Coronavirus: why are some people experiencing long-term fatigue?

The Conversation blog post: Coronavirus: why are some people experiencing long-term fatigue?, by Prof Frances Williams, 16 July 2020

 

People who have been seriously unwell and treated on intensive care units can expect to take some months to recover fully, regardless of their ailment. However, with COVID-19, evidence is mounting that some people who have had relatively mild symptoms at home may also have a prolonged illness. Overwhelming fatigue, palpitations, muscle aches, pins and needles and many more symptoms are being reported as after-effects of the virus. Around 10% of the 3.9 million people contributing to the COVID Symptom Study app have effects lasting more than four weeks.

Chronic fatigue – classified as fatigue lasting more than six weeks – is recognised in many different clinical settings, from cancer treatment to inflammatory arthritis. It can be disabling. If 1% of the 290,000 or so people who have had COVID-19 in the UK remain under the weather at three months, this will mean thousands of people are unable to return to work. They will probably have complex needs that the NHS is ill-prepared to address at present.

COVID-19 is not the only cause of chronic fatigue. Prolonged fatigue is well recognised after other viral infections such as the Epstein-Barr virus, which causes infectious mononucleosis (also known as glandular fever). Post-viral fatigue was also seen in a quarter of those infected with the original Sars virus in Hong Kong in 2003.

When it comes to treating chronic fatigue, the emphasis previously has been on effective treatment of the underlying disease, in the belief that this would diminish the fatigue. However, for most viral infections there is no specific treatment, and because COVID-19 is so new, we don’t yet know how to manage post-COVID fatigue.

What might be causing post-COVID fatigue?

Although we know that lasting fatigue can sometimes follow other viral infections, detailed mechanistic insight is, for the most part, lacking. An ongoing viral infection in lung, brain, fat or other tissue may be one mechanism. A prolonged and inappropriate immune response after the infection has been cleared might be another.

However, a previous study has given us some insight. When a chemical called interferon-alpha was given to people as a treatment for hepatitis C, it generated a flu-like illness in many patients and post-viral fatigue in a few. Researchers have studied this “artificial infection response” as a model of chronic fatigue. They found that baseline levels of two molecules in the body that promote inflammation – interleukin-6 and interleukin-10 – predicted people’s subsequent development of chronic fatigue.

Of particular interest, these same pro-inflammatory molecules are seen in the “cytokine storm” of severely ill COVID-19 patients. This suggests there might be a pattern of immune system activation during the viral infection that is relevant to ongoing symptoms. Further support for interleukin-6 playing some sort of role comes from the successful use of tocilizumab – a treatment that lessens the impact of interleukin-6 and reduces inflammation – to treat severe COVID-19.

Read the full article for info about Covid-19 research at Kings College, London and the need to pace when managing chronic fatigue. Prof Williams recommends Dr Muirhead’s ME/CFS course for clinicians at StudyPRN.

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‘I need to start listening to what my body is telling me’: Does mindfulness-based cognitive therapy help people with CFS?

‘I need to start listening to what my body is telling me.’: Does mindfulness-based cognitive therapy help people with Chronic Fatigue Syndrome? by Bridie O’Dowd & Gemma M Griffith in Human arenas 2020, July 16 [https://doi.org/10.1007/s42087-020-00123-9]

 

Research abstract:

Mindfulness-Based Cognitive Therapy (MBCT) was lightly adapted for participants diagnosed with chronic fatigue syndrome (CFS). The aim of the study was to explore participants’ experiences of the MBCT course, with a particular focus on how they applied MBCT to living with and coping with the symptoms of CFS.

Nine participants with CFS who completed the MBCT course were interviewed using semi-structured interview methods. Inductive thematic analysis, a methodology designed to generate themes from the ‘bottom up,’ was used.

Four superordinate themes were generated from the data: (1) awareness of unhelpful
behavioral patterns associated with CFS, (2) benefits of group solidarity, (3) use of mindfulness tools to facilitate shifts in behavioral patterns, and (4) a sense of change and agency.

Participants became aware of three specific transformative changes that contributed
to a more skillful way of living with CFS: development of acceptance, improved self-care and self-compassion, and reduction in heightened stress response. MBCT appears to enable people with CFS to actively work with their symptoms, and make transformative changes in their behavioral patterns, resulting in benefits to well-being.

