Sandra Finley

Oct 292024
 

According to grant documents obtained by Children’s Health Defense via a FOIA request, the NIH is spending $2.2 million in taxpayer money to test personalized “nudges” to coax older people into getting more vaccines.

brain and vaccine bottle

Using U.S. taxpayer dollars, researchers at two universities are identifying older people behind on their recommended vaccines and testing personalized “nudges” to coax them into getting more shots. nih-nudge-more-vaccines-feature.jpg

According to grant documents obtained by Children’s Health Defense (CHD) via a Freedom of Information Act (FOIA) request, the National Institutes of Health (NIH) is funding the $2.2 million “BE IMMUNE” clinical trial, which began in 2020 and will run through 2025.

Researchers at the University of Pennsylvania and the University of Washington are using Electronic Health Records (EHR) data — the electronic records from doctors’ offices containing patients’ detailed health and demographic data — to target African American, Hispanic and Asian people with lower flu, pneumococcal and herpes zoster vaccination rates.

The ongoing study blames the “poor vaccination rates” on patients’ and clinicians’ “widespread decision-making biases.” The trial is testing strategies drawn from behavioral economics, which uses insights from psychology to understand — and in this case to “nudge” or direct — people’s decision-making behavior.

The randomized controlled study is headed up by Dr. Shivan Mehta and a team of healthcare management experts who combine medical and business-based strategies to run studies like these.

The trials often are based in Penn Medicine’s in-house “Nudge Unit,” where behavioral design teams are dedicated to figuring out how to influence patient choices.

The grant is part of a massive initiative by the NIH to increase vaccine uptake by changing how people make decisions. The initiative has included hundreds of millions of dollars in grants since 2020 to create “culturally tailored” pro-vaccine materials to promote COVID-19 and flu vaccines.

It also included more than 50 grants worth $40 million designed to increase HPV vaccine uptake.

 

Testing the ‘ladder’ of behavioral interventions

The study is testing different “nudges” at more than 100 primary care practices at Penn Medicine, University of Washington Medicine and the Veterans Affairs Health System, one of the world’s largest EHR vendors in the world.

Over 1,000 primary care physicians and thousands of eligible patients at those practices are involved in the trial.

The range of tested interventions is scaled on a ladder.

Nudges lower on the ladder try presenting people with information so they can make their own decisions about vaccines —- methods that typically are not very effective for increasing vaccine uptake, the researchers said.

Nudges higher on the ladder either prompt people to make decisions, or simply plan their decisions for them.

For example, one nudge automatically sets up vaccination appointments for people, compelling them to go to their appointment and get vaccinated unless they intentionally opt out.

Credit: NIH

The “opt-out” framework has been effective in other areas of healthcare, such as colorectal cancer screening or persuading more people to take their flu shots, the researchers reported.

Netflix uses prompts to encourage binge-watching — healthcare should prompt people to get more shots

Penn’s “Nudge Unit,” which bills itself as the “world’s first behavioral design team embedded within a health system,” houses the study, which is also being conducted in a similar unit at the University of Washington.

Economist Richard H. Thaler and legal scholar Cass R. Sunstein popularized nudging in their 2008 book, “Nudge: Improving Decisions About Health, Wealth, and Happiness” as a method to create a “choice architecture” designed to influence people’s behavior in a predictable way “but without restricting choice” — particularly for policies or measures that might otherwise be unpopular.

Penn launched its Nudge Unit in 2016, inspired by British Prime Minister David Cameron’s Nudge Unit, established in 2010 to shape citizen behavior in the United Kingdom — a strategy the Penn researchers thought should also be applied to healthcare.

Penn’s Nudge Unit founders argued in a 2018 New England Journal of Medicine article that healthcare should use the same strategies businesses use to influence consumer behavior.

For example, they said, airlines require consumers to actively choose whether to purchase trip insurance before they can buy a plane ticket. Netflix changed its default settings to automatically play the next episode in a TV series to encourage binge watching.

“Similar opportunities exist to direct clinicians and patients toward better health care in situations where there’s consensus about desired behaviors,” they wrote, citing effective drugs, vaccines and targeted therapies as examples.

The strategy is being implemented globally — management consulting firm McKinsey reported that about 400 “nudge units” had been established globally by 2021.

However, even the Bill & Melinda Gates Foundation-backed Gavi concedes, “the theory has its critics — detractors argue that nudges can be paternalistic, invasive, ideological, and coercive in ways that erode public trust.”

The researchers behind this study also found that often the nudge approach doesn’t work.

In those cases, they argue “a stronger intervention—a ‘shove’—may be needed.”

October is Vaccine Injury Awareness Month. It’s also the launch of CHD’s Million-Dollar Match campaign. Please donate today to help Children’s Health Defense raise $1 million by October 31.
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EHR — an opportunity to scale up the nudge

The researchers celebrated EHR for offering a unique opportunity to develop and rapidly scale up personalized nudges.

The records increasingly are used for research and clinical trial recruitment because they contain a wealth of data. And new technological tools now allow researchers to “mine, assimilate, analyze, link, reproduce and transmit information” gleaned from that data.

Twila Brase, a registered nurse and author of “Big Brother in the Exam Room: The Dangerous Truth about Electronic Health Records,” told The Defender most people think the privacy of their EHR is protected by the Health Insurance Portability and Accountability Act, better known as HIPPA — but that’s not the case.

HIPPA only guarantees your data will be secure as it is passed among the various entities that have access to it, including researchers, Brase said. And that access can be provided without your consent.

“Nowhere in the law does HIPPA give you control over your medical records,” she said.

Because the records contain massive amounts of personal information that can be used and linked in many different ways, researchers studying EHR-based research argue that the use of EHR also raises “pressing questions concerning privacy, confidentiality, and patient awareness.”

They say that the use of one’s EHR data for research reasons can be confusing or even impossible to opt out of because often the provision of healthcare is linked to accepting a policy allowing researchers to use EHRs.

