A Disorder For Everyone!

By Sophie Olson @TheFlyingChild

Yesterday I delivered my first workshop for A Disorder For Everyone AD4E. The workshop was aimed at those working in therapeutic and support settings and we explored how to best support CSA survivors without pathologising and retraumatising them.

I discussed how the ‘help’ I received in the mental health system was medicalised from the start. I was told the ‘issue’ was in my head, that I was ill and there was ‘a chemical imbalance’ in the brain. This scientific validity of psychiatric diagnosis is now widely disputed, but I had no ability to challenge it at that time. I knew deep down that abuse was the crux of the issue but thought it had caused my brain to ‘go wrong’. I trusted my consultant.

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Surviving in Stormy Seas

By Sophie Olson
A Poem by Sophie Olson that reads:

do you drink every day?
and she recalled
how heavy the weight 
of her coat
a stumbling trudge under street lamps at dusk
blank faces of commuters
as she stood on the edge
and waited
hopeless in her head
debating
the pull of motherhood
considering
milk-mouthed babies
starfishes in warm beds

There were so many days like this. Too many days. It feels like a lifetime of surviving. Often I wonder why I did survive. Sometimes I feel so very old.

This poem reflects a point in my life where I had reached out for help more times than I can remember. I had tried to be stronger, happier – more resilient. I had tried to focus on, and be grateful for the good things – there were many good things – but I was drowning and help wasn’t forthcoming.

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The Flying Child CIC celebrates after receiving National Lottery Community funding

The Flying Child CIC celebrates after receiving National Lottery Community funding

Press Release: November 2022

A Surrey-based Community Interest Company, The Flying Child is celebrating today after being awarded three years of funding from The National Lottery Community Fund, to support survivors of child sexual abuse (CSA) in Surrey and to continue providing professional training through The Flying Child Project.

Founded in 2020, the survivor-led project has reached over 1000 professionals to date, across the U.K. in Education, Social Work, and healthcare settings, improving understanding of trauma resulting from CSA and the confidence of professionals in supporting both children and adults in a trauma informed way. In a recent participant survey, 100 percent of attendees said they felt better equipped to manage a disclosure of CSA, with all likely to recommend the training to a colleague.

“The training was fantastic. It openly addressed difficult conversations through real life experiences and first-hand conversations. It really highlighted the volume of CSA in the community, some not dealt with. We haven’t had training like it. I would recommend every [professional setting] to participate”.

Training participant (Primary School Teacher)

The new National Lottery funding will allow The Flying Child Project to continue their training, aiming to reach thousands more over the three-year period. It will also fund The Flying Child peer support and creative well-being groups for survivors of CSA in the local community.

The groups will consist of a 12-week therapist-led programme, co-facilitated by a lived experience support worker. In addition, creative groups for survivors will be offered, providing the opportunity to express trauma through art and writing, meet other survivors and build networks in a supportive space. Over the next three years The Flying Child aims to support 360 survivors of CSA – with initial groups starting in the new year.

Sophie Olson, founder and managing director of The Flying Child, said: 

“Thanks to National Lottery players, this grant means we have a fantastic opportunity to improve outcomes for both child victims and adult survivors of CSA. As an organisation we normalise speaking about an ‘unspeakable’ subject and challenge the societal culture of silence. Lived experience in training helps to break down barriers and dispel myths that lead to victims of abuse being overlooked, and their normal reactions to trauma being misunderstood. The current statistics estimate there are 11 million adult survivors of CSA in the UK, equating to 1 in 6, yet are a large, hidden, and marginalised group, with services often not adequately trauma informed or accessible.

 CSA is a devastating form of abuse with long-lasting consequences on mental and physical health, and wellbeing. Peer support groups play a vital role in the community. Because CSA is considered a taboo subject, stigma and shame silences the majority with many believing they are the only one. This is something we aim to change. This grant will make a big difference to people’s lives.”

 The Flying Child encourages the local community to engage on Twitter and Instagram @flying_project, and to become survivor ‘allies’ – helping to challenge the silence surrounding CSA. Sophie Olson’s story can be heard on the BBC Radio 4 documentary The Last Taboo. For more information about the training or peer support groups, please visit www.theflyingchild.com.

During the pandemic, in 2020 alone, The National Lottery Community Fund distributed almost £1 billion to charities and community organisations across the UK.

To find out more visit www.TNLCommunityFund.org.uk  

Drop The Disorder Poetry Night

I consider myself a survivor of CSA and the psychiatric system, and was pleased to take part in an event by Drop The Disorder: an evening of spoken word performances to challenge the culture of psychiatric diagnosis and the pathologising of emotional distress.

One of the most significant moments of my journey was the time I reached out to a GP as I was leaving an appointment. She was kind, but as there was no screening for trauma, I was set on a path that delayed recovery for an entire decade. She didn’t intend to cause me further harm, she probably had little idea of what else to do with me. Trauma-informed pathways are long overdue and it is time for change. It is hard to have conversations like these without being accused of stigmatising mental illness but those who are harmed by the system must feel able to speak. When I do, I’m not denying the experiences of those who benefit from treatment, I’m validating my own experiences as someone who was failed by that system.

