Last week I emerged from hibernation (life is a bit tough right now for lots of reasons) to attend a ‘Psychology at the Movies’ screening of 55 Steps – an important and hard-hitting film based on a true story of Eleanor Reise (a lady repeatedly drugged against her will, played by Helena Bonham Carter) and Collette Hughes (her lawyer, played by Hilary Swank) that has been effectively buried. What I write here is based on a series of tweets I made, trying to explain why we need to work together to resurrect it.
The opening scene was far more familiar than the 80s US asylum should be. Whilst our wards in the UK are often more modern and I’ve never seen someone tied to their bed, ‘physical restraint’ is very much alive & kicking. I have been bundled into seclusion, forced to the ground, had my pants pulled down & been injected with a drug that stole my will. I’ve felt humiliated, desperately needing a wee and being left for hours.
In response to Collette’s opening gambit of her being there to help, Eleanor said: ‘Everybody’s here to help me. That’s why I need help’. This cuts to the heart of it. Most people working in mental health want to ‘help’. Most family members agree to hospitalisation hoping it’ll ‘help’. Wider society is able to avert their eyes because good and kind people are trying to ‘help’. By framing restraint and forced drugging as an intervention to give treatment we have created a guided mask for what is essentially state-sanctioned GBH (Grievous Bodily Harm).
In almost any other situation, pinning people down and injecting them would be cause for investigations and criminal charges. The perpetrators would be seen as aggressors. Those who fought back would be seen as courageous. Those who accepted their fate would be understood. Against such odds, fighting back isn’t always the best option. Those who said they deserved such treatment, or that it was in their best interests, would be heard … but we would not send them back for more. We would draw a line.
We try not to draw comparisons with sexual assault, or allow ourselves to fully recognise or feel the profound degradation involved. We focus on the kindness and professionalism of the staff, the training provided, the illness of the person and that it is an intervention of last resort. We resort to the idea that lives are at risk if we do not act. That it is the only option available.
Yes – lives are at risk. Our lives. Systemising and reducing the risks of restraint only makes sense if we accept such coercion is necessary and ethical. It’s about making something less crap. It helps us feel better, but avoids the important dialogue – what do we need to do to stop this? How do we bring our mental health system back from the edge? How do we stop traumatising patients and staff in this way?
Investment, alternatives, attitude change, resourcing .. there’s much to be done. As long as we accept that holding people down to force them to take drugs is OK, will this change? It’s a plaster concealing a gaping wound that doesn’t cease to bleed just because we no longer have to look at it.
This might all sound dramatic – it is. It needs to be.
My experiences are mild comprised to many. I’m white, female and mostly related to coercion with compliance. I learned the game and the limits of my free will early into my journey. I was not Eleanor Reise. I did not call a lawyer and fight for the rights of me and my fellow patients. Together, her and Collette did something amazing. I want to celebrate that. It’s a tonic. I want to drink it in and feel that change is possible. That it’s possible to fight and win.
Eleanor died before this film was made. The impact of these drugs on her body was too much and, eventually, led to her early death. Despite the hard hitting realisation that the quality and length of people’s lives are at stake, this is not an anti-meds movie. It acknowledges that, even with informed choice, many would agree to take medication voluntarily. I think they would. But the concept of informed choice is key.
I re-started on Quetiapine last year after the birth of my baby. I know a lot about the drug. I knew it would probably help me (it does). I knew it’s possible adverse effects. I was not held down and forced to take it. I was not under a section. Yet, it was not a choice. Having been coerced in the past, I have always made a calculation about how far professions would let my decision to not take meds stand. The fact I could eventually be forced was a factor in my decision to agree. That is not true consent. It’s not choice. There was no other alternative. Now, a year later, I’m dealing with Tardive Dyskinesia – a topic featured in the film – and, yet again, withdrawing.
From the opening scene to its final thought, the film sets out the systematic dehumanisation of people diagnosed with ‘severe mental illness’ and the terrible cost borne by those who are deemed ‘mad’ and our society as a whole.
