Introduction
The death-positive movement, the most recent manifestation of the death awareness
movement, contends that modern society is suffering from a “death taboo” and that
people should talk more openly about death (Koksvik and Richards, 2021). This movement
is striving to shift the dialogue about (and place of) death and dying into community
spaces (Breen, 2020).
People are dying at older ages and over longer periods of time, as a result of chronic
disease trajectories and advances in medical interventions, generating new demographic,
and epidemiological trends. In many circumstances, death and dying processes are over-medicalized
due to aggressive treatments and practices in hospitals and residential eldercare
facilities (Becker et al., 2014). Most deaths happen within such institutions, leaving
communities frequently “in the dark” regarding processes of care and illness at the
end of life (Breen, 2020). There is a widespread belief that community-based solutions
in palliative care and support for the bereaved are needed (Richards et al., 2020).
However, as argued by Park et al. (2022), scant attention has been given to community-level
interventions for death, dying and grief, or to the public's readiness to fully participate
in these interventions.
The COVID-19 pandemic highlighted the global need for communities to be prepared for
illness, death and grieving. As a result, the general population and health and social
care professionals became keenly aware of a variety of issues connected to mortality
and the end-of-life, challenging tendencies to avoid discussions about death and dying.
Two related concepts attempt to counteract this reluctance to consider or discuss
death: death literacy and grief literacy.
Death literacy is defined as a set of skills and knowledge enabling people to learn
about, understand, and act on end-of-life and death-care options (Noonan et al., 2016).
People and groups with a high level of death literacy have a context-specific comprehension
of the death system and can more easily adapt to it, becoming better equipped to provide
care for others or to gain access to critical services necessary for high-quality
end-of-life support (Noonan et al., 2016).
Grieving often accompanies loss, which is typically, but not always, tied to death.
Grief literacy has been defined as knowledge, skills, and values that promote compassion
for self and others in the face of loss (Breen et al., 2022). The aims of the grief
literacy movement are to understand and normalize grief, improving everyone's ability
to recognize and effectively respond to loss. Increased public awareness of loss will
organically encourage greater emotional and practical support around grief, with clear
benefits for the bereaved as well as frontline health and social care professionals,
who often have limited time and resources to sufficiently attend to these issues.
Grief literacy can be viewed as a natural extension of death literacy, and increasing
individual capacities in both areas may help reduce the effects of death avoidance
and death anxiety (McClatchey and King, 2015).
One approach that may enhance both death and grief literacies is the Death Café. Inspired
by the work of Crettaz (2010), Death Cafes are a global social franchise, with locally-organized
public events that encourage discussion of all aspects of death, dying and mortality.
These discussion events, often taking place in cafes, restaurants, libraries or other
public spaces and facilitated by volunteer hosts, adhere to one vital rule: cake or
other culturally-appropriate celebratory foods should be enjoyed by participants to
honor our precious “finite lives” (Death Café, 2022). The Death Café approach, currently
used in more than 81 countries worldwide, allows individuals to discuss difficult
topics, increasing their self-awareness, potentially reducing death anxiety, and augmenting
compassionate connections through conversation and personal sharing (Miles and Corr,
2015; Fong, 2017; Chang, 2021).
We argue that the Death Café approach can be a useful strategy to improve both death
and grief literacy levels and may help promote the burgeoning concept of compassionate
communities as part of palliative care (Graham-Wisener et al., 2022).
Death cafés and compassionate communities
The Death Café movement, through its promotion of open discussion about the human
realities of death and grief, has strong links to the compassionate community model.
Public Health Palliative Care International (Compassionate Cities, 2022) defines a
compassionate community as a community development initiative associated with global
palliative care. A compassionate community consists of groups of neighbors/members
of a community who come together to help people in their network living with a terminal
illness, along with caregivers and the bereaved. Compassionate communities attempt
to follow the 95% rule, wherein the dying person spends only 5% of end-of-life with
formal medical services and the remaining time with their caregivers and connections
in the community (Kellehear, 2013). Based on the premise that death and dying are
shared communal concerns, care networks are created from within the existing community
to support its members. Compassionate communities are framed as a public health response
to death and bereavement, raising public awareness, and preparing people for death
by discussing their wishes in advance and fostering compassionate behaviors toward
those in the community who are nearing death or have recently experienced bereavement
(Koksvik and Richards, 2021). Innovative community-based strategies, such as Death
Cafes, may appeal to a wide variety of groups within the population, and can be adjusted
to fit local culture and practices. The Death Café model allows for informal sharing
of intimate stories and experiences within a social and convivial atmosphere (Leland,
2018). These kinds of activities may help community members better engage with the
Compassionate Communities ethos (Liu et al., 2022).
