Dr Ian Lipkin says 3-5 years to solve ME/CFS

Cort Johnson reports: Ian Lipkin: Three to Five Years* to Solve Chronic Fatigue Syndrome (ME/CFS)  December 26, 2015

Ian Lipkin flew to Lake Tahoe this December to fundraise for joint projects with Simmaron Research Foundation. In a talk covering his virus hunting career, the threat of pathogens to humanity, and his work with chronic fatigue syndrome (ME/CFS), he dropped a bombshell:  he stated that he believes it’s possible to solve ME/CFS in three to five years.

On that hopeful note, let’s learn more about Dr. Lipkin, his work, and his collaborations with Simmaron.

Dr. Peterson’s Introduction

Lipkin’s Columbia Center for Infection and Immunity (CII) has established close ties with the Simmaron Research Foundation. Only a couple of months before, his chief collaborator, Mady Hornig (and Simmaron Scientific Advisory Board member) had given a talk.  Now Ian Lipkin was here.

Tea-Time at Simmaron I: Mady Hornig on the “Peterson Subsets”, Immune Exhaustion and New Gut Findings In ME/CFS

Dr. Peterson started his introduction of Ian Lipkin by noting that he’d known him since they crossed paths in the 1980’s when Dr. Peterson sent him patients suffering from HIV/AIDS.

Ian Lipkin was the first to isolate Borna disease virus. He identified the West Nile Virus, developed technologies to identify SARS and then hand carried 10,000 test kits to Beijing at the height of the outbreak. He most recently discovered a highly dangerous virus that recently jumped into humans called MERS (Middle Eastern Respiratory Syndrome Coronavirus).

Lipkin has pioneered many technological breakthroughs in finding pathogens including the use of MassTag-PCR, the GreeneChip Diagnostic, and High Throughput Sequencing. His latest breakthrough is the development of a new screening technique that enhances researchers ability to find viruses 10,000 fold.

Called the top virus hunter in the world, Ian Lipkin runs the Center for Infection and Immunity at Columbia, and is the director of the Center for Research in Diagnostics and Discovery (CRDD) at the NIH. He also worked closely with Steven Soderbergh on his film Contagion.

Ian Lipkin talks

Who says brilliant scientists can’t be a hoot to listen to as well?
Ian Lipkin’s presentation was both enlightening and at times hilarious. Exhibiting a wry sense of humor, Lipkin poked fun at himself and virtually everyone around him.

The last time he was in Lake Tahoe, he said, was in 1984 and he hearkened back to the HIV/AIDS patients Dr. Peterson sent him in the early 1980’s.

“When you come to a fork in the road – take it!”

He stated the guiding principle in the search for pathogens could be summed up by the great Yogi Berra’s adage “When you come to a fork in the road – take it!”.

HIV/AIDS was the beginning of many changes. Even after the medical community knew it was being passed in the blood it still took them 2 1/2 years to find it. Why did they know a pathogen was present?  Because of the infectious nature of the spread of the disease and the cytokine abnormalities found.

In a Discover interview,  Lipkin noted that he ran the first clinic in San Francisco that would treat HIV/AIDS (then called GRID) patients with neurological problems. (Note the iconoclastic element to Lipkin that showed up early in his career: he was willing to see patients others wouldn’t see. Check out Lipkin’s fascinating story of how HIV/AIDS lead to him to study infectious diseases.)

Lipkin then worked on a virus which demonstrated the effects a persistent viral infection can have on the central nervous system. The virus alters how nerve cells work but doesn’t kill them.

Next, in another story with possible overtones for chronic fatigue syndrome (ME/CFS), he investigated patients who’d come down with what appeared to be a mysterious psychiatric disorder. It took him two years but using a new method involving genetic cloning he uncovered the Borna disease virus. It was the first virus discovered using genetic means.

The Borna virus discovery was a game-changer for pathogen community.
Jump forward thirty years (after it took the medical community almost three years to find HIV) and viruses are being discovered using molecular means all the time. The Center for Infection and Immunity itself discovered 700 new viruses from 2009-2015.

