.

Yet through it all, you have stood tall, a rock to me and countless others, the world over.

The other Lazarus, the one that Jesus rose from the dead, the one Jesus wept for -tears of compassion, tears of anger, that is me, in the mystery of our marriage and the power of our love, more alive than ever, never giving up.


(This is taken from :
Severe ME : Notes for Carers” :
  1. Many world-class clinicians state that ME is either an infectious disease, or an auto-immune disease as a direct result of infectious insult and recognise ME as a complex neuro-immune disorder accompanied by chronic low-grade inflammation, increased levels of oxidative and nitrosative stress.(Maes et al 2014), requiring a skilled biomedical response.
  2. ME was recognised as a specific disease entity by The Royal Society of Medicine in 1978 and by the World Health Organisation since 1969 as an organic neurological disease, ME is currently classified under ICD code G93.3. In the USA, ME ranks second only to HIV as the cause of serious, long-term illness. (Hooper 2004)
  3. Cycles of severe relapse are common, as are further symptoms developing over time. Around 30% of cases are progressive and degenerative and sometimes ME is fatal. (National CFIDS Foundation). Two reviews have concluded that, “Substantial improvement is uncommon and is less than 6%"(Anderson et al. 2004); and "Full recovery... is rare". (Cairns & Hotopf, 2005)
  4. According to the Chief Medical Officer (DH 2002) people with Severe ME in the UK currently receive "seriously inadequate health care”.
  5. There is a significant body of compelling published evidence, demonstrating the involvement of the central nervous system, the autonomic nervous system and the peripheral nervous system in the pathogenesis of ME, as well as immunological and vascular disruption. (Williams 2004)
  6. There are known to be so many issues with the body’s defence against pathogens, the Immune System, in ME that it has also been called CFIDS, Chronic Fatigue and Immune Dysfunction Syndrome. When the immune system has been seriously disrupted, all kinds of bacteria can no longer be eliminated.
  7. ME is not a somatoform, “all in the mind”, psychiatric disorder. The documented biochemical, metabolic, vascular, neurological and muscle abnormalities in ME/CFS patients (Williams 2004) have led to the WHO classification of ME as a neurological illness. The UK Department of Health and the WHO Collaborating Centre at the Institute of Psychiatry have agreed that ME is undoubtedly neurological. There is no published evidence whatsoever, as opposed to opinion, that ME (as distinct from chronic fatigue) is a psychiatric disorder. (Williams 2004)
  8. ME is not ‘medically unexplained.’ ME is a multi-system disease with many organ and bodily systems affected, producing a myriad of symptoms [and] many aspects of the pathophysiology of the disease have, indeed, been medically explained in volumes of research. (ME Society of America)
  9. Cognitive Behaviour Therapy (CBT) and Graded Exercise Therapy (GET) are potentially harmful to anyone with ME. The Chief Medical Officer (2002) warned that exercise-based regimes advocated for less severely affected patients tend not to have been studied among those most severely affected. Shepherd (2001) warns that as much care should be taken in prescribing exercise as in prescribing pharmaceuticals, for ME patients do not respond to exercise in a manner that is expected of healthy people. (Streeten et al 2001)
  10. It is not 'fatigue' or 'tiredness' that is the one essential characteristic of ME/CFS but central nervous system (CNS) dysfunction (Bassett 2006). As leading ME expert Dr Byron Hyde MD (2003) explains: “The one essential characteristic of M.E. is acquired CNS dysfunction, [not] chronic fatigue. A patient with M.E. is a patient whose primary disease is CNS change, and this is measurable”
  11. It has been shown that ME, alongside a wide range of seemingly unrelated disorders, such as Alzheimer’s, Diabetes, may have mitochondrial dysfunction in common (Pieczenik and Neustadt 2007); the research appears to be suggesting that blood flow problems are affecting the mitochondria’s ability to produce energy instead of the mitochondria themselves being messed up in ME. (Johnson 2013). It has been estimated that people with ME are about a litre short of blood.