And EHR research often operates on the same logic as the nudge — an “opt-out” approach where permission is assumed unless a patient explicitly indicates they want to revoke it.

Oct 292024
 

 

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Oct 272024
 

A speech by The Prince of Wales on the 150th Anniversary …

The Royal Family
https://www.royal.uk › clarencehouse › speech › speech-…
– – – – – – – – – – – – – – – – –
Jul 5, 1991 — We will build a better future for the mentally ill because we know what ‘better’ means, and it means radical change in society’s assumptions.

. . .    forcing yourselves to listen to me. However, I can only assume that if your professional reputation is anything to go by, I should at least be guaranteed the best audience I have ever had!

Personally, I think I need my head examined for coming all the way to Brighton merely to reveal my lamentable ignorance about the complex problems with which you have to deal in your professional lives. By the time I have finished this morning, I dare say it shouldn’t be too difficult to diagnose what is wrong with me, and no doubt you will then all argue furiously over the course of treatment to be prescribed. My guess is that you will recommend complete rest for another two weeks accompanied by a total abstinence from stress-inducing speeches…!

Talking of stress-inducing speeches, I am afraid I don’t have a very good record when it comes to the 150th anniversaries of professional bodies. The British Medical Association and then the Royal Institute of British Architects discovered, too late, the folly of their invitation to such an unreliable speaker! I can only imagine you have invited me under the delusion that you can actually cure me! Whatever the case, please know that I come here today as someone who is honoured to be your Patron, who brings you heartfelt congratulations on the achievement of such a distinguished anniversary and who makes no pretence of speaking in any other capacity than as a layman. But you must forgive me if I speak from time to time from the heart – it is a congenital defect!

In this spirit I want you to know how much I sympathise with you in what must be, at times, a literally soul-destroying task. As a profession your calling is to try and bring a measure of healing and comfort to the mental anguish and suffering of countless numbers of people. And yet you have to operate in an environment which I suspect most people who consider themselves sane and ‘normal’ (whatever that is!) prefer to shun or make jokes about. Not only that, but you are also working within the confines of current society, whose attitude and outlook must necessarily colour your approach.

I know that there have been many debates both within and without psychiatry as to what is a helpful definition of mental health, but as yet no proposal has won general agreement. I can imagine, therefore, that psychiatrists are often left with having to respond to people with acutely disturbed behaviour and to try to offer treatment that will lessen or eliminate the extreme behaviour presented – for the person and those around them.

I know, too, of the countless debates there have been within the profession regarding the nature of the task you have set yourselves in the last 150 years – in particular the arguments about psychotherapy and psychiatry, the latter having grown out of a branch of general medicine and which therefore is concerned with finding a physical basis for the major psychiatric disorders.

A hundred and fifty years ago, people had very limited, but nevertheless clear and important, definitions of madness. They had little idea or understanding of the causes but were quite clear that madness was to do with unacceptable behaviour. The term described certain forms of violence, and unacceptable responses to social situations. It constituted a failure to relate to other human beings. In some respects this is a definition from which we have not advanced, but during that time generations of psychiatrists have made major progress towards understanding and treating mental illness. It is, therefore, perhaps disappointing that society’s understanding and acceptance of mental illness has developed so little during the same period, and that there is still somewhat of a social stigma attached to it.

A stigma is ‘a distinguishing mark of social disgrace’, and ultimately comes from a Greek word meaning ‘to tattoo’. This appropriately conveys the image, for the mentally image person, of being branded; perhaps the one who causes a disturbance on the Underground, or someone whose unacceptable behaviour embarrasses family and friends. The quiet, unobtrusive sufferer from depression understandably fears being tarred with the same brush. As a result he dares not admit to symptoms and so does not receive treatment until he or she has suffered greatly for an unnecessarily long time. This stigma makes the whole of life even more difficult for both the mentally ill and the mentally handicapped; it affects the patients themselves, their relatives and all who deal with them. This tends to include mental health professionals, who themselves can become subtly tainted.

I know that the Royal College of Psychiatrists aims to try and remove this stigma altogether and is working to lessen its effect. Providing the facts for the general public about the different mental illnesses is helpful, and efforts in public education such as the College’s ‘Beat Depression’ campaign can certainly help. The media obviously have an important part to play in the process and there are shining examples of what can be done, such as the series of articles by Marjorie Wallace in The Times which not only aid the foundation of contemporary understanding of schizophrenia, but also led directly to the formation of a charity called SANE, of which I am Patron. As Professor Anthony Clare said in his keynote speech two weeks ago, at the start of your celebrations: ‘What SANE has done is to strip back the curtains surrounding mental illness, so that the condition is no longer so mystifying. As a result sufferers and families no longer need to feel so neglected and isolated.’

There are, is has to be said, sections of the media which do not take such an enlightened view and (perhaps reflecting the views and prejudices of their readers) will go to great lengths to avoid any serious discussion of mental illness. I believe that the difficulty sufferers have in talking about their illness and treatment, and the secrecy surrounding it, gives an added responsibility to professionals like yourselves to speak up, and in terms that everyone can understand. Heart by-pass operations and transplant surgery attract enormous interest, and there is no shortage of ex-patients to testify to the success of the techniques. But disorders such as severe depression and schizophrenia are largely ignored and opportunities for us all to learn anything about their nature and treatment are virtually non-existent.

This same taboo on the public discussion of what are, afterall, common illnesses has led, I believe, to a general undervaluing of the work of psychiatrists. Not unnaturally, the brilliant work of our best surgeons attracts a certain sort of glamour. We marvel at, and are grateful for, their successes and share their sorrow when a patient cannot be saved. But psychiatry remains largely unsung – perhaps because it is also, inevitably, unseen. Its triumphs are, almost by definition, private; invisible to the public eye. And when there are significant failures how often does anyone register the impact they have on the psychiatrists who have done their best? On the contrary, the public perception is all too often negative, driven by the same stigma which attaches to their patients and, quite possibly, to people who are rash enough to make speeches about the subject!

