Uncategorized

CDC the Puppeteer and the UK BPS Connection to Bury ME

/ Gabby Klein / 1 Comment

wood-doll-2679701_1280

My thanks to advocate Eileen Holderman for her consultation on this blog post

Fake Media Attacks on #PwME

In the past week, there has been a media onslaught of biased and stinging articles maligning 17 million disabled men, women and children worldwide who suffer from the acquired neurological and immunological disease myalgic encephalomyelitis (ME).  The false media stories about the disease betray the ample scientific evidence that this is an acquired, infectious, biologically based disease which appears in the outbreak (50+ worldwide) and a sporadic form.

For decades the biopsychosocial (BPS) UK force, led and assisted by the US Centers for Disease and Control (CDC) hijacked a biological disease and falsely depicted it with their false BPS indoctrination.  The seeds were planted decades ago by CDC, and BPS proponents worldwide jumped on the bandwagon.  Powerful forces whether in the insurance industry or government health agencies have a financial stake in making this disease disappear.  With their science denialism, they are saving massive amounts of money by withholding medical testing, treatments, research and disability payments.

In 2011, the costly UK PACE Trial recommending GET and CBT as treatments for “CFS” was published.  It was met by severe criticism from the medical, scientific, advocacy and patient communities for the poor use of cohort selection (Oxford Criteria), faulty study design, changing protocol midway – including criteria and outcome measures. Recently, the UK BPS propagandists’ trophy, the PACE Trial, has been experiencing a blitz of increased criticism from scientists, academics, and advocates – discrediting the study for its poor design and unreliable findings.  To save embarrassment for their failed study, UK BPS promoters are instead deviously accusing the victims (17 million severely disabled people) with the crime of daring to complain about being forced to take harmful bogus treatments – treatments which ME experts agree in consensus are harmful to people with ME.

In the Reuters’ article Special Report: Online activists are silencing us, scientists say,  the author writes a one-sided, distorted piece which not only tells the BPS slant but attempts to legitimatize the false narrative that ME is just an ailment of the mind.  The facts, that over 10,000 scientific papers have been published showing biological abnormalities and that nearly 100 ME clinicians, researchers, and academics signed a letter in opposition of the PACE trial and its findings, were purposefully left out of the piece.

And of course, just like earthworms who mysteriously appear after an intense rain, other media outlets published articles this week with the same insulting and shameful propaganda.  I’m not surprised by this.  It’s the BPS proponents’ last major lost battle cry!

Victim blaming and falsely defaming a group of advocates are classical silencing methods which I wrote extensively about in my blog: “Resisting Attempts to Silence #PwME.”   This well-known manipulation method is reprehensible but, when directed at a vulnerable, very ill patient community, it is particularly cruel and shameful.

Reuters Quotes CDC’s Dr. Unger

The Reuters piece quotes CDC’s Dr. Elizabeth Unger who reveals CDC’s true colors when it comes to GET and CBT.  The article states:

The head of the CDC’s chronic viral diseases branch, Elizabeth Unger, told Reuters this [the removal of GET & CBT terms] was done to remove jargon and medical terms that are not widely understood by the public. “We received feedback that the terms were confusing and too frequently misinterpreted,” she said in an email response to questions.

Unger said the CDC’s advice stresses that each CFS/ME patient’s needs are different. “For some, carefully managing exercise and activities can be helpful,” she said. “Likewise, some patients may find that talking with a therapist helps them.”

Dr. Unger could have used this opportunity to condemn GET and CBT as harmful to patients with ME but, chose not to.  Instead, Unger claims that CDC removed the labels of these therapies because it was “confusing” and frequently “misinterpreted”!

What she goes on to recommend sure sounds like CBT and GET!

The organization MEadvocacy.org and independent ME advocates have been strong proponents in pointing out that CDC’s claims of an improved website are not that at all. They just removed some trigger labels yet, the message is the same old (see my blog – Emperor CDC’s New Clothes).

CDC’s Ongoing Malfeasance

In the US, for over three decades the CDC with intent and malice took measures to bury the disease ME.  They did this by controlling the narrative of the disease.  They consistently refuse to acknowledge that this is an infectious disease which appears in outbreaks and refuses to adopt the criteria created by international ME experts – the International Consensus Criteria (ICC).  Instead, they repeatedly re-define the disease with overly broad meaningless definitions.

CDC’s leadership decided from the start that they were going to bury the distinct disease ME.  Their malfeasance was revealed through an FOIA request by advocate Craig Maupin.  Craig obtained a copy of a letter written by Stephen Straus (NIAID) to Keiji Fukuda (CDC) after he authored the 1994 Fukuda criteria.

Straus writes:

Now that the definition is revised we could project at leisure what will come of it. I’d be very interested in your frank opinion on the matter when convenient.  My own sense is that a few years of use in the field will once again verify that there is no demonstrable or reproducible differences between individuals who meet the full CFS criteria and those who can be said to suffer Idiopathic Chronic  Fatigue. This would beg the question of whether additional revisions to the definition are warranted, or its entire abandonment.

I’ve felt for some time, Kieji, that those that have CFS are at a certain point along a continuum of illness in which fatigue is either the most dominant symptom or the most clearly articulated by virtue of impression on the part of the patient or physician that such a complaint is important. I predict that fatigue itself will remain the subject of considerable interest but the notion of a discrete  form of fatiguing illness will evaporate. We would then, be left with Chronic Fatigue that can be distinguished as Idiopathic or Secondary to an identifiable medical or psychiatric disorder. I consider this a desirable outcome.

The desired outcome – the evaporation of the disease!

Timeline of CDC’s Burial of ME Through the Creation of Inappropriate Names and Overly Broad Definitions

In 1988 – CDC created the Holmes Criteria.  The CDC’s definition emphasized “fatigue” and required 8 out of 11 symptoms for diagnosis with no explicit exclusion for all [edited to add “all” 3/22/19] psychiatric conditions.  This is also when the demeaning moniker “chronic fatigue syndrome” was stamped on us, creating the false narrative that people with ME are just lazy and choose to complain about a common complaint of fatigue.

In 1994 – CDC redefined the disease using the Fukuda Criteria.  This time, CDC engaged the aid of BPS proponents –  Michael Sharpe, Simon Wessely, Andrew Lloyd, and Ian Hickie in writing this watered down definition.  The new definition reduced the number of symptoms required for diagnosis to only 4 out of 8. The stress was still on fatigue, and the hallmark symptom post-exertional malaise (PEM) was not required (only optional).

In 2005 – CDC created the Reeves Criteria (also called the Empirical definition). The authors, William Reeves, Elizabeth Unger, and Suzanne Vernon also promoted the Reeves’ self-reported questionnaires which were all about subjective feelings of fatigue. This latest definition was so broad (basically if you had long term fatigue, you received a diagnosis of “CFS”) that it substantially (and falsely) increased the prevalence of the disease.

CDC’s Ongoing BPS Propaganda with the Creation of the Toolkit

On November 3, 2006, the CDC launched its toolkit for health care professionals at the National Press Club Conference.  The toolkit, which Kim McCleary of the CFIDS Association of America (now called Solve ME/CFS Initiative) helped write, features and details recommendations for graded exercise therapy (GET) and cognitive behavior therapy.

Dr. Anthony Komaroff who spoke at the conference stated: “But the good news is that there are now over 4,000 published studies that show underlying biological abnormalities in patients with this illness. It’s not an illness that people can simply imagine that they have and it’s not a psychological illness. In my view, that debate, which was waged for 20 years, should now be over.” (This – nine years before the IOM Report was published)

Yet, perversely, almost the entire CDC toolkit is about psychological treatments for “CFS” such as GET and CBT. It talks about coping methods and emotional issues.  CDC’s toolkit for clinicians was featured on the CDC’s ME/CFS website as well as tens of thousands of hard copies that were sent out to medical practitioners nationwide.  It was also translated and disseminated into Spanish.

