I reached my limit on a cloudy day in March 2025. I reached it not because of one dramatic event, but because of the slow, persistent erosion of dignity I’d experienced over time – an erosion caused by small but painful encounters with fellow healthcare professionals. As a Diagnostic Radiographer with more than 35 years’ experience working in healthcare, including 15 years in the NHS, I never expected that becoming a patient would be the hardest experience of my life.
My personal journey through breast cancer began in 2022 with a diagnosis that changed everything. Then, in May 2024, I received a second diagnosis – this time on the contralateral breast, discovered during my two-year routine surveillance. Since that first diagnosis, I have endured surgery, radiotherapy and ongoing systemic treatments, including an aromatase inhibitor. I’ve undergone biopsies guided by both ultrasound and MRI, and RF tag placements using stereo mammography. I carry the physical scars, tattoos and lymphoedema that tell the story of survival and pain. But those are only part of the story. The emotional bruises, the psychological toll of dismissive and impersonal care, are just as lasting.
I’ve seen the NHS at its most brilliant: efficient, kind and deeply human. But I’ve also seen it at its most disconnected. During my second round of radiotherapy, I chose private healthcare because the thought of enduring another NHS experience like the first was too much. That choice was right for me, but it shouldn’t have had to be that way.
My lived experience
Across the 35 months since my initial diagnosis, I have felt increasingly invisible. My dignity and individuality were repeatedly overlooked. I was made to feel like an inconvenience, a task to be managed rather than a human being needing care. I was forced to get off a trolley while still under the effects of anaesthesia. A drug reaction was casually dismissed. I was discharged post-operatively before I could safely walk unaided. I wasn’t allowed a gown during radiotherapy. These may seem like administrative or procedural failures but, to the patient on the receiving end, they are deeply dehumanising.
I’ve been told my body habitus is awkward. A radiographer leaned their full weight onto my back during an MRI, pushing me into a hard device corner while I lay prone with my breast in a clamp and cannulated. I was told about potentially needing more extensive genetic testing – again, while I was clamped into a machine mid-MRI biopsy. This same biopsy team casually discussed how far apart the samples were being taken – again, while I was undergoing the procedure. In these moments, I wasn’t a person with fears and feelings. I was an object being processed.
Even moments that should have brought comfort instead delivered cold detachment. A nurse specialist gave me difficult news without even closing the door. A qualified nurse told me to stop crying when I broke down at a pre-op assessment. My concerns about lymph nodes were dismissed – by one of my own colleagues. And then, the final straw: a surgical registrar instructed me with a dismissive wave to undress behind a curtain, without a smile, a name badge or even a trace of empathy.
Because I’m a radiographer
As a radiographer, I experienced these moments with an additional layer of awareness. I knew the protocols, the systems and the pressures my colleagues were under. I recognised when things were done well and when they weren’t. I understood when a comment was inappropriate, when a procedure lacked explanation or when empathy was completely absent. This professional insight heightened my sense of vulnerability. I wasn’t just upset by these failings, I knew exactly how preventable they were. I knew the standards we are all trained to uphold, and it was deeply painful to see them ignored.
A better way
None of this was inevitable. Every interaction could have been an opportunity for connection and compassion. I wish I had been treated like the vulnerable human being I am – someone navigating the profound fear, grief and exhaustion that comes with a cancer diagnosis.
I wish people had said hello. I wish they had introduced themselves, worn their name badges clearly and taken just a moment to acknowledge that I was scared. It would have meant everything to hear: ‘I know this is hard; I’ll take good care of you.’ A few simple words, offered sincerely, can profoundly alter how a patient experiences treatment.
I wish healthcare professionals remembered that a cancer patient isn’t just physically wounded – they are emotionally raw. Thoughtless words, brusque actions or rushed procedures all become emotional burdens that patients carry long after their physical wounds begin to heal.
For me, the hurt was compounded by the knowledge that I would never have treated a patient in this way. That discrepancy – between what I knew was possible and what I experienced – created a powerful sense of disillusionment. The knowledge that I was both a colleague and a patient made the indifference that much more painful.
What can radiographers learn from my experiences?