We need public will to fight again this and create the humane and ethical alternatives we need so badly. That takes money and rethinking our whole approach to supporting those in distress. Without a public outcry can you really imagine any government taking on such an initiative, especially as previous outcries have generally led to more coersion.
If you can, please check out 55 Steps. At the moment you can find it on Amazon Prime and Google Play.
Let yourself really feel what this treatment did to Eleanor and don’t avert your eyes. Value her strength, and the determination of her lawyer. Use that to stand up and say ‘NO’. Write to your MP. Write to your local mental health charities. Push for it to be screened in your local independent cinema. Tell any advocacy, patient experience, user-led, feminist, campaigning, legal, mental health, social justice, bird watching or social group you’re involved with about it. Group together and host a DIY screening, even.
Please do something. Don’t just watch it and go on with your lives. We are the ones who allow this to continue. We need to make our voices heard and let people know that this is not, in any way, mental health care.
Thank you to all those who arranged it, took part in the panel and allowed themselves to be affected by it. Including: Dr Sara Tai (Uni of Manchester), Prof. Peter Kinderman (Uni of Liverpool), Bryan Bonaparte (Uni of Westminster), Helena Bonham Carter CBE, Colette Hughes, Norman Lamb MP and Mark Bruce Rosin (the witer and producer of 55 Steps).
me too <3 ty <3
Psychiatry is changing at last, albeit, slowly…
Yes, yes, yes!
I am deemed crazy, strapped to a bed and imprisoned for demanding my rights…not violently, just not in the helpless, compliant way people expect me to be.
Those that harm me, break the law, don’t follow policies, are experts doing their jobs. If they are challenged by someone with power, I am thanked for my feedback.
In Australia the lawyers won’t look at mental illness cases. “If they’d followed the law you may still have been traumatised.” Our rights are only considered if we die…and again our role is educating others.
People are wilfully blind, or scared; my rights are sacrificed so the caring profession can remain comfortable and ignore my distress…except patients and staff alike know this corrupt system serves none of us and traumatises all of us. Now that is crazy.
I cannot understand how “normal” people’s consistent delusions about evidence, efficacy and best practice are not deemed INSANE in the face of actual humans dying, distressed and unable to live in this heartless paradox. At the same time, protesting against inhumane, illegal, unhelpful and unkind treatment leads to me losing my freedom because of lack of mental capacity and reason.
It’s like a huge absurd nightmare where the punchline for me has been realising I will never be a human to the community, even though, in fact, I am human.
I desperately need to see this film. I need that tonic to give me hope that one day we who can see, on both sides of the locked doors will unite and call the B S so we can all enjoy a safe and meaningful life. I need to see someone with power stand and fight with someone who has been treated badly in the name of “care”
I’m sorry that you are having added consequences from your “cures”. Parenting and surviving takes heaps of hope and energy. I hope you have the supports you need.
I have four children now adult…”adopted baby”, “tricyclics baby”, “ECT baby” and “Prozac baby”.
They all survived and are decent, resilient, compassionate, creative men.
Totally agree having experienced some of the above in Scotland. It’s hidden inside these hospitals and there are no real alternatives. Don’t know any lawyers who would challenge it as it’s state sanctioned but am willing to help to change things.
Hallo Rachel. I was looking you up after watching the Oxford Q&A) from 2018 following the screening of the “Mad to be Normal” film.
I didn’t know of you before (I did know of Marjorie and Bob and definitely R D Laing).
You made the most sense.
I’m now going to buy the film you are trying to get noticed. Have watched the trailer. Helene BC is very good as ever.
What I particularly liked about what you said on the table – why search for genes so that they can be eradicated? Agreed! My brother was diagnosed with Schizophrenia 50 years ago (his diagnosis has never been changed). He will always be as he is but with a medication that he is willing to take he can be himself safely.
I’ll be back in due course.
Best wishes
Thankyou! I remember that event … I had only recently had a baby, so was surprised I made any sense at all 🙂 I am glad your brother is finding a way of being himself. My diagnosis is back, not that I agree with it 🙂 But I think the medical profession are not so good at responding to the variety in what it is to be human and how we process our distress. With warmth, Rai