Lipkin was aware of and interested in ME/CFS in the eighties but there was no money. In 1999 he and Britta Evangaard found no evidence of the Borna disease virus in ME/CFS. From there we jump forward to 2010 when NIH Director Francis Collins tasked Lipkin to determine if a retrovirus, XMRV, was present. XMRV turned out to be a laboratory artifact, and the paper was retracted – something that Lipkin said was not all that unusual in science. (He emphasized that he and Dr.
Peterson were very careful to put out studies that would stand the test of time.)

The XMRV discovery tanked but proved to be a boon for ME/CFS by heightening the attention around it. Lipkin had kept an eye on ME/CFS for years and after being hired by the Chronic Fatigue Initiative to take it on, he was back in a big way.

In the next portion of his talk he turned to viruses and humans.

Viruses and Humans

How are most viruses getting into humans? From animals. After it’s jump from primates to humans, HIV is, of course, the most familiar example, but viruses are also escaping from bats, birds, pigs, rodents, insects and even camels into humans.

A sea change in the viral field occurred in 1999 when a mosquito-borne virus – the West Nile Virus – was so bold as to attack the residents of the New York. Lipkin shifted his work from the West to East coasts and ultimately identified the virus. As the outbreak spread, it got the attention of Senator Joesph Lieberman who sponsored the first big initiative to learn how viruses spread from animals to humans.  Politicians, Lipkin said, can be very important allies.

If viruses are going to get spread around the world, New York City may very well be the best place to do that. Twenty-one million passengers traveling to and from 72 countries pass through New York airports every year. Animal products including bushmeat – all potentially contaminated with nasty viruses – pour into New York City regularly.

How many viruses remained to be discovered? A survey of one species of bats found fifty-five viruses, fifty of which were new to science.
Lipkin estimated 320,000 viruses were still unknown. He then covered virus’ able to escape from bats, ticks  and rats into humans.

Bats – Called in to investigate an ill Saudi Arabian man (with four wives), he uncovered a new virus called MERS (Middle East respiratory syndrome coronavirus) which was similar to those found in bats. (Asked if there were any bats in the area, he was told no. The next video showed bats flying every which way in the area :)). If the bats weren’t biting the humans, though, how was the bat virus jumping into people?

MERS appears to have been present in bats for quite some time. It spread to camels in the 1990’s and then jumped from camels to humans around 2010.

MERS is not particularly easy to transmit but when it gets transmitted, watch out. Death rates are high. It took one Saudi Arabian to spread MERS to South Korea this year where it killed several dozen people, put several thousand into quarantine and basically threw the country into a panic. Schools were closed, tourists stopped coming, and parts of the economy slumped as South Korea fought off the virus. MERS is the kind of virus that keeps public health officials up at night.

It’s not surprising that Lipkin is wary of pathogens. He noted that he rarely shakes hands but darting a glance at Dr. Peterson said he’d made an exception that evening. (If you haven’t seen Steven Soderbergh film “Contagion” and can handle apocalyptic scenario’s you might want to give it a try. Lipkin consulted extensively on the movie which involved a worst-case scenario of a virus wiping out much of humanity. The film was praised for its scientific accuracy. (Spoiler alert – we do survive in the end :)).

Ticks –  Lipkin believes chronic Lyme patients who are not recovering from antibiotics probably got another infection from the ticks. Lipkin found that over 70% of the Ixodes scapularis ticks associated with Lyme disease carried at least one pathogen and 30% carried more than one in New York. Last year he identified a rhabdovirus (Long Island tick rhabdovirus) new not just to ticks but to science itself. A small survey suggested that 15% of residents may carry antibodies to the virus.

Rats- Lipkin’s study of New York City’s second most common resident – rats – revealed they carried an amazing array of pathogens including Escherichia coli, Clostridium difficile, and Salmonella enterica, Bartonella spp., Streptobacillus moniliformis, Leptospira interrogans, and Seoul hantavirus.

Lipkin is understandably wary of pathogens. He noted that he rarely shakes hands but darting a glance at Dr. Peterson said he’d made an exception that evening.