I regret hesitating at the door. This poem is called Door Handle Moment

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Why didn’t you say anything before?

Why didn’t you say anything before? Were the words said when I disclosed. I didn’t know how to respond to that. The things I wanted to say spun inside my head and stuck in my throat but I couldn’t say them. I swallowed my words and looked at the floor instead.

Why didn’t you…?… you could have… you should have…

The events of that disclosure day unfolded violently, like a bomb exploding and glass embedding itself in our hearts. It was one of the hardest and worst things I’ve ever had to do. I tried to say why I hadn’t, I really did but I was mute with shame, regret and fear.

My fault was how I interpreted these responses. It’s my fault.

I was probably in shock too. Disclosure might be shocking for the recipient but it’s far worse for the one saying the terrible words we hoped we might never have to actually say – no more hoping that someone would just notice, ‘get it’ instead. It felt like peeling the skin from my bones, exposing the essence of me to the world. It hurt. I wanted to run away and hide. I wished I’d never said anything at all.

It was impossible to explain why I hadn’t because where would I begin? How could I describe my inability to retrieve the correct words and to speak them aloud? I didn’t say much after I disclosed. I couldn’t answer their questions and some of them made me feel so unsafe I wanted to die. I stayed silent and scrutinised their faces and body language. I was looking for any nuance of behaviour for a sign they didn’t believe me.

I waited to be cast out of the family and shunned for saying these terrible words.

Why didn’t you say anything before?

Now I have my words and if I could go back in time and do it all over again I would say,

I did.

I had been non-verbally disclosing since childhood but nobody was listening. They didn’t understand what I was trying to say.

Dentists Need To Know

Over the last few weeks I have been using my own lived experience as a survivor activist, working with The University of Bristol, Bristol Dental School and activists Viv Gordon, Patricia Debney and Hazel Larkin to coproduce research ‘Improving Access to Oral Health Services for Adult Survivors of Child Sex Abuse.’ It has been a wonderful and empowering project to be part of, beautifully and safely held by all, and I’m excited by the change already on the horizon. Many survivors (including myself) find accessing dentistry almost impossible and I look forward to the day in which survivors’ needs are recognised. We can be perceived as ‘nervous’ patients but this is not the case. We are traumatised by our experiences of abuse and going to the dentist can be triggering and re-traumatising, leaving many of us avoidant. The fault does not lie with us for not being able to ‘overcome our fear’, it lies with a system that doesn’t (yet) understand and accommodate our needs. Many thanks to Brigstow Institute and Bristol and Weston Hospital Charity for funding such valuable and vital research, and to Viv for setting this ball in motion.

This is my response to one of the creative writing tasks from the workshops. We were asked what we thought ‘Dentists need to know.’

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Catching the Feather:

A short story of CSA

There was a brown flower on the cups we drank our tea from.

I once filled the brown flower cup with water and around thirty soluble aspirins. I then used that vile mixture to wash down around twenty paracetamol tablets, I was 11 years old and I never, ever, told a soul… The hospital staff looked for reasons for my illness, from kidney stones (which I was ultimately plagued with) to appendicitis (had appendix out on another attempt, and never told a soul), but they could not find anything. Just that my liver wasn’t working and I was a very poorly girl. I was allowed home with no diagnosis.

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On the Crest of a Wave

Content: Child sexual abuse. Suicide.

This week I have been considering why it’s so hard for survivors to reach out even when our support network is strong. I feel that I’m an old hand at this and it should be easy to say when I’m triggered but it’s not. Some triggers grind me to a halt and I need to take a few days to reflect on what it was, process the memory and wait for the wave to pass.

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ACE’s: Proceed With Caution

I recently watched an online discussion about ACE’s and outcomes for the individual. As a survivor of childhood sexual abuse, it made me feel a bit uncomfortable. Trauma; how we react to trauma, and the consequences of trauma will vary between individuals. We are all different, and labelling trauma survivors must be done responsibly and with caution. Most would agree that support for trauma survivors is lacking and inconsistent and must be more widespread, but care should be taken when striving for a trauma-aware society, not to inadvertently end up with a one-size fits all model of care. 

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Why a child (or adult) survivor might not disclose abuse (and how to word a question in a way that may promote disclosure)

By Sophie Olson

This blog post stems from an email to lady who asked a question on a tweet. The tweet emphasised the need to ask a child again, if you think they may be being abused but they deny they are. She asked how these questions could have been worded to encourage disclosure. I sent her a couple of first-hand accounts from survivors of CSA along with my own. This is my (edited) reply.

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Trained Thoughts…

Some of the most desperate in society have suffered more than you can possibly imagine.
I live near an organisation that provides help for the homeless, many of whom have challenging mental health needs. A lot, if not all of these people will have suffered trauma
in the past and now face daily judgement.

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