CDC has tentacles all over the world and after the media presentation, the CDC toolkit started to appear on medical websites all over the world causing clinicians in different countries to spread the abuse.  Additionally, CDC’s toolkit linked to London’s St. Bart’s Hospital where Psychiatry professor Peter White worked and propagated the BPS misinformation.

To this date, CDC has not officially retracted the toolkit nor have they issued a black-box warning against using GET and CBT for pwME. 

CDC’s Latest Attempt at Entombing ME with the IOM Criteria and SEID Name

Against the urging of the medical, research, advocate and patient communities, CDC  contracted – for a million dollars – with the Institute of Medicine (IOM) (now called National Academy of Medicine (NAM)) to redefine the disease yet again. This was in direct violation of the recommendation of the Chronic Fatigue Syndrome Advisory Committee (CFSAC), doctors, researchers, ME advocates, and patients.  ME clinicians, researchers, and advocates wrote open letters (experts’ open letter and advocates open letter) to HHS urging them to cancel the IOM contract and instead adopt our ME experts criteria (the Canadian Consensus Criteria (CCC) with the aim of working toward the adoption of the International Consensus Criteria (ICC)).

CDC refused to adopt and use our experts’ criteria because it would mean relinquishing their hold on the puppets spewing the false BPS narrative of the disease and admitting to the actual reality of the biological disease ME.

In 2015, the IOM authors delivered their report.  They complied with CDC’s wishes and created another overly broad definition with a small checklist of 4 out of 5 common subjective symptoms.  The IOM authors did not specify any specific testing to aid in diagnosis (the ICC does) and, most importantly, no psychiatric exclusions are required.  This will result in many people, some with psychiatric disorders, to be misdiagnosed and muddy the waters.  Not only did the IOM authors deliver, per CDC’s directive, a loose meaningless definition but, they also recommended a new absurd name – systemic exertion intolerance disease (SEID).

MEadvocacy.org and ME advocates have repeatedly informed the community about CDC’s ongoing malfeasance and how this will continue to adversely affect people with ME worldwide.  Since the 1980’s CDC’s stronghold and perversion of the narrative of the disease have driven the lack of large scale serious biological studies, proper medical care, appropriate medical testing, and promising FDA approved treatments.  They used methods to accomplish their aim of burying ME by redefining the disease over and over again and really blurring the line whether this is a biological or psychosomatic disease.  CDC engaged the aid of UK BPS proponents to help carry out their harmful recommendations, and they continue on this contemptible path.

The media outlets have jumped on all this misinformation and have caused untold harm to people with ME by misrepresenting the disease and by mischaracterizing pwME as lazy malingerers.

CDC remains the puppeteer – still pulling the BPS strings worldwide!

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Reasons Why #PwME Should Sign the Petition to HHS for Recognition of ME as Defined by ICC

/ Gabby Klein

lady-justice-2

“I don’t recall anything in the IOM report that states that the term myalgic encephalomyelitis, or ME, can not be used to describe who meets published ME criteria” – Lucinda Bateman – Global Chronicle 009 p 24

The Institute of Medicine/systemic exertion intolerance disease (IOM/SEID) criteria which the US Centers for Disease Control and Prevention (CDC) is currently promoting on their website and to medical professionals for diagnostic purposes does not define the distinct disease myalgic encephalomyelitis (ME).  The National Institutes of Health is inaccurately recommending the use of the diagnostic IOM/SEID criteria as one of several choices of research criteria for studies at the NIH-funded ME/CFS Consortium Centers.  Some NIH-funded researchers are already incorrectly selecting people for their studies using the IOM/SEID diagnostic criteria.

The criteria for chronic fatigue syndrome (CFS-Fukuda), systemic exertion intolerance disease (SEID-IOM) and the deceptive combination  ‘ME/CFS’ do not define the disease ME. 

What is ME?

Myalgic Encephalomyelitis (ME) is an acquired distinct disease, recognized and defined by international ME experts (Ramsay Criteria, Canadian Consensus Criteria (CCC), and the International Consensus Criteria ( ICC).  ME is classified as a neurological disease by the World Health Organization (WHO).  ME has appeared in 50+ outbreaks worldwide and in sporadic form – severely disabling millions of men, women, and children worldwide.  It is a polio-like disease attacking the nervous system, reactivating viruses, and causing muscle weakness and pain.  It becomes systemic, eventually affecting many body systems such as the immune, endocrine, metabolic, energy systems, and the heart.

What is CFS/SEID?

CFS and SEID are government constructed vague entities defined based on the common subjective symptom fatigue.  HHS has repeatedly attempted to control the narrative about this disease with creations of overly vague definitions and demeaning names. HHS hoped that with their efforts in obfuscating the scientific and historical evidence, they will accomplish the disappearing of the disease (See evidence in a document obtained via FOIA request here).

ME is not CFS

The 2015 IOM report states in its opening paragraph: “Myalgic encephalomyelitis (ME) and chronic fatigue syndrome (CFS) are serious debilitating conditions that impose a burden of illness on millions of people in the United States and around the World.” (ME and CFS are described as two separate “conditions” – even though ME is a distinct disease and CFS is an assortment of conditions which are based on the subjective symptom- fatigue)

The ICC definition for ME is based on neuroimmune pathology which is consistent with the neurological classification of ME in WHO.  It includes specific testing to aid in diagnosis including immunological and cardiology testing.

The IOM/SEID definition does not demand any neurological nor immune dysfunction. It is a simple checklist of 4 out 0f 5 subjective symptoms common to many chronic illnesses and does not require specific testing for diagnosis.

Reasons to Insist on Recognition of ME as per the ICC:

  • Vague criteria such as the CDC’s Fukuda and IOM/SEID result in many people misdiagnosed with the disease.  This harms everyone involved.  Those who suffer from another condition will be stuck with a wrong diagnosis and wrong treatments.  Those with the actual disease will get recommendations for inappropriate and possibly harmful treatments such as graded exercise therapy (GET) and cognitive behavioral therapy (CBT).
  • The ICC, unlike the IOM/SEID definition, does not require a 6 month waiting period for diagnosis.   The sooner one gets diagnosed, the sooner they can get recommendations for appropriate treatments.  We know from experience that the sooner pwME start treatments such as rest, antivirals, immune modulators, the better their chances of improvements. 
  • Unlike the IOM/SEID which includes the symptom of post-exertional malaise (PEM), the ICC includes Postexertional neuroimmune exhaustion (PENE pen′‐e) which is a more accurate description of what pwME experience. The ICC acknowledges and addresses brain inflammation, whereas the IOM/SEID states there is no evidence of brain inflammation.
  • The ICC was created for both – diagnostic and research purposes.  The ICC authors knew that HHS has misused the intention of previous criteria.  They, therefore, took the precaution of creating a set of criteria which could be used for both.  In direct opposition of what ME stakeholders were promised, HHS is already recommending the use of their newest diagnostic criteria for research purposes.
  • The problem with the use of overly broad criteria for research is that it creates confusing results because it is not targetting a specific disease.  The lack of meaningful study results stunts scientific advances and recommendations for appropriate treatments for the disease.
  • The IOM/SEID authors clarified that they did not take severe ME into consideration when creating their criteria.  It is impossible to accurately define a disease by omitting 25% of the most severely affected.  The resulting simple checklist of common subjective symptoms in the IOM/SEID does not describe ME.
  • The IOM report states on page 23: “Because of the large number of results, the committee reviewed only papers published during the past 10 years with the understanding that older research is considered and cited in the introduction and discussion sections of more recent literature.”  Dr. Ramsay’s important work and the critical evidence of ME worldwide outbreaks were not looked at by the IOM/SEID authors.
  • The ICC recommends specific testing to aid in diagnosis. The IOM/SEID does not.  The lack of directed testing will impede the ability of pwME to get insurance to pay for particular tests for ME.  Additionally, it will be hard/impossible to get insurance coverage for ME treatments like antivirals because the IOM/SEID criteria do not include any symptoms of viral or inflammatory nature.