Later Lipkin referred to the hamburger and French fries lunch that he and Peterson usually have saying do as we say not as we do. How does Lipkin reportedly like his meat? “Burn it” he tells the waiter. The man is taking no chances – he knows too much.

Infection and Disease

A pathogen is just one of the players, however, in a vast swirl of factors which ultimately determines whether one is going to have a chronic illness. Timing, for instance, is a key factor. If you expose a mouse to a pathogen at one stage of pregnancy, it’ll stop moving around its cage. If you expose the same mouse to the same pathogen later in pregnancy, it will run round and around its cage unceasingly.

A large autism study underscored the complex role timing plays. The 120,000 person autism birth cohort study found that if a mother comes down with a fever after the first trimester, her chances of giving birth to a son with autism go up three-fold.  If she treats the fever with acetaminophen, her chances of giving birth to an autistic child drop significantly.  If she takes acetaminophen for any other problem than a fever, her risk of giving birth to an autistic child goes up again.

Three to Five Years – An ME/CFS Timeline

How does all this relate to ME/CFS? Likpin cited the findings of their work to date.

  • The suspected pathogens don’t appear to be the problem (the CII is reportedly looking further at herpesviruses.)
  • Evidence suggests altered microbiomes (gut flora) are present
  • Striking differences in immune expression between shorter and longer duration patients appear to be present
  • Preliminary evidence suggests that levels “X” and “Y” metabolites and, at least, one immune protein are significantly altered in ME/CFS.
    (Lipkin embargoed this information pending publication of the paper.
    One of them is highly unusual.)

Lipkin emphasized, though, that ME/CFS is not a one-size fits all disease. For instance, it’s possible that fungi may be a problem for some patients. That’s an intriguing idea given the recent fungi funding in Alzheimer’s disease published in Nature.

Then Lipkin made his bold declaration “We’re going to solve this in three to five years”, with a big proviso. Provided the resources are made available, he believes science can crack ME/CFS fairly quickly.  That sounds really fast, but Lipkin’s time-frame is not that far off from Ronald Davis’s 5-10 time-frame (provided he gets the resources as
well.) (or Dr. Montoya’s).

These eminent researchers believe that given the technology present today we could understand ME/CFS fairly quickly – if enough resources were brought to bear.  Lipkin pointed to a slate of researchers in his lab working on ME/CFS to signify the major shift that’s occurred. He said “I couldn’t have gotten them five years ago”.

He highlighted two places the patient community can make an impact:

  • Funding Pilot Studies –   The community can fund pilot studies
    which can be turned into big grants
  • Advocacy – Lipkin is a savvy researcher. He knows how the NIH works and once again he emphasized the need for the ME/CFS community to push harder legislatively – to talk to their representatives in the House of Representatives, in particular – and get them to push the NIH for more funding.

Lipkin’s Bucket List

Ian Lipkin has clearly developed a special relationship with ME/CFS, Dr. Peterson, the Simmaron Research Institute. He hadn’t been in the Lake Tahoe area for decades, yet he and two of his assistants had flown across the country to support the Simmaron Research Institute’s spinal fluid work. He was even shaking hands.

I shook my head – not for the first time – about Lipkin. How had we gotten so lucky? Lipkin oversees the work of 65 researchers in the U.S. and 150 more across the globe. The New York Times reported that on any given day his lab had 140 viral research projects underway. The head of the National Institute of Allergy and Infectious Disease, Anthony Fauci said, “Lipkin really stands out from the crowd.”

Yet, here he was in Truckee in mid-December exhorting the audience to support an important Simmaron study that he believed needed funding.

What had driven the “The World’s Most Celebrated Virus Hunter” to take on our disease? I asked his assistants. They told me that Ian Lipkin wants to do two things more than anything else before he retires: he wants to solve ME/CFS, and he wants to solve autism. We’re on his bucket list.

That floored me even more (:)) so I asked – but, but…..doesn’t  he care what other people think about this neglected disease? That question left them almost gasping for breath. After they had been able to calm down, they assured me: no he doesn’t.