It is sad that society does not generally seem to recognise what it asks of its psychiatrists. Of all the areas of specialist medicine, you cover perhaps the broadest range of disorders, only outdone by the GP, who also has a key role in the identification and treatment of mental illness. You certainly deal with what is by far the most complex organ in the body. In the absence of anyone else, we would like you to solve all the problems of society. We confront you with the most complex problems, part biological, part psychological, part social and part spiritual, and expect you to unravel them, treat all the parts that belong to psychiatry and at the same time somehow make better all the parts that don’t belong to psychiatry.

I am sure it would be helpful if more people understood that a psychiatrist’s first problem is to decide how to reach out to a patient, how to make them feel understood, cared for, and safe. Frequently, patients are frightened, not only by their pain, suffering or madness, but also by the image of psychiatry which they may have gained from films or highly biased sources. I am told that a recent film ‘The Silence of the Lambs’ portrays psychiatrists in a quite terrifying manner, which is no doubt a help at the box office, but is none at all to the psychiatrists – or to those in need of their help.

In our contemporary society there is every incentive to believe that suffering can be banished, avoided or at worst postponed. Psychiatrists have to confront the evidence to the contrary every single day. Just being with a patient who is frightened or frightening must be incredibly difficult and takes immense courage and dedication; the human contact can awaken shadows in the doctor’s own psyche, testing that inner strength which has the most profound influence on the patient. To listen and share in someone’s pain takes great bravery and it deserves recognition.

In a day’s work psychiatrists and psychotherapists will doubtless hear many dark and terrible stories; of loneliness, isolation, poverty and bereavement. Despite the best efforts of social services, and other caring agencies, children do suffer at the hands of their parents, guardians or other adults. Physical and mental abuse are not uncommon and tend to be perpetuated from one generation to the next. Other children and adults suffer not through the deliberate will of others, but through misfortune, accident, bereavement or other crisis.

Many people are somehow able to re-direct this neurotic energy into creativity, perhaps at work, or through various forms of artistic expression, or in spiritual understanding and healing. But for reasons that you and your colleagues are only slowly unravelling there are also people for whom suffering leads to pain, anxiety, depression, drug abuse and other forms of mental illness.

Between these two groups are a great many other people who respond to medication, and yet at the same time are influenced by the amount of stress or suffering to which they are exposed. I am told that before modern drugs were available patients with schizophrenia were routinely admitted to hospital and for some of them their symptoms would be ameliorated by providing a structured, peaceful and caring environment. Similarly, it is now known that schizophrenia patients receiving medication need more medication if they are in a family environment which is highly stressed and less in a family which is supportive, and yet accepting, and where there is understanding of the illness.

As I said at the beginning of my lecture, it is not surprising that there has been a lot of discussion about the relative merits of the biological and psychosocial approaches to problems of the psyche. One school of thought claims that mental illness is in the last resort a physical disorder to be treated by physical means. New drugs make this a powerful and effective approach, which has certainly led to a dramatic relief of symptoms and greatly reduced periods of hospitalisation. At the same time the power of the technique is such that a psychiatrist faced with a distressed or unhappy person, and probably in a crisis situation, may have to resort to a ‘chemical cosh’ too readily, in order to calm someone quickly – substituting drugs (which can lead to dependence) for the time and understanding which could conceivably rescue the patient from his predicament.

The other school of thought believes, as you all know better than me, that mental illness is primarily a behavioural malaise, to be treated by methods appropriate to such a disorder. It uses drugs and physical techniques as sparingly as possible, and relies on reaching a close rapport with the patient, helping him or her by psychological analysis in depth to integrate apparently conflicting emotional drives. This view, too, has its undeniable quota of success, but is difficult to apply on a large scale, if only because of the prohibitive cost in time and medical manpower.

Having made my own views on over-reliance on medication known to the British Medical Association some years ago, and having spent time since then in encouraging what I prefer to call complementary practice, it will not surprise you to hear that I am concerned, for what it is worth, that the psychological approach to mental illness should not be forgotten or discounted.

I know that this College recommends the lowest possible dosage of drugs and encourages the use, wherever possible, of psychological techniques, but all the enquiries I have been able to make have suggested that the training of psychiatrists is heavily weighted towards the medical approach. This may be a reflection of a society which some people would say is overly materialistic, with the emphasis too much on doing and changing, and not enough on being and accepting. The power of the medical techniques is undeniable. They have brought real benefits and no-one would wish to deny that. But I would have thought that over-emphasis on drugs can also enable us as a society to lose sight of problems which have their roots in the way we treat each other.

A teenager with hallucinations and strange beliefs may be diagnosed as schizophrenic and be provided with the extensive help and support he or she needs. But another similar teenager may have other serious difficulties – perhaps an inability to form stable relationships, a tendency to violence or to take overdoses during outbursts of uncontrollable rage. Both teenagers need care. The schizophrenic fits neatly into the medical model, whilst the other may be labelled as ‘delinquent’ or assessed as having a personality disorder. Both conditions are treatable and both require a great deal of time and resources, not only from psychiatrists. One is understandable in terms of illness, the other only in much broader terms, which may involve facing unpleasant realities about our society. No doubt there are people who would say that the patient with a personality problem is not the concern of the psychiatrist. But without proper help and discretion such adolescents may go on to deprive and, perhaps, even abuse their own children.

