Very few people know.
Quite a few people think they know … but they don’t.
So, as is often the case, education is the answer.
If there is genuine understanding of an issue, most people’s needs will be met. So, in endeavouring to ensure that the needs of those affected by severe and complex adolescent mental health issues are met, those advocating for the right services are gathering information from the people who know – the people who’ve experienced those issues.
If this is you or someone you know, we need your input … so that we can make sure YOU and those close to you … AND others like you … get the best help in future.
We need to put together stories, snapshots, insights into what it’s like living with severe and complex mental health issues during adolescence – for the young people, for their carers, for their families and their friends.
So if you can tell us just a little, we can put together some examples that resonate with truth but without identifying any individual or contravening anyone’s privacy. We can paint a clear picture of what it feels like to:
- be turned away from an Emergency Department
- be denied access to services because you’re TOO unwell
- have to retell your history over and over again to psychiatrists, psychologists, CYMHS staff
AND what it feels like to:
- get the right support so that you can attend school
- work with a clinician who respects your input and acknowledges your strengths
- build a life with functional relationships and moments of peace
Only your own stories can describe what it’s like. And we know that it’s not easy to tell those stories. So Health Consumers Qld have put together some questions to provide a framework for people to provide their insights. So that we can educate people – the people in positions that will determine the services available to support those dealing with severe and complex adolescent mental health issues.
Click on the links below to have your say – the good, the bad, the unimaginable. If the government officials, medical professionals and bureaucrats don’t know what’s happening to you, they can’t improve the system, the type/amount of support or the approach/attitude of clinical staff etc.
The good things must be replicated and shared.
The bad things must be prevented from impacting people’s lives ever again.
So please fill us in about your significant experiences and knowledge of what works/doesn’t work (AND/OR encourage others to do so) via: