Monday, October 22, 2012

CFSAC testimony - Dr. Joan Grobstein on Responsibility

The CFSAC committee met again on October 3-4, 2012. Public testimony can be seen in the above youtube clip and an accompanying one. As usual the testimonies of patients and advocates were varied, heartfelt and stirring. Over the years these presentation have done a great deal to publicly give a face to ME/CFS and to elaborate, in the most personal and often harrowing terms, the toll that it takes on patients. Collectively these testimonies are the strongest evidence of the case against the government for   their weak response to this medical emergency. This year there is some slight evidence that the CFSAC committee and the federal government itself, principally the FDA, is waking up from their long slumber and beginning to take ME/CFS seriously.

Many years ago I came to realize that the testimonies of Dr. Joan Grobstein are particularly articulate and insightful. Dr. Grobstein has the capacity to distill various problems down to their essential matter - and to cut out the crap. Dr. Grobstein has repeatedly clarified the central issues and constructed a path that will lead us out of the quagmire impeding research and treatment into this illness. It has always been my opinion that this woman should be given a position where she could "make things happen". Certainly her background as a physician gives her a unique and important perspective. When concerned people are gathered to design a plan of how to attack this illness, Dr. Grobstein's name should be first on the list.

Dr. Joan Grobstein's oral presentation at the October CFSAC meeting begins at 38:50 on the youtube video . Previous testimonies of Dr. Grobstein are available elsewhere on this blog or on youtube. Each of them is noteworthy.

In no way should this focus on Dr. Grobstein be seen as diminishing the myriad fine efforts of all the participants in the public testimony. Their testimonies do us all a very great service and I thank these individuals for the special time and effort that it takes to give testimony.
  • Two important items of Dr. Grobstein follow: The first is a transcript of Dr. Grobstein's oral statement delivered at the CFSAC meeting. The second is Dr. Grobsteins' five-page written submission.

"Hello.  I’m Dr. Joan Grobstein.  I’m a physician.

My topic is responsibility.

Recently we’ve seen accomplished scientists honestly and courageously admit that their original findings about XMRV were mistaken.  They took responsibility for an error.  At its best, this is how science works:  form a hypothesis, test the hypothesis, revise the hypothesis.  We would like to see the same honesty and courage from scientists at CDC about the empiric definition.  The hypothesis that the empiric definition defines the same disease as either Fukuda or the Canadian definitions has been tested and found to be wrong.  Scientists at CDC must take responsibility for this error.  The original paper on XMRV in ME/CFS patients has been retracted. CDC should retract all papers using the empiric definition or, at least, rename them to indicate that they are studies of Idiopathic Chronic Fatigue and major depression, not ME or CFS.

NIH must also take responsibility:  fund studies that will clarify the definition controversy, as it did with XMRV.  Because we saw money appear quickly to study XMRV, we know that funds are available.  It’s clear that CDC’s new study about the definition is unlikely to be impartial.  They are vigorously defending their position.  During a recent phone contact with patients Dr. Unger said CDC could be “lumpers one day and splitters the next”.  This is a remarkably unscientific statement.  The scientific method demands that we rigorously define the conditions of our investigations.  Without understanding this, how can Dr. Unger be trusted to undo the harm to ME and CFS patients that the definitional conflict has caused?  Leaders at CDC must take responsibility and ensure that science done at CDC is impeccable.  There are biomarkers for Canadian-defined ME/CFS patients.  Does CDC wish to conceal that these biomarkers are not found in empiric-defined CFS patients?

Turning now to the responsibilities of the voting members of CFSAC, its staff, and its ex officio members, we’re all aware that very few recommendations made by this Committee have been implemented.

For example, CFSAC made three specific revenue-neutral recommendations  which have been ignored.  The first, from 2009, condemned the use of the empiric definition.  Despite this recommendation, CDC continues to publish studies using the empiric.  The second recommended removing the Toolkit from the CDC website.   The third recommended making IACFS/ME’s Primer widely available.  These last two recommendation were made 4 months ago.  Today, the Toolkit remains on the CDC website.  Meanwhile, CFSAC’s own website has a new link to the Toolkit and no link to the Primer.