 

Excerpts from Discussion:

During the course, participants described how they became aware of specific vulnerabilities that are particular to CFS, and with the support of the group and specific mindfulness tools, reported a change in habit patterns which maintain and perpetuate CFS, such as perfectionism, being driven, people-pleasing, and tendency to catastrophize. There were three very specific transformative changes that occurred as a result of the MBCT course, which were supported across the four superordinate themes. These were the development of acceptance, a cultivation of self-care, and a reduction in heightened stress reaction.

Development of Acceptance
Given the chronic, unpredictable nature of CFS and the lack of curative treatment, cultivating a stance of acceptance of “what is,” shifted the participants’ agenda from a goal of “getting rid” of their condition to working skillfully with it. Crane (2008) describes the goal-driven “doing” mode as being cognitively focused and future orientated. This creates a tendency to discrepancy monitor, that is, monitoring the mismatch between where one actually is and the goal of where one wants to be (Bishop et al. 2004; Segal et al. 2013). The participants developed awareness that this striving to close the gap of how they found themselves and how they wished themselves to be, often demanded large amounts of draining energy.

The shift to acceptance, as a valid mode of coping with CFS, was enhanced by the mutual, supportive learning environment of the class. For some participants, acceptance involved acknowledging the fundamental truth of their current disability. For others, it was a recognition of the impossibility of meeting previous high standards and a welcome letting go of the exhausting maintenance of habit patterns. After the course, participants recognized that these patterns such as perfectionism, people pleasing, and feeling guilty were not only counterproductive but also potentially instrumental in the etiology of their condition (Hambrook et al. 2011; Luyten et al. 2011; Van Houdenhove and Luyten 2008).

Cultivation of Self-Care
The extant research which explores MBPs for CFS populations reported significant shifts in self-reported measures of anxiety, somatization, and unhelpful cognitions and behaviors (Rimes and Wingrove 2013; Sampalli et al. 2009; Surawy et al. 2005). However only the latter of these studies measured and reported improvement in self-compassion scores (Neff 2003). This study showed that increased self-care and self-compassion were fundamental to the shift participants experienced in managing their CFS.

This shift to enhanced self-kindness appeared to arise from a willingness to step out of the driven, energy-draining personality traits of perfectionism, high standards, conscientious, driven working style, and a strong susceptibility to self-criticism (Hambrook et al. 2011; Luyten et al. 2011). The mechanisms by which the mindfulness training enabled this shift appeared to be threefold. First, there was an increased awareness and an intention to “listen” to symptoms rather than ignore them. This led to a more gentle, kindly, and forgiving attitude towards their bodies experiencing fatigue and pain.

Second, the participants developed metacognitive awareness (Bishop et al. 2004; Teasdale 1999), allowing them to observe their thought processes more clearly. This allowed them to recognize the critical, driven nature of their self-narrative and enabled them to create a kinder less judgmental inner-dialog. Third, the kindness and care developed within the group acted as a medium in which a “permission to self-care” was cultivated. This permission frequently translated into a license to rest, previously un-granted because striving and pushing was so ingrained and prevalent. This shift frequently resulted in protection and preservation and replenishing of limited energy.

Reduction in Stress Reaction
As the course progressed, many participants became aware of an exaggerated stress response, felt physically in the body as pain and fatigue, emotionally as anxiety, and cognitively as fast, racing thoughts. This awareness led participants to actively apply mindfulness to reduce their stress response. First, they found the breath gave them a sense of grounding, calming, stepping back, and providing rest from stressful experiences and reactions. Second, they found everyday mindfulness allowed them to shift attention from catastrophizing thoughts, which would inevitably generate a high stress response onto the more neutral actuality of what they were doing in that moment. Third, they developed a self-soothing inner-dialog that encouraged them to move attention to the breath, remember that thoughts are not facts, and recognize that there may be a habitually exaggerated response going on that they could disengage from. As a result, many of the group reported a reduction in pain and fatigue.

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Cognitive function declines following orthostatic stress in adults with ME/CFS

Cognitive Function declines following orthostatic stress in adults with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), by C Linda M C van Campen, Peter C Rowe, Freek W A Verheugt, Frans C Visser in Front Neurosci. 2020 Jun 26;14:688. [doi.org/10.3389/fnins.2020.00688]

 

Research abstract:

Introduction:

Orthostatic intolerance (OI) is common among individuals with myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS).

