Power, irony and the ‘sorry’ ship…

‘Sorry’ or an absence of sorry has been a consistent feature of the last few years. We’ve collected a right old rag bag of non-apologies including ‘I’m sorry for any distress you may have felt…’ ‘Please accept my condolences for your loss‘ and ‘I’m sorry if [fill in whatever here]. Last week Valerie Murphy finally ‘found remorse’ and produced an apology for the MPTS panel.

The Murpy effect

At LB’s inquest, one of the barristers, Mr Fortune, offered Murphy the opportunity to say sorry to us when she was giving evidence. An eminently sensible and kind man, he’d obviously helped his client Winnie Betsva come to the decision to do so when she earlier gave evidence. Winnie said sorry. Clearly and unambiguously. Murphy’s non-response lead Fortune to dramatically say “I specifically did not ask we, I addressed the question to you. Dr Murphy please answer.” After further procrastination she stated “It was the right decision. I don’t believe there were failings”. On the inquest recording you can hear the courtroom door slam as I walked out. [I didn’t slam it, it closes loudly.]

Fast forward to yesterday and an email from the GMC. Murphy’s solicitor said she wants to write to us and are we willing to allow the GMC to pass on our home address.

When the ‘sorry’ ship has sailed…

There comes a time when the space to say sorry expires. How long that window remains open will vary but given we went into the MPTS tribunal last August fully expecting and prepared to accept an apology from Murphy four years after LB died it lasts some time.

That ship has sailed now. It sailed for me when instead of saying sorry she allowed her barrister to unnecessarily cross-examine me for nearly two hours.

I had to leave that room too when he told me she was upset. For a brief break before returning to more of the same. While Murphy sat next to him. Feet away.

I’d hazard a guess that Murphy wants to apologise to us now because this absence is repeatedly referred to in the sanction decision. The focus of the MPTS process is on finding demonstrations of insight and remorse by the doctor and the panel helpfully suggest what she might produce before the hearing next year. Including

A reflective account addressing what you have learned and done in respect of the Tribunal’s findings of facts, impairment and sanction demonstrating your level of insight;

[As a bit of an aside, in my thoughts about this I had a sad chuckle earlier remembering LB’s approach to unwanted stuff like hex bugs, broken watches, the egg of trust. He just binned em. Without hesitation.]

The panel should have drawn a dotted line under a potential apology at this stage. It really doesn’t take much insight or reflection to realise that it is probably too late. There’s heavy irony here that the panel are prepared to drag an apology out of Murphy in pursuit of evidence of insight without themselves showing any insight or reflection of the continuing brutality of the process for us. Murphy, likewise, is demonstrating no insight into her actions if she’s prepared to suddenly fashion an apology after everything she’s done and hasn’t done.

Final thoughts

Power is, as always, at the heart of this sorry business. The power to withhold a genuine sorry or to give a half baked non-apology. The power to choose to send ‘the sorry’ a circuitous route to the recipient or simply to others. The power to give a medic – who catastrophically failed a patient by not providing the most basic of basic medical care – chance after chance to buck her ideas up. The erasure of any consideration of the impact of the whole process – including actions taken and decisions made – on the family and wider.

This is an extract from one of the responses sent to the Professional Standards Association expressing concerns about the panel sanction decision.

The Equality Act requires public sector agencies to make reasonable adjustments such that the service offers a similar standard to groups such as disabled people to that experienced by other people. Using learning difficulties as a mitigating factor points in a direction contrary to the Equality Act, seeming to accept that standards are lower for medical professionals working with people with learning disabilities.

I can’t help thinking the MPTS process has descended into some kind of farce. Underpinned by an inability to see LB as a person, demonstrated by using ‘learning difficulties as a mitigating factor’.  It’s the only way I can make any (non)sense of it.

[As a postscript, as I’m struggling to make sense of this, if anyone has any different thoughts please chip in below.]