Who’s responsible for the lack of action?  Committee members have fulfilled their responsibilities.  It says on the website they “asked” that these three things be done.  On the contrary, they are experts, and, as such, they made recommendations to the Secretary.  Yet neither the ex officio members nor the staff have apparently worked on implementation.  Dr. Koh’s comments gave no indication that he is aware of the importance of these recommendations.  In a letter to advocates explaining his refusal to meet, Dr. Koh said, “CFSAC provides a mechanism to ensure stakeholders are engaged and have the
opportunities to offer input.”  Instead, it appears that CFSAC provides a mechanism to ensure stakeholders are contained and have opportunities to offer input that will be ignored.  So what is the point of CFSAC?  If it cannot accomplish these small, high impact tasks how can it accomplish what we really need:  significantly increased funding for research, better education and improved clinical care?  CFSAC costs $235,000 annually.  That sum could fund a study of natural killer cell function in Canadian-defined patients, or create a mechanism to identify an undiagnosed low-income patient, or educate a few more physicians.  I’m a taxpayer.  I’m concerned that we’re spending almost a quarter of a million dollars each year on a committee whose recommendations are routinely ignored by DHHS.

Here’s a suggestion.  Ask ex officio members to take responsibility.  Ask staff members to assign each recommendation to the agency or agencies with responsibility for implementing that recommendation.  Ask each ex officio member to report on activities to implement each recommendation at every meeting.  If nothing is happening ask for explanations from higher levels within the agencies.

We need to see progress. 

[Please read my written testimony which contains other suggestions for progress.]

If you fund it they will come.

Progress in our understanding of ME and CFS has been hampered by a lack of funding for good research.  We have been told by the NIH that funding levels are low because very few high quality applications are received addressing these diseases.  Yet we are told by researchers who have had repeated success in obtaining NIH funding for research in other areas that their applications for funding for projects concerning CFS have been repeatedly rejected.  Funding for clinical trials has been rare.  This has resulted in a vicious cycle:  few people enter the field out of fear that they will not be able to obtain funding, and thus there is a smaller pool of high quality applicants and applications.  It is time to break that cycle with dedicated funding for ME and CFS research.

Following the model that resulted in Requests for Applications issued on September 21, 2012, by the National Cancer Institute, I suggest that several Institutes at the NIH develop a list of provocative questions (PQs) about ME and CFS that then lead to Funding Opportunity Announcements, using RO1 and R21 mechanisms.  The total funding available in the NCI announcements was $64-84 million.  In addition, $21 million was made available for a Clinical Trials Network, something that is also desperately needed to further our knowledge of ME and CFS.   The relevant institutes that should be involved in developing the PQs are:  National Cancer Institute (increased incidence of early malignancy),  National Eye Institute (multiple ophthalmologic problems), National Heart, Lung, and Blood Institute (orthostasis, post-exertional malaise and altered blood volume), National Human Genome Research Institute (increased incidence in family members), National Institute of Allergy and Infectious Diseases (multiple co-infections, possible infectious etiology, immunological abnormalities), National Institute of Arthritis and Musculoskeletal and Skin Diseases (joint and muscle involvement), National Institute of Child Health and Human Development (pediatric ME and CFS), National Institute on Deafness and Other Communication Disorders (hyperacusis), National Institute of Diabetes and Digestive and Kidney Disorders (associated irritable bowel syndrome), Nation Institute of Environmental Science (associated chemical sensitivity), National Institute of General Medical Science (basic processes of cellular energy allocation), National Institute of Mental Health (adjustment of patient, family and community to chronic disease), National Institute on Minority Health and Health Disparities (no access to diagnosis or treatment for minorities and low-income individuals), National Institute of Neurology Diseases and Stroke (cognitive dysfunction, sleep disorders, autonomic nervous system dysfunction, possible disorders of glymphatic system), National Institute of Nursing Research (need for nursing care for homebound and bedbound patients, quality of life in a chronic illness), National Center for Complementary and Alternative Medicine (patients forced to use alternative medicine because no mainstream treatments available), NIH Clinical Center (clinical studies of bedbound patients), and National Center for Advancing Translational Sciences (need for rapid implementation of bench science in these diseases).

