Evidence map›Paper›PMID 42146972›Full record

ArticlePalliative care and social practice2026

'I'm tired of justifying why my life has stopped': A qualitative analysis of the experiences and support needs of young people caring at the end of life and into bereavement.

Emily Harrop, Zoe Abbott, Noreen Hopewell-Kelly, Silvia Goss, Charlie Byrne, Jane Bayliss, Kerry Jones, Oliver Clabburn, Rachel Warren, Alison Penny and 1 more

Abstract read
In one paragraph

Article in Palliative care and social practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Emily HarropMarie Curie Research Centre, School of Medicine, Division of Population Medicine, Cardiff University, UK.ORCID https://orcid.org/0000-0003-2820-0023
Zoe AbbottMarie Curie Research Centre, School of Medicine, Division of Population Medicine, Cardiff University, UK.ORCID https://orcid.org/0000-0002-2354-0291
Noreen Hopewell-KellyMarie Curie Research Centre, School of Medicine, Division of Population Medicine, Cardiff University, UK.ORCID https://orcid.org/0000-0002-0699-0178
Silvia GossMarie Curie Research Centre, School of Medicine, Division of Population Medicine, Cardiff University, UK.ORCID https://orcid.org/0000-0002-9728-5756
Charlie ByrneMarie Curie Research Centre, School of Medicine, Division of Population Medicine, Cardiff University, UK.
Jane BaylissMarie Curie Research Centre, School of Medicine, Division of Population Medicine, Cardiff University, UK.
Kerry JonesSchool of Health, Wellbeing & Social Care, Open University, Milton Keynes, UK.ORCID https://orcid.org/0000-0003-2756-8029
Oliver ClabburnOliver Clabburn Social Research, Taunton, UK.
Rachel WarrenMarie Curie, London, UK.
Alison PennyChildhood Bereavement Network/National Bereavement Alliance, National Children's Bureau, London, UK.
Helen LeadbitterYoung Carers Initiative, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Family carers play an essential role in caring for terminally ill relatives, but evidence regarding the experiences of young/young adult carers is limited. Objectives: To explore the experiences and support needs of young/young adult carers when caring at the end of life and into bereavement, and identify ways of improving support. In the 'Discussion', we apply the Dual Process Model of coping with bereavement (DPM) to help conceptualise our findings. Design: A mixed-methods study comprising; an online survey of statutory, voluntary and community sector professionals/volunteers working with current or bereaved young/young adult carers ( Results: Our three main themes centre around; providing care at the end of life; navigating bereavement; and managing daily life and relationships. When caring, young/young adult carers struggle with a lack of emotional and practical preparedness for death, caregiver burden and changing roles and relationships within the family. Post-bereavement, they experience complex emotions relating to the death and the loss of their caring role/identity, alongside difficulties dealing with administrative/practical tasks and changes to living situations and family roles. Pre/post-bereavement young carers experience difficulties opening up and seeking help and lack of understanding or support from family, peers and schools/colleges, whilst also struggling with school attendance and performance. Transitioning between education and work/unemployment creates support gaps and needs unique to young adult carers, alongside a general lack of preparation for adult life. Conclusion: Young/young adult carers experience multiple challenges and support needs, which can be usefully theorised using an adapted version of the DPM. Cross-sector changes, reflecting public health approaches, are needed to improve the informal and formal support available to young people when caring and bereaved.

Indexed as

bereavementchildren and young peoplefamily caregivinggriefpalliative carequalitativeyoung carers

Identifiers

PMID42146972
PMCPMC13172680

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.