Constructing remorse…

I’m not sure where I’m at right now. An odd mix of physical and emotional pain, despair, rage, intensity, incredulity, powerlessness. A heady mix of summat there’s no name for. Four years on from referring Valerie Murphy to the GMC. Seven months since her tribunal started in August 2017. My cross-examination during that first hearing. The drawing out of this process across two weekends in November and three days this week. Being battered with further evidence, excuses and shite.

A slow and inexorable torture.

Enter ‘remorse’

Remorse arrived in Manchester this week. Late in the day but Murphy’s barrister explained ‘the blessing’ of insight can take time for some doctors. [Yes really.]

George Julian carefully traced the crystallisation of this remorse over 4.5 years.

Short version here:

A remorse drenched reflective statement signed days before the hearing was shared with the panel.

Murphy even pitched up with a new version of the yellow card story. An exemplar in how ‘facts’ can be retrospectively squeezed into newly discovered remorse spaces. Bit of a fakery giveaway here with her aim ‘from’ rather than ‘of’ this project:

Someone has to drive this through she told the panel between sniffles, ‘a bad headache’ and having been apparently “emotionally broken” by these events.

The yellow card narrative. A redemption song.

Sense and sensibility

Stepping back, it’s obviously not possible to raise awareness of your own failings until you recognise you’ve failed. Given this recognition only happened in the last week or so it’s unlikely Murphy has been openly talking about her failings while spreading the news about the yellow card. [While off work sick].

Anyone calmly sitting next to their barrister tearing strips off a mother whose son died under their care is not ‘open about their personal failings’.

The panel must know this. They were there. They’ve read the mountain of documentation which includes shifting the blame to anyone or anything that moves.

Followers of the live twitter feed collectively groaned on Monday morning when after light questioning it transpired that the pioneering yellow card team of four had never met. A slow collapsing into vague reference to a chance meeting with one of the team at a conference back in 2014/5 and, the ultimate farce, regular meetings with the second who happens to be Murphy’s husband.

George live tweeting the proceeding was pulled up for ‘audible expression’.

The absurdity of the evidence presented on Monday and the subsequent acceptance of the panel to swallow this was more than apparent to those following.

The decision

The decision was published mid afternoon on Wednesday. 12 months suspension and another review. The sanction document (I’ve only managed to read up to page 8 so far) captures so much horror it’s difficult to understand the decision. Or this process really.IMG_3513

And then. Under mitigating circumstances on p7. This.

‘The difficult field of adult learning difficulties.’

It was the ‘difficult field of learning difficulties’ what did it for LB [for Danny Tozer, Edward Hartley, Thomas Rawnsley, Stephanie Binchcliffe, Anthony Dawson, Sarah Burnley… and so many others].

‘Difficult’ which, in this context, means less than. Less than human. Entitled to less than care in shoddy, substandard surroundings. Murphy was never going to be struck off for a less than death. She might have done nothing remotely resembling being a doctor but she only had to whip out a bit of made up remorse and a shabby incoherent story at the 11th hour to avoid erasure.

This damning statement by the panel effectively endorses the idea that certain people can expect to be treated appallingly. Utterly, utterly shameful.

Taking Mildred, Murphy and North Parade

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Rich and I walked down to North Parade yesterday so I could stock up on wool to help me get through the final section of the GMC tribunal. A process started in May 2014 when we referred LB’s responsible clinician to the GMC. The tribunal has spread out across two weeks in August, two weekends in November and a further three days from this Monday. 

The consultant, Valerie Murphy, relinquished her licence in 2014 and returned to work in Ireland. When we referred her we knew nothing about the patient who died seven years before LB in the same bath. A death she raised with the Trust in March 2014 and then 18 months later at LB’s inquest. A death dismissed in life.  Another layer of grim wrongness discarded as easily as a dirty wrapper in a street bin.

I already feel queasy that the sanction will be decided this week. The impairment decision makes for a devastating read and the process has been brutal. George Julian is back in Manchester tonight ready for the 9.30am start. She will be live-tweeting the proceedings at @JusticeforLBGMC shedding light on these processes (and allowing us to follow from home).

