Maeve Boothby O'Neill - articles about her life, death and inquest

Discussion in 'General ME/CFS news' started by dave30th, Jan 27, 2023.

  1. Amw66

    Amw66 Senior Member (Voting Rights)

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    Sadly, professions where there is a power imbalance can attract some dodgy people. Nursing is one of them.
    There are wonderful nurses, but there are also toxic individuals.
     
  2. dratalanta

    dratalanta Established Member (Voting Rights)

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    TLC? That name is quite the sick joke. The opposite of tender, loving care.

    The internet suggests that in a nursing context TLC should stand for "Timely: Proactive rather than reactive approach to avoid prolonged unnecessary suffering; Team oriented: Nurses, social workers, trained laypersons, and others involved; Longitudinal: Balance of palliative and curative measures evolves with time; Collaborative: Patients, family members, and providers share decisions".

    Possibly helpful concepts like "avoid prolonged unnecessary suffering" and "balance of palliative and curative measures" get abused in an overstretched system so it is not TLC but LTC: Leave To Croak.
     
  3. Eleanor

    Eleanor Senior Member (Voting Rights)

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    The enormous difference it can make when someone sees you as a person rather than a case.
     
  4. Arnie Pye

    Arnie Pye Senior Member (Voting Rights)

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    My father was put on the Liverpool Care Pathway (LCP). He had a lot of health problems but his final issue was a stroke which made swallowing and chewing difficult or impossible. He couldn't talk by that stage. It seemed that as soon as hospital staff realised this was the case he had food and water withdrawn. I managed to get to the hospital about two hours before he died. There were sticks with small pink sponges on them in a jug of water to moisten his mouth with. One of the things that upset me was that dad was desperately sucking water out of these sponges, lifting his head off the bed to get at them. When I decided to try and give him some water a nurse appeared and shouted at me. Nobody had told me that the whole point was for my dad to die as soon as possible. From my point of view this was entirely for the hospital's convenience. By the time he died he'd been on the LCP for 2 or 3 days. I've since read that he went fairly quickly compared to some who last for a week. Given that thirst which can't be quenched is torture I think it is a really cruel way to go.

    The other thing that I noticed was that when he actually died dad clutched his chest, suggesting to me that he was having a heart attack. Yet his death certificate said he'd died of cerebrovascular accident (aka stroke). I don't think the doctor who certified my father's death actually looked at him. He (the doctor) was an aged old codger himself and he was not seeing living patients any more, he was just seeing the dead ones. I think the fees for certifying death were just a nice adjunct to his pension.

    At least when my mother died quite a few years later she had stopped eating and drinking under her own steam. Then she was given what seemed to be a lot of sedative injections throughout her last day - I don't know what they actually consisted of. It almost felt like watching her die had become a spectator sport for the family members who turned up because nobody could say anything to her and get a response. It was horrifying.
     
    Last edited: Aug 30, 2024 at 9:09 PM
  5. Trish

    Trish Moderator Staff Member

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  6. Arnie Pye

    Arnie Pye Senior Member (Voting Rights)

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    I've seen articles that say that the LCP has continued in many places, just under another name :

    https://www.bmj.com/content/350/bmj.h555

    Unfortunately I don't have a link to the whole article.

    What I'm now wondering about is how people in hospital died, say, 40 or 50 years ago. It isn't something that would ever have crossed my mind at the time. I certainly would never have guessed that medical staff would hasten someone's death by depriving them of food and water.
     
  7. SNT Gatchaman

    SNT Gatchaman Senior Member (Voting Rights)

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    Here are a few relevant passages —

    Good to see there is precedence for Government banning the NHS from using a harmful practice when they themselves have failed to correct their systemic error. Looking forward to them tackling ME/CFS usefully in the delivery plan and then they should feel free to take on psychosomatic medicine more generally ...

    The point made about "brave patients or carers who try to jump up and down" is very relevant to this thread. At great cost to Sarah and Sean.