Kellehear (2020) developed a model of person-centered care and the concept of Compassionate
Cities for end-of-life patients. The person is surrounded by circles of care, namely
(outward from the center): a closer internal network; supported by a wider external
network; then the community, social and health services; and, lastly, the local and
national authorities. When the Compassionate Community model is followed, family members
and caregivers are more resilient and less exhausted during an individual's final
days of life, and the dying person can have a better quality of life at home (Librada-Flores
et al., 2020). Community support for patients and their caregivers is performed through
tasks, such as spending time with the patient (e.g., reading a book, talking) or providing
direct care, thus allowing the informal caregiver to rest or perform tasks outside
their caregiver role. The care network may also assist by completing household chores,
such as cooking, cleaning the house, pet care, shopping, etc. The idea is to create
an intentional, but natural, external support network that enhances the direct care
system for the individual (Librada-Flores et al., 2020). This intentional network,
forming the circles of care around the dying and the bereaved, requires a high degree
of comfort with intimacy and trust in the ability of community members to both offer
and accept care from non-professionals during a vulnerable time in life. We believe
that the personal sharing and interaction that takes place at Death Café events can
help build the foundations of compassion and comfort that, over time, will allow this
exchange of care to occur more naturally in groups and communities.
More compassionate connections within a community, augmented by initiatives like Death
Cafes and Compassionate Communities strategies, should result in a better quality
of life and death for all (Richards et al., 2020). Darwin suggested morality as the
defining feature in the human-animal divide, and it can be argued that compassion
within a human community is a powerful variable in survival (Wilson, 2019). Hypothetically,
a person integrated into a more compassionate and generous community may survive longer
and thrive within a high-quality social system. Opportunities to build compassion,
and understanding and openness about death and grief within heterogeneous and constantly-evolving
community structures are crucial to improving end-of-life and bereavement care for
all (Abel, 2018).
Death cafes: Sharing stories and conversations about loss, death, and grieving
The Death Café model encourages the relaxed mutual sharing of personal memories, thoughts,
beliefs, and feelings about mortality and grief (Chang, 2021). Participants tell stories
about their experiences of losing loved ones and funerals they have attended, anticipate
their own deaths, discuss preferences for their own death, beliefs in the afterlife
and many other aspects of death, dying, and bereavement. Recalling these experiences,
articulating a narrative from them, and listening to the narratives of others is a
unique compassion-building benefit of Death Cafes (Mitchell et al., 2021).
According to Mroz et al. (2020), narrating adverse life situations within a supportive
community is associated with increased subjective well-being and resilience. Following
a loss, facing the experience may imply both positive and negative reframing, and
the ability to integrate these experiences into one's life story will depend on how
they are remembered (Neimeyer, 2001; Mroz et al., 2020). Individuals often retrospectively
reconcile the stress of loss by retelling events that emphasize personal progress
(Mroz and Bluck, 2018) and communion with others. We argue that participating in Death
Cafes allows the sharing of life experiences connected with dying and grief, that
can contribute to this increased sense of well-being. Narratives about loss tend to
include more references to personal connections than those about other life issues,
particularly fond memories and recollections of intimacy with a dying or deceased
loved one (Bluck et al., 2008). Furthermore, recalling personal interactions with
those involved throughout the process of loss can alleviate feelings of isolation
(Mroz and Bluck, 2018, 2019).
The abrupt and unexpected death of a loved one can be extremely difficult for the
bereaved, and this context of death is relevant given the present pandemic scenario
(Gesi et al., 2020; Morris et al., 2020). Previous research has indicated that dealing
with fatalities that are discordant with the natural life cycle, such as those caused
by an accident or a sudden illness, is severely challenging (Shear, 2012; Keyes et
al., 2014). The unexpected death of a loved one may worsen the sense of meaninglessness
that bereavement can bring and heighten existential anxiety (Tang and Xiang, 2021).
Due to isolation and social distancing during the pandemic, patients dying from COVID-19
had limited physical contact at their bedside and restricted emotional comfort and
consolation at end-of-life, while the bereaved endured a lack of access to, or absence
of, conventional culturally-acceptable rites and social or community resources (Cardoso
et al., 2020; Laranjeira and Querido, 2021; Petry et al., 2021). These restrictions
affected the dying person's care options, and fostered feelings of regret among family
members, who missed the opportunity to “be there” in those final moments (Breen, 2020;
Wallace et al., 2020; Laranjeira et al., 2022). By emphasizing personal sharing in
an informal social environment, Death Cafes offer a space for people to talk about
death and mortality and process the unprecedented challenges encountered during COVID-19.