  12. Cardiovascular dysfunction in ME patients has been well documented for many years. (Williams 2008)
  13. Cardiac output in normal people will vary from 7 litres per min to 5 litres per min between standing and supine. In healthy people this drop is not enough to affect function. But in ME sufferers Peckerman found that the drop may be from 5 litres lying down to 3.5 litres standing up. At this level, people with ME may be in borderline heart and organ failure.(Peckerman et al 2003)
  14. Studies have shown that the baroreflex response that regulates blood pressure is under performing, particularly in Severe ME. (Peckerman et al 2003) The heart’s job is to maintain blood pressure. If the blood pressure falls, organs start to fail and are shut down in terms of priority.
  15. A study showing that the mean age of ME patients dying from heart failure is significantly lower than the age of those dying from heart failure in the general US population, implies that ME is a risk factor to cardio-vascular disorder.( Maes and Twisk 2009 )
  16. Maes et al (2009) found that Coenzyme Q10 deficiency in ME is related to fatigue, autonomic and neurocognitive symptoms and is a risk factor explaining the early mortality in ME due to cardiovascular disorder.
  17. Neurocognitive problems, strikingly similar to those of patients presented with D-lactic acidosis (linked to Short Bowel Syndrome) reported to be made worse by physical or mental exertion, are one of the most frequent and disabling symptoms associated with ME. (Sheedy et al 2009)
  18. In 2009 a study found vitamin D levels to be considerably lower in ME patients than in healthy people. Soon after an investigation at the University of Dundee discovered an association between lower vitamin D levels and arterial stiffness, dysfunction of the endothelium (the lining of blood vessels) and inflammation, in ME patients. (Breakthrough Spring 2015)
  19. ME is not depression. Research, for example, shows that ME patients show more alpha electroencephalographic activity during non-REM sleep, but this is not seen in dysthymic or major depressive disorder (Whelton, Salit, & Moldofsky, 1992). There are five major clinical tests of depression, all related to disturbances of the HPA (Hypothalamic-Pituitary-Adrenal) axis; they are, increased levels of Overnight Cortisol, 24-hour urinary cortisol, Corticotropin-releasing hormone, Arginine vasopressin and Adrenocorticotropin hormone (ACTH), ACTH is a hormone that is often released in response to stress, high ACTH levels can be an indicator of depression. ME patients, generally, show none of these signs, that is because ME, contrary to what many doctors wrongly believe, is not depression. (cf. Komaroff 2015)
  20. SPECT cerebral blood flow studies of persons with ME show decreased blood flow in several key areas such as frontal lobes and brain stem which are different from both healthy controls (Barnden et al, 2001Costa et al, 1995) and depressed subjects (Schwartz et al, 1994, Fischler et al, 1996). PET scan studies have reached similar conclusions. (Tirelli et al, 1998)
  21. The neurocognitive impairment in ME has been found to be rooted in physical dysfunction, not maladaptive thinking, related to decreased cerebral blood flow velocity. (Ocon et al 2011)
  22. Hickie (1991) found that general characteristics of depression: anhedonia (lack of pleasure in life); weight loss; suicidal ideation; severe psychomotor change; pathological guilt; and severe anxiety, are not typical in ME.
  23. ME is not deconditioning. The predominant psychiatric paradigm, still seems to be that patients have medically unexplained chronic fatigue, and that their problems derive from deconditioning consequent on physical inactivity at best and simple avoidance behaviour (underpinned by abnormal illness beliefs) at worst. (Scottish Cross Party Submission 2005).
  24. What happens in ME has little to do with cardiovascular deconditioning (Spence & Stewart 2004) and is more related to chronic orthostatic intolerance/postural tachycardia syndrome (POTS), caused by vascular dysfunction.
  25. Studies have shown that most patients do not avoid minimal activity and that lack of fitness is not related to the fatigue in ME (Bazelmans et al 2001 ). Moreover, deconditioning cannot explain the documented delay between the end of exertion and the exacerbation of symptoms, the upregulated immune system etc. (De Merlier et al 2000)
  26.  Although, as with lupus, multiple sclerosis and ovarian cancer for example, there is no medical test available to confirm a diagnosis of ME, it is absurd to claim no objective or quantifiable abnormalities can be found in patients with Severe ME. (Bassett 2006) “Tests will only all be normal in M.E. patients – as with all illnesses – if completely the wrong tests are done, or if those tested do not in fact have M.E. in the first place.” (Bassett 2006)
  27. A 2015 study at Stanford University, comparing brain MRI images, found that the brains of people with ME differ from healthy subjects in at least three distinct ways: white-mater content was reduced by about 7%, a consistent abnormality in the right arcuate fasciculus was identified with links to the severity of illness and there was a thickening of grey matter, where the two areas of the brain connect at the right arcuate fasciculus. These results, showing strong evidence for Central Nervous System defects, were reported widely around the world. (Breakthrough Spring 2015)
  28. Certain aspects of immune system dysfunction, dysregulation of the RNase L pathway, hyperactive NF-kappaB leading to disturbed apoptotic mechanisms and oxidative stress or excessive nitric oxide, for example, appear to be present in both Cancer and in ME and may play a role in the two diseases and in the physiopathology of the common symptom fatigue. (Meeus et al 2009)
  29. There is evidence that ME is characterised by increased oxidative stress (Maes et al 2011). Researchers at the University of Dundee have found that people with ME have high levels of reactive oxygen molecules which can harm blood vessels and muscles. (Breakthrough Spring 2015)
  30. There is good evidence that ME patients have a generalised hyperalgesia (an increased sensitivity to pain throughout the body which increases after stressors and following exercise – this is unusual because sensitivity to pain normally decreases in people during physical activity. (Breakthrough Spring 2012)
  31. Problems with eyes and vision are common feature of ME, including eye pain (which is severe or very severe in one third of cases), prominent eye movement dysfunction and visual processing issues. (ME Research 2015)
  32. Studies examining the microecology of the gastrointestinal (GI) tract have identified specific microorganisms whose presence appears related to ME, which is associated with marked alterations in the gut microbiota, with lower levels of Bifidobacteria and higher levels of aerobic bacteria. A CFIDS Association of America pilot study, for example, found greatly increased ratios of Firmicute/Bacteriodetes bacteria before and after exercise in ME. (CIFDS 2013)
  33. It has been found that a significant subset of ME patients may have a chronic, non-cytolytic form of enteroviral infection which could be diagnosed by stomach biopsy. (Chia 2008)
  34.  Reports also suggest that ME patients may have a major drop in all E.Coli species - in contrast to Crohn’s Disease where over 95% of the invasive species are E.Coli. (Lassesen 2013)
  35.  One of the most consistently observed abnormalites in ME is hypocortisolism (low cortisol levels); there is evidence for reduced cortisol and ACTH production/responsiveness in ME, alongside evidence of reduced adrenal gland productivity. A mutation in the cortisol binding globulin gene (CBG) has also been found in people with ME, this impaired CBG functioning would exacerbate any cortisol deficiencies already present. (Torpy et. al. 2001)
  36. New Scientist magazine reported in July 2015 that nearly two thirds of people, diagnosed with “ME/CFS” who have taken Rituximab, a drug normally used to knock out white blood cells in people with lymphoma and rheumatoid arthritis, have experienced a major remission of their symptoms. We are not sure, however, if Rituximab really is a potential treatment for ME; it could be that the two thirds of patients it helped have “CFS”, not ME, for “ME/CFS” is an umbrella term, subject to many different interpretations, incorporating a wide range of meaning and poorly identified conditions. If you have ME, caused by an enterovirus, the John Richardson Group (2013) warn, it could be very dangerous indeed to take Rituximab, which suppresses the immune/virus balance.