What You Can Do

ME is in danger of being erased by the efforts of HHS.  Please take the time to read, join the over 4,400 who already signed and sign the petition for recognition of ME as per ICC.  Please share widely. If each one of you gets another individual to sign, we can double the number of signatures.

Petition in English here

Petition in Dutch here

Petition in French here

Petition in Spanish here

Petition in Italian here

Petition in German here

 

 

 

 

 

 

 

 

 

 

 

 

Emperor CDC’s New Clothes

/ Gabby Klein / 3 Comments

fairy-tale-1750666_1280

The much-anticipated revision of CDC’s website on ‘ME/CFS’ section “Information for Healthcare Providers” was unveiled July 12, 2018.  The main reason for the revision was to adopt and educate medical professionals to diagnose people using the government-sponsored clinical IOM/SEID criteria and to update the toolkit based on current scientific data. 

The result of the CDC website update is full of deceptions and in many ways worse than the old toolkit for medical professionals.

Problems and Danger with Adopting and Using the IOM/SEID Criteria

ME advocates have warned that the 2015 government-sponsored IOM/SEID criteria are even worse than the failed and highly criticized government 1994 Fukuda definition.  Critics of the Fukuda definition argue that it was overly broad with too much emphasis on the one common symptom ‘fatigue’. The IOM/SEID definition is even more vague.  Unlike the Fukuda, it doesn’t specify exclusions which means that many people suffering from primary psychiatric and psychological conditions will get a diagnosis of IOM/SEID.

Even worse, the new criteria do not demand any neurological nor immune dysfunction symptoms! Investigators (Dr. Leonard Jason, Frank Twisk and Asprusten et al) who have looked into the IOM/SEID criteria and published papers comparing it with other definitions have warned that it does not define the neuroimmune disease myalgic encephalomyelitis (ME) as defined since 1969 by the World Health Organization (WHO) and coded under Neurological disorders as ICD – G93.3.

The IOM authors clarified this distinction as well.  They stated that the entity they were defining was not a neurological one.  It was a broader entity with subsets which remain to be defined.  They were clearly not defining the distinct disease ME as per our international non-government medical ME experts with their 2011 International Consensus Criteria (ICC). This comparison chart created by the patient organization MEadvocacy.org is an easy visual tool that illuminates the difference.

The danger of using the broad IOM/SEID definition is that the pool of patients diagnosed will be a muddied group.  It will be harmful to those who suffer from ME as per ICC and those who suffer from other conditions for which they lack proper diagnosis.  To properly treat patients one needs to identify precisely the disease they suffer from. It would be like throwing people who suffer from rheumatoid arthritis and osteoarthritis together under one rubric because they share many of the same symptoms. This conflation would be dangerous because as we know, the treatments are entirely different.

Even more alarming, ‘ME/CFS’ investigators working at NIH funded ‘ME/CFS’ consortia are currently using the clinical IOM/SEID to select their cohorts in their studies!  Using this faulty criterion will cause the group to be made up of people suffering from different conditions. The results will be skewed whether searching for a biomarker or successful treatment options. It will be impossible for future researchers, who are unfamiliar with the criteria issues, to duplicate studies as they will have no way to know how to select patients correctly.

Harmful GET recommendation Without the Name Remains on Website

CDC’s previous toolkit for providers recommended graded exercise therapy (GET), stating: “Graded exercise therapy (GET) has shown to be very helpful to some CFS patients. Graded activity and exercise are defined as starting from a very low, basic level of exercise and/or activity and gradually increasing it to a level where people can go about their daily life. NOTE: the level of activity may not be the same as before the CFS diagnosis.”

CDC’s current toolkit treatment section recommends: “Patients who are tolerating their current level of activity and have learned to “listen to their bodies” might benefit from carefully increasing exercise to improve their physical fitness and avoid deconditioning Some healthcare providers with expertise in ME/CFS refer their patients to an exercise physiologist who understands ME/CFS and uses an individualized and flexible approach to advancing activity levels.” [bolding for emphasis]

CDC is in effect still educating doctors to recommend people with ‘ME/CFS’ exercise incrementally.  This description is what graded exercise is, and it is genuinely devious of CDC who many in the community have hailed for supposedly removing GET from their toolkit, only to see them re-introducing it in a concealed manner.  ME advocates and patients who have been on this road with CDC for decades are not surprised at their repeated deceptions. Their malfeasance has no bounds, and they will do anything to cover-up the reality of the neuroimmune disease ME which has appeared in many worldwide outbreaks and the sporadic form.

Dangers of Conflation Which Result in the Burial of ME

CDC states: “There is no consensus on whether CFS and ME are synonyms, different spectrums of the same illness, or distinct conditions.”

These words describe the crux of the problem with the government’s attempts to cover-up ME.  It benefits HHS to keep it all a big, muddied, confused heap of nothing.  It has been their intention from the start – to make ‘CFS’ go away. As a 1994 letter obtained through FOIA effort by advocate Craig Maupin from NIAID’s Dr. Straus to Dr. Fukuda states:

“I’ve felt for some time, Kieji, that those that have CFS are at a certain point along a continuum of illness in which fatigue is either the most dominant symptom or the most clearly articulated by virtue of impression on the part of the patient or physician that such a complaint is important. I predict that fatigue itself will remain the subject of considerable interest but the notion of a discrete form of fatiguing illness will evaporate. We would then, be left with Chronic Fatigue that can be distinguished as Idiopathic or Secondary to an identifiable medical or psychiatric disorder. I consider this a desirable outcome.“

HHS and its agencies have purposefully acted to conceal the fact that this is a distinct disease with its distinguished history.  They have repeatedly misbranded (CFS, ME/CFS, SEID), misdefined (Fukuda, Reeve’s, IOM/SEID) the disease to keep the confusion going.  They have also falsely combined ME with CFS as in ME/CFS to perpetuate the confusion. It’s like calling a disease lung cancer/cold!

In the same vein, HHS repeatedly refuses (in contrast with other diseases) to accept and adopt criteria created by the international non-government experts in the disease [Canadian Consensus Criteria (CCC) and ICC] which clarify and distinguish ME.  With the same concealment tactic, CDC erased our experts’ criteria CCC and ICC from their resource section.

Other Tactics Used by CDC to Minimize the Disease

  • CDC prides itself on the use of evidence-based scientific data, yet they state on their new website “Some patients return to full function” as if that is a scientifically proven fact.  Which evidence-based studies is CDC relying on when making this positive statement?  I would argue that there is more evidence of people with ME #(pwME) dying from ME than fully recovering from the disease.
  • In their Spectrum of ‘ME/CFS,’ CDC states: “For example, patients mildly impaired by ME/CFS may be able—with careful planning and activity management—to keep a job or continue their education, participate in social and family activities, and attend to daily life.” This statement gives the false impression that pwME if managed well, can perform normal activities of life.  It is a false assumption and does not ring true with pwME. For an ME diagnosis, pwME need to have extensive reductions in previous activity.  Activity management might ensure that they do not aggravate their condition and avoid crashing but, it does not improve their base condition.
  • CDC states: “From a clinical perspective, case definitions are used to make the appropriate diagnosis and guide therapy and management. From a research perspective, case definitions are used to identify the appropriate study population. Multiple case definitions may be required for different applications and can co-exist if there is a good understanding of how they are being used.” Historically, HHS has conflated the purpose of criteria.  They have used definitions whose goal was for research, in clinical settings and vice versa.  ‘ME/CFS’ investigators are already using the clinical IOM/SEID definition for studies at the NIH funded ‘ME/CFS’ research consortia – despite assurances it by HHS they would solely be used for clinical purposes!
  • In CDC’s attempt to conceal any possibility of an infections agent playing a role in ME, they have omitted the history of ME and the fact that it appears in the epidemic for with 50+ worldwide outbreaks.

It is alarming to see this revised CDC criteria in 2018 – more than 30 years after CDC was called down to investigate the massive Lake Tahoe outbreak.  The name, definition and data do not reflect the findings at Lake Tahoe nor the WHO 1969 defining  ME under neurological disorders nor the 2011 International Consensus Criteria defining the distinct disease ME.