The medically trained psychiatrist could be forgiven for feeling at a loss when faced with a disturbing and frightening young person who neither needs nor responds to medication. I believe there is a need for training which emphasises to psychiatrists that there will be times when they will feel overwhelmed when faced with people who have suffered greatly; that there will be times when it is important to remain with and be with and comfort such a person in their suffering. Psychiatrists rightly emphasise the importance of communicating clearly and skilfully, and I welcome the growing importance being given to listening and counselling skills in all branches of medicine. Sometimes there is a need for doing, but equally there are times for being with, for waiting, for being patient and for allowing spiritual healing to occur. There is a sense, too, in which suffering, if handled sensitively, can be transmuted into a positively redeeming process. I was talking recently to the wife of a Church of Scotland Minister who told me that as often as not she and her husband are left to pick up the pieces with people who have failed to respond to psychiatric treatment. She told me that she has only witnessed a true transformation in such people when they finally discover within themselves that transfiguring dimension we define (or perhaps I should say that some of us define!) as God. Above all, perhaps, students need to be taught that growth and healing are natural processes. Science can accelerate them, but it can also retard or prevent them.

Ladies and gentlemen, I was interested to observe that the motto of your College is ‘Let wisdom guide’. For what it is worth, I believe we need to be reminded occasionally that wisdom has a far more profound meaning than just the acquisition of knowledge in the modern scientific-materialist sense. Should we not be asking ourselves pretty carefully where scientific materialism has been leading us – and, indeed, what kind of society it has been creating? Is there not an imbalance that needs correcting; an abandoned element that requires rehabilitation? It is perhaps worth recalling that Jung himself told one of his associates that he did not want anybody to be ‘Jungian’. “I want people above all to be themselves. As for ‘isms’, they are the viruses of our day, and responsible for greater disasters than any medieval plague or pest has ever been. Should I be found one day only to have created another ‘ism’ then I will have failed in all I tried to do.”

At the risk of being controversial, (which at least has the advantage of providing a useful source of conversation over lunch!) I would like to pose a few thoughts to you.

In Ancient Greece, sickness of the soul or psyche needed not the care of ancient medicine or a physician, but exclusively a god or saviour named Asclepius. The reason for this was that classical man saw sickness as the effect of a diving action, which could be cured only by a god or another divine action. Thus a clear-form of homoeopathy was practised, where the divine sickness was cast out by divine remedy. “When the sickness is vested with such dignity, it has the inestimable advantage that it can be vested with healing power.” Thus said CA Meier in his ‘Healing Dream and Ritual’.

Such explanations, of course, run totally counter to ‘modern’ explanations of mental illness. The modernist will doubtless accuse the proponents of theocentric views of wanting to tip psychiatry back into the dark ages, and bring back ghouls and ghosts and other irrational explanations that muddy our scientific understanding. But perhaps, then, we can ask for an explanation as to how and why such illness does arise? Although it may be categorised and its manifestations damped down, I would suggest it is very hard to explain its intrinsic cause.

Is it not because the irrational forces of the universe have been ignored so completely for so long that they can come with such power into the lives of people who have no conception of what is happening? Without experienced people who work in those worlds, containment, transformation and healing are surely very difficult.

It seems to me that the meaning that illness has for us is, to a large extent, conditioned by our view about the purpose and goal of the life we are given on this planet. In other words, for the materialist, enlightened self-interest would lead us to see illness as of no value and with no meaning, whereas someone with a religious view of Creation will need to think about it in a much larger frame than merely the restriction of the individual’s ability to do all that he or she could. If wisdom is to be your guide then Shakespeare makes a few salient points when Macbeth speaks to the doctor about Lady Macbeth, thus –

‘Canst thou not minster to a mind diseased, Pluck from the memory a rooted sorrow, Raze out the written troubles of the brain, And with some sweet oblivious antidote Cleanse the stuffed bosom of that perilous stuff which weighs upon the heart?’

The conclusion of the matter was ‘more needs she the divine than the physician’. I do not expect you to agree with me, but I believe that the most urgent need for Western man is to rediscover that divine element in his being, without which there never can be any possible hope or meaning to our existence in this Earthly realm. As Wordsworth wrote with such profound insight –

‘And I have felt A presence that disturbs me with the joy Of elevated thoughts; a sense sublime Of something far more deeply interfused, Whose dwelling is the light of the setting suns And the round Ocean and the living air, And the blue sky and in the mind of man; A motion and a spirit that impels All thinking things, all objects of all thought, and rolls through all things.’

At the heart of many religious, psychological and psychiatric writings is a recognition of the importance of the way in which all the members of our society are inter-connected and inter-dependent, and the need to look at the whole person in the whole society. This, of course, runs directly contrary to our natural instinct to attempt to deal with the complexities of contemporary life by breaking it down into different components. Yet experience shows that if we do not address the whole of a person’s needs within the whole of the society in which that person lives, treatment will fail.

I do believe that we are in danger of cutting ourselves off into a world that recognises only mind and body. But in the treatment of mental illness we must surely recognise the importance of understanding and respecting the culture and beliefs of the individuals concerned and of those close to them. When – as is too often the case in our generation – there seem to be no beliefs, but simply a spiritual vacuum, there are no foundations on which to build an acceptance of our own weakness, respect for the unique worth of others, and a reconciliation between those classed as mentally ill and the society in which we must all live.

To take just one example, I believe that one of the conditions most commonly encountered by psychiatrists is depression and anxiety. One of the main causes seems to be the lack of acceptance of suffering in a society which focuses on immediate gratification. We find it hard to accept that there is a need to adapt to loss, and to grieve, and we are intolerant of people who are emotionally distressed. Often their distress is made worse because they do not have the inner resources and spiritual development which would enable them to see that there is a meaning beyond themselves.

Treating the whole person within the whole society should perhaps be easier to achieve under the policy of community-based care, with local services designed to help people live as fully and productively as possible, despite their problems or disabilities. I know there are problems and challenges in making the new system work properly, but it does seem that the debate about whether community-based services (in which the role of the hospital is clearly defined) are right in principle, is over. The challenge now is to put those locally-based services in place in every district, in keeping with the need for them.