As radiographers, we are often the first or only point of contact for patients undergoing terrifying and life-altering tests. Our role is not just technical, it’s profoundly human. Every time we position a patient, explain a procedure or guide them through imaging, we are part of a story they will never forget. We may perform the same task many times a day but, for that patient, it may be their first, or most frightening, experience.
I reached my limit on a cloudy day in March 2025. I reached it not because of one dramatic event, but because of the slow, persistent erosion of dignity I’d experienced over time – an erosion caused by small but painful encounters with fellow healthcare professionals. As a Diagnostic Radiographer with more than 35 years’ experience working in healthcare, including 15 years in the NHS, I never expected that becoming a patient would be the hardest experience of my life.
My personal journey through breast cancer began in 2022 with a diagnosis that changed everything. Then, in May 2024, I received a second diagnosis – this time on the contralateral breast, discovered during my two-year routine surveillance. Since that first diagnosis, I have endured surgery, radiotherapy and ongoing systemic treatments, including an aromatase inhibitor. I’ve undergone biopsies guided by both ultrasound and MRI, and RF tag placements using stereo mammography. I carry the physical scars, tattoos and lymphoedema that tell the story of survival and pain. But those are only part of the story. The emotional bruises, the psychological toll of dismissive and impersonal care, are just as lasting.
I’ve seen the NHS at its most brilliant: efficient, kind and deeply human. But I’ve also seen it at its most disconnected. During my second round of radiotherapy, I chose private healthcare because the thought of enduring another NHS experience like the first was too much. That choice was right for me, but it shouldn’t have had to be that way.
My lived experience
Across the 35 months since my initial diagnosis, I have felt increasingly invisible. My dignity and individuality were repeatedly overlooked. I was made to feel like an inconvenience, a task to be managed rather than a human being needing care. I was forced to get off a trolley while still under the effects of anaesthesia. A drug reaction was casually dismissed. I was discharged post-operatively before I could safely walk unaided. I wasn’t allowed a gown during radiotherapy. These may seem like administrative or procedural failures but, to the patient on the receiving end, they are deeply dehumanising.
I’ve been told my body habitus is awkward. A radiographer leaned their full weight onto my back during an MRI, pushing me into a hard device corner while I lay prone with my breast in a clamp and cannulated. I was told about potentially needing more extensive genetic testing – again, while I was clamped into a machine mid-MRI biopsy. This same biopsy team casually discussed how far apart the samples were being taken – again, while I was undergoing the procedure. In these moments, I wasn’t a person with fears and feelings. I was an object being processed.
Even moments that should have brought comfort instead delivered cold detachment. A nurse specialist gave me difficult news without even closing the door. A qualified nurse told me to stop crying when I broke down at a pre-op assessment. My concerns about lymph nodes were dismissed – by one of my own colleagues. And then, the final straw: a surgical registrar instructed me with a dismissive wave to undress behind a curtain, without a smile, a name badge or even a trace of empathy.
Because I’m a radiographer
As a radiographer, I experienced these moments with an additional layer of awareness. I knew the protocols, the systems and the pressures my colleagues were under. I recognised when things were done well and when they weren’t. I understood when a comment was inappropriate, when a procedure lacked explanation or when empathy was completely absent. This professional insight heightened my sense of vulnerability. I wasn’t just upset by these failings, I knew exactly how preventable they were. I knew the standards we are all trained to uphold, and it was deeply painful to see them ignored.
A better way
None of this was inevitable. Every interaction could have been an opportunity for connection and compassion. I wish I had been treated like the vulnerable human being I am – someone navigating the profound fear, grief and exhaustion that comes with a cancer diagnosis.
I wish people had said hello. I wish they had introduced themselves, worn their name badges clearly and taken just a moment to acknowledge that I was scared. It would have meant everything to hear: ‘I know this is hard; I’ll take good care of you.’ A few simple words, offered sincerely, can profoundly alter how a patient experiences treatment.
I wish healthcare professionals remembered that a cancer patient isn’t just physically wounded – they are emotionally raw. Thoughtless words, brusque actions or rushed procedures all become emotional burdens that patients carry long after their physical wounds begin to heal.
For me, the hurt was compounded by the knowledge that I would never have treated a patient in this way. That discrepancy – between what I knew was possible and what I experienced – created a powerful sense of disillusionment. The knowledge that I was both a colleague and a patient made the indifference that much more painful.
What can radiographers learn from my experiences?