ME advocates worldwide are rightfully aligning in their fight against the PACE Trial with their recommendation of the harmful treatments of graded exercise therapy and cognitive behavior therapy.  ME advocates need to do the same with CDC’s revised website which is deceptive because like the Emperor’s New Clothes – it is just more of the same wrongdoing. ME advocates need to rigorously fight CDC’s dangerous recommendation of GET and their use of the vague IOM/SEID definition which will result in the burial of the distinct disease myalgic encephalomyelitis. 

Beware of Aiding in the Burial of ME!

/ Gabby Klein / 2 Comments

dangerous-1040641_640

Since the Lake Tahoe outbreak of the distinct neuroimmune disease myalgic encephalomyelitis (ME), the US Centers for Disease Control and Prevention (CDC) has extended all their efforts in minimizing, conflating, misbranding, wrongly defining the disease in an attempt to bury the facts and reality of this severely disabling chronic disease affecting an estimated million American men, women and children.  The purpose of their malfeasance is to evade and deflect responsibility for this burdened pandemic.

One of CDC’s methods of cover-up is to refuse to adopt and to diverge from the authentic criteria for ME authored by international ME experts (Ramsay’s, CCC & ICC).  They have managed this by producing and/or acquiring faulty, overly broad criteria that do not describe the actual immunological, neurological and infectious nature of the disease.  Their latest offense is the acquisition of the IOM/SEID criteria. They have used the Institute of Medicine (IOM) (now called National Academy of Medicine) which is perceived to be an independent private organization when in effect most of their work is paid for by HHS – not exactly an unbiased partner. The charge and parameters of the IOM work were set up and controlled by HHS (leaving out many studies into the immunological and infectious nature of the disease) They have done this in an attempt to give their re-branding and redefining effort false legitimacy.  In actuality, this new criteria is yet another vague, ill-defined, fatigue-based definition.

Organizations who claim to represent #pwME like SMCI and MEAction have banded together with the CDC to aid in legitimizing this bad definition which is overly broad and does not define ME.

They have done this by:

  • Sponsoring and arranging a press briefing immediately after the release of the report.
  • Collaborating with CDC with their Technical Development Workgroup (TDW) to aid in embracing and inscribing the faulty definition to the CDC website (list of participants).  MEadvocacy, the patient organization representing #pwME issued a blog explaining why they opted OUT of this workgroup.
  • Collaborating with CDC to work on the new toolkit for healthcare providers and medical continuing education to teach and disseminate the IOM/SEID criteria.

Their latest “service” to the CDC is with their guileful inclusion of the ‘consideration of the recommendation from the IOM relating to ME/CFS’ in their proposed Senate resolution S.Res.508 – dated May 15, 2018,  introduced by Senator Markey and co-sponsored by Senators Collins, King, and Van Hollen to raise awareness about ME/CFS of the following language:

“Resolved, That the Senate

…

(3) encourages—

(A) the National Institutes of Health and other Federal agencies to work with experts, stakeholders, and individuals with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome to—

(i) consider the recommendations of the National Academies of Sciences, Engineering, and Medicine relating to Myalgic Encephalomyelitis/Chronic Fatigue Syndrome;

…”

Remember the National Academies of Sciences was formerly called the “Institute of Medicine”.  So, the Resolution which was drafted by MEAction and SMCI includes a push to implement the IOM recommendations.  Since these organizations were the ones who suggested the draft of the Resolution, they could have added anything, yet they proactively suggested adopting the IOM recommendations. [edited to include exact wording of the specific part of the Resolution and to clarify]

These are the IOM recommendations they are alluding to:

1 – Physicians should diagnose ME/CFS (with IOM criteria), and a new ICD code should be assigned. (please note that  “SEID” or  “ME/CFS” has no US ICD classification or code. The ill-defined conflated term violates ICD rules by combining diagnoses from different ICD sections).

2 – HHS should develop a toolkit for medical practitioners (based on the IOM).

3 – A multidisciplinary group should reexamine the IOM criteria when firm evidence supports modification, or in no more than 5 years.

4 – The committee recommends that this disorder be renamed “systemic exertion intolerance disease” (SEID). SEID should replace ME/CFS for patients who meet the criteria set forth in this report.

The above Senate Resolution is in recognition of May International Awareness month for the disease.  It details some basic stats (some faulty one like women are 4 times more likely to get the disease and neglects to include the cluster outbreaks and blood donation bans due to infectious components and/or etiology as well as state this disease kills patients), the financial burden and the general need for funding, medical care, and education.  Why not just stop it at that? Why did MEAction and SMCI insert the IOM recommendations in this resolution – except for aiding CDC in their burial of the disease, myalgic encephalomyelitis?

Myalgic encephalomyelitis is the distinct severely disabling, multi-system chronic disease that appears in epidemic and a sporadic form.  The symptoms of ME are numerous and include but are not limited to the following: post-exertional collapse, muscle and joint pain, enlarged lymph nodes, chills, low-grade fever, vertigo, extreme fatigue and weakness, cognitive impairment (delayed processing, aphasia, short-term memory loss, etc.), cardiac problems, orthostatic intolerance, sleep dysfunction, headaches, allergies, mold and chemical intolerance, frequent reactivated infections and co-infections.

Myalgic encephalomyelitis is not chronic fatigue syndrome nor is it systemic exertion intolerance disease nor is it chronic fatigue. One cannot claim to represent the entire community when, in effect, not only are they advocating for and promoting recommendations for faulty criteria but, they are aiding in the full burial of the distinct disease ME.

NOTHING ABOUT US WITHOUT US

Organizations and advocates who promote the IOM criteria DO NOT represent #pwME-ICC.  Falsely branding themselves as ME organizations and advocates is deceptive and harmful to this severely ill patient population.  Their attempt to speak for #pwME-ICC when approaching government officials or serving on government or private committees concerning the disease is not authorized by #pwME-ICC.  They are in effect aiding CDC to conflate and confuse while attempting to bury ME-ICC.

The ‘Mah Nishtanah’ of ME

/ Gabby Klein / 14 Comments

question-mark-1495858_640

The Jewish Holiday of Passover celebrated this past month, as it is every spring, commemorates the liberation of the Israelites from slavery in Egypt.  Its feature is the Seder when family and friends join together for an elaborate festive meal with specific customs and rituals. For many families, one of the highlights of the Seder night is the Mah Nishtanah, the “four questions” recited by the youngest members of the family.  The questions are about the difference between this night as opposed to all other nights and its purpose is to stimulate interest and thought about the history and traditions involved with Passover.

Isidore Rabi, a winner of a Nobel Prize in physics, was once asked why he became a scientist. He replied, “My mother made me a scientist without even knowing it. Every other child would come home from school and be asked, ‘What did you learn today?’ But my mother used to ask a different question. ‘Izzy,’ she always used to say, ‘did you ask a good question today?’ That made the difference.”

In the tradition of the questions of  ‘mah nishtanah’, I would like to stimulate thought about the history, actions, and state surrounding the acquired neuroimmune disease Myalgic Encephalomyelitis (ME) which manifests itself in epidemic and sporadic form and affects an estimated million American men, women, and children.  There is no FDA approved treatment to date regardless of the fact that it leaves the majority of sufferers disabled from work, housebound or bedbound – some for decades.

From the beginning, when representatives of the CDC were called down to investigate the outbreak at Lake Tahoe in the 1980’s, CDC and other US health agencies have mistreated this disease which has resulted in incalculable harm to the million American men, women and children with ME.  Every item questioned below are actions the government has taken or refused to make based on their attempt to disappear the reality and facts of the real acquired neuroimmune disease ME.

Following the form of ‘mah nishtanah’ questions as in “on all other nights we eat leavened or unleavened bread; tonight we eat only matzah”, here are the questions for ME.