The Simmaron Research Foundation’s Next Spinal Fluid Study

Lipkin was at the event to support the Simmaron Research Institute’s next spinal fluid study. The results of the first one – the most extensive spinal fluid study ever done in ME/CFS – were eye-opening. A comparison to multiple sclerosis (MS) found evidence of immune dysregulation almost equal to that found in MS. The difference was that instead of being raised, the cytokine levels were reduced in ME/CFS.

For more on the Peterson’s subsets and Lipkin and Hornig’s Simmaron Work

That finding surely left a big smile on Lipkin’s and Hornig’s faces.
Earlier they had found evidence of a profound reduction in immune functioning in the blood of later-duration ME/CFS patients. Now a similar reduction was found in their spinal fluid. Having findings in two different systems match has rarely happened in ME/CFS. That suggested they were uncovering system-wide problems.

No wonder Lipkin was eager to begin a new and larger spinal fluid study. It’s part of achieving his bucket list.

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Gait automaticity in women with CFS

Research abstract:

Patients with chronic fatigue syndrome (CFS) report difficulties walking for a prolonged period of time. This study compares gait automaticity between women with CFS and nondisabled controls.

The “stops walking with eyes closed with secondary cognitive task” test is based on the classic “stops walking while talking” test but compares walking with eyes closed while performing a secondary cognitive task in a female CFS population (n = 34) and in female nondisabled controls (n = 38).

When initiating gait, 23.5% of patients with CFS looked toward the ground compared with only 2.6% of nondisabled controls.  After 7 m, subjects were asked to close their eyes, and after another 7 m, they were asked, “How much is 100 minus 7?” Of the patients with CFS, 55.9% stopped walking compared with 5.3% of nondisabled controls.

Less automated walking was observed in patients with CFS than in nondisabled controls (p < 0.001). The test-retest reliability is moderate for global stopping. This simple test observed reduced gait automaticity in patients with CFS for the first time. Dual tasking could be helpful to address the functional limitations found in this particular study.

Reduced gait automaticity in female patients with chronic fatigue syndrome: Case-control study, by JB Eyskens, J Nijs, K Wouters, G Moorkens in J Rehabil Res Dev. 2015;52(7):805-814

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New year greetings from WAMES

New year greetings from the WAMES team. We hope you had the Christmas you needed and we wish you a healthier, happier, safe and dry 2016!

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Lucy’s practical ways to show compassion to someone who is continually ill

Telegraph article: Living with chronic fatigue: How I wish my friends would treat me, by Lucy Mayhew , 21 December 2015.

Lucy Mayhew_pre-illness

Bear Grylls and I have virtually nothing in common – the survival expert has a GTI turbo-charged body, whereas seven years ago, mine became my jailor.

Grylls recently name-checked  kindness as an overlooked quality “critical to survival,” and in the midst of paralysing physical pain, fear and despair I have learned how true this observation is. But also, because compassion doesn’t cure suffering, it is absurdly easy to neglect precisely when it is most urgently needed.

In 2008 I was in my twenties living in London leading a busy, fulfilling life working as a journalist, surrounded by a large circle of friends. Then an atomic bomb exploded wiping out virtually all physical function and destroying my life.

There is no tidy diagnosis or cure for my complex immune and gastrointestinal condition. It has most in common with the severest cases of Chronic Fatigue Syndrome where, as immunologist and AIDS and CFS specialist Dr Nancy Klimas explains, “patients experience a level of disability equal to that of patients with late-stage AIDs”.

A few weeks ago leading scientists around the world met at a global compassion conference in Shrewsbury where plans were unveiled for a new research institute dedicated to study and application of compassion.

The International Institute for the Study of Compassion has the support of Charles Darwin’s descendants. His great-great-granddaughter, Ruth Padel was at the conference where she spoke enthusiastically about the growing body of evidence that build’s on Darwin’s observations that compassionate behaviours are critical for human flourishing and even our very survival as a species.

Dr James Doty, a Stanford University neurosurgeon, also at the conference, highlighted research demonstrating compassion – and its kindred traits of understanding, kindness and connection – settles fear at a physiological level. My own experience attests to this. But I also know that our aversion to suffering leads us to denial – ‘she looks fine she must be just depressed’- or to reject, because we can’t stand to witness someone on a treadmill of suffering.