  It should be stressed that any registered medical practitioner, consultant or GP, in the UK, who chooses to dismiss or ignore widely available biomedical evidence for ME, may be in breach of the legal requirement for doctors to keep up to date with developments in medicine and medical science and this consequently raises issues of medical indemnity.(Hooper 2010 )
  In the UK, there is no act of parliament setting out patient’s rights, however the NHS must take account of law made by parliament (e.g. Human Rights Act etc.) or by court judgements. Health professionals must use reasonable care and skill and patients are entitled to receive care of a standard which a “responsible body of medical opinion” considers to be appropriate to their condition. If the duty of care is breached, the patient may be able to sue for negligence.(NHS 2006)

 Greg Crowhurst (c) 201
 From : Severe ME : Notes for Carers

References :

1 Whiting J (2015) The Doctor’s Dilemma (free download), Stonebird,
2 Ellis C (2015) The End ME/CFS Project: History Taking Root, Phoenix Rising
3 Hooper M (2010) Magical Medicine
4 NHS (2006) Rights to Treatment Mental Illness/Assets/RightstoNHStreatment.pdf
5 A report of the CFS/ME Working Group
6 Handel B (2015) Validity of chronic fatigue bolstered by research. The Lawyers Weekly
7 Maes M & Morris G (2014) Mitochondrial dysfunctions in Myalgic Encephalomyelitis/chronic fatigue syndrome explained by activated immuno-inflammatory, oxidative and nitrosative stress pathways.
9 Andersen MM et al (2004) Illness and disability in Danish CFS patients at diagnosis and 5-year follow-up. J Psychosomatic Research 2004; 56: 217-229."
10 Cairns R and Hotopf M(2005) A systematic review describing the prognosis of chronic fatigue syndrome
11 Williams M (2004) Issues re the use of the Oxford criteria for the MRC “CFS” Trials
12 Streeten DH (2001) Role of impaired lower-limb venous innervation in the pathogenesis of the chronic fatigue syndrome. Am J Med Sci 2001 Mar;321:163-167.
13 Bassett J (2006) A Hummingbird’s Guide to CFS/ME . The Effects of CBT and GET (on patients with ME)
14 Hyde, Byron M.D. (2003) The Complexities of Diagnosis in (ed) Jason, Leonard at et al. 2003 Handbook of Chronic Fatigue Syndrome by Ross Wiley and Sons, USA
15 Pieczenik SR, Neustadt J (2007) Mitochondrial dysfunction and molecular pathways of disease Exp Mol Pathol. 2007 Aug;83(1):84-92. Epub 2007 Jan 18
16 Johnson C (2013) The Splitter: Researcher Asserts ‘Brain-damaged’ Subset Present in Chronic Fatigue Syndrome (ME/CFS)
17 Williams M (2008) Evidence of cardiovascular problems in ME/CFS that NICE disregarded
18 Peckerman A, LaManca JJ, Qureishi B, Dahl KA, Golfetti R, Yamamoto Y, Natelson BH.(2003) Baroreceptor reflex and integrative stress responses in chronic fatigue syndrome.Psychosom Med. 2003 Sep-Oct;65(5):889-95.
19 Maes et al (2009) Coenzyme Q10 deficiency in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is related to fatigue, autonomic and neurocognitive symptoms and is another risk factor explaining the early mortality in ME/CFS due to cardiovascular disorder.
20 Sheedy JR, Wettenhall RE, Scanlon D, Gooley PR, Lewis DP, McGregor N, Stapleton DI, Butt HL, DE Meirleir KL. (2009) Increased d-lactic Acid intestinal bacteria in patients with chronic fatigue syndrome. In Vivo. 2009 Jul-Aug;23(4):621-8.
21 Breakthrough (Spring 2015)
22 Whelton, C.L., Salit, I., & Moldofsky, H. (1992). Sleep, Epstein-Barr virus infection, musculoskeletal pain, and depressive symptoms in chronic fatigue syndrome. The Journal of Rheumatology, 19, 939-943.
23 Komaroff AL (2015) Chronic Fatigue Syndrome: Biology, Diagnosis, and Management
24 Costa,D.C., Tannock,C., & Brostoff,J. (1995) Brainstem perfusion is impaired in chronic fatigue syndrome. QJM, 88, 767-773
25 Schwartz,R.B., Komaroff,A.L., Garada,B.M.,Gleit,M., Doolittle,T.H., Bates,D.W., Vasile,R.G., & Holman,B.L. (1994) SPECT imaging of the brain:comparison of findings in patients with chronic fatigue syndrome, AIDS dementia complex, and
