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"All I needed was for somebody to care"

About: Crisis Mental Health / Crisis Resolution Home Treatment Team (CRHTT) Crisis Mental Health / Decisions Unit (DU) Crisis Mental Health / Liaison psychiatry Northern General Hospital / Accident and emergency

(as a service user),

I struggled with my mental health for many years before finally seeking help. A diagnosis of autism and several years of repeated recoveries and relapses from depression followed. In 2023, after an escalation of events in my personal life, I took an overdose. Perhaps something deep down in me didn’t really want to die, because I woke up the next day. A conversation with my GP took me to A&E, the CDU, the Decisions Unit, and then home under the Home Treatment team.

2 years later, I am in a far better place. But this is despite rather than thanks to mental health services, who I genuinely believe caused psychological trauma; it was one of the worst experiences of my life and I remain scared of any future need to use the service.

I hope my story can be learnt from.

I turned up at A&E alone (I had nobody to call) and unable to speak (I had my details written down). I was triaged quickly, tests were done, and I was taken to CDU. I was seen by a doctor. All staff were polite.

But then I waited, alone, for almost 12 hours.

Nobody spoke to me. Nobody told me if the tests were ok, or what I was waiting for. I wasn’t able to ask.

The noise, the beeping, the phones, the lights were like a drill through my skull. I hid beneath my coat, fingers in ears, stress building, building, building. Nobody noticed.

I didn’t eat, drink, use the bathroom; I wasn’t able to ask. Nobody noticed.

I didn’t know what was going on. When I tried to leave, it was explained that I would be seen by psychiatric liaison soon, next.

Hours passed, stress built from the uncertainty, and from what they’d said would happen not happening. Nobody noticed.

I was eventually seen by the psychiatric liaison team and, after more uncertain waiting, taken to the Decisions Unit in the middle of the night.

I was not in a fit state to work out how to recline the chair, or get the duvet in the cover. I still had a cannula in; I pulled it out myself. Nobody noticed.

Next day came; nobody spoke to me.

I didn’t eat and barely drank; nobody noticed.

Another night passed.

Stress was building again; another patient was now in the room so I couldn’t relax; the uncertainty of what was happening was gnawing away inside and the on-edge-ness becoming bigger and bigger.

I finally found myself able to knock on the office door and ask what was happening.

I was shouted at. Told they’d already told me, I knew what I was waiting for. And that if I was upset, I could leave, they weren’t keeping me there.

Implosion imminent, I managed to communicate a need for a private space.

A meeting room was opened.

I curled up in a ball on the floor in the corner.

I was shouted at again.

I melted down. I scratched my arms until they bled. Nobody noticed.

I was finally seen by the home treatment team. Sent home with a plan.

A taxi arrived next day to take me to Crisis House.

But they didn’t tell me the address. I knocked on the wrong door. Was not expected and couldn’t communicate when I knocked on the right one. So I walked several miles home.

Future home visits were unhelpful; just handouts about activities inaccessible to me (autism and social anxiety go hand in hand).

One visit upset me so much that I shut myself in another room and seriously contemplated another overdose. Noone noticed.

After two weeks I was discharged. That was it.

It could have, should have been so much better.

What did I need?

I needed understanding within the context of autism.

Yes, I got up in the morning and showered. That did not mean I was ok; it meant I could not cope without some semblance of routine.

Yes, I was agitated about not being seen for a long time. But this did not mean I needed appeasement; it meant I needed clarity about the length of time I’d be waiting, some semblance of certainty.

Yes, I looked like I could communicate. But this was autopilot, perfected through years of masking and pushing through. I could keep a neutral expression. But behind this I was on the edge of shutdown. I was unable to take in anything you told me. I was unable to approach you, to ask for anything, to express any needs.

I needed you to understand this. To be patient. To not shout at me. To help me meet my own basic needs.

More than anything else, I needed you to care.

To the person who noticed that my lips were cracked from dehydration and encouraged me to drink, thank you. You were the only person who made me feel like someone cared.

Apart from this, the experience, far from helping me, made everything worse.

I knew my reason for being there was self-inflicted. I was racked with guilt for wasting your time when others were genuinely unwell. I knew that my overdose had been more a cry for help than a committed suicide attempt, an act of desperation to end the unbearable loneliness, rejection, worthlessness.

I just needed you to speak to me, to ask me if I was ok. To check in with me, to reassure me I wasn’t alone. To tell me that it was ok for me to be there, that I wasn’t unworthy of care. To tell me not to feel guilty; that you had heard and understood my desperate cry for help.

You didn’t. By leaving me alone and ignored, you reiterated and validated every single one of the negative feelings that had brought me there in the first place.

You made me feel simultaneously invisible and like a burden, unworthy of help.

What you didn't do was care; and this should be such a simple thing.