My circumstances are neither as cruel nor visible as those countless others are forced to endure. Nonetheless life has ceased to be life; rather it is an endless round of endurance I yearn to escape.

St Augustine said that physical pain was the greatest evil and he was right. I didn’t have a humour bypass or decide it might be diverting to become a hermit for almost a decade. I am extremely fond of life but this version needs returning to sender.

My illness has left me totally unable to speak due to a chronically sore throat. And the annihilating exhaustion which is impossible to describe, keeps me almost permanently in bed, often too weak to sit up. My gastric condition frequently delivers attacks which prevent eating for days.  I have cardiac and neurological symptoms and excruciating migraines but nothing breaks me like my seventy-two hour gut pain attacks which not even opiate pain medication can sate.

“Today I am sicker than ever and am currently casting about for viable medical help. Two things keep me going: stubborn determination that there is a path to recovery and savouring small gifts of compassion.”

I have worked with practitioners of conventional, alternative and integrated medicine based on every continent bar Africa and encountered kind, bullying and indifferent consultants. I’ve taken cannabis juice, cannabis suppositories; undertaken stool transplants; been brought to my knees by the side-effects of conventional and holistic medications. I’ve seen shamans and charlatans; tried to invent past lives; get good at meditation and coax forth a belief in God or the power of my own mind in an attempt to heal myself.

Today I am sicker than ever and am currently casting about for viable medical help. Two things keep me going: stubborn determination that there is a path to recovery and savouring small gifts of compassion.

Last week, in response to sharing my current state, my dearest friend emailed: “Nothing to say as all words, advice or sympathy from all parties are useless at this stage, but thanks for the update nonetheless.”

My friend is not callous, we adore each other and she wants me well but, as Dr Doty, concedes, being “truly compassionate when someone is suffering takes an immense amount of strength”.

Loss of physical function is hell but acute pain takes you to hell’s basement where you doubt life, goodness and yourself.  Alone, one employs legion strategies to keep buoyant.  Nothing, however, is as effective as the faith drawn from another’s warmth – it wards off desolation and revives one’s resolve to keep fighting.

The reply I sent my friend was to urge her that her input is never without value. I explained that the single, stand-out moment of my seven year illness was last November. She was visiting on the third day of one of my suicide-inducing gastric pain attacks.

‘You came into my room,’ I wrote. ‘As I cried you hugged me and said you knew what a huge amount I had done and how endlessly hard I had been trying to find a path back to health. That explicit recognition of the breadth and depth of my delving and the connected salute to how vile this situation was, did more good than anything else could possibly have done. It didn’t stop the pain or banish the fear but it helped. A lot. It’s what people mean when they talk about bearing testimony to a person’s suffering. It transcends pity. It’s love as understanding which is priceless.

Sometimes there are no viable suggestions but you can repeatedly let a person in distress know you are holding the space for brighter times for them. It never gets old or tired. It never becomes unnecessary. It can be spoken and unspoken — both is best.

“We may be unable to affect the outcome of a hellish circumstance, but the way it is experienced can always be altered and improved.”

Strip a person of everything they have and they will be left with two things — the instinct to survive, and the instinct of love, both given and received.

Philosopher A.C Grayling calls love ‘a baggy concept’, but its very roominess allows it to be expressed and experienced in a hundred different ways. Such caring does not require grand gestures, special gifts, and it doesn’t need to impinge on the day of a busy person, but it does need showing.

Eleanor Roosevelt also suggested the shortness of life meant it was a good idea to learn from other people’s mistakes. So I am sharing these hard-learned, unoriginal reflections in case some of their sentiment might imprint and suffuse where pithier, more eloquent words may only fleetingly register.

So whenever you might be faced with a situation where you feel useless, remind yourself this isn’t so. A legitimately frightened person knows they cannot look to another for rescue but they will be soothed, albeit imperceptibly, by small bids of solidarity. We may be unable to affect the outcome of a hellish circumstance, but the way it is experienced can always be altered and improved.

If a person is alive, they will still have hope because hope is an instinct. Even the condemned man being marched to his execution has hope of a last-minute reprieve; so if he knows that someone else also holds that hope, and, at the very least, wishes the circumstances were different, that helps; so much. Believe me.