Mah Nishtanah ME Questions

Why is it that:

  • All other complex chronic diseases are named with people’s names, geographical locations or distinctive feature; this complex chronic disease is falsely branded “chronic fatigue syndrome” – after a common symptom of fatigue? (see how diseases are named here)
  • All other complex chronic diseases are defined by non-government medical experts in that specific disease;  this complex chronic disease is repeatedly ill-defined by the government (CDC)? (see Frank Twisk paper here)
  • All other complex chronic diseases are taught in depth in medical and nursing schools; this complex chronic disease is either not taught at all, or mentioned dismissively?
  • All other complex chronic diseases have a medical expertise assigned to them with ample nationwide practitioners caring and treating patients;  this complex chronic disease does not have a distinct medical expertise assigned to it and has very few knowledgeable doctors caring and treating patients?
  • All other complex chronic diseases are placed in a specific NIH Institute who claims responsibility for funding research for it; this complex chronic disease has not been placed in any particular NIH Institute?  (it is currently situated in the Office of Research on Women’s Health which has no specific budget set aside for research)
  • All other complex chronic diseases receive NIH funding commensurate with the disease severity and burden;  this complex chronic disease gets a pitiful fraction of appropriate funding? (see table here)
  • All other complex chronic diseases that render patients unable to of a fair chance to secure Social Security Disability payments; this complex chronic disease has a high rate of denial for SSD, regardless of the severity of symptoms and the disabling nature of them?
  • All other complex chronic diseases that appear in epidemic form are studied for their infectious nature; this complex chronic disease which has appeared in over 50 outbreaks worldwide since the 1930’s (see list here) yet its infectious nature is mostly ignored and covered up by CDC?
  • All other complex chronic diseases have appropriate recommendations for FDA approved treatments; this complex chronic disease has no FDA approved treatments and has recommendations for treatments that are harmful to people with ME (graded exercise therapy [GET] and cognitive behavioral therapy [CBT])? (see a warning about GET from Workwell Foundation here)
  • All other complex chronic diseases that are biological in nature are described, defined and studied as a biomedical disease; this complex chronic disease is falsely labeled, defined and studied as a psychosomatic condition?

Once is happenstance.  Twice is coincidence.  Three times, it’s enemy action.  – Ian Fleming

All these discrepancies and discriminatory actions by HHS are not coincidental.  They all serve the purpose to minimize, marginalize this disease and deflect responsibility from the health agencies whose charge it is to “for protecting the health of all Americans and providing essential human services, especially for those who are least able to help themselves.”

The month of May is awareness month for ME.  It is time to ask the hard questions such as:

  • Why have the government health agencies ignored, neglected and covered up this severely disabling acquired multisystem disease for decades?
  • Why did the government health agencies enable the psych lobby to highjack this disease when they have known for decades that this is a biomedical disease?
  • Why are they so reluctant to properly name and define this disease as recommended by the medical experts and community?
  • How much money has the government withheld with their refusal to properly fund this disease and by their continuous denial of disability coverage?  

This May patients and advocates need to ask deep-seated questions and demand answers. With the insistence and demand that the proper name (myalgic encephalomyelitis) with the appropriate definition (ICC) be used, it will force the government to finally distinguish ME from fatiguing and psychosomatic conditions. It is with this most important distinction that meaningful change will take effect.

CDC’s Staged Call

/ Gabby Klein / 5 Comments

recording studio

I wish to thank advocate Eileen Holderman for her consultation with this blog post.

In 2012, The U.S. Centers for Disease Control and Prevention (CDC) instituted the “ME/CFS Stakeholder Engagement and Communication conference calls (SEC)” (previously called PCOCA) series with the stated purpose of sharing information with those interested in ME/CFS as part of their regular outreach and communications efforts. These calls are billed as a form of engagement with the community, but this is just by name – not reality.

CDC’s Phantom Engagement

CDC’s claims of transparency and stated desire to engage with the ME/CFS community is debunked by their consistent underhanded actions.  Their “engagement” call is, in fact, an hour-long one-sided communication.  CDC placed all callers – a group of very sick disabled people – in a silent mode for the hour-long call. CDC falsely alleged they can’t take live calls when many large government events take live questions all the time.

CDC’s 60-minute call devoted 50 minutes to their invited speakers – leaving only a couple of minutes in the end to cover the many crucial questions sent in by ME patients and advocates.  CDC kept us in the dark as to whose questions they selected – never giving us the actual names.

CDC refuses to make the recordings available on their website, even though they tell us that they are being recorded.  CDC is very well aware that this is a community of people who are severely sick and it is too taxing for them to listen in at the appointed time and for a full hour-long call.

Conclusions about CDC’s lack of engagement and consideration of people with ME:

  • CDC stages the call so that they are in complete control of the narrative
  • CDC manipulates the timing of the call as to leave minimal time for public questions
  • CDC refuses to take live calls because they are apprehensive of challenging questions
  • CDC is more concerned about the perception of engagement than an actual one
  • CDC is not worried about federal rules that call for accommodations for the disabled
  • CDC does not want a record of the meeting because they want to avoid activists’ criticism

 

November 2, 2017, CDC Call

The latest  CDC call took place on November 2, 2017.  The topic was:“Take Home Messages from the 2015 Institute of Medicine Report on ME/CFS” with Drs. Lucinda Bateman, Ellen Clayton, and Peter Rowe.  All three speakers served on the IOM panel to create new government-sponsored criteria and a new name – systemic exertion intolerance disease (SEID).

Background of the HHS/IOM Implementation and Stakeholders’ Protests

October 2012

In October 2012, the Chronic Fatigue Syndrome Advisory Committee (CFSAC) sent the following recommendation to Dr. Sebelius, the Secretary of The US Department of Health and Human Services (HHS):  “CFSAC recommends that you will promptly convene (by 12/31/12 or as soon as possible thereafter) at least one stakeholders’ (Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS)experts, patients, advocates) workshop  in consultation with CFSAC members to reach a consensus for a case definition useful for research, diagnosis and treatment of ME/CFS beginning with the 2003 Canadian Consensus  Definition for discussion purposes.”

HHS highjacked and distorted CFSAC’s recommendation, turning their backs on their own advisory committee of experts.  In Septemeber 2013, HHS secretly contracted, sponsored and charged the Institute of Medicine (IOM) to create yet again, another government-controlled clinical definition and a new name for the disease.  Myalgic Encephalomyelitis (ME) stakeholders were outraged at HHS’ deception and exploitation.  Fifty International ME researchers and clinicians wrote an open letter to Secretary Sebelius urging her to stop the IOM contract and to adopt the 2003 Canadian Consensus Criteria (CCC) for clinical and research purposes.  Sixty six ME advocates worldwide signed a letter in support of the Experts’ Letter.   ME patients sent letters to their congressional representatives with the same message – stop the IOM, adopt the CCC.

But, HHS continued to disregard the voice of the international ME community and ignored the continued protests taking place such as a new letter dated December 2013 signed by 197 professionals and advocates with detailed objections to the IOM process.  Advocates also continued their protests in the form of public testimonies at the IOM January 13, 2014, open meeting (see article here).

In February 2015, the IOM panel published their report including new clinical criteria and a new name – systemic exertion intolerance disease (SEID). The new criteria have been heavily criticized by CFSAC, experts, advocates, and patients for:

  • no list of exclusions
  • no objective tests and measures
  • not including exhaustion of the central nervous system after minor physical activity
  • omitting core symptoms such as pain and immune dysfunction
  • the core symptom of cognitive dysfunction is only listed as an option.
  • signs of the infectious nature of the disease such as flu-like symptoms, sore throat, swollen lymph nodes and headaches are absent
  • no autonomic and neuroendocrine symptoms
  • no specificity toward different stages and levels of the disease

In the preface to the ICC, its authors state: “There is a poignant need to untangle the web of confusion caused by mixing diverse and often overly inclusive patient populations in one heterogeneous, multi-rubric pot called ‘chronic fatigue syndrome’. We believe this is the foremost cause of diluted and inconsistent research findings, which hinders progress, fosters skepticism, and wastes limited research monies.”

The new IOM clinical criteria are just another in the string of CDC vague, overly inclusive criteria which have and will continue to confuse and hinder progress in the science and understanding of ME.   In Dr. Leonard Jason’s estimation, the IOM criteria are even broader than the previous CDC criteria – the Fukuda definition.

Alarmingly, the new clinical criteria are now being recommended and used for research.  Dr. Bateman, who served on the IOM panel to create the new vague clinical criteria, has stated she will be using the IOM definition in her studies at the new  NIH ME/CFS Collaborative Research Centers – disregarding the false promise that it will only be used for diagnostic purposes – never for research!

Pushing and Defending the IOM Criteria

Dr. Lee, the previous DFO of CFSAC,  stated at one of their meetings – ‘it is not the job of the government to create definitions for diseases, it has to come from the community of experts.’  Yet, since the 1980’s the CDC has perpetually ignored the name and criteria authored by experts and has produced one faulty definition after another (Holmes, Fukuda, Fukuda, and IOM).

ME experts have developed and have successfully been using the CCC and the International Consensus Criteria (ICC) for years in clinical practice and for research.  It is the government who has repeatedly refused to do so – opting instead to use their own faulty CDC definitions.

CDC refuses to adopt the ME experts’ definitions citing that it is too hard for clinicians to understand. Ironically, Dr. Bateman defended the weaker IOM definition with its 280-page report! She advised clinicians to look at selected chapters of the report to find what should have been part of the core symptoms of the disease.  In reality, reinforcing the fact that the new criteria are inadequate and impractical.

CDC’s patient engagement call was an epic fail.  It was a long infomercial for the faulty CDC/IOM criteria. It was a farce as far as engagement is concerned – there was none!  They refrained from making accommodations to a community of disabled and cognitively challenged people. They falsely claimed they could not take live questions.  They spent a few minutes, in the end, answering four questions for which the origin is unknown.

CDC did not answer these questions – among many others:

Question for Dr. Bateman – from Gabby Klein

You were an author of the 2011 International Consensus Criteria (ICC) which recommended removing CFS from ME.  The ICC states the following: “Not only is it common sense to extricate ME patients from the assortment of conditions assembled under the CFS umbrella, it is compliant with the WHO classification rule that a disease cannot be classified under more than one rubric”.

You were an author of the IOM criteria as well which stated regarding coding: “A new code should be assigned to this disorder in the International Classification of Diseases, Tenth Revision (ICD-10), that is not linked to “chronic fatigue” or “neurasthenia.”

Since the IOM report did not ask to replace the WHO classification of ME, do you, therefore, agree that the IOM criteria do not define the disease Myalgic Encephalomyelitis (ME)?

Question for Dr. Bateman – from Colleen Steckel

The IOM panel was charged by its sponsor, HHS, to ”recommend clinical diagnostic criteria that would address the needs of healthcare providers, patients, and their caregivers.”  In addition, in an interview with Phoenix Rising regarding the IOM criteria, Dr. Bateman stated: “SEID criteria are intended for current use, for doctors to do better at making the diagnosis in a clinical setting. There was no discussion of anything but using them for this purpose.”

Yet, NIH is currently recommending the use of the IOM criteria for their new ME/CFS (myalgic encephalomyelitis/chronic fatigue syndrome) competitive consortium grants.  Can you explain why new clinical criteria will now be used for research?

The expert criteria ICC would ensure the disease myalgic encephalomyelitis would be the focus of any studies.

Question for Dr. Unger – from Colleen Steckel

Are there any plans to address the concerns raised by MEadvocacy.org in their recent blog labeled “CDC’s Website Revision is No Reason for Celebration”?

Patients continue to be told by doctors that this is just a fatigue illness and refuse to look into immunological, cardiology, and neurological issues.  Patients continue to fend for themselves with little care from mainstream doctors. This continues to lead to despair and suicide within the community.  The CDC needs to do much more in order to change this reality.

Questions to Dr. Unger – from Eileen Holderman

What are the official case definitions for ME that CDC endorses for research and clinical?

As former CFSAC member and Chair of Subcommittee for CDC Website Review, when will CDC take down Toolkit and Resource Guide from the CDC website Stacks? 

Questions from Guido Den Broeder

(1) Will you please once more distinguish between ME and CFS, as you did before?

Myalgic encephalomyelitis (at G93.3 in the ICD-10) is a specific post-viral brain disorder. Much is known about its causes, diagnostics, and treatment.

Chronic Fatigue Syndrome (R53.82 in the ICD-10-CM) is a term for unexplained fatigue and malaise. It is not a disease. In clinical practice, patients with a variety of diseases start out with a diagnosis of CFS, even though this is not a clinical diagnosis.

(2) What are you going to do to prevent ME?

Will Coxsackie B be added to polio vaccinations?

Are you going to follow mononucleosis patients and test their immune system for post-mono abnormalities?

(3) What are you going to do to reduce the clinical use of the CFS label?

Will you increase awareness among physicians of diseases such as ME, EDS, Lyme, Hashimoto, etc.?

Are you going to promote the clinical use of the SEID label as defined by the IOM?

These are only some of the many questions from patients and advocates that CDC has not answered!

 

 

 

Resisting Attempts to Silence #PwME

/ Gabby Klein / 4 Comments

woman-1445917_1920

Methods of Silencing Dissent to Control a Specific Agenda

Globally, government agencies and officials as well as private sector companies, and organizations use known astroturfing and silencing methods to achieve their intended goals.  They use media to spread propaganda to manipulate opinions. They employ specific tactics to squash dissent to institute their desired agenda. 

In the myalgic encephalomyelitis (ME) community, this method of controlling a specific intention is used by government health agencies, medical interest groups, and those supporting them.  They advance the false narrative that ME is not a distinct disease but, a collection of fatiguing conditions.  They also perpetuate the myth that ME is imagined – a functional somatic condition.

This government deceit harms people with ME (pwME).  The underhanded conflation of ME with chronic fatigue syndrome (CFS), chronic fatigue (CF), and psychosomatic conditions results in falsely depicting the disease as a benign condition, possibly just in the mind of the patients.  The medical community has therefore in the main dismissed this ‘vague condition,’ neglecting to care or study it. 

Those whose interest lies in perpetuating this myth because of financial benefits or other motives use established methods to advance their biased goals by spreading misinformation and falsely accusing those who dare to speak out about the malfeasance. 

Methods of Silencing a Group of Activists

Ron Duchin, research analyst at Mongoven, Biscoe & Duchin Inc., in Washington DC, created and utilized specific techniques to break up activists groups who were fighting for social justice such as environmental groups, animal rights groups and consumer affairs groups. His famous legacy was breaking up civil rights activists groups fighting the tobacco industry.  He later used this plan advising other industry giants in how to fight any dissent which was adversely affecting their objectives.

Duchin explained that activists fall into four categories: radicals, opportunists, idealists and realists, and that a three-step strategy was needed to bring them down.

  • First, you isolate the radicals; those who are vocal in their desire to change the corrupt system and promote social justice. Then use methods of character assassination to discredit them – such as exaggerations, lies, trumped up charges to marginalize them.
  • Second, you carefully cultivate the idealists; those who are quieter and are not as direct in their methods and objectives as the radicals. You do this by gently persuading them that their advocacy has negative consequences for some groups, thus transforming them into realists.
  • Finally, you co-opt the realists (the pragmatics willing to work within the system) into compromise. “The realists should always receive the highest priority in any strategy dealing with a public policy issue . . . If your industry can successfully bring about these relationships, the credibility of the radicals will be lost, and opportunists can be counted on to share in the final policy solution.” Opportunists, those who are motivated by power, success, or a sense of their celebrity, will be satisfied merely by a sense of partial victory.