Do you have a similar story to tell? Tell your story & make a difference ››

Responses

Response from Zoe Dodd, Head of engagement, experience and peer support, Engagement and Experience, Sheffield Health Partnership University NHS Foundation Trust last month
Zoe Dodd
Head of engagement, experience and peer support, Engagement and Experience,
Sheffield Health Partnership University NHS Foundation Trust
Submitted on 15/12/2025 at 17:02
Published on Care Opinion at 17:02


picture of Zoe Dodd

Good afternoon Goldfish7,

Thank you so much for taking this time to feedback on your experience in 2023. I am pleased to hear that you are in a better place but sorry to hear you have been let down by services.

Since 2023 we have made a number of changes within our psychiatric liaison team and Decisions Unit. We have introduced a triage to ensure people are not waiting 12 hours in an ED department with no contact.

There are a number of issues that you have raised which I would like to discuss further with you to understand your experience more if that would be helpful for you. My contact email is zoe.dodd@sheffieldpartnership.nhs.uk then we can arrange to speak further in a way which suits you best and feels safest for you.

I have also been in touch with current leadership in these services who will also be in touch. We are keen to listen and learn from experiences and thank you again for posting.

Kind Regards,

Zoe

  • {{helpful}} {{helpful == 1 ? "person thinks" : "people think"}} this response is helpful

Update posted by Goldfish7 (a service user)

Good afternoon, thank you for your response. I appreciate you providing your email address, and I hope your willingness to discuss this means some things have now changed within the hospital. I think, however, that at this stage it is a can of worms that I prefer not to reopen. I submitted feedback at the time through a survey sent to me with further details but don't want to go through them all again.

The main point of my feedback here was to raise the importance of feeling like someone cares and just being checked in on maybe every hour or 2 when struggling with mental health, and also to raise the need for awareness about autism amongst staff because difficulties can be internalised and not outwardly visible. I hope these messages can be taken on board.

Response from Zoe Dodd, Head of engagement, experience and peer support, Engagement and Experience, Sheffield Health Partnership University NHS Foundation Trust last month
Zoe Dodd
Head of engagement, experience and peer support, Engagement and Experience,
Sheffield Health Partnership University NHS Foundation Trust
Submitted on 18/12/2025 at 17:52
Published on Care Opinion at 17:52


picture of Zoe Dodd

Thank you for your response. I absolutely understand and take on board what you are saying. It is absolutely critical that people are supported through their distress with particular consideration to autism. There has been a huge amount of work in SHPU to address this including mandatory staff training, co-production and review of therapeutic environments.

Thank you again for taking the time to post and I wish you well.

Best Wishes,

Zoe

  • {{helpful}} {{helpful == 1 ? "person thinks" : "people think"}} this response is helpful
Response from Sheffield Teaching Hospitals NHS Foundation Trust last month
We have made a change
Sheffield Teaching Hospitals NHS Foundation Trust
Submitted on 22/12/2025 at 13:53
Published on Care Opinion at 14:00


Thank you for taking the time to share your experience. We are very sorry to read how distressing your time in the Emergency Department was, particularly during such a vulnerable period in your life. It is clear from your account that you felt overwhelmed, unheard and alone, and we are truly sorry that we did not meet your needs or provide the care, understanding and reassurance you deserved.

We want to acknowledge how difficult it must have been to attend the Emergency Department on your own, unable to communicate verbally, while experiencing a mental health crisis. Long periods of waiting without clear information, reassurance or regular check-ins can be extremely distressing, particularly in a noisy and stimulating environment. We are sorry that you were left feeling unseen and unsupported.

Your feedback highlights the importance of understanding autism, including how distress may not always be outwardly visible, how masking can occur, and how difficult it can be to ask for help. We recognise that agitation or quietness should not be misinterpreted, and that what is often needed is clarity, consistency, patience and compassionate communication.

Since your experience in 2023, we have made a number of changes to improve the care and support we provide to autistic people and those attending the Emergency Department in mental health crisis. These include the introduction of the Yellow 5 sensory room, which offers a quieter, more supportive environment for patients who are overwhelmed by noise, lighting and activity within the Emergency Department. We have also implemented the Oliver McGowan Mandatory Training for our staff, which is a powerful and important programme that helps staff better understand autism and learning disability, challenge assumptions, and provide more person-centred, compassionate care.

Alongside this, we continue to emphasise the importance of regular communication, proactive check-ins, and support with basic needs for patients who may struggle to advocate for themselves.

Your story is powerful, and we are grateful that you shared it with us. It helps us reflect on where we must do better and reinforces the importance of kindness, understanding and care in every interaction. No one should ever feel like a burden for seeking help.

We are very pleased to hear that you are now in a far better place, and we wish you all the very best for the future. Please be assured that your feedback has been shared with our Emergency Department and mental health teams so that learning continues.

Thank you again for taking the time to tell us about your experience.

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