The thing is that REGULATED professionals in the psychiatric/psychotherapeutic field are very, very aware of the risk of transference, strong feelings of attachment engendered when people are disclosing such traumatic events.
Should anyone be soliciting /even allowing the disclosure of such traumatic experiences outside of very clear structures / referral paths etc?
Actual frontline clinicians would be aware of the risk of being seen as a saviour, as the only person who *gets it*, the person to whom the devastated can disclose information they struggle to tell even those closest to them.
In an appropriate setting they should have the skills to detach without devastation for the already traumatised individual.
MH services are not without serious flaws but they do get this. And as one prominent Psychiatrists implied the CMHT will still be there if stickers & journaling don't work.
This x 1000.
I've been a research psychologist for most of my career (I'm on clinical training now). Even as a researcher who doesn't provide therapy or treatment, it is a reasonable expectation that you would be very aware of people's vulnerabilities when recruiting participants or securing consent.
Jessica received a distressed Facebook message from Sally Ann in which she shared her experiences as a victim of child sexual exploitation and talked about how her trauma had been exacerbated when her keyworker made her watch a graphic film about abuse. She contacted Jessica because she had seen her speak out against these films, and she wanted to help the campaign.
Someone with limited knowledge of psychology and research ethics might reasonably assume that this message was consent to share. On a journalistic level, using journalistic standards of consent, it would have been OK. But for a researcher claiming specialist expertise in trauma, that is not a reasonable assumption and the bar for consent is significantly higher. If someone reached out to me over Facebook and was clearly very distressed, my first thought would have been, "Is this person able to consent to publication right now? Do they understand the process, and can they weigh up the possible risks and benefits to themselves?" I would explore these questions with them when they were calmer and send them a proper participant information sheet and a consent form to sign. This is the bare minimum standard for ethics in research. No matter how Jessica tries to twist and dodge, she got it wrong here. And this whole situation arose because she couldn't just acknowledge that to Sally Ann and remedy her mistake. She can't admit she's wrong, ever, and Sally Ann isn't the only woman to have suffered for that weakness of character and professional integrity.
A teenage girl who had participated in my PhD research withdrew her consent for something she had written to appear in the book I was publishing. She was happy for it to be in the thesis and in academic articles, but not the book. I was disappointed, because her written contribution was very powerful and I knew the chapter would be weaker without it. I also didn't really see why someone would be OK with having their story in a thesis but not in a book. But my disappointment didn't matter. Whether or not this girl's reasoning made sense to me was irrelevant. What mattered was that I respected the participants who had been gracious enough to let me interview them. I wouldn't even have known that this girl had changed her mind if I hadn't contacted all my participants as I was doing the final edits to double-check they were still happy. Technically I would have been on solid ground to press ahead with publication without the final check - the original consent form explained that I would be writing articles and a book, after all. But if you're working with vulnerable people and you care about them as individuals, you owe them more than the bare minimum. Jessica can't call herself trauma-informed so long as she tries to excuse terrible decision-making based on technicalities.