Friday, June 15, 2012

Mary Schweitzer's 6/13/12 CFSAC Testimony

CDC must end the use of the Toolkit and the Reeves "empirical" definition

Testimony to the Chronic Fatigue Syndrome Advisory Committee of the
U.S. Dept. of Health and Human Services
Wednesday-Thursday June 13-14, 2012
Mary M. Schweitzer, Ph.D.

Thank you for allowing me time to speak.

I'd like to express my admiration for the young people who testified today – I know how hard it was for them, and they did a great service. Thank you.

When you talk about educating people – whether teachers or physicians or the public in general – it comes down to the CDC's website on CFS. Despite the changes you have made, that website remains both wrong and dangerous to patients.

CDC's website on CFS continues to promote one particular viewpoint on CFS – that the disease can somehow be managed with cognitive behavior therapy and graded exercise. I was glad to hear the toolkit and brochures are going to be retired – but they should be burnt. That should be shut down NOW. Continuing the effective promotion of what is in there is simply wrong, and it harms patients in the real world –now. Why on earth are they still around?

The reference to cognitive behavior therapy signals the reader that the disease is really a somaticizing disorder – psychiatric, to be solved with psychiatric methods. Cognitive behavior therapy, or CBT, is very different from the pacing, or "envelope theory", that most of us are taught to prevent the dangerous push-crash cycles we suffer. Saying that CFS can be fixed with CBT implies what British psychiatrists say out in the open – we appear to be sick because we are deconditioned; we are deconditioned because we have inappropriate beliefs about illness and CBT is necessary to teach us we really aren't sick any more. That's when the second half of the equation comes in – Graded Exercise, with the combination often called CBT/GET.

While the emphasis on CBT is misleading and a nuisance, promoting graded exercise therapy is downright dangerous. Researchers in the past few years have shown that patients with this disease do not operate normally in aerobic metabolism. We do not utilize oxygen in our cells as normal people do, and we do not expel carbon dioxide as normal people do. Without an understanding of this mechanism, graded exercise is dangerous.

Other research articles suggest that there are significant cardiac abnormalities in groups of patients with "CFS" (Fukuda 1994). Again, without understanding how this works, or how badly the patient is affected by it, graded exercise is dangerous.

Finally, studies conducted by patient organizations in the UK have consistently demonstrated that Graded Exercise harms more patients than it helps. If it were a drug – with more patients suffering adverse events than experiencing improvement - it would never get past FDA.

But – the CDC recommends graded exercise – on its website, and in the published material that is sent to anyone asking for information. This is not okay. End it NOW.

And please, end your relationship with British psychiatrists who work for insurance companies.

In fact, the only hard link to an institution outside the CDC remains in the section recommending graded exercise. It links to Dr. Peter White's psychiatric CFS clinic at St. Bartholomew's Hospital in London. White is chief medical officer of two insurance companies: Scottish Provident and Swiss RE.

What does Dr. White think of CFS? This is from an article published last month in the British Medical journal: "The requirement that conditions should be classified … either mental or physical … causes particular difficulty in the context of the functional somatic syndromes or somatoform disorders, in which physical symptoms are often assumed to have a psychological explanation. […] For example, chronic fatigue syndrome may be classified as myalgic encephalomyelitis (ME) within the neurology chapter (G93.3) of ICD-10, or as neurasthenia, a psychiatric disorder (F 48.0)."

Really? Does CDC believe that? CFS is a somatoform disorder? It may be classified as neurasthenia?

While CDC helpfully links us to Dr. White's website, there are no links to American researchers or clinicians. None, zero, zippo, zilch. Why?

The most obvious reason – and another major critique I have of CDC's website – is that the only research on that website is their own, often in conjunction with Emory University. For years the research was about childhood traumas somehow causing CFS. I see they have branched out to include cytokines – but I see no references to the researchers who have worked on the relationships between cytokine abnormalities and CFS for twenty years. If you go to the website, it looks as if CDC discovered it all by themselves.

We need CDC to give a balanced perspective on information about this disease. We need professional summaries of research in different disciplines – not the tiny little slices of the research pie that CDC allows us to see. And they should make use of the researchers and clinicians who have represented us on CFSAC (and the CFSCC) for almost twenty years. Why not?

Dr. Unger replied that they didn't have to have a balanced bibliography or depiction of the disease because that is not what their website is for. It was just for saying what they were doing, period.

However, recently I heard from two different friends that there are new PSAs on the radio for "CFS". Now, normally I would have been pleased with this. But at the end of the PSA, the listener is referred to … the CDC– to its website and/or the old toolkit for professionals and/or the new brochure, all of which remain woefully inaccurate.

It matters that CDC has deep biases in what it places on its website, and in its publications. Outsiders go to the CDC website and learn that we need cognitive behavior therapy and graded exercise – which does not in any way reflect the approach of American experts on the subject.

When I heard CDC's testimony today, I had to wonder – where do I fit? Where do people like me fit? I have a diagnosis of Myalgic Encephalomyelitis and fit both the Ramsay and WHO definitions, as well as the 2011 International Definition (Carruthers et al, Journal of Internal Medicine). I have immune defects and am beset by viruses, some of which are in my spinal fluid. If you could not find anybody with viruses, then your subset was not patients like me. Why? Where do I belong then? What was wrong with your collection process that people like me were missing? Or if we were not missing, what was wrong with the way you did the research that we didn't show up? Why are you hiding us? Why do you say this disease is such a mystery when it is not; that there are no treatments when there are?

Why isn't there an MEAC - Myalgic Encephalomyelitis Advisory Committee?

There are at least one million Americans, of every class and ethnicity, with this disease. There have been cluster outbreaks in the past and there will be cluster outbreaks in the future.
This disease ruins whole lives. Children get it. Teenagers get it. It ruins families. Yet both CDC and NIH continue to spend virtually nothing on this disease. This has been going on thirty years – more than a generation. When will it end? How long do you think you can keep it a secret?

Postscript on definitios:

The Fukuda definition (1994) was only intended to be temporary until subsets of patients had been identified using biomarkers. If you actually READ the article itself, you will see that. CDC has done nothing in this regard. 18 years. Nothing.

The Reeves definition, sometimes misleading called "empirical," is without any basis at all. In the lone article where he used his questionnaires on a set of 58 Kansas patients who had been diagnosed with CFS using Fukuda, he could only come up with SIX who met his definition. I would hardly call that a ringing endorsement. It should be dumped.

The Canadian definition of 2003 was created by a committee of seasoned clinicians after Canada adopted its own version of ICD-10 and placed both CFS and M.E. in the same category. It is intended for clinical use, but it has already been useful in research. If nothing else, use this definition.

Dr. Reeves always said there would be no references to different names or definitions until the community of scientists came up with one. Well – they have. Last summer a group of researchers and clinicians led by Bruce Carruthers published an article in the Journal of Internal Medicine, defining Myalgic Encepalomyelitis and offering a way to diagnose it. (I should note that Melvin Ramsay had a textbook describing M.E. in the 1980s – this has been ignored by CDC.) The new M.E. definition makes post-exertional exacerbation of symptoms – which can be measured objectively – the center of the disorder – not chronic fatigue.

This is what we need = acceptance of the diagnosis of Myalgic Encephalomyelitis with a scientific definition. For those diagnosed with chronic fatigue syndrome who do not meet the criteria for Myalgic Encephalomyelitis, I would recommend the Canadian definition – and if they don't meet that, find out what they really have. And treat them.

CFS was a misstep. When the cluster outbreaks occurred around the United States in the 1980s, American clinicians did not know about M.E. because it was not used in the United States – epidemic neuromyesthenia had been used to mean the same thing, but there had been little about it after the 1970s.

Had those cluster outbreaks occurred in Surray, England, instead of lake Tahoe, or Lyndonville NY, or Rockville Maryland, or Hollywood, or Cherry Hill NJ – the patients would have been diagnosed with M.E. We would be much further along (I would hope) on diagnosing and treating patients.

Instead, CDC and NIH (represented by the late Stephen Straus) went its own way, adopting a made-up name for a disease that already had a name, a definition, and research. We have been set back 30 years by this misstep.

Time to go back to the name in place before that misstep – M.E. – time to accept that there already exist formal definitions for the disease, and time to quit saying its so mysterious, because it is not. Thank you.

Mary M. Schweitzer, Ph.D.

Thursday, June 14, 2012

Llewellyn King interviews Dr. Peterson

In Episode #26 of ME/CFS Alert, host Llewellyn King interviews Dr.
Daniel Peterson of Simmaron Research.


Tuesday, June 12, 2012

Dr. Judy

All criminal charges against Dr. Judy have been dropped!

Monday, June 11, 2012

Fibro, CFS and Disability Insurance

Note: This is a press release from a law firm. The key graph is this:
Recently, a court decision reviewing a denied disability claim for a
fibromyalgia sufferer took a step towards holding large insurance
companies accountable for fully evaluating claimants seeking
disability compensation. They did not hold that fibromyalgia and
chronic fatigue syndrome should receive coverage, but that insurance
companies owe their policy holders a duty to conduct a full,
independent investigation.

Fibromyalgia/Chronic Fatigue: Diagnosis Difficult, Benefits Often Denied
Large insurance companies often deny disability claims based on
fibromyalgia and chronic fatigue syndrome.