Cognitive dysfunction has been demonstrated during head-up tilt testing (HUT) in those with ME/CFS: worse scores on cognitive tests occur with increasing tilt angles and increasing complexity of the cognitive challenge. The aim of our study was to determine whether cognitive impairment persists after completion of HUT.

Methods and results:

Eligible participants were consecutive individuals satisfying criteria for ME/CFS who underwent HUT because of OI. The 2- and 3-back tests were performed before the start of HUT and within 5 min after completion of HUT. We measured the percentage of correct responses and raw reaction times before and after HUT for both the 2- and 3-back tests. We studied 128 ME/CFS patients who underwent HUT and had a complete set of N-back data before and after HUT.

Compared to pre-tilt responses, the percentage of correct responses on the 2-back test decreased post-HUT from 77(18) to 62(21) and of the 3-back test from 57(17) to 41(17) (both p < 0.0001). The raw reaction time of the 2-back test increased post-HUT from 783(190) to 941(234) m/s and of the 3-back test from 950(170) to 1102(176) (both p < 0.0001). There was no difference in the N-back test data for subgroups dichotomized based on disease severity, the presence of co-morbid fibromyalgia, or the presence of postural orthostatic tachycardia syndrome.

Conclusion:

As measured by the N-back test, working memory remains impaired in adults with ME/CFS following a 30-min head-up tilt test.

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Severe ME in children

Severe ME in children, by Nigel Speight in Healthcare Vol 8, #3 p 211, July 14, 2020 [This article belongs to the Special Issue ME/CFS]

 

Guideline abstract

The current problem regarding Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome (ME/CFS) is the large proportion of doctors that are either not trained or refuse to recognize ME/CFS as a genuine clinical entity, and as a result do not diagnose it. An additional problem is that most of the clinical and research studies currently available on ME are focused on patients who are ambulant and able to attend clinics and there is very limited data on patients who are very severe (housebound or bedbound), despite the fact that they constitute an estimated 25% of all ME/CFS cases.

This author has personal experience of managing and advising on numerous cases of severe paediatric ME, and offers a series of case reports of individual cases as a means of illustrating various points regarding clinical presentation, together with general principles of appropriate management.

 

4. Possible Clinical Features of Severe and Very Severe ME/CFS

  • Minimal energy levels, resulting in the patient being housebound or bedridden;
  • Paralysis;
  • Severe generalised continuous pain;
  • Severe continuous headache;
  • Hyperaesthesia/extreme sensitivity to touch;
  • Abdominal pain, worse after food—this may be so severe as to interfere with nutrition;
  • Sleep disturbance, possible hypersomnolence or difficulty sleeping on account of pain and headache;
  • Major problems with cognition, concentration and short-term memory;
  • Extreme sensitivity to light and sound;
  • Multiple chemical sensitivities;
  • Problems with eating and drinking—this can be due to either general weakness or actual dysphagia, and this may necessitate tube feeding;
  • Aphonia (mechanism unclear);
  • Myoclonic jerks;
  • Incontinence.

 

17. Take Home Messages

  • Severe ME constitutes a major challenge for both patient and doctor.
  • Mismanagement in the form of “activation regimes” can result in permanent harm or even death of the patient.
  • The patient deserves the total commitment of one doctor, who is willing to visit at home on a regular basis.
  • Referral to a psychiatrist who does not believe in ME/CFS can be harmful.
  • The patient should be protected from sensory overload.
  • The doctor should resist the temptation to overinvestigate, or involve too many other professionals.
  • Nursing at home is usually far preferable to admission to a busy general hospital.
  • Tube feeding is indicated when the patient has problems with eating and drinking.
  • Urinary catherization may be helpful in reducing the stress of having to micturate.
  • Symptomatic treatment for pain and sleep problems is worthwhile.
  • Full recovery is possible.
  • The role of immunoglobulin deserves further study [10].
  • There is a need to improve both undergraduate and postgraduate medical training in this area, and to provide greater resources for the patient population affected.
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Health Care responsibility & compassion-visiting the housebound patient severely affected by ME/CFS

Health Care responsibility and compassion-visiting the housebound patient severely affected by ME/CFS, by  Caroline Kingdon, Dionysius Giotas, Luis Nacul and Eliana Lacerda in Healthcare 2020, 8(3), 197 [doi.org/10.3390/healthcare8030197]
[This article belongs to the Special Issue ME/CFS – the Severely and Very Severely Affected]

 

Research abstract:

Many people with severe Myalgic Encephalopathy/Chronic Fatigue Syndrome (ME/CFS) commonly receive no care from healthcare professionals, while some have become distanced from all statutory medical services.