major unipolar depression. AJR Am.J Roentgenol., 162, 943-951.
26 Fischler,B et al (1996) Comparison of 99m Tc HMPAO SPECT scan between chronic fatigue syndrome,major depression and healthy controls: an exploratory study of clinical correlates of regional cerebral blood flow. Neuropsychobiology, 34, 175-183.
27 Tirelli et al (1998) Brain positron emission tomography (PET) in chronic fatigue syndrome: preliminary data. American Journal of Medicine, 105, 54S-58S.
28 Ocon AJ et al (2011)Research: orthostatic stress impairs neurocognitive functioning,
29 Hickie I (1991) Psychological Aspects of ME, Emerge, September 1992,
31 Spence V and Stewart J (2004) Standing up for ME
32 Bazelmans E, Bleijenberg, G, van der Meer, JWM and Folgering, H (2001) Is physical deconditioning a perpetuating factor in chronic fatigue syndrome? A controlled study on maximal exercise performance and relations with fatigue, impairment and physical activity. Psychol Med, 2001, 31; 107-114.
33 De Meirleir, K., Bisbal, C, Campine, I, De Becker, P, Salehzada, T, Demettre, E and Lebleu, BA.(2000) 37 kDa 2-5A binding protein as a potential biochemical marker for chronic fatigue syndrome. Am J Med, 2000, 108; 2: 99-105.
34 Breakthrough (Spring 2015)
35 Meeus M, Mistiaen W, Lambrecht L, Nijs J. (2009) Immunological similarities between cancer and chronic fatigue syndrome: the common link to fatigue? Anticancer Res. 2009 Nov;29(11):4717-26.
36 Maes M et al (2011) Lower whole blood glutathione peroxidase (GPX) activity in depression, but not in myalgic encephalomyelitis / chronic fatigue syndrome: another pathway that may be associated with coronary artery disease and neuroprogression in depression. Neuro Endocrinol Lett. 2011;32(2):133-40.
37 Breakthrough (Spring 2012) ME Research (Autumn 2012) ME Research
38 CIFDS Association of America (2013) The Role of the Gut Microbiome in ME/CFS
39 Chia JK and Chia AY (2008)Chronic fatigue syndrome is associated with chronic enterovirus infection of the stomach.
Chia JK1, Chia AY.
40 Lassesen K (2013) Fertile Flora: the Gut Microbiome and the Infection Connection in Chronic Fatigue Syndrome and Fibromyalgia
41 Torpy, D., Bachman, A., Grice, J., Fitzgerald, S., Phillips, P., Whitworth, J. and R. Jackson. 2001. The Journal of Clinical Endocrinology and Metabolism 86, 3692-3700.
42 The John Richardson Research Group’s
43 Crowhurst G(2005) Submission To The Parliamentary Inquiry Into Progress In The Scientific Research Of M.E. By The 25% Severe ME Group
44 Hemmingway P (2006) The Risks to Health from Electromagnetic Radiation (EMR)
45 Chew Graham C et al(2009) Practice Nurses' views of their role in the management of Chronic Fatigue Syndrome/Myalagic Encephalitis: a qualitative study BMC Nurs. 2009; 8: 2.Published online Jan 22, 2009. doi: 10.1186/1472-6955-8-2
46 Nightingale F (1860) Notes on Nursing
47 Crowhurst G(2005) Submission To The Parliamentary Inquiry Into Progress In The Scientific Research Of M.E. By The 25% Severe ME Group
49 Crowhurst G (2011)Perrin's point found !
50 Myhill 2008 Muscle Pain in Chronic Fatigue Syndrome (ME/CFS) – Causes and Treatment
51 Robinson S (2010) ME/CFS Pain & Fibromyalgia Pain – Can You Distinguish Between the Two?
52 Dellwo A (2010) Fibromyalgia, Chronic Fatigue Syndrome & Comorbid (Overlapping) Conditions As If One Illness Isn't Enough!
53 Bell David (2008) ME/CFS as a Mitochondrial Disease
54 Sampson DP (2010) Close analysis of a large published cohort trial into fatigue syndromes and mood disorders that occur after documented viral infection International Association for CFS/ME
55 Bassett J (2006) A Hummingbird’s Guide to CFS/ME . The Effects of CBT and GET (on patients with ME)
56 Hornig M(2015) Distinct plasma immune signatures in ME/CFS are present early in the course of illness
57 Ross A et al (2013)What is brain fog? An evaluation of the symptom in postural tachycardia syndrome
58 Breakthrough (Spring 2012) ME Research

