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  1. Peter T

    Open University of Oxford: CFS study: Researching the biochemistry of Chronic Fatigue Syndrome, closes 30th Dec 2022

    Philip Cowen PROFESSOR OF PSYCHOPHARMACOLOGY Dept of Psychiatry, University of Oxford See https://www.psych.ox.ac.uk/team/phil-cowen He is a psychiatrist with historic links to Kings College, London. His research interest seems to primarily relate to psycho pharmacology of depression...
  2. Peter T

    Open University of Oxford: CFS study: Researching the biochemistry of Chronic Fatigue Syndrome, closes 30th Dec 2022

    I don’t know if this is the same study, but Neurochemistry of CFS and post-COVID-19 fatigue Named contact Phil Cowan See https://www.hra.nhs.uk/planning-and-improving-research/application-summaries/research-summaries/neurochemistry-of-cfs/
  3. Peter T

    An Observational Study Comparing Fibromyalgia and Chronic Low Back Pain in Somatosensory Sensitivity, Motor Function & Balance, 2021, Mingorance et al

    Migraine, brain tumour, raised intracranial pressure and carbon monoxide poisoning have some symptom overlap, ie headache, does this mean that they have a ‘shared pathophysiology’ and any differences between them can therefore be treated as psychogenic?
  4. Peter T

    Reclaiming terminology for ME/CFS

    Though I am not a fan of the word ‘fatiguability’, it or an alternative should be used in conjunction with PEM. Only if it is made very clear that PEM is different to just tiring, even tiring quicker than an well person, will people understand what is meant by PEM. Also hopefully this will...
  5. Peter T

    Is it too early to create a medical specialty for m.e.-like diseases?

    Is historically the problem not the lack of a specific ME medical specialism, as much that we do not fit easily within the existing structure of medical specialisms and no one existing specialism has taken ownership of us?
  6. Peter T

    Is it too early to create a medical specialty for m.e.-like diseases?

    Creating a medical specialism is I think something of a boot strap operation. You create specialists posts of various sorts, which then train others and conduct research, which hopefully prompts other services to follow suit. In the UK, in theory the creation of the specialist ME/CFS services...
  7. Peter T

    UK House of Lords/ House of Commons - relevant people and questions

    Aren’t ministers meant to issue a statement any correcting errors of fact they make in Parliament? There has been a fair amount of fuss recently when ministers and the Prime Minister have just ignored requests for them to do this. Unfortunately there does not seem to mechanism to oblige...
  8. Peter T

    Development and User Experiences of a Biopsychosocial Interprofessional Online Course on Persistent Somatic Symptoms, 2021, Rosmalen et al

    What does this tell us? I imagine if you did an analogous study looking at training people in spiritual healing or mediumship you would get very similar results. Doesn’t this miss out one important component? If you are looking at communication between professionals and patients, don’t you...
  9. Peter T

    UK: Priority Setting Partnership for ME/CFS

    A problem is that sometimes people may have more than one condition. A friend, with an under active thyroid condition, experienced years of distress and confusion and problematic thyroid drug management of her condition, before she suspected she had concurrent ME and then persuaded her...
  10. Peter T

    The Times: My Mother, Munchausen’s and Me by Helen Naylor review — the tyrant in the sick bed

    This is what the Times article says of the mother’s ’Parkinson’s’ and her death: The article does not give enough information for us to be able to conclude if the mother did or did not have ME, and given the potential variability of the condition even within an individual, I don’t see how we...
  11. Peter T

    Psychotherapy and Psychosomatics: Psychosocial Factors Predict COVID-19 Vaccine Side Effects,2021, Geers et al

    How disappointing. I did not win the Lottery, despite the peer pressure to do so via on line support groups.
  12. Peter T

    The Times: My Mother, Munchausen’s and Me by Helen Naylor review — the tyrant in the sick bed

    I don’t know if there have ever been any unambiguous cases of either Münchhausens or Münchhausens by proxy, despite its popularity in drama and popular fiction. Personally I would have thought that if you were planning to fake an illness for attention and a need for medical validation you would...
  13. Peter T

    Life insurance

    Yes, I have always since diagnosis declared ME on insurance forms, as not to do so could invalidate the policy. But I have never had any requests back for further information or any restrictions on cover added. In relation to driving beyond notifying insurers, I have not notified the DVLA, but...
  14. Peter T

    Ken Ware - Neurophysics therapy

    [Note, I wrote this response a couple of hours ago, but managed not to post it though I thought I had. One benefit of the software used for S4ME is that it hangs onto drafts we leave hanging rather than such as Facebook that will delete a draft if you just look away or accidentally sneeze. I...
  15. Peter T

    United Kingdom: News from BACME - British Association of Clinicians in ME/CFS

    I agree this is an important issue, and would be happy to work with anyone to achieve this, though individually going beyond comments to collating larger amounts of information, adding sources and references, etc, I quickly hit my personal cognitive limits so would struggle to achieve/lead...
  16. Peter T

    United Kingdom: Petition: Set up a national harms reporting scheme for non-pharmacological treatments

    A side issue that indicates a pressing need for recording harms from behavioural and psychological interventions, is the relatively recent BACME members survey that could be interpreted as indicating a widespread introduction or ‘pacing’ and ‘pacing up’ as therapeutic techniques by British...
  17. Peter T

    Life insurance

    I don’t currently have life insurance, but do suspect that in the past when I have had travel insurance and currently my ongoing motor insurance, have been cheaper than they might have been because of insurance companies misunderstanding of the nature of ME.
  18. Peter T

    United Kingdom: News from BACME - British Association of Clinicians in ME/CFS

    My first take home is that for the UK specialist services GET was already on the way out before the NICE guidelines were published, though we don’t know how much this was happening because it was observed not to work within clinical practice or because of the developing recognition of just how...
  19. Peter T

    The new NICE guidelines - do they affect benefits at all?

    Wasn’t there some evidence several years ago that the contracted assessor companies were operating a target system to reduce claim levels, though this was denied both by the DWP and the companies involved?
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