Astroturfing Methods to Manipulate and Control an Agenda

What is astroturfing? (Astroturf and manipulation of media messages by Sharyl Attkisson – see video here)

Astroturfing is the attempt to create an impression of widespread grassroots support for a policy, individual, or product, where little such support exists. Multiple online identities and fake pressure groups are used to mislead the public into believing that the position of the astroturfer is the commonly held view.  The goal is to neutralize any opposition.

Tactics:

  • give the impression that there is widespread support for or against an agenda when there’s not
  • seek to manipulate and change opinions by making some feel like outliers when they’re not
  • seek to malign those who openly disagree with the intended view
  • attack those who publish articles they don’t like or whistleblowers who tell the truth
  • intentionally shove so much confusing and conflicting information into the mix that you are left to throw up your hands and disregard all of it, including the truth

How to Recognize Signs of Propaganda and Astroturfing

  • use of inflammatory language such as crank, quack, nutty, lies, paranoid, pseudo and conspiracy theorists
  • personal attacks on individuals and organizations surrounding an issue rather than addressing the facts
  • reserve all public skepticism for those exposing wrongdoing rather than the wrongdoers
  • instead of questioning authority, question those who question authority.

Methods of controlling an agenda and minimizing dissent in the ME Community

  • Labeling ME patients with a demeaning name – chronic fatigue syndrome – to reduce impact and cause marginalizing of patients (See HHS Refuses to Correct their Wrongful Branding).
  • Defining the disease with government-produced vague criteria which include many who suffer from fatiguing, psychiatric, psychological and other conditions, – with the aim of burying the neuroimmune disease ME. Then, accuse #pwME of somaticizing and catastrophizing. 
  • Quieting criticism by spreading rumors that the patients are an “angry and crazy” group –  rumors that are never substantiated with evidence – to legitimize their own biased objectives and to dissuade clinicians and researchers from treating patients and studying the disease.
  • Media articles that miseducate about the disease and misrepresent the community such as this article in the Guardian titled “Chronic fatigue syndrome researchers face death threats from militants.” The author uses classic astroturfing methods when writing: “In addition, activists – who attack scientists who suggest the syndrome has any kind of psychological association – have bombarded researchers with freedom of information requests, made rounds of complaints to university ethical committees about scientists’ behaviour, and sent letters falsely alleging that individual scientists are in the pay of drug and insurance companies.”  Notice the inflammatory language: “attack” – for disagreeing; “bombarded” – for requesting information from the government as if that is a terrorist act; “falsely alleging” – when there is actual evidence.
  • Mis-educating by highlighting the ‘fatigue’ element of the disease (even though it is just one symptom of many in this systemic disease).  Choosing to educate the misconception that this is a condition of the mind even though science proves otherwise. Encouraging harmful treatments such as GET and CBT which still appear on CDC’s website (see toolkit and guide to medical professionals) Educating with overly broad, inaccurate criteria as in the revised CDC website promoting the IOM criteria.  (See “CDC’s Website Revision is No Reason for Celebration”)
  • Marginalizing or disparaging clinicians and researchers who show interest in treating or studying the disease, by denying their applications for government funding and refusing their requests to serve on federal committees. Dr. Jose Montoya, a professor at Stanford University and one of the leading ME clinicians and researchers today, told The Guardian what his mentor told him when starting his work with ME patients:  “You are committing academic suicide. You’re turning your career into a mess.”  
  • Giving the illusion that patients have a platform for input and engagement when in reality their voice is consistently ignored.  HHS creates puppet committees and working groups, such as the Chronic Fatigue Syndrome Advisory Committee (CFSAC) and various working groups yet, very few (if any) of their members’ recommendations are implemented.  Stakeholders’ oral and written testimonies to CFSAC are sought but readily ignored and dismissed.
  • Threatening those who dare to ask critical questions – as in the threat of eviction of three CFSAC voting members – two of which went public – Eileen Holderman (patient advocate)and Dr. Mary Ann Fletcher (scientist) (See video here, letter from advocates calling for an investigation here).
  • Rewarding those who support the biased government agenda by giving them preferential treatments, whether with a coveted seat at the table or with funding opportunity perks.  Some in the co-opted interest groups aid the government with attempts to silence opposing voices by telling them not to complain and to ignore the malfeasance.
  • Rejecting grant applications to fund biomedical research, in deference to studies using a psychological/psychiatric view.  World renown ME investigators, such as Drs. Ronald Davis, Ian Lipkin, Nancy Klimas, Jose Montoya, Mark Davis and Robert Naviaux have each received rejections for their research grant applications from NIH. Yet, funding studies by Psychologist Fred Friedberg, Ph.D. such as home-based management are accepted (See study).

As currently seen with the University of Bristol Professor Esther Crawley’s upcoming TEDx talk “Dare to Disrupt”, the desire by these groups to propagate their false narrative about ME is powerful.  In her write up on TEDex website, Crawley writes: “I dare to disrupt because …We need to disrupt views of this illness.Those who are ill with CFS/ME do not have a voice – they are too unwell. We need to provide their voice, and we need to speak up about this illness. Because we, as a community, as a society, as friends, as neighbors and as parents should look after children who suffer.”

Yet, the ME community did not choose Crawley to be their voice.  The opposite is true. Esther Crawley is a proponent of the unscientific GET, CBT, and lightning process treatments in children with ME and is involved in studies using these harmful therapies.  She was an author on a study which promoted the diagnosis of pervasive refusal syndrome (PRS) for children with severe ME.  UK patients and advocates have spoken out against these studies taking place because of their potential for harm. Crawley fought back by using the astroturfing method of character assassination. She spread allegations that she was being attacked and harassed by ME patients.  These charges were debunked by Tyme Trust who obtained FOI requests from the University which revealed that no reports of harassment were made (See Adam Lowe’s article, “Esther Crawley claims harassment, university has no record”).

The nefarious methods of control by those with a false narrative about myalgic encephalomyelitis and their supporters will continue. To prevent the disappearing of ME, we need to recognize and expose these treacherous acts.  Our advocacy efforts should focus on demanding the use of proper criteria for diagnostic and research purposes ( ME-ICC criteria and ME-ICC Questionnaire), and for appropriate NIH funding ($250mil a year in the US) to effectuate impactful studies leading to an acceptable biomarker as well as FDA approved treatments for #pwME.

References:

Astroturf and manipulation of media messages | Sharyl Attkisson – video –https://www.youtube.com/watch?v=-bYAQ-ZZtEU&feature=youtu.be

Transcript of the Attkinson’s video – https://www.facebook.com/notes/anne-liconti/transcript-astroturf-and-manipulation-of-media-messages-sharyl-attkisson-tedxuni/10155251065525277?hc_location=ufi

Mongoven, Biscoe & Duchin: destroying tobacco control activism from the inside – http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1763840/pdf/v011p00112.pdf

Eileen Holderman, CFSAC Comment – January 13, 2017

/ Gabby Klein / 1 Comment

Good morning to the Committee Members and to the stakeholders.

I’m Eileen Holderman, an advocate for ME, GWI, and other neuroimmune diseases.

I formally served as the Patient Advocate on CFSAC and chaired 2 subcommittees – one was for the review and improvement of the CDC Web Site.

While I believe advocates’ efforts should always be ongoing to improve Government policies, I am dismayed when I see efforts that are redundant and seemingly futile. Specifically, I am referring to the efforts advocates are asked to make in regard to the TDW for the improvement of the CDC Web Site, not only because of my subcommittee’s work for 4 years, but because of the efforts of all my predecessors.

Today, I will read into the public record excerpts from an open letter I wrote to Dr. Beth Unger of CDC, at the time I completed my 4 year term on CFSAC.

Here are excerpts, which unfortunately, still apply today:

Dear Dr. Unger:

As I prepared to write my thank you letter, I checked out the CDC Web Site so my final remarks would be accurate. To my surprise and dismay, I noticed CDC created a new web page to feature May 12 Awareness Day. I say ‘surprise’ because there was no mention of it to me or my Review Panel; and there was an opportunity to mention it as recent as last Friday during my Subcommittee Teleconference when I asked if there were any announcements from HHS – you will recall that my inquiry was met with an awkward silence. Had CDC communicated to me that they planned to feature May 12 Awareness Day with the erroneous content of the CDC Web Site, I would have objected. Furthermore, our national and international ME/CFS and FMS organizations do an exceptional job of raising awareness for these diseases so CDC need not undermine those efforts. I appeal to CDC to remove the new web page as advocates have already begun to voice their justified criticisms of the content.