Five practical ways to show compassion to someone who is continually ill

  1. Be patient and constant: Like regular meals, a person in distress needs repeated comfort and, as time passes, that need intensifies. It is human nature to hold on to hope even when the outlook looks pretty futile; and to feel that someone else cares and is holding on too is a great tonic.
  2. Share your life: Visits and phone-calls aren’t always possible but record a voice message on your smartphone or send a chatty email – these can light up the world for days. Don’t worry how pedestrian or dull you think your news is because it’s the inclusion – the human connection – that’s cherished. Likewise an out of the blue, three-word text: ‘thinking of you,’ can really lift a pain-filled day.
  3. Be sensitive: We still want to hear your happy news – engagements, pregnancies, career successes, as well as your problems, even if they seem trifling. A short simple acknowledgement of how hard it must also be to be denied the joys (and trials) of ordinary life, shows sensitivity that deeply nourishes.
  4. Avoid belittling commentary: ‘I wish you’d try to overcome this depression; get some fresh air; ignore the pain. You certainly look well.’  Implying this is a chosen circumstance that stems from weakness, lack of willpower and moral fibre, hurts. When quality of life is so diminished there is nothing one won’t do to feel well.
  5. Show you believe: Pain and poorly understood illnesses are frequently stigmatised and discredited. Simply naming the presence of  suffering brings enormous relief, as does a sympathetic smile or hand on the arm. The confidence arising from your acknowledgement also provides space for lightness and laughter.
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DOPE: Delayed Onset Post Exertional fatigue

Dr John L Whiting explains why he thinks the term DOPE is better than PEM or PENE:

One of the biggest nuisances that ME/CFS sufferers have to contend with is the post exertional fatigue component.

This issue was an aspect of my own questionnaire for CFS in 1992, and that I presented a poster on the this as one of the 4 main CFS fatigue subtypes that I had recognized at the time in Dublin, Ireland to the International Symposium there in 1994. This information was inadvertently missed by attendees at the time.

Post exertional malaise etc now has been recognised as a cardinal problem in more recent years by those who study the disease, but it does not appear to have gained the traction that it deserves as a key issue in this setting by many of those who you would expect to know better.

My own acronym for this strange phenomenon (before the acronym PENE etc came into being at a rather late juncture in the 30 year history of CFS) was and still is the term DOPE.

DOPE stands for:

Delayed Onset Post Exertional fatigue.
DOPE contrasts significantly with other fatigue subtypes in that there is a time gap of 1-3 days (occasionally longer) between the exertion (or even exertion WITHOUT a sense of any intra-activity difficulties, such as having an enjoyable night out and not recognising it as exertion) and the symptoms that follow later.

This unusual GAP IN TIME

… is the diagnostic giveaway in terms of saying ah-ha, this is CFS/ME.
… is not part of normal physiology

What is strange is that the exertion in question may be FULLY tolerated symptomatically AT THE TIME of activity, with no clues or forewarning as to what is to follow later.

Thus, it does not necessarily feel like exertion in real time, but the body interprets the activity as exertion nevertheless. Consequently, caution or care with ones energy envelope are not considered during the activity, especially in patients who are new to the illness.

DOPE is a nuisance because it takes the patient by surprise. In addition, observers before the fact (of observing the consequences) see such patients activities as representing normality and assume or fail to consider any delayed onset penalty effects.

The more troublesome issue is that WHEN DOPE hits, it happens in such an unexpected way that it is difficult for patients to keep to previous promises, which in turn then creates the impression of unreliability in that person – for all the wrong reasons. Appointments have to be cancelled at the last minute, as there were no advanced warning symptoms. This can be and often is socially unacceptable and is a strike against ones own character in many home and work settings.

In my clinical notes, I record DOPE in my patients in this manner:
DOPE 1, DOPE 2-3, and so on, where the numeral represents the day of onset of symptoms and also their duration. I also circle the number when symptoms peak, say Day 3 for example.