At this point and at the risk of repeating what you already know only too well, it may be worth reminding ourselves of the scale of the problem of mental illness. Quite apart from the cost in terms of human misery, the Mental Health Foundation has calculated that in 1989 no less than 71 million working days were lost in the United Kingdom because of mental illness; this represented 17% of all sickness absences from work, and cost this country nearly £4 billion in lost working days. Other research has shown that in every thousand people, 250 will suffer from a diagnosable mental illness. Of those 250, 17 will go to a psychiatrist and six will subsequently enter hospital. That is perhaps a salutary reminder of how much larger the problem is than even you encounter, and I have no doubt at all that some of those you do not see are just as ill as those you do.

But what sort of service do the mentally ill want, what do their relatives want? As you know, most want to live at home, to live their separate lives as far as possible like the rest of society. Patients tell me that they do not wish to go to hospital, and yet relatives tell the most awful stories of the deprivation, suffering and terror that they endure in trying to help their loved ones through their illness at home. It seems to me that if community-based care is really going to provide proper support we will need to find ways of giving greater strength, solidity and dependability to local services. But there must also be proper provision for those patients whose overriding need is for refuge and asylum. There will always be people who need a place of sanctuary where they can work through their pain and suffering, with professional support available 24 hours a day, and learn to adjust to their illness and all that it means in terms of loss of ability and potential. To recognise this would be a useful step forward in national policy.

I realise how difficult it must be to make such a complex and far-reaching change in the system as the current move to a community-based service. Though the mental hospitals could be stultifying and disabling, they must have been easier to manage than a network of smaller, sometimes almost invisible, local services. Developing and coordinating all these different community services is difficult, too, in part because many of the critical variables are outside the direct control of mental health professionals, planners or managers. Housing, for example, is a vital ingredient which regrettably is often lacking at present, causing all sorts of problems for individuals and for those who are trying to provide the service. It must be very depressing and de-motivating for psychiatrists to do their best for their patients and then be unable to discharge them to decent housing and the prospect of work. At the moment I know there are times when some of you have to discharge patients into poor accommodation, without supervision, often in a deprived area, and without the knowledge that this is going to aggravate their illnesses and result in their return to hospital. Clearly we need to forge new partnerships, not only between health and social services, but also involving housing authorities and housing associations.

What is also frustrating is how confusing the reports on all this tend to be. No one seems to know on a national basis what is really happening to people being diverted or discharged from mental hospitals. Studies of those resettled from hospital are generally very encouraging, but we know much less about those who have fallen through the cracks and those who might have been hospitalised in a previous era. I believe there is a need to monitor what is happening more carefully in order to get the national picture into focus. As a BBC Panorama programme earlier this week illustrated, there are undoubtedly people appearing in the accident departments, the courts and the prisons who represent the casualties from current policies.

These problems should not lead us to suggest, however, that we abandon the idea of locally-based care. But we do need to find a constructive middle path between over-protection in institutions and abandonment to uncaring communities, impoverished lives and, at worst, homelessness or incarceration.

I am told that good examples of such progress can already be seen here in Brighton, , but also in such places as North Lincolnshire, Exeter, Torbay, central Birmingham, Nottingham, Bath and Newcastle. The need now is to speed the spread of this good practice throughout the country.

I realise that accomplishing all this in a time of financial stringency is far from easy. But I do think it is important for all the key players to come together in a variety of ways at national, regional and local levels to clarify what needs to be done and how best to do it. This will require a general spirit of collaboration that cuts across old territorial boundaries – never, I realise, an easy thing to achieve.

In this connection I very much welcome the setting up of the Centre for Mental Health Services Development as part of the Institute of Health at King’s College London. I understand that this is supported enthusiastically by both the Mental Health Foundation and the Department of Health and that its Advisory Board is graced by the presence of your President.

So far as money is concerned, the re-shaping of the mental hospitals really does release a lot of money, on which the first call, I suspect, ought to be funding community care for the mentally ill. At present, I understand that over half of the £1.5 billion spent on hospital and community services supports just 40,000 patients in the remaining large hospitals. Less than half supports many hundreds of thousands of patients in the community, many of whom are at least as disabled by their illness as those in hospital.

I believe it is also important sometimes to listen to those who actually use the mental health services. I have been impressed by what I have heard about what is known as the ‘self-advocacy’ movement. In a previous era no one would have believed that people diagnosed as schizophrenic or manic depressive could eventually be capable of providing advice on policy and planning. But this is just what is now happening. Clearly, even people with very real illnesses and disturbances don’t remain so all the time. And some get very much better and can become an inspiration for others. It is therefore encouraging to learn that the College has already set up a Patients’ Liaison Group.

Another group with a major contribution to make is the General Practitioners. Very many people with psychological symptoms consult their family doctor, but in about half of all cases the GP does not recognise the condition as a psychiatric disorder, and even where the condition is regarded as psychiatric it may go untended. This is hardly surprising as it is still possible to enter general practice as a Principal with as little as eight weeks experience of studying psychiatry. I would have thought that there was an urgent need for training for GPs in psychiatry, both in the identification of mental illnesses and in their effective treatment. Since I am about to become next year’s President of the Royal College of general Practitioners (they need their heads examining as well!), I was interested to learn about an exciting development in community psychiatry which aims to foster close working ties between these two groups of professionals. The Liaison in Community Psychiatry programme (known as LINC-UP) begins with a nationwide survey of all psychiatrists at this conference, and I hope you will all be able to give it your support.

Another area which I hope you will support and encourage is the perhaps somewhat undervalued task of research. This country has a proud reputation in this area, and I know that biological researchers in psychiatry and allied fields are currently beginning to make significant inroads into our understanding of the functioning of the brain. Of course such research is expensive, and last month SANE asked me to launch an appeal to enable the founding of an International Schizophrenia Research Centre in this country. It was the most wonderful start to be able to announce immediately that no less than £1.75 million has been pledged to the Centre by King Fahd of Saudi Arabia. The task now is to match this most generous contribution from other sources.

Ladies and gentlemen, I would like to end by suggesting that any vision of a better future for people who are afflicted by mental illness must have its roots in a better understanding of mind and body, and in values that go far beyond the material. We will build a better future for the mentally ill because we know what ‘better’ means, and it means radical change in society’s assumptions.