    June 10, 2012 /24-7PressRelease/ -- Fibromyalgia and chronic
fatigue syndrome are two frequently misunderstood medical conditions.
According to the National Institutes of Health people often think they
developed overnight and exist only within a person's mind. The truth
is that these diseases have been around for centuries, although they
were commonly believed to be a single condition known as muscular

With technological advances, physicians and medical researchers have
been able to specifically categorize these two unique diseases. The
recent ability to diagnose these ailments allows patients an increased
chance of managing the disorder and returning to their daily routines.

A diagnosis is often achieved using an 18-point test. The challenge
for people with these diseases is that even with a positive diagnosis
the level of pain and fatigue resulting from these diseases cannot be
quantified. As a result, many large insurance companies frequently
deny disability insurance claims.

The companies argue that the patient is not truly disabled and support
this statement with the fact that it is very difficult for doctors to
objectively list the level of pain and fatigue suffered by the

Basics of Fibromyalgia and Chronic Fatigue Syndrome and Treatment by Insurers

Fibromyalgia is a disorder that causes pain in the victim's muscles
and includes symptoms of fatigue, anxiety, depression and headaches.

Chronic fatigue syndrome is a complicated disorder that shares many
similarities with fibromyalgia. Symptoms include fatigue, loss of
memory, unexplained muscle pain, poor sleep and extreme exhaustion
lasting more than 24 hours.

Insurers Employ Sneaky Tactics to Avoid Paying Fibromyalgia Claims

Unfortunately for both of these diseases the symptoms are subjective.
There are no tests to determine the exact level of patients' pain or
fatigue. Many insurers attempt to circumvent coverage of these
diseases by requiring objective tests. This technique is often
successful, because it is near impossible to objectively prove that a
person suffering from either of these disorders is in pain.

Recently, a court decision reviewing a denied disability claim for a
fibromyalgia sufferer took a step towards holding large insurance
companies accountable for fully evaluating claimants seeking
disability compensation. In the case, a large insurance provider
denied a policy holder disability benefits without conducting an
independent medical examination. Instead, they based the denial on an
investigation carried out by one of the company's employees.

The court ultimately found the insurance company's denial was
unreasonable. They did not hold that fibromyalgia and chronic fatigue
syndrome should receive coverage, but that insurance companies owe
their policy holders a duty to conduct a full, independent

Although the holding works in the policy holder's favor, the road to
approval of a disability insurance claim is still long and

The future of ME Community


The future for the M.E. Community

I am acutely ill with a flu-like virus, causing shivering, aches &
pains, headache and I am sleeping, irregularly, about 12 hours a day.
When awake, I am weak, unable to concentrate or function normally. Since
this is a repetitive cycle, I have decided to take an indefinite period
of time away from the work of the M.E. Community, for the sake
of my own health and because I do not have sufficient help or support to
continue, even at the lowest practical level.

I shall return with a revamped campaign based on divorcing M.E. (Myalgic
Encephalomyelitis) from "fatigue" as part of the sleep cycle, whether as
a single word, or sandwiched between "chronic" and "syndrome". It is the
acceptance of Chronic Fatigue Syndrome (or any other name, with
"fatigue" as a component) that has been at the root of maintaining
people ill with M.E. for 25 years and there is no sign of any change so
long as it gets support for the medical and political establishments, as
well as from CFS/ME patient organisations. This is because it is:
logically untenable to consider a single illness (M.E.) exactly the same
as several other conditions (CFS), or one as a subset of the other,
either CFS/ME or ME/CFS; doing so leads to research design that is
invalid (does not measure what it purports to measure) and unreliable
(cannot be repeated within and amongst subjects) and, worst of all,
applying untrustworthy conclusions about treatments, such as Cognitive
Behaviour Therapy (CBT) and Graded Exercise Therapy (GET) to people with
M.E., who were not tested, is at least ineffective, often harmful and
morally reprehensible.

This will require the support of a majority of the M.E. community, in
both effort and subscription to funding, or nothing will change because
those who perpetuate the CFS construct are either, ignorant of their
invalid work or, more selfishly, concerned with career interest or
profit motive of their sponsors. If we do not bring about a change,
proven by properly designed research work, I shall see it as a victory
for institutionalised bullying over patient apathy and I shall be the
latest of a number of generations of campaigners to be forced into
retirement - but at least I shall have one more last try.

Please do not contact me, with the expectation of a reply, unless it is
with practical help towards this project, for which you have the time,
energy and commitment to put more in than you take out, or unless you
have a no-strings donation (I'm thinking of £1 million, or a large part
thereof) as I cannot cope with reading messages, let alone responding to
them at this time but please do feel free to forward and republish this
letter anywhere for optimum benefit.

Best wishes
Dr John H Greensmith
ME Community
36a North Street
BS16 5SW
United Kingdom
+44 (0) 117 956 0150

RIP Karen Sherlock

She spent her last months fighting for the "security" of £96 a week and the reassurance that it couldn't be taken away.