Paradoxically, it is often the most seriously ill and needy who are the most neglected by those responsible for their healthcare. Reasons for this include tensions around the complexity of making an accurate diagnosis in the absence of a biomarker, the bitter debate about the effectiveness of the few available treatments, and the very real stigma associated with the diagnosis.

Illness severity often precludes attendance at healthcare facilities, and if an individual is well enough to be able to attend an appointment, the presentation will not be typical; by definition, patients who are severely affected are home-bound and often confined to bed.

We argue that a holistic model, such as ‘‘Compassion in Practice’’, can help with planning appointments and caring for people severely affected by ME/CFS. We show how this can be used to frame meaningful interactions between the healthcare practitioners (HCPs) and the homebound patient.

Common symptoms affecting people with severe Myalgic Encephalopathy/Chronic Fatigue Syndrome (ME/CFS) seen by CureME:

  • Unrefreshing sleep
  • Disabling fatigue
  • Sleep problems
  • Exercise intolerance (PEM)
  • Pain after exertion/activity
  • Muscle pain
  • Intolerance to standing
  • Concentration problems
  • Difficulty in finding words
  • Difficulty in making decisions
  • Brain fog/cognitive dysfunction
  • Slow thinking
  • Short-term memory problems
  • Difficulty in understanding
  • Difficulty in retaining information
  • Unusual sensitivity to light and/or noise
  • New sensitivities to food, medication, chemicals or odours
  • Intolerance to heat and cold
  • Allergies/hypersensitivities
  • Gastrointestinal symptoms
  • Sickness and nausea               [See Table 1 for more information]

Conclusions

We believe that compassion is central to the care of people with ME/CFS. Despite the current absence of curative treatments for people with severe ME/CFS, the HCP has a responsibility to provide care through a relationship based on empathy, respect and dignity. By supporting the individual with compassion and competence and acknowledging and learning from the patient’s experience, the encounter with the housebound patient can be both effective and worthwhile.

The first step in the therapeutic relationship is to believe and trust the individual: to articulate that you, the practitioner, hear what your patient is saying and recognise that their experience is legitimate.

This severe, complex multisystem disease has long been misjudged by the healthcare profession. Educating practitioners about the needs of those most severely affected by ME/CFS will help drive the step change in understanding and belief, compassion and empathy required to care for all patients with ME/CFS.

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WAMES Facebook interruption

Apologies, if you follow WAMES on Facebook. We are currently unable to access the site to post. The reason is unclear.

 

Bear with us as we seek a solution. We will continue to post on this blog and twitter.

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Environmental accommodations for university students affected by ME/CFS

Environmental accommodations for university students affected by myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), by Lily Chu, Lynn R Fuentes, Olena M Marshall and Arthur A. Mirin in Work pp. 1-12, 2020[DOI: 10.3233/WOR-203176]

 

Research abstract:

Background:  Today, 24% of college and university students are affected by a chronic health condition or disability. Existing support programs, including disability services, within colleges and universities are often unaccustomed to addressing the fluctuating and unpredictable changes in health and functioning faced by students with severe chronic illnesses.

This situation is especially difficult for students with lesser-known, invisible diseases like myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), a complex disease affecting up to 2.5 million Americans which often begins in late adolescence or young adulthood.

Objective:  Educate occupational therapists (OTs) about ME/CFS and steps they can take to assist students

Methods:  This work is based on a review of the scientific literature and our collective professional/ personal experiences.

Results:  ME/CFS’ effects on multiple organ systems combined with the unusual symptom of post-exertional malaise frequently and substantially decrease function. Currently, no effective disease-modifying treatments have been established.

Nevertheless, OTs can help students maximize their participation in university life by identifying potential obstacles, formulating practical solutions and negotiating with their institutions to implement reasonable, environmental accommodations.

Conclusions:  Through understanding this disease, being aware of possible support options, and recommending them as appropriate, OTs are in unique position to greatly improve these students’ lives.