It is terrible to have made you sit here for so long (you will all end up with bad backs before I’ve finished!) but there are just three main points that I would like to leave you with. Firstly, my encouragement and admiration for your intensely difficult, undervalued work with the large group of people who bear the stigma of mental illness.

Secondly, it is clear that the current national and international policies in psychiatry are moving firmly away from the large closed institutions. That is understandable, but we still need places of sanctuary and we must make community care work. There are now good models of success; projects where community care is working really well. But we have a long way to go before those models of excellence are the universal pattern. That is the challenge in our generation.

Finally, my feeling that there is a need for greater recognition, even among such an enlightened group as yourselves, that mental and physical health are not simply about medical repairs. We are not just machines, whatever modern science may claim is the case on the evidence of what is purely visible and tangible in this world. mental and physical health also have a spiritual base. caring for people who are ill, restoring them to health when that is possible, and comforting them always, even when it is not, are spiritual tasks. Training people for your profession and maintaining your professional skills are not simply about understanding and administering the latest drugs but about therapy; in the original Greek sense of healing – physical, mental and spiritual, and also about wisdom, in the ancient sense of understanding the true nature of our existence enabling those who are ‘seeing through a glass darkly’ then to see face to face. If you lose that foundation as a profession, I believe there is a danger you will ultimately lose your way.”

Oct 272024
 
ASIDE:    HHS = The United States Department of Health and Human Services is a cabinet-level executive branch department of the U.S. federal government created to protect the health of the U.S. people and providing essential human services. Its motto is “Improving the health, safety, and well-being of America”. Wikipedia
Founded: April 11, 1953
Annual budget: $1.631 trillion (2022)
Employees: 83,202
– – – – – – – – – – – –

The House report on HHS Covid propaganda is devastating. 

The Biden administration pushed falsehoods about Covid vaccines, boosters, and masks.

 

Thanks to Dan for submitting.  He writes:  Hind sight is 20/20. But the damage is done.

– – – – – – – –

Sandra speaking: Brownstone text is copied below, in case the link does not work.

Page 85 of the actual Report.  My SURVEILLANCE RADAR picked this paragraph up in skimming.  (Confession:  I didn’t really read all the 113 pages! – – Brownstone did that, but using different radar.)

The scale of the public relations campaign raises serious questions over further entrenching
Big Tech’s role in surveilling Americans and in seeking to influence public opinion. Without more
answers from Google and HHS, it is unclear whether personally identifiable information was in
any way used by Google in the development of the Campaign for the custom search dashboard,
and to what extent children’s viewing habits were involved in the Campaign. Google, like other
Big Tech companies, has been able to bury in their privacy policies what they do with Americans’
information in the absence of a federal data privacy and security standard. Current data privacy
protections have been limited to just minors under the age of 13.  Even with that limited privacy
protection, Google and other Big Tech companies have been dogged for not doing enough . . .

The Most Devastating Report So Far Brownstone Institute

🔗 https://brownstone.org/articles/the-most-devastating-report-so-far/

The House report on HHS Covid propaganda is devastating. The Biden administration spent almost $1 billion to push falsehoods about Covid vaccines, boosters, and masks on the American people. If a pharma company had run the campaign, it would have been fined out of existence.

HHS engaged a PR firm, the Fors Marsh Group (FMG), for the propaganda campaign. The main goal was to increase Covid vax uptake. The strategy: 1. Exaggerate Covid mortality risk 2. Downplay the fact that there was no good evidence that the Covid vax stops transmission.

The propaganda campaign extended beyond vax uptake and included exaggerating mask efficacy and pushing for social distancing and school closures.

Ultimately, since the messaging did not match reality, the campaign collapsed public trust in public health.

The PR firm (FMG) drew most of its faulty science from the CDC’s “guidance,” which ignored the FDA’s findings on the vaccine’s limitations, as well as scientific findings from other countries that contradicted CDC groupthink.

The report details the CDC’s mask flip-flopping through the years. It’s especially infuriating to recall the CDC’s weird, anti-scientific, anti-human focus on masking toddlers with cloth masks into 2022.

President Biden’s Covid advisor Ashish K. Jha waited until Dec. 2022 (right after leaving government service) to tell the country that “[t]here is no study in the world that shows that masks work that well.” What took him so long?

In 2021, former CDC director, Rochelle Walensky rewrote CDC guidance on social distancing at the behest of the national teachers’ union, guaranteeing that schools would remain closed to in-person learning for many months.

During this period, the PR firm FMG put out ads telling parents that schools would close unless kids masked up, stayed away from friends, and got Covid-vaccinated.

In March 2021, even as the CDC told the American people that the vaxxed did not need to mask, the PR firm ran ads saying that masks were still needed, even for the vaxxed. “It’s not time to ease up” we were told, in the absence of evidence any of that did any good.

In 2021, to support the Biden/Harris administration’s push for vax mandates, the PR firm pushed the false idea that the vax stopped Covid transmission. When people started getting “breakthrough” infections, public trust in public health collapsed.

Later, when the FDA approved the vax for 12 to 15-year-old kids, the PR firm told parents that schools could open in fall 2021 only if they got their kids vaccinated. These ads never mentioned side effects like myocarditis due to the vax.

HHS has scrubbed the propaganda ads from this era from its web pages. It’s easy to see why. They are embarrassing. They tell kids, in effect, that they should treat other kids like biohazards unless they are vaccinated.

When the Delta variant arrived, the PR firm doubled down on fear-mongering, masking, and social distancing.

In September 2021, CDC director Walensky overruled the agency’s external experts to recommend the booster to all adults rather than just the elderly. The director’s action was “highly unusual” and went beyond the FDA’s approval of the booster for only the elderly.

The PR campaign and the CDC persistently overestimated the mortality risk of Covid infection in kids to scare parents into vaccinating their children with the Covid vax.