 Greg Crowhurst (c) 2016
From : Severe ME : Notes for Carers

There is little hope...

How did we get to this :

An article on CoCure calling for "CFS/ME/SEID to be properly incorporated into mainstream medicine. "

You know, we stand on the shoulders of giants,the Ramsays, the Dowsetts, the Hennesy's, but when the IOM, ignoring the volumes of research outlining the Neurological, Autonomic, Neuroendocrine and Immune system malfunctions that constitute M.E, ignoring Severe ME, claimed that M.E. and CFS “denote conditions with similar symptoms” and proposed "SEID", it was as if they had effectively done what the psychiatric lobby have been trying to do for years... bury ME under fatigue :…/a-tragic-mishmash-of-id…

There is NO SUCH THING as "CFS/ME/SEID" !!!

All the time that ME, as defined by Ramsay and the WHO , is confused with Chronic Fatigue, or is ignored or wrongly misrepresented as Chronic Fatigue Syndrome, or SEID, there will continue to be little hope of proper medical investigation or representation, especially for the most severely affected, we fear.

An Exercise in Social Engineering

The PACE Trial was an exercise in Social Engineering : see Hooper and Williams :

The Pain in Caring

Few are able to bear the pain of watching, waiting, being with the person who suffers, especially if that
pain is drawn out over years and years.
There is pain in caring for someone as ill as my wife; I made this list:

1. The pain of my presence, my voice, my thinking even, my attempts to try and be quiet, increasingly being too much for her to bear.
2. The pain of her total suffering, paralysis, deep isolation from anyone and everything, the absolute littleness of her life.
3. The pain of the immensity of the illness, in its face we are only a dot - at least that is what came to me in a reflective drawing recently- a powerful dot of fire though, that will never give up!
4. The pain of the hours spent coping, my wife never comfortable, never finding any relief anywhere, moving from lying to sitting, always being pulled back into paralysis and exacerbation of symptoms.
5. The pain of feeling less and less confident, hopeful, certain of a cure one day.
6. The pain of getting older, it has been more than two decades now, realising my body is slowing, is not as strong as it used to be, to help.
7. The pain of witnessing the psychiatric lobby still going from strength to strength, in contrast to our diminishing situation.
8. The pain of being so alone; knowing there is not one ME group that is waging an effective fight.
9. The pain of fighting so hard, yet the illness is still left untreated and is taking its tragic course, regardless.
10. The pain of my wife whispering to me, at 2am that the pain is too much to bear.
We have found that love gives strength in the bleakest,
most barren, pain-wracked place.
(from "Severe ME; Notes for Carers")