Many of these divisions are already represented on the Trans-NIH ME/CFS Research Working Group.  This group should be tasked with formulating the Provocative Questions with the input of both expert clinicians, who have been working with affected patients for years, and also expert patients.  Because patients have been largely abandoned by the scientific and medical communities, many have developed considerable expertise in pathophysiology and available therapeutics. We know which Questions are the most Provocative, because we live with these questions every day.

The Working Group is currently reported to be meeting monthly.  An accelerated schedule will be necessary to develop and prioritize the Provocative Questions, so that RFAs can be issued as soon as possible.  A high priority should be given to studies of potential therapeutic agents, because there are no therapeutic agents currently approved for the treatment of ME or CFS.  Similarly, there are no validated biomarkers to use for diagnosis or to follow responses to therapies.  This is also a very high priority.  Of note, expert clinicians are using therapies that they believe to be effective and also use biomarkers to evaluate those therapies.

Unlike cancer, which has been well-funded and extensively studied for decades, ME and CFS have largely been ignored.  Although there are over 5000 published studies, most are small and many have not used rigorous criteria for inclusion of subjects.  The required funding for this first initiative is therefore larger than in the cancer initiative described above.  It is, of course, impossible to know how much funding is needed to advance our knowledge of ME and CFS to the point where patients’ lives will be measurably improved.  However, it is possible to make an educated guess based on current NIH funding for Multiple Sclerosis, a disease which causes a similar level of disability and may well be a related or overlapping condition.  MS is estimated to affect approximately 400,000 Americans and receives $121 million per year from NIH for research.  ME and CFS are estimated to affect at least 1,000,000 Americans.  It therefore seems reasonable to allocate $302 million annually to ME and CFS research.

A Barrier to Productive Research Besides Funding

The biggest problem for ME and CFS research has been a somewhat esoteric one:  there have been multiple definitions of the disease, some of which have been overly broad, have not focussed on the most important and unique features of the diseases, and have been shown to include large numbers of patients with other disorders as their primary diagnosis.  This has resulted in wildly varying results  and has made it appear that there are no consistent biomarkers or responses to therapeutic agents.  It has also given an erroneous picture of the diseases.  For example, because large numbers of patients with major depressive disorder were included in cohorts defined by a definition developed by the CDC (the empiric definition) and probably also by another definition developed by physicians in the UK (the Oxford criteria), it has appeared that ME and CFS could be psychological disorders which may respond to cognitive behavioral therapy and a program of increasing exercise intensity (called graded exercise therapy or GET).  However, even in this diluted population the benefits of these therapies are quite minimal.  There is evidence that GET is actually harmful to patients with ME and CFS defined by more stringent criteria preferred by expert clinicians.  It is therefore extremely important that research funded by the NIH use an appropriate definition during patient selection.

The International Association for Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (IACFS/ME), an organizations of clinical and research experts, has recommended using the Canadian Consensus Criteria (CCC) to define ME/CFS in its CFS/ME Primer for Clinical Practitioners.  Patient groups also support this definition.  Thus, it seems reasonable to use this definition in NIH research.

Most (but not all, as noted above) research in the past has used the Fukuda definition, developed at the CDC in 1994.  The problem with Fukuda is that it does not insist on post-exertional malaise, which is probably the cardinal symptom of ME.  It also does not give a higher priority to the presence of other very important features of ME:  orthostasis (not even mentioned in Fukuda), cognitive dysfunction and sleep disorders.  Until the issues in the definition are clarified, it will be necessary for every study funded by the NIH to also classify patients using Fukuda and, in addition to standard data analysis, to separately analyze the data for patients who meet Fukuda criteria and those who meet Canadian criteria (many will meet both).  Thus, over time it will get clearer if there are distinctions between groups defined by these two criteria.  It seems likely that CCC defines ME and Fukuda defines a less-specific group that has been called CFS.  However, only consistent data analysis will provide this clarification.