We walked down Cuckoo Lane. Passed the John Radcliffe hospital where LB didn’t die. The Oxford Brookes University nursery where he went as a tot (before being ‘released’ with a ‘too difficult for us’ stamp). Across the Marston Ferry Road and along the river to University Parks. Roaming around various North Oxford roads until we emerged opposite North Parade.

The small wool shop (Oxford Yarn Store) for a novice but seriously hooked crocheter was dazzling. Like a cave of brilliant jewels arranged and heaped on every surface, from floor to ceiling.The woman was reassuringly helpful showing me what wool I should use and a photo of the end result if I used the wool I liked. I suspect I’ll be a long term spiky novice on the stitching front (I have history here) but she was quietly encouraging.

After some careful questions about my recent turn to crocheting she said she was following what happened to LB and her nephew was autistic. She wished me luck and looked sad.

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Over on twitter (which constitutes about 15% of my current non-working life if I include the early hours of the morning) reverberations about Hadiza Bawa-Garba continue.  This is the doctor recently struck off by the GMC. I relentlessly stand on my timeline with a faulty light sabre (alongside a number of other family members, lay people and the rare medic) hitting back at what seem to be outlandish, extreme and inappropriate claims by hopefully a vocal minority of medics (though given the shedload of cash raised overnight to challenge the GMC decision I’m not sure). 

I don’t have any personal feelings about Bawa-Garba being struck off. I’ve consistently said that a legal process has been followed to the max and until further details of the original manslaughter trial are known there’s little point in speculating about ‘scapegoating’ or miscarriages of justice. I worry that Jack’s Down’s syndrome was a feature simply because of the dire mortality figures around learning disabled people. Certain people receive differing care across health and social care settings.

The tone of the challenge by the medical profession is grim; little or no consideration of Jack and his family (or worse), exclamation marks, unsavoury and sometimes inconsistent comments.  There has also been condemnation of dissenters to the ‘We are all Hadiza” calls. Among other things this week I was called Mildred from Three Billboards.  ‘A woman past caring’ said the medic dismissively erasing the intense love, complexity, humour and strength of McDormand’s character. I’ll take that, I thought. I’ll bloody take Mildred.

And hope the right decision is made this week.

The fish tank, gotes and dressing up

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An old mate Jill called round unexpectedly this afternoon while I was crocheting in the back room. I’m getting not too bad at crocheting squares with wobbly sides.

We had a bit of a reminisce over a cuppa and hob nob or two. The time we first met. About 20 years ago when Rosie, and Jill’s son Tristan, started at primary school together. Jill and I randomly sat on a wooden bench by the fish tank in the foyer so absorbed in chatting we missed the talk the headteacher was giving to new parents in the school hall. We laughed (in part horror) when they filed out passed us.

Failing our first ever school-related parental task.

The headteacher explained in the talk we missed that the bench by the fish tank was where kids would wait when no one turned up to collect them at the end of the day. The cone of shame bench. Rosie was to sit there a few times over the next four or five years. After what now seem like capers in the overly complicated and convoluted world of family life when a child is labelled as disabled.

ConnorWe remembered how Tristan became a regular fixture at ours after school typically wearing his Thunderbirds outfit. Virgil. Captain Tracey… The outfits.

I’d forgotten about the outfits. LB was a sucker for dressing up. Captain Scarlett, Woody from Toy Story, a racing driver, the Early Learning Centre policeman tabard. Batman to Tom’s handed down Spiderman.

Washing up gloves, school shoes and wobbly masks. The full gear.

Jill’s younger son Will became one of Tom’s bezzy mates. He was with us on the visit to the rare breeds farm when LB let the goats out.  I still chuckle when I remember being in that tiny space with LB and those cheeky goats. I recently found his school holiday diary where he’d written:

‘I let the gotes out’.

You did matey. And I should have seen it happening.

We didn’t half laugh though. That memory is priceless.