I do not believe that there are immune mediators involved in DOPE. I have multiple sentinel markers of inflammation that I use routinely, that can indicate immunological changes, none of which I have observed to ever alter in the course of DOPE, either before, during or after DOPE occurs.

My feeling is that DOPE is either neurotransmitter related, metabolically mediated, or microcirculatory in origin. There are ways to reduce or prevent DOPE, that support my theories on the matter.

Iron status is one of the most critical factors of all, and has been totally neglected in ME/CFS research.

Simply calling the problem post exertional malaise says absolutely nothing to the novice in this field as to what is being implied. For example, when does exertion NOT have after-effects in a normal population? Is it not true that immediately after exertion it is normal to notice the body is tired, exhausted or in a state of recovery (catching ones breath, say). Agreed that malaise is not the same as catching ones breath, but who is to say WHAT this malaise we talk about, is, how it is defined, and what is its underlying mechanisms and/or pathology?

If PENE is to be characterised as pathognomonic of ME/CFS, surely its phenomenology should be described in the utmost detail in the published literature by now? This is a very very serious and very odd omission.

I much prefer the acronym DOPE over PENE as it is more specific and more correct. It more accurately highlights the issue at hand, which PENE does not unambiguously do.

This is very relevant. For example, the idea of walking distance as in the PACE trial, does not take DOPE into consideration. A person could easily exceed his/her safe exertion limits and then experience severe DOPE a number of days later, and fail to have this recorded in the study.

Furthermore, DOPE is highly unlikely to be psychosomatic, as there is neither primary nor secondary gain, as just about no one is sympathetic to the individual who seemingly has performed ‘well’ a few days before, and then says “Sorry, I’m not up to doing what you just asked me to do”. In other words, DOPE has the opposite effect to what psychosomatic theory argues to be true.

How does one characterise a person who can do something ‘normally’ (in the visually overt behavioural characterisation of what the term normal means) but who is sick in bed or housebound several days later?

Is such a person sick or is this person well? It all depends on the day one is evaluated, and whether or not the phenomenon is typical or atypical for such a person. If it is a regular occurrence, DOPE MUST be taken into account. I have seen many many clinical and medicolegal or welfare instances where DOPE is ignored, is dismissed or is considered irrelevant, simply because the evaluator SEES nothing wrong with the patient at the time.

Another noteworthy point is that the test-retest exercise testing protocol of Stevens et al. is on the money but may miss many patients where day 3 is the day of DOPE onset. Also, DOPE is itself unreliable in that sometimes it does not eventuate as expected – thus, testing for it with exercise tests may miss these uncommon absences of DOPE.

Finally, weakness post exertion, exhaustion post exertion, somnolence post exertion, apathy post exertion as well as orthostatic fatigue, cumulative fatigue and cyclical fatigue are all phenomenological subsets of fatigue, each of which has DIFFERENT pathophysiological underpinnings and treatments. What happens instead, is that the research community lumps these all together as one (!!!), diluting the chances of identifying anything meaningful from within the data collected. There is so much in this field of science that needs to be rectified. If we as experts can’t get it right, then how can we expect anyone else to accurately understand what ME/CFS is all about?

Therefore, in any research project or research paper, the type of fatigue (as subsumed into the diagnosis of ME/CFS) MUST be specified if anything is to be gained from such work.

Dr Whiting Summarises Some of the Latest Research into CFS,  30 September 2015

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BBC TV show Doctors features ME

The BBC1 tv series ‘Doctors’ featured a very positive and very well researched programme on Dec 4 2015, which includes a segment with a man who has ME or CFS. Tony Britton from the ME Association advised the producers.

Series 17 Episode 152 The power of you

Available for 29 days

 

 

 

 

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Close to collapse – Shocking report exposes failings in ME social care

Shocking’ report exposes failings in ME social care, By Raya Al Jadir in Disability News Service, November 13, 2015

A tiny proportion of disabled people with the neurological condition ME are receiving the social care they could be entitled to, according to a “shocking” new report from a charity.

Action for ME surveyed 850 people with ME* (myalgic encephalomyelitis), and found 97 per cent of them could be entitled to state-funded care and support, but only six per cent had been given a care package by their local authority, while only 16 per cent had been given an assessment of their needs.