In Aug. 2021, the military imposed its Covid vax mandate, leading to 8,300 servicemen being discharged. Since 2023, the DOD has been trying to get the discharged servicemen to reenlist. What harm has been done to American national security by the vax mandate?

The Biden/Harris administration imposed the OSHA, CMS, and military vax mandates, even though the CDC knew that the Delta variant evaded vaccine immunity. The PR campaign studiously avoided informing Americans about waning vaccine efficacy in the face of variants.

The propaganda campaign hired celebrities and influencers to “persuade” children to get the Covid vax.

I think if a celebrity is paid to advertise a faulty product, that celebrity should be partially liable if the product harms some people.

In the absence of evidence, the propaganda campaign ran ads telling parents that the vaccine would prevent their kids from getting Long Covid.

With the collapse in public trust in the CDC, parents have begun to question all CDC advice. Predictably, the HHS propaganda campaign has led to a decline in the uptake of routine childhood vaccines.

The report makes several recommendations, including formally defining the CDC’s core mission to focus on disease prevention, forcing HHS propaganda to abide by the FDA’s product labeling rules, and revamping the process of evaluating vaccine safety.

Probably the most important recommendation: HHS should never again adopt a policy of silencing dissenting scientists in an attempt to create an illusion of consensus in favor of CDC groupthink.

You can find a copy of the full House report here. The HHS must take its findings seriously if there is any hope for public health to regain public.



Published under a Creative Commons Attribution 4.0 International License
For reprints, please set the canonical link back to the original Brownstone Institute Article and Author.

 

Author

  • Jay Bhattacharya

    Dr. Jay Bhattacharya is a physician, epidemiologist and health economist. He is Professor at Stanford Medical School, a Research Associate at the National Bureau of Economics Research, a Senior Fellow at the Stanford Institute for Economic Policy Research, a Faculty Member at the Stanford Freeman Spogli Institute, and a Fellow at the Academy of Science and Freedom. His research focuses on the economics of health care around the world with a particular emphasis on the health and well-being of vulnerable populations. Co-Author of the Great Barrington Declaration.

Oct 222024
 

A Netherlands court last week ruled that Bill Gates can stand trial in the Netherlands, in a case involving seven people injured by COVID-19 vaccines. Other defendants include Albert Bourla, CEO of Pfizer, and the Dutch state.

bill gates and gavel and covid vaccine bottles
00:00/06:05

A Netherlands court last week ruled that Bill Gates can stand trial in the Netherlands, in a case involving seven people injured by COVID-19 vaccines.

According to Dutch newspaper De Telegraaf, the seven “corona skeptics” sued Gates last year, along with former Dutch prime minister and newly appointed NATO Secretary General Mark Rutte, and “several members” of the Dutch government’s COVID-19 “Outbreak Management Team.”

Other defendants include Albert Bourla, Ph.D., CEO of Pfizer, and the Dutch state.

“Because Bill Gates’ foundation was involved in combating the corona pandemic, he has also been summoned,” De Telegraaf reported.

According to Dutch independent news outlet Zebra Inspiratie, the plaintiffs allege that Gates, through his representatives, deliberately misled them about the safety of the COVID-19 shots, despite knowing “that these injections were not safe and effective.”

Dutch independent journalist Erica Krikke told The Defender that the seven plaintiffs — whose names are redacted in the lawsuit’s publicly available documents — “are ordinary Dutch people, and they have been jabbed and after the jabs they got sick.”

Krikke said that of the seven original plaintiffs, one has since died, leaving the other six plaintiffs to continue the lawsuit.

The lawsuit was filed in the District Court of Leeuwarden. According to De Telegraaf, “Gates had objected because, according to him, the judges did not have jurisdiction.” Accordingly, the court first “had to rule in the so-called incident procedure,” De Andere Krant reported.

Zebra Inspiratie reported that the hearing in this “incident procedure” took place on Sept. 18 and that Gates’ representatives disputed jurisdiction, but not the claim.

According to De Andere Krant, Gates was represented by the Pels Rijcken law firm, based in The Hague, described as “the largest and the premier litigation law firm in the Netherlands.” Gates did not appear at the Sept. 18 hearing, but attorneys for Gates argued that the court “had no jurisdiction over him because he lives in the United States.”

However, in its Oct. 16 ruling, the Leeuwarden court ruled it does have jurisdiction over Gates. De Andere Krant reported that the court found “sufficient evidence” that the claims against Gates and the other defendants are “connected” and based on the same “complex of facts.”

Other defendants who reside outside of the Netherlands, including Bourla, did not challenge the court’s jurisdiction.

The court ruled Gates must pay attorneys’ fees and additional legal costs totaling 1,406 euros (approximately $1,520). A hearing is scheduled for Nov. 27.

‘Even if … your name is Bill Gates, you still have to go to court’

In remarks shared with De Andere Krant, Arno van Kessel, one of the plaintiffs’ attorneys, welcomed the ruling. “In its verdict, the court has clearly recorded the basis of our conclusions of claim,” van Kessel said.

Dutch attorney Meike Terhorst told The Defender it is “quite interesting” that the plaintiffs filed the lawsuit in Leeuwarden instead of The Hague, where normally, all cases against the government related to COVID-19 are filed.

“In general, COVID-19 court cases have been very unsuccessful in the Netherlands,” Terhorst said. “There is a slim chance it will be successful.”

She added:

“I think most judges support the COVID-19 vaccination agenda and will find it hard to believe the vaccinations have caused injuries. So, we have a long way to go, regardless of the case.”

Krikke shared a more optimistic outlook, saying that the court sent a message that “even if you are rich and your name is Bill Gates, you still have to go to court.”

New Zealand-based independent journalist Penny Marie, who has closely followed the proceedings in this case, told The Defender she hopes the Oct. 16 ruling “will hopefully set a precedent and help plaintiffs in similar cases around the world regarding jurisdiction,” in cases “where the defendant does not reside in the country of the plaintiff.”