As radiographers, we are often the first or only point of contact for patients undergoing terrifying and life-altering tests. Our role is not just technical, it’s profoundly human. Every time we position a patient, explain a procedure or guide them through imaging, we are part of a story they will never forget. We may perform the same task many times a day but, for that patient, it may be their first, or most frightening, experience.
‘We must all take the time to reflect and ask what we can do to improve care’
Charlotte Beardmore, SoR executive director of professional policy
Thank you for sharing your experience and for taking the time to do so. We’re truly sorry to hear what you went through. Sadly, we know from national patient experience surveys, as well as from conversations with friends and colleagues, that your experience is not unique.
These are undoubtedly challenging times in healthcare, and it’s more important than ever that we keep patients at the centre of everything we do. We must strive to provide the kind of care we would want for our own loved ones.
Listening to and reflecting on feedback like yours is essential. It helps us understand what truly matters to patients and how we can continue to improve the services we provide. As the author rightly points out, it’s often the simplest actions—those that require no extra time—that can have the greatest impact. These actions are fundamental to what it means to be a radiography professional.
Improving and enhancing patient care remains a shared responsibility. As an organisation, our strategic priorities are focused on both patients and professionals. The Education and Career Framework, published in 2022, sets out the standards for the radiography profession. Importantly, patients from our advisory group played a key role in shaping this framework, ensuring that education and training remain grounded in patient and public needs.
All graduate radiography programmes approved by the College of Radiographers must demonstrate meaningful patient involvement in their design. Learning outcomes are expected to reflect the high standards necessary to support excellent patient care.
Our recently published strategies from the Society and College of Radiographers reaffirm our commitment to supporting patients and improving care. We also recognise that some of our existing guidance, such as Patient, Public, Practitioner Partnerships, hasn’t been as widely known or used as intended. That’s why our Patient Advisory Group will soon begin reviewing and updating this guidance to ensure it better supports the profession.
Looking ahead, our incoming President, Katie Thompson, will lead a year-long campaign to encourage all members of the radiography workforce to introduce themselves clearly—using phrases like “Hello, my name is… and I’m a diagnostic/therapeutic radiographer/sonographer.” This simple act of introduction can help build trust and connection with patients.
We must all take the time to reflect on the experiences shared and ask ourselves what more we can do to improve care. We have a collective responsibility.
Our patients deserve nothing less.
Thank you for sharing your experience and for taking the time to do so. We’re truly sorry to hear what you went through. Sadly, we know from national patient experience surveys, as well as from conversations with friends and colleagues, that your experience is not unique.
These are undoubtedly challenging times in healthcare, and it’s more important than ever that we keep patients at the centre of everything we do. We must strive to provide the kind of care we would want for our own loved ones.
Listening to and reflecting on feedback like yours is essential. It helps us understand what truly matters to patients and how we can continue to improve the services we provide. As the author rightly points out, it’s often the simplest actions—those that require no extra time—that can have the greatest impact. These actions are fundamental to what it means to be a radiography professional.
Improving and enhancing patient care remains a shared responsibility. As an organisation, our strategic priorities are focused on both patients and professionals. The Education and Career Framework, published in 2022, sets out the standards for the radiography profession. Importantly, patients from our advisory group played a key role in shaping this framework, ensuring that education and training remain grounded in patient and public needs.
All graduate radiography programmes approved by the College of Radiographers must demonstrate meaningful patient involvement in their design. Learning outcomes are expected to reflect the high standards necessary to support excellent patient care.
Our recently published strategies from the Society and College of Radiographers reaffirm our commitment to supporting patients and improving care. We also recognise that some of our existing guidance, such as Patient, Public, Practitioner Partnerships, hasn’t been as widely known or used as intended. That’s why our Patient Advisory Group will soon begin reviewing and updating this guidance to ensure it better supports the profession.
Looking ahead, our incoming President, Katie Thompson, will lead a year-long campaign to encourage all members of the radiography workforce to introduce themselves clearly—using phrases like “Hello, my name is… and I’m a diagnostic/therapeutic radiographer/sonographer.” This simple act of introduction can help build trust and connection with patients.
We must all take the time to reflect on the experiences shared and ask ourselves what more we can do to improve care. We have a collective responsibility.
Our patients deserve nothing less.
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