    "re-badge their approach or their use of the Liverpool care pathway, call it something else, and carry on as before". Looking at you FND.
     
  8. Binkie4

    Binkie4 Senior Member (Voting Rights)

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    I'm wondering what evidence Dr Shenton will give when she responds to the written questions posed to her by the coroner at Maeve's inquest.

    What she writes will depend on the questions asked- unless she wishes to introduce her own perspective beyond that requested by the coroner. Will she be allowed to do this?

    Do we know what questions the coroner has posed to Dr Shenton?

    Dr Shenton presumably has views on how her patient was treated/ not treated in the hospital, and on Dr Weir's advice on treatment. Will she be asked to or choose to comment on this. Sarah ( I think it was Sarah) has already said what Dr Shenton said to her about Maeve's treatment.

    edit: Apologies. I am clinging to straws in an effort to be hopeful about 27th Sept. @MrMagoo has reminded me that the Coroner covered Dr Shenton's written replies on the Fri afternoon.
     
    Last edited: Sep 1, 2024 at 1:24 PM
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  9. lunarainbows

    lunarainbows Senior Member (Voting Rights)

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    I watched my Grandpa die just last month, in exactly the way the Liverpool pathway is described. This is in a big well known hospital here. His food was withdrawn first, even though he was at the time still able to swallow/eat small amounts. He was drinking a bottle of fortisip at a time, although he was unwell, but still they withdrew it and put him on nil by mouth. Later, as he deteriorated for several days without any food (and we were continually asking the nurses / doctors if they would actually feed him some other way), they kept fobbing us off and told us he was “very old”, and gave us the sponge with sticks. And then they withdrew water IV too, and we watched him waste away to a living skeleton state in front of our eyes.

    In the end all of us - his family - knew that it was not his cancer that killed him, but starvation and dehydration that killed him quickly. At the time nothing was explained to us and they never told us what they were doing or why. So yes hospitals still do this to some patients. :( :( it is the worst thing I have ever witnessed.
     
    Last edited: Sep 1, 2024 at 2:20 AM
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  10. JemPD

    JemPD Senior Member (Voting Rights)

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  11. bobbler

    bobbler Senior Member (Voting Rights)

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    I’m confused - I thought there was already something from her? Faint memory of discussion of how she corrected the line ‘worst I’ve ever seen a patient treated’ like

    is there more to come from this?
     
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  12. bobbler

    bobbler Senior Member (Voting Rights)

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    I’m so sorry, that’s awful :hug:
     
  13. Sly Saint

    Sly Saint Senior Member (Voting Rights)

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    a good friend of mine had to watch her mother, who had alzheimers, go thro the same in hospital.
     
  14. Binkie4

    Binkie4 Senior Member (Voting Rights)

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    I remember Sarah commenting on what Dr Shenton said to her but I am more interested in how she responded to the coroner's questions....and what they were.
    I too remember a bit of a sense of disappointment at something that was later attributed to Dr Shenton. Perhaps she did retract her earlier comment? My memory of the inquest is fading and I fear being too hopeful about 27th Sept.
     
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  15. MrMagoo

    MrMagoo Senior Member (Voting Rights)

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    Yes Dr Shenton gave written replies which were covered on the last day of the inquest hearing.
     
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  16. Binkie4

    Binkie4 Senior Member (Voting Rights)

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    Thank you @MrMagoo. My memory has erased all but a faint trace of that. i think I was looking for something to be hopeful about but in the process clinging on to straws. I am feeling rather gloomy today after the encouragement of the LBC and BBC Breakfast programmes.
     
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  17. MrMagoo

    MrMagoo Senior Member (Voting Rights)

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    It was a bit disappointing so I wouldn’t bother searching it out. It was very “the whole system isn’t geared towards ME” very restrained and nothing explosive.

    I am hoping the 27th September brings something up about the need for systemic changes, I’m hoping there is a Prevention of Future Deaths report but that’s my heart leading. My head is preparing me for disappointment.
     
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