There was recently an effort among researchers, including the CDC, to establish a minimal data set for ME and CFS research in order to begin to answer some of the questions about differences between definitions and also basic information about the diseases.  However, I have recently heard that this effort has stalled, for unclear reasons.  This is unfortunate.  This could be one of the Provocative Questions:  what data should be collected in every study in order to make patient cohorts uniform (or at least clarify when they are not) and enhance our understanding of these diseases?  An NIH-funded review of the 5000 studies already done to see whether the definition used correlates in any way with the results would be very helpful.

The only study that is currently being done about the definition is a study by the CDC.  This is problematic, because the CDC is the originator of both the Fukuda and the empiric definitions.  They have continued to publish research using the empiric definition as recently as this year, although it has been condemned by CFSAC (see below), and most researchers now agree that it is overly broad and that research using the empiric definition is biased toward demonstrating psychopathology in CFS.  Although it is possible that the next CDC definition will be an improvement, this seems unlikely.  In a recent question-and-answer session with patients, the head of the CDC’s CFS program, Dr. Elizabeth Unger said that she thought the CDC could be “lumpers one day and splitters another” (lumpers referring to more inclusive definitions and splitters to more precise ones).  She also said that she thought that heterogeneity has been the barrier [to moving forward in our understanding of ME and CFS].  It is unnerving that she thinks that heterogeneity is the barrier, and yet she is unwilling to improve consistency by promoting a splitter-definition over a lumper.  She may feel more of an allegiance to past failed efforts of the CDC to appropriately define the diseases than she does to rapidly advancing research that will help to alleviate the suffering of patients.

It is obvious that more research must be done to specifically address the problems that the multiple definitions have created.  NIH should be actively promoting this effort.  A possible solution is an NIH-funded symposium whose task would be to address the definition problem and the resulting methodological challenges with the goal of creating standards for research within a year.   

It is important that outside groups either validate or challenge CDC’s efforts.  However, this should not delay other research, especially in the areas of biomarkers and therapeutics.  Patients should not have to wait for therapies because researchers are squabbling over the small details of definitions.  We have two serviceable definitions:  Canadian and Fukuda.  For now, the best solution is probably to recruit only patients who meet both sets of criteria, but it may also be possible to use a study design that incorporates patients who meet one and/or the other.  It is also possible to improve Fukuda by requiring post-exertional malaise.  In any case, it must be very clear what definition is used, and it will be important to analyze data collected in such a way that it can be leveraged to clarify the definition problem.  It is vital that the definition used be stated in the abstract to the article, so that clinicians and researchers can rapidly ascertain the study’s relevance to their patient population.  Continuation of the effort to delineate minimal data sets is also very important. 

Yet another barrier:  will

To members of the patient community it does not appear that HHS is really interested in promoting research or other solutions to the problems and challenges that American citizens with ME and CFS face.  We have asked to meet with high level officials in the Department and have been told that our only avenue of communication with the Department is the Chronic Fatigue Syndrome Advisory Committee (CFSAC).  Patients have attended meetings of the Committee with great difficulty and at great personal cost.  The Committee has made some excellent recommendations to the Secretary, but these recommendations have mostly not been implemented.  Most recently, three revenue-neutral recommendations have been ignored:  a condemnation of the empiric definition (2009), a recommendation to remove the CDC’s clinical guidelines from their website (2012--see Mary Dimmock’s testimony about the Toolkit), and a recommendation to post the IACFS/ME Primer instead (2012).  There have also been multiple recommendations to increase funding for research and for centers of excellence for research and clinical care.  NIH research funding for CFS is currently $6 million per year.  This level of funding is 220th out of 232 diseases.  There is no funding for ME, i.e., no funding that requires using the Canadian definition.  There are no centers of excellence.