Excerpts:

1.3. The valuable role of occupational therapists

A major goal of occupational therapy is to help individual patients live life to its fullest despite injury, illness, or disability [24]. OTs possess the unique skills and experience to assess the obstacles facing students, formulate possible solutions to overcome them, and advocate for those solutions to be put in place. According to one definition of advocacy carried out by OTs,

“Advocacy is a client-centered strategy involving a variety of actions taken by the client and therapist, directed to the client’s environment to enact change for the client such that engagement in occupation is enhanced through meeting basic human rights or improving quality of life” [25].

OTs also bring professional authority that students, families, and caregivers may not possess when advocating for and negotiating accommodations with professional staff and faculty of higher education institutions. This document is intended to serve as a brief, practical resource for OTs working with adult students afflicted by ME/CFS. We will describe what ME/CFS is, basic principles of medical treatment, and how OTs can help. This document is also relevant and helpful for university staff and faculty members.

 

3. Recommended accommodations

3.1. Maintain overall awareness of the fluctuating nature of ME/CFS

(A) Maintain awareness of the waxing and waning nature of ME/CFS and its unpredictability

3.2 Advise students to negotiate accommodations in advance

(B) Ensure that affected students are aware of the need to register with the disability office as early as possible.

(C) Advise students to schedule an appointment with an academic adviser/consultant early in their university years.

(D) Encourage students to communicate with instructors prior to beginning a class.

(E) Encourage students to request assignment flexibility when possible, emphasizing mastery over quantity of work

(F) Help students to minimize travel

3.3. Requests directed to disability and other university offices

(G) Request lecture notes and/or recordings when lectures are not online or otherwise available for review. If no recordings are available, allow students to record lectures on their own

(H) Request examination accommodations ahead of time.

(I) Request flexible scheduling when possible and the ability to miss or leave classes  without penalty when medically necessary.

(J) Request easily accessible rest areas on campus and the right to take opportunities for rest where and when needed.

(K) Request ergonomic furniture and devices, such as desks, chairs, computers, keyboards, computer mice, etc.

(L) Request as much flexibility as allowable for students who have a work assignment, such as a teaching assistantship, or another type of work-like experience, such as an experiential learning course requirement

(M) Facilitate the use of wheelchairs, mobility aids, and other power-driven mobility devices (OPDMDs)

3.4. Advocating for students at a systemic level

The next three accommodations are not under the direct purview of OTs. However, if asked, OTs can bring up systemic changes that universities can implement to improve the situation campus-wide for all students with ME/CFS and even students with other chronic illnesses. OTs can also offer to be a resource for the university.

(N) Provide awareness training to relevant university staff

(O) Arrange for support services,

(P) Ensure that the various university offices that serve students with ME/CFS are working synchronously and in harmony with each other.

Read full paper [uncorrected author proof]

NB Read about the law requiring ‘reasonable adjustments’ in UK education 

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Two-Day cardiopulmonary exercise testing in females with a severe grade of ME/CFS: comparison with patients with mild & moderate disease

Two-Day cardiopulmonary exercise testing in females with a severe grade of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: comparison with patients with mild and moderate disease, by  C (Linda) MC van Campen, Peter C Rowe and Frans C Visser in Healthcare 2020, 8(3), 192; [doi.org/10.3390/healthcare8030192] ne 2020
(This article belongs to the Special Issue ME/CFS – the Severely and Very Severely Affected)

 

Research abstract:

Introduction:

Effort intolerance along with a prolonged recovery from exercise and post-exertional exacerbation of symptoms are characteristic features of myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS). The gold standard to measure the degree of physical activity intolerance is cardiopulmonary exercise testing (CPET).

Multiple studies have shown that peak oxygen consumption is reduced in the majority of ME/CFS patients, and that a 2-day CPET protocol further discriminates between ME/CFS patients and sedentary controls.

Limited information is present on ME/CFS patients with a severe form of the disease. Therefore, the aim of this study was to compare the effects of a 2-day CPET protocol in female ME/CFS patients with a severe grade of the disease to mildly and moderately affected ME/CFS patients.

Methods and results:

We studied 82 female patients who had undergone a 2-day CPET protocol. Measures of oxygen consumption (VO2), heart rate (HR) and workload both at peak exercise and at the ventilatory threshold (VT) were collected. ME/CFS disease severity was graded according to the International Consensus Criteria.

Thirty-one patients were clinically graded as having mild disease, 31 with moderate and 20 with severe disease. Baseline characteristics did not differ between the 3 groups. Within each severity group, all analyzed CPET parameters (peak VO2, VO2 at VT, peak workload and the workload at VT) decreased significantly from day-1 to day-2 (p-Value between 0.003 and <0.0001).