“For parties who make claims against those involved in the implementation of the Great Reset and other international actions, such as the COVID-19 emergency response initiated by the WEF [World Economic Forum] and imposed on all U.N. member nations, I hope that this ruling provides an opportunity for others to follow suit,” Marie added.

Collage of Rally and Events

Father of vaccine-injured plaintiff made ‘emotional plea’ to the court

At the Sept. 18 hearing, plaintiffs also delivered statements. According to Zebra Inspiratie, “One of the victims, who is very ill, was also given the opportunity to make a plea. She was no longer able to speak and was represented by her father. It was an emotional plea.”

Krikke said the plaintiff’s father told the court that his daughter, who was previously healthy, fell ill after getting the COVID-19 vaccine and could no longer speak, telling the judge that he “would really like to speak to Bill Gates directly” to ask him what happened to his daughter.

“After that, the judge was really quiet,” Krikke said.

The Oct. 18 ruling also addressed the plaintiffs’ claims about Gates’ role in the WEF’s “Great Reset” project.

“The Bill & Melinda Gates Foundation is also affiliated with the World Economic Forum … an international organization whose statutory objective is to unite ‘leaders from business, governments, academia and society at large into a global community committed to improving the state of the world,’” the ruling states, adding:

“This is a project aimed at the total reorganization of societies in all countries that are members of the United Nations … as described by [WEF founder and executive chairman Klaus Schwab] in his book Covid-19: The Great Reset. …

“Characteristic of this political ideology is that this forced and planned change is presented as justified by pretending that the world is suffering from major crises that can only be solved by centralized, hard global intervention. One of these pretended major crises concerns the Covid-19 pandemic.”

The ruling also states, “The Bill & Melinda Gates Foundation is affiliated with ‘Gavi, the Vaccine Alliance‘ … an international partnership in the field of vaccinations between various public and private entities.”

Oct 222024
 

PREVIOUS WAS:   For Your Selection  October 02

 

For Your Selection OCTOBER 23, 2024

COVID

  1. ***   2024-10-16 Covid – VERY IMPORTANT THAT YOU WATCH. Could a new class-action lawsuit offer justice for COVID-19 vaccine victims? (Carrie Sakamoto case and others) Tamara Ugolini, Rebel News***
  2. 2024-10-22 B ill Gates to Stand Trial in Netherlands in COVID Vaccine Injury Lawsuit. Michael Nevradakis, CHD

  3. 2024-10-18 Death by Covid Vaccine, Umar Sheikh lawyer – Suing Pfizer & the Govt. For 17-year-old Sean Hartman. Interview by Jason Lavigne

  4. 2024-10-21 Pfizer’s ‘Crimes Against Humanity’ — and Legacy Media’s Failure to Report on Them. Naomi Wolf. CHD, by Brenda Baletti.

  5. 2024-10-17 Charges dropped against 50 Freedom Convoy truckers from Coutts protest. From LifeSiteNews By Anthony Murdoch

  6.  2024-09-24 Alberta Premier Danielle Smith announces province will amend Bill of Rights to include vaccine refusal. Legislation will be tabled in the coming weeks. Video’d press conference.

UPDATE:   By the end of October the draft legislation was tabled and in public debate.

TYRANNY

7.  2024-09-16 The Amish (American side of border): A Control Group for Technofeudalism, By Tracy Thurman, Brownstone Institute

8.  2024-08-16  (Canadian side of the border)  Ontario’s Amish community faces unprecedented fines ($400,000) and legal hurdles, because of the ArriveCan App. They don’t use phones, let alone smartphones; “Apps” are unknown. By Rebel News.

(There is an update on this case.  I’ll find and get it posted.)

 

We are all warriors.

Sandra

Oct 222024
 

Important to watch AND forward to others.  /S

A new class-action lawsuit is providing Albertans injured by the “safe and effective” COVID shots with renewed hope for justice.

Marking the legacy of the so-called pandemic was the widespread suspension of our civil liberties and the establishment of a bio-security nanny state that forcefully pushed mass vaccinations on every man, woman and child to the benefit of Big Pharma and their bureaucratic accomplices inside all levels of government.

The fevered push to get shots into arms saw the government change regulatory due process and rush these novel products to market. As a result, an untold number of people were left injured or dead and entirely forgotten by the system.

At the heart of this lawsuit is Carrie Sakamoto, a young mother from Lethbridge whose personal $10.5 million vaccine injury lawsuit pivoted into a class action, representing potentially thousands of Albertans facing debilitating, long-term effects from the widely promoted but highly controversial COVID-19 mRNA vaccines.

Lawyers Jeff Rath and Eva Chipiuk from the firm Rath and Co. are the lawyers behind this massive lawsuit. They recently joined me for an interview to explain how the Alberta government took part in “unlawful, negligent, inadequate, improper, unfair, and deceptive practices” to convince people to put their health, safety, and employment on the line under the guise of the greater good.

Click here to watch.

Rath pointed out that the government of Alberta, including Health Officer Deena Hinshaw, ignored important safety data before the rollout of these shots:

“[Pfizer] clearly demonstrated that if you put these shots into the arms of children, that the vaccines themselves would kill more children than COVID.”

This lawsuit is more than just a legal battle — it’s an urgent call for accountability and a potential precedent for future public health responses. As legal action unfolds, will this be Canadians’ only hope for the government to take responsibility for the widespread harm caused by their hasty vaccine rollout?

You can find updates on this lawsuit and our other facts-based reports on this issue at NoMoreShots.ca.

On that website, we’ve also set up a petition you can sign demanding our government immediately revoke market authorization for these shots.

Yours truly,

Tamara Ugolini

P.S. In response to the government’s “safe and effective” narrative, we’ve launched a campaign at NoMoreShots.ca where you can find credible and well-researched reports on the safety and efficacy of COVID-19 vaccines and sign our petition to revoke market authorization of these shots before more people are hurt.