Recently, there has been a surge of interest in narrative strategies for dealing with
loss (Rolbiecki et al., 2021). Self-narrative framing around loss connects significant
events and data into a series of components that span time and create a personal story
(Ratcliffe and Byrne, 2022). Storytelling is what makes these events and facts intelligible;
it gives them a function, place, and meaning, establishing the order of events in
the past, present, and anticipated future. Death Cafes can offer this meaning-building
activity of mutual storytelling and sharing at the community level.
We argue that death and grief literacies can better emerge within a population that
engages with the Compassionate Communities concept and with social experiences such
as Death Cafes. In the Death Café model, a person can remember and maintain a connection
with a deceased loved one and share stories with other participants that can instill
a positive reflection upon their own life, i.e., gaining a sense of personal growth,
avoiding rumination, and focusing on positive social connection (Mroz et al., 2020).
Therefore, Death Cafes are arguably aligned with both death and grief literacy and
Compassionate Community efforts.
The pandemic has drawn attention to the need to develop grief literate societies and
compassionate communities (Table 1). Although there is no single solution for assisting
someone who is grieving, we provided some tips that may allow for mutual understandings
and interdependent support both in the bereaved's day-to-day settings, as well as
in broader society (Fang and Comery, 2021; Breen et al., 2022).
Table 1
Strategies to promote grief literate societies and compassionate communities (Bartone
et al., 2019; Breen et al., 2022; Hasson et al., 2022).
• Solidarity actions, such as illuminating landmarks during significant cultural or
religious occasions.
• Dedicated support groups for grieving individuals and families by faith communities
and social groups.
• Develop awareness on the nuances of grief among health and social professionals,
so they can provide appropriate health education and, if necessary, refer patients
to psychosocial care.
• Incorporate psychosocial education about loss, grief, and bereavement into employee
wellness programs, providing additional opportunities to recognize and talk about
loss.
• Broadcast stories of loss, anguish, and grief in the media, as well as stories of
hope, healing, and recovery.
• Increase opportunities for creative exploration of grief, emphasizing an art and
health approach to death, dying, bereavement and grief.
• Establish universal teaching and learning about death and grief at all educational
levels, from primary school to university and adult education (lifelong learning).
• Consider the creation and implementation of a national, European or International
Day of Grieving and Commemoration to acknowledge grief and raise global public awareness
of death and grief literacy.
• Give special emphasis to unique contexts of death and grieving, including suicide,
overdose, homicide, neonatal loss, miscarriage, stillbirth, etc.
• Create more opportunities for individuals to identify what kinds of support they
would want at the end-of-life and during periods of grief. For example, advance healthcare
directives can assist in promoting discussions around end-of-life care and bereavement.
Final remarks
Community-level interventions are a crucial component of a multifaceted public health
strategy regarding end-of-life, particularly given the increasing challenges imposed
by the changing demography of death and COVID-19. Promoting death and grief literacy
through education, health promotion, and community development strategies is essential
to attain the skills and culturally appropriate values for a compassionate community.
Achieving improved levels of these literacies for both the general public and health
and social care professionals is a process that should be prioritized.
Researchers, health professionals, and social educators must collaborate with communities
in the design of death and grief literacy projects. Rather than focusing on individual-level
acute grieving, initiatives like Death Cafés can promote community-wide literacy around
all facets of death and loss. We suggest a dual approach: developing specialist resources
while also investing in community capacity to understand grief, give empathetic care
and reduce the stigma of death and bereavement.
Finally, there can be unforeseen consequences of making bereavement care a societal
responsibility. Presently existing services in government, religious, and charitable
sectors may decide to dispense with grief care, if they view the community as the
sole source of such assistance. Ultimately, effective joint procedures and true community
partnerships among professionals and the public are vital to developing death and
grief literacy for all.
Author contributions
All authors listed have made a substantial, direct, and intellectual contribution
to the work and approved it for publication.
Funding
This work was funded by national funds through FCT – Fundação para a Ciência e a Tecnologia,
I.P (UIDB/05704/2020 and UIDP/05704/2020) and under the Scientific Employment Stimulus—Institutional
Call—[CEECINST/00051/2018].
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial
or financial relationships that could be construed as a potential conflict of interest.
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