The magnitude of the change in CPET parameters from day-1 to day-2 was similar between mild, moderate, and severe groups, except for the difference in peak workload between mild and severe patients (p = 0.019). The peak workload decreases from day-1 to day-2 was largest in the severe ME/CFS group (−19 (11) %).

Conclusion:

This relatively large 2-day CPET protocol study confirms previous findings of the reduction of various exercise variables in ME/CFS patients on day-2 testing. This is the first study to demonstrate that disease severity negatively influences exercise capacity in female ME/CFS patients. Finally, this study shows that the deterioration in peak workload from day-1 to day-2 is largest in the severe ME/CFS patient group.

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“That’s why they don’t believe you, you don’t look sick!”: creating medical credibility & patient visibility for ME/CFS through television

“That’s why they don’t believe you, you don’t look sick!”: creating medical credibility and patient visibility for ME/CFS through television, by Giada Da Ros

 

Article abstract:

Since the end of the 20th century, the Myalgic Encephalomyelitis / Chronic Fatigue Syndrome community tried to create medical credibility and patient visibility for a chronic, controversial disease with many symptoms, no cure, and no diagnostic test. Not taught in medical schools, it relied on television to make itself visible fighting stigma and prejudice, challenging the political system and the philosophical approach we use to think about illness itself, having patients re-appropriate the discourse. Keeping a cultural approach to health communication as a phenomenon that maintains, produces, and transforms health and illnesses, I analyze news, fictional and talk-show programs.

My aim in this paper is to show how, since the end of the 20th century, the ME/CFS community tried to create, through traditional and original television spaces, medical credibility and patient visibility for what has historically been a very controversial disease, fighting stigma and prejudice, challenging the political system and the philosophical approach we use to think about illness itself, having the patient ri-appropriate the discourse.

I will also show, through the Italian experience (and my own personal one), how non-traditional spaces were used as viable, fecund means for disseminating health knowledge, also pushing for a virtuous model of relationship between physician and patient.

In doing so I will mainly focus on programs that aired at the turn of the century. This is not just for historical reasons, but for two other strong motives: if it’s true that new spaces, like the Internet and social media, opened up and gained strength in the meantime regular TV still maintains a broader and less topic-focused approach that can reach outside the intended foreseeable target audience; also, with regards to ME/CFS, some of the main communication issues are now still the same as in the beginning, and it is worth looking at the roots of how we talked about it to draw inspiration on what worked and what should be done differently.

 

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Dr Anthony Fauci says that post-covid syndrome “is highly suggestive of” ME

#MEAction blog post: Dr. Anthony Fauci says that post-covid syndrome “is highly suggestive of” Myalgic Encephalomyelitis

 

Blog post extract:

Terri asked Dr. Anthony Fauci (Director of the National Institute of Allergy and Infectious Diseases and member of the White House Coronavirus Task Force), what NIH is doing to address Covid-19 “long-haulers” risk of developing ME and CFS and pointed out that there has been very little funding invested in research into ME and few medical providers know how to take care of people with ME. There are still no FDA approved drugs to treat ME.

Dr. Fauci said Terri Wilder’s question was very relevant.

Dr. Fauci went on to say,

“If you look anecdotally there is no question that there are a considerable number of individuals who have a post-viral syndrome that really in many respects can incapacitate them for weeks and weeks following so-called recovery and clearing of the virus….you can see people who’ve recovered who really do not get back to normal that they have things that are highly suggestive of myalgic encephalomyelitis and chronic fatigue syndrome. Brain fog, fatigue, and difficulty in concentrating so this is something we really need to seriously look at because it very well might be a post-viral syndrome associated with covid-19.”

Read the full blog post

ME association: America’s top covid doctor turns ME/CFS into a subject for general discussion as the pandemic deepens

MEpedia: Anthony Fauci

CNN: Coronavirus may cause fatigue syndrome, Fauci says

Forbes: Fauci pushes back On Trump’s false claims, says he hasn’t briefed
president in 2 months

Dr. Anthony Fauci pushed back on President Trump’s claim that 99% of
coronavirus cases are ‘totally harmless,’ and confirmed that a
post-viral syndrome associated with Covid-19 has incapacitated some
patients for prolonged periods and as the ongoing debate over the
seriousness of the pandemic, between the president and the country’s top
doctors, continues to play out publicly.

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