No HHS official has given an explanation as to why the three important, revenue-neutral recommendations (empiric definition, toolkit and primer) have been ignored.  To date, Dr. Koh’s comments have given no indication that he is aware of those recommendations or of their importance.  At this point, many patients are asking, what is the point of this committee?  If it cannot accomplish small tasks that probably only require a single bureaucrat’s signature how can it ever accomplish something more substantive like significantly increased funding for research, education and clinical care?  What, then, is the purpose of this committee?  CFSAC costs $234,532 annually. This money could fund a study of natural killer cell function in Canadian Consensus Criteria-defined ME/CFS patients and/or a study to determine appropriate dosing of rituximab for ME.  As a taxpayer, I am extremely concerned that we are spending nearly a quarter of a million dollars each year on a committee whose recommendations are routinely ignored by HHS.  We have begun discussions about this problem with our legislators.

We feel that CFSAC, as it is currently functioning, is not meeting our need for an urgent, coordinated and fully funded federal response to ME and CFS.  Here is a link to the reply we received from Dr. Koh, Assistant Secretary for Health, when we asked to meet with him and key deputies to discuss our concerns: .  The full text of the letter can also be read in testimony submitted to CFSAC by Denise Lopez-Majano.  Of note, in response to a request for patients to have direct input on the Ad Hoc workgroup Dr. Koh stated, “While the [Ad hoc] workgroup and its charge are inherently internal to HHS, some of the members are also ex officio members of the CFSAC where they hear the stakeholder perspective. CFSAC provides a mechanism to ensure stakeholders are engaged and have the opportunities to offer input.”  I would suggest that CFSAC keeps stakeholders engaged in activity that consistently leads to no results and gives the opportunity to offer input that is consistently ignored.  This has to change.

If CFSAC is to become a more effective avenue for cooperation between the patient, clinical and research communities and the federal government that produces substantive action to rapidly improve the lives of citizens with ME and CFS, we need to see some changes in how it functions.  We need to be able to question the ex officio members and Dr. Koh directly.  We need frequent updates on the activities of the Ad hoc workgroup (we have had none to date).  We need to see the promised report from the NIH the State of the Knowledge conference 18 months ago.  We need to discuss many other important issues.  We need to see substantive recommendations implemented.  We need to see progress.  If CFSAC continues to be ineffective and its recommendations are ignored, it should be disbanded.  A more productive process must be implemented.  We need to meet with Dr. Koh and key deputies from HHS to discuss these issues.

We look forward to a better future.

Wednesday, October 10, 2012

"See you later"

The news comes that XMRV Global Action  (0n Facebook) is saying "Auf Wiedersehen". This is a bit of disappointing news to say the least. It seems that the world of ME/CFS information and communication is shrinking dramatically in the last few weeks.

Since late 2009, XMRV Global Action has been a clearinghouse for information on neuro-immune illness. They did a first-rate job and their site was the go-to site for many of us. Somehow they were able to consolidate the important current issues without a lot of clutter. This of course is useful to many who cannot spend a long time on the computer - or for those who have trouble focussing.

This website was extremely useful to me over the years and I am not sure how I am going to replace their information feed. I can say the obvious. I won't be able to. I am going to miss a great deal of information now - information that was essential to form an opinion and a course of action with this difficult illness.

As a daily reader of the site I want to thank the six or eight sponsors, those who ran the site, for their generous daily efforts. What they did was just great. It could not have been done better and many of us are indebted to their joint enterprise. Hopefully someone else will be able to step forward and fill the void left by their departure. Certainly those who ran this site have given others a fine matrix to follow.

Friday, October 5, 2012

Mold – “A Tough Tussle”

The fantastic writer Ambrose Bierce wrote a short story, a quite frightening piece, called “A Tough Tussle”. The story concerns a Civil War soldier’s deadly nighttime struggle with an unseen or unknown terror. “A Tough Tussle” and Brainerd Byring’s frightening incident come to mind when I think of my own experience with another unknown or unseen terror: Mold.

My daughter got sick with a neuro-immune illness in 2002 and stayed about half sick for three or four years when she went downhill.  Prior to her downhill crash in 2006 she moved to St. Paul, MN from NYC.  In St. Paul she lived in the same apartment until May 2012.

