My name is Sophie Olson.

I’m from the United Kingdom. I decided to take part in Victorious Voices because I believe our stories are the key to breaking stigma, which in turn is a form of prevention. One person speaks, then the next...and on it goes. There is a ripple effect to speaking out about child sexual abuse that has the potential to change lives in extraordinary ways. 

I challenge the myth that child sexual abuse is rare or that it only happens ‘somewhere else.’ Child sexual abuse occurs in all communities and suggesting otherwise not only risks demonising specific groups but also harms survivors who don’t fit the prevailing stereotypes. I challenge the widespread belief that our responses to surviving child sexual abuse are reflective of ‘disorder,’ and I advocate for trauma-responsive, non-pathologising support for ALL survivors, including professionals expected to respond to and support victim/survivors.

I was sexually abused in the family home, up to the age of 14, by a close family member. As well as sexual abuse, I was subjected to other forms of abuse (much of it hidden from others in the family), that continued into adulthood. I am from a middle-class background and was privately educated. As a child and young person, I showed many signs and indicators of child sexual abuse, but they were misunderstood or dismissed by family, schools, and healthcare professionals. I made partial disclosures to professionals at 18, 25, and 30, but I don’t consider these moments full disclosures, because most of the words I needed to say -especially the word rape - I couldn’t.

 Like many survivors in distress I reached out for help and ended up in the mental health system. It was a system that caused immense harm. When the ‘treatment’ made no difference to the distress of child sexual abuse, my Psychiatrist said my ‘illness’ was ‘severe and enduring’ and that I would never recover or live without community support or medication. I was also told I’d be on lifelong benefits. 

The turning point for me was the death of someone I knew. She died by suicide after giving evidence in court. I rang a helpline and was told about a local charity that could help me. 

Accessing peer support helped me to find some sense of validation. I connected with other survivors and for the first time felt like I was less alone with my experience. A few years later I disengaged from the mental health system entirely and asked the facilitator - Pat - if she could take me on as her private client.

 

I tried different creative methods in therapy to speak the ‘unspeakable’ - art, collage and eventually (and most successfully), writing. I wrote about the abuse in the style of a fairy tale - immersing myself in my own story, with a lot of support from Pat. Speaking the words and sharing my story was the most vital part of the healing process. I wrote a lot of poetry too, always to express the words I find harder to say. Regular writing practice continues to help me, as healing from child sexual abuse doesn’t have an end point. The impacts of child sexual abuse are lifelong, which is why I am passionate about improving the current response to victims and survivors.

Pat worked intuitively, was safely flexible with her boundaries and able to offer more in terms of communication between sessions. She didn’t stick to scripted platitudes or a formulaic approach. After previous failed attempts at therapy, for me this was what made the difference. It wasn’t a linear process. In processing my story, I fell backwards into the familiar abyss. It was overwhelming to reveal, accept and process the abuse because I had minimised it for many years, mainly as a protective factor. Overcoming these setbacks were only possible because of the support of a skilled, patient, experienced and wise practitioner who not only helped me process the abuse, but believed I could achieve my highest dreams and potential.

Up until therapy with Pat, I had been waiting for someone else to ‘fix’ me because I was told I needed fixing by a mental health system who diagnosed survival as mental illness. It was a lightbulb moment when I realised Pat might be able to guide me from the darkness, but she couldn’t save me. Only I could do that. Over time I realised I didn’t need fixing because I wasn’t broken. I had been sexually abused. I was reacting normally to trauma. Because of her empathy, understanding, kindness, and non-pathologising support I found a way to tell the whole story. Finding the words set me free. 

But in sharing my story with a wider circle, I realised not everyone was able to stand by me. A couple of friends ghosted me. This was devastating because it made me feel ashamed of speaking out. Then it made me angry. Why as survivors are we so hard to see and hear? Yes - the subject is difficult, but negative societal responses to survivors, in workplaces, communities and families, exacerbate often deep-seated feelings of shame. The shunning, pathologising, disbelief and victim-blaming serves only those who commit these crimes against children.

 Over time, my experiences both pre and post disclosure became the driving force behind the set up of my own community interest company: The Flying Child CIC. I was determined that survivors receive better in terms of recognition, opportunities and support. We received National Lottery Community Funding to provide support for adult survivors, and our training arm - Side By Side CSA - works across all sectors to improve professional confidence in the subject. We support professionals to explore and overcome their own barriers to engaging with a deeply uncomfortable subject, and invite them to respond to the needs of survivors in a way that does not compound trauma. Our training is delivered by those with lived experience, and professional allies from within the system. As of September 2026, we will be working internationally. My first book - The Flying Child, A Cautionary Fairy Tale For Adults was published in 2024, by ZunTold. It documents my journey through therapy, and is co-authored by my therapist Patricia Walsh.

Today, my work as a writer, researcher, educator and speaker means more to me than I can even put words to. This is because my own education was cut short by a university professor who threw me out of my degree rather than asking why I was struggling and falling behind. I started far later in life than I would have preferred, but I am proud of my professional achievements. For so long I believed I was incapable of work. 

I have a few words of advice to other CSA Survivors on their healing journey. Firstly, we are all different and what helps one survivor might not help the next, so don’t give up if whatever you’re trying isn’t helping. It says less about you and more about a systemic rigidity in terms of what support is offered to survivors (for example - in my case, a medicalised ‘meds and diagnosis’ type of support did nothing to help me - but I wasn’t aware there were other options, as no professional ever said). There is always another option, but sometimes it takes a while to find it.

 Secondly there is no such thing as a ‘perfect survivor.’ Try not to compare yourself to others. Life can be very challenging, and sometimes, simply putting one foot in front of the other is enough. Survivors sometimes contact me and say, “I can’t do what you do.” I really do understand this mindset and the erosion of hope that can happen over time, but I would say: Never say never. You might come across people who make you believe you are too ‘damaged’, ‘complex’ or ‘fragile’ to ever live a ‘normal’ life. Don’t buy into it because it’s simply not true. There are doors open to me today as a survivor of child sexual abuse that I never knew were there. Good support, plus building up relationships within the survivor community led me to places I once believed were firmly out of reach. I continue to reclaim a sense of identity and agency through working and contributing to society, in a way I believed (and was told) was impossible. 

I’m not a fan of self-care - as I still find it hard to recognise my own needs in this respect, but things that are important to me are: Writing. Working. Advocacy. Activism. I do not see myself as ‘recovered’ as I will always be a survivor - and of course my experiences still impact me in many ways, but there is a strong sense of purpose that was missing before. I loved (and still do) being a mum of four, but I also needed something for me.

You can find out more about The Flying Child CIC - a nonprofit organisation leading conversation about survivor-led training, campaigning and support, at www.theflyingchild.com, and on our socials @TheFlyingChild.

 #SocietysShameNotMine #SideBySideCSA #TheFlyingChild

Sophie Olson Victorious Voices
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