The report, Close to Collapse, will form the basis for a formal inquiry led by the charity and supported by the all party parliamentary group on ME,  which will examine the challenges faced by people with ME and chronic fatigue syndrome in accessing support.

The report also found failings in provision of advocacy support for people with ME, with nearly four in five of those who responded to the survey not having access to an advocate.

Action for ME is now seeking funding to establish a national advocacy service.

One survey respondent**, who lives in the south-east of England, told the charity that the “mental strain” of having to undergo two separate hour-long assessments – the second one had been ordered after her original social worker left and was replaced by a student on a placement – had left her “broken” and in “severe physical pain”, and failed to address the problems she faced.

She said: “I was told that any help I got would have to be paid for myself, out of DLA [disability living allowance]. The sum total of social services assistance amounted to fitting safety grab rails.

“I feel very badly let down. I don’t have the strength to organise anything for myself, so I am just struggling through doing what little I can.

“I manage to wash or bath about twice a month. My house is filthy and I am smelly. My meals are limited to the most simple, mostly microwave-ready meals. At times this makes me suicidal.”

The disabled researcher and campaigner Catherine Hale, the report’s lead author, said: “Many of the individuals who shared their experiences with us have been left feeling truly desperate by the lack of support available to them.

“The difficulties they face in engaging with the assessment process because of their disabling symptoms, and the lack of education about the condition among social care professionals, is a double whammy.”

Sonya Chowdhury, chief executive of Action for ME, added: “People with ME are being left isolated and neglected by this shocking failure to provide the social care support to which they are entitled.

“Those most severely affected by the condition – around a quarter of people with ME – are house- or bed-bound, and for them the situation is truly dire.”

Disability News Service asked the Department of Health to comment, but it had not responded by 7pm today (12 November).

*ME is a long-term, chronic, fluctuating illness that causes symptoms affecting many body systems, particularly the nervous and immune systems

**It is not known whether the respondent was male or female

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Evette’s life with ME – a living torture

Severely affected Evette describes having ME as a living torture in ITV news on 30 October 2015.  Reporter Rob Osborne interviews Christalla Davies from support group MESiG and a local doctor about the seriousness of ME.

Youtube video [2 mins 48 secs]

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Interview with Ronald W Davis about his search for cure for sick CFS son

BBC interview with Ronald W Davis, Professor of Biochemistry and Genetics at Stanford University USA: Scientist dad searches for cure for sick son

Whitney Dafoe was a healthy, well-travelled photographer until he contracted an illness that has been identified as chronic fatigue syndrome. His father, Ronald W Davis, is one of the world’s leading biomedical scientists and is now putting all his resources into finding a cure for his son.

Washington post article, by Miriam E Tucker, Oct 5 2015: With his son terribly ill, a top scientist takes on chronic fatigue syndrome

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ME: symptoms & biomarkers

Review abstract:

Myalgic Encephalomyelitis (ME) continues to cause significant morbidity worldwide with an estimated one million cases in the United States. Hurdles to establishing consensus to achieve accurate evaluation of patients with ME continue, fueled by poor agreement
about case definitions, slow progress in development of standardized diagnostic approaches, and issues surrounding research priorities.

Because there are other medical problems, such as early MS and Parkinson’s Disease, which have some similar clinical presentations, it is critical to accurately diagnose ME to make a differential diagnosis.

In this article, we explore and summarize advances in the physiological and neurological approaches to understanding, diagnosing, and treating ME. We identify key areas and approaches to elucidate the core and secondary symptom clusters in ME so as to provide some practical suggestions in evaluation of ME for clinicians and researchers.

This review, therefore, represents a synthesis of key discussions in the literature, and has important implications for a better understanding of ME, its biological markers, and diagnostic criteria. There is a clear need for more longitudinal studies in this
area with larger data sets, which correct for multiple testing.

Myalgic Encephalomyelitis: Symptoms and Biomarkers, by Leonard A Jason, Marcie L Zinn, and Mark A Zinn in Curr Neuropharmacol. 2015 Sep; 13(5): 701–734 [Published online 2015 Sep]

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