I became suspicious of the building in which my daughter lived after reading about mold as a complication for neuro-immune illnesses. I went through her entire building, attic and basement, and saw no evidence of water damage or water intrusion. I spoke to her landlord who has owned the house for thirty years, and he said that there had been no water intrusion in the time that he owned the building. Upon closer questioning he did reveal that when he first bought the building, he looked into a square hole (no longer there) in the floor of the basement and was surprised to see water, and that something floated by on the surface of the water indicating that the water was moving. This gave me an idea and I went to the historic society of St. Paul and found a map of the property prior to the house being built in 1920. It appeared from this map that the house had been built on a stream bed.

Over a period of several years I did two ERMI tests of my daughter’s apartment and they were both high. They registered 11 and then 7, both with an extremely high Aureobasidium pullulans.  As with all molds it is difficult to find out much about this strain  - except that it is associated with water. This made sense if the house was actually built on a stream bed. Aureobasidium pullulans does not seem to be a dangerous mold, but who knows?

During these years my daughter was too sick to consider moving from the premises.

Circumstances led me to move into the apartment below my daughter. It is a two apartment building so I had control of the entire building. I was shocked in October 2011 to get an even higher ERMI test for the ground floor apartment, which I now occupied – 17, including another sky-high Aureobasidium pullulans.

With this test I decided to do what I could to remediate this building. In the next month I went over every square inch of the building, first cleaning it and then spraying every surface with a concoction of vinegar, borax, oil of oregano, vodka and clove. I cleaned and did the mold treatment on all floors, walls and ceilings including the basement and the attic. I found a small amount of mold in the basement eaves that I remediated myself.

I did another ERMI test that came down significantly but was still irritatingly high. Of course, with my remediation, I was unable to get into the walls or the floors.

At this point I bought a number of dehumidifiers and was able to lower the humidity in the basement to about 40%. It is believed that mold does not grow under 50% humidity. I was shocked to find the humidity in the attic was close to 100%. The reason for this was that the landlord had put insulation down on the floor of the attic, a short-term solution for insulation, but one that will lead to the roof rotting. I pointed this out to him, did him a favor, and took up the insulation. Thus, I was able also to lower the humidity in the attic below 50% with a dehumidifier.

This remediation was completed in November 2011, and the low humidity in the building continued until my daughter was able to move out of the apartment in May 2012.  Over that time, November 2011 to May 2012, she made slow but steady improvement with one major setback. However, she was strong enough on May 2, 2012 to make this move to an apartment ten blocks away – and the move went without incident. 

There are various other reasons – beyond mold remediation - that one might point to for her improvement – primarily the introduction of the probiotic formula MAF 314. This occurred simultaneously with the mold remediation – in October 2011.

My daughter’s slow progress has continued in her new apartment. While she is better, she still remains quite ill.  I have not done an ERMI test in the new space.

Over the last few years she has done a number of tests that measure global cytokine activity or inflammation or NK cell function. Among them are:

c4a – at Jewish National lab, Denver

In 2011 my daughter’s c4a was 15,210 (0-2830). In March 2012 it had come down to 7,377 (0-2830). I imagine that it would be even lower now. I will find out soon.

MMP-9 – at Quest

In 2010 her MMP-9 was 888 (0-985).  Disregarding the Quest lab's normal parameters, Dr. Ritchie Shoemaker says that anything over 332 is high. In March 2012 her MMP-9 was 1325 (0-985). In September 2012 her MMP-9 dropped to 272.

Functional NK (LU30) - at Focus lab

Over the past year my daughter's functional NK cell has gone from 17 to 21 to 34 (9/2012).

There is another useful test which I need to repeat. It is a urine test from Realtime labs and measures three mycotoxins.

Do I think my daughter’s illness was caused by mold? No, I do not think that mold caused her illness. Do I think that mold was a complicating factor? I think the evidence points to this, but, like all things with this illness, we will never really know. I think she lived in a sick building.