For the past 4 years, my Review Panel and I have made countless suggestions to improve the CDC Web Site. While CDC did make changes to the general sections of the web site, my opinion is that most of the changes were cosmetic, not substantive. The CDC Web Site still resembles a web site for the condition of chronic fatigue instead of a web site for the neuroimmune disease of Myalgic Encephalomyelitis (aka CFS).

Below, are my specific (though not my complete list of) recommendations to improve the CDC Web Site that need to be, but have yet to be, implemented:

* remove the Resource Guide

* remove the Toolkit

* remove the expired and needless Emergency Preparedness Webinar

* remove the expired CDC/Medscape video online course

* remove all references to the Oxford Case Definition in the CME online courses

* remove references to CBT

* remove references to GET

* remove references to St. Bart’s and NICE Guidelines

* remove all links to CDC psychosocial published studies on ME/CFS

* remove all implications both subtle and overt to ME/CFS as a psychogenic and/or a fatigue “condition”

Hopefully, the CDC Web Site will get on board with our 50+ ME/CFS experts and adopt the CCC in their CME courses and in all of their content, and reference the 5000+ biomedical papers on ME/CFS, and offer links to the IACFS/ME Primer and the ME ICC Primer and a section on Pediatric ME/CFS. The CDC Web Site needs to reflect the serious, disabling nature of this neuroimmune disease affecting nearly one million American men, women, and children and 17 million worldwide.

Again, thank you for the time and consideration you, Ermias, and John have given me and the Review Panel in regard to improving the CDC Web Site.

Best regards,

Eileen Holderman                                                                                                                                                          

Thank you for the opportunity to speak today and I wish all of you well.

 

CFSAC Comment, Gabby Klein – January 13, 2017

/ Gabby Klein / 7 Comments

The Chronic Fatigue Syndrome Advisory Committee (CFSAC) met January 12 and 13, 2017. Here is the meeting agenda.  The following was my call-in testimony.

Hi, my name is Gabby Klein.  I am a patient advocate and blogger.  I have been ill with ME for 14 years.

As I sat down to write, I thought of our current situation as ME patients at the start of the year 2017. I thought about the comparison of the state of  ME patients today to a decade or three ago and became aware that there have been next to no improvements made throughout the years.  Due to HHS neglect and misdeeds, over 30 years after the Lake Tahoe outbreak:

  • Few doctors nationwide have the knowledge and experience necessary to properly diagnose and care for patients.
  • The same harmful GET and CBT therapies continue to be recommended by HHS.
  • There are no FDA-approved drugs.  
  • NIH still spends a minuscule amount of money on a disease with an enormous economic, mortality and quality of life burden.
  • The CDC and other HHS agencies continue to spread incorrect, harmful information on their website and in their continuing medical, educational material.
  • The unscientific and demeaning name, CFS, is still being used and the government still controls and fabricates incorrect and overly broad definitions – like the IOM.
  • HHS continues to cover up their negligence and malfeasance with the creation of more committees, workshops, and working groups – giving the false impression that they are actually doing something for the patients.
  • There is a continuing lack of transparency as well as a withholding of crucial information from the patient community.  The recent incident of NIH’s invitation – by Dr. Walitt with Dr. Nath’s approval, to ME denier Dr. Shorter to lecture on the false history of the disease, was a prime example.
  • False promises are frequent as in Dr. Collins promise of a considerable increase in funding for ME/CFS. It has in reality resulted in mere crumbs – an increase of $7 to 8 million for a million US disabled patients!  Moreover, in his eight years of service as NIH director, Dr. Collins has never mentioned ME/CFS when speaking to the Senate Appropriations Committee advising on specific increases in NIH funding.

Until HHS publically apologizes to the ME community for their three decades of neglect and malfeasance and until the time when HHS

  • exclusively uses our expert criteria – such as the CCC, ICC, or Ramsay’s
  • uses the correct name myalgic encephalomyelitis (ME)
  • properly educates medical practitioners
  • and appropriates NIH funding to the figure of a minimum of $250 million a year- which is on par with other similarly burdened diseases

I will continue to challenge and hold the federal government accountable.

 

My Comment to MEAction’s #MillionsMissing Protest Demands

/ Gabby Klein / 17 Comments

The organization, MEadvocacy , their supporters and independent advocates who advocate for the disease Myalgic Encephalomyelitis (ME) and for the criteria CCC and ICC represent a significant percentage of the ME community.  According to Jason’s latest study (as shown below), the majority of the community prefers the name Myalgic Encephalomyelitis (ME) over CFS, ME/CFS  or SEID and selects the CCC and ICC criteria over the IOM criteria.

Therefore, MEadvocacy and independent advocates such as myself, have repeatedly communicated the name and criteria preferences to MEAction to include them in the protest demands but have been cut out of the process time and time again.  Additionally, MEadvocacy and their supporters were excluded when MEAction met with high-level staffers at HHS recently – again shutting out a significant voice in the ME community.

For over 30 years, HHS has used these silencing tactics on ME advocates and now our own “community platform” (MEAction) is using the same tactics against MEadvocacy and independent advocates to silence our voices.

I left a comment on their website Friday afternoon, but unfortunately, it has not come out of moderation yet.  *edit – my comment was just posted 11:24pm along with a reply from MEAction (although the timestamp for my comment shows 9/23/2016 at 4:12pm – which is the time that I posted my comment to their website)

You can read my comment below:

On August 12th, 2016, I sent the following letter to MEAction regarding their MillionsMissing demands:

MEadvocacy sent you a letter before the May 25 protest letting you know that they and their supporters would not endorse demands from the ME community that do not include as a priority the name myalgic encephalomyelitis in conjunction with the ME criteria (CCC and or ICC) – not the CDC or IOM criteria.

Even though I am an independent advocate now, I advocate for the same demands as MEadvocacy.org and their supporters.

I do not support demands to HHS that do not start off with demanding recognition of the real neuroimmune disease ME.  Without this recognition, we are causing harm to the ME patient community.

In addition, to use the name ME without advocating for criteria created by our ME experts is deceitful.  The IOM panel themselves distinguished IOM/SEID from ME and recommended separate coding.

Sincerely,

Gabby Klein

ME advocate – relatingtome.net.

MEAction did not address MEadvocacy’s concerns about the demands in May, nor have they addressed my concerns in my letter to them dated August 12th, 2016.

Their current demands have not changed the wording in section #3 about Education.  They still demand the CDC amend their website and educational information to comply with 2014 IACFSME Primer and with the IOM report supplemented by CFSAC recommendations.

MEadvocacy has shown in their blog – Analysis of CFSAC August 2015 Recommendations for the IOM Criteria that the IOM criteria – even if the CFSAC recommendations are incorporated will result in inferior criteria to the CCC and the ICC.

The majority of ME patients prefer the CCC and ICC criteria over the IOM as outlined by Dr. Leonard Jason’s recently published paper: Patient Perceptions Regarding Possible Changes to the Name and Criteria for Chronic Fatigue Syndrome and Myalgic Encephalomyelitis.  Over a thousand global patients filled out questionnaires about the name and criteria for the disease. The results revealed that 32-35% of respondents approved of the IOM criteria, compared to 58-64% approval of the CCC, and 55 to 58% approval of the ICC.

In addition, myalgic encephalomyelitis was the preferred name chosen by a majority of patients 65-68%.  This demand is not even mentioned in MEAction’s demands to HHS!  

I therefore, cannot endorse MEAction’s demands and would ask MEAction to make it publicly very clear that these demands do not reflect the demands of the majority of ME patients.