OAR@UM Collection:/library/oar/handle/123456789/231872025-12-28T22:00:29Z2025-12-28T22:00:29ZSurrounded by predators : the lived experiences of online harassment by male public figuresBezzina, MalcolmSammut, FrancescaScerri, Josianne/library/oar/handle/123456789/1420892025-12-10T13:13:48Z2025-01-01T00:00:00ZTitle: Surrounded by predators : the lived experiences of online harassment by male public figures
Authors: Bezzina, Malcolm; Sammut, Francesca; Scerri, Josianne
Abstract: Online harassment is a pervasive threat to public figures, with journalists and politicians facing heightened exposure due
to their visibility and engagement in public discourse. While international research has explored the gendered nature of
cyberharassment, little is known about the lived experiences and coping strategies of male public figures. This study focuses
on the lived experiences of cyberharassment among male journalists and Members of Parliament (MPs) in Malta. Online
semi-structured interviews were conducted with three MPs and three journalists, aged between 28 and 70 years. Data were
analysed using Interpretative Phenomenological Analysis (IPA). Findings reveal substantial commonalities between journalists
and MPs in both the impact of harassment and the coping mechanisms employed. Two superordinate themes emerged: “A
gladiator among tigers”, which captures a range of adverse physical, psychological, and emotional effects, as well as concerns
for others and about the changing online environment; and “From ‘standing the heat’ to firefighting”, which examines the
problem-solving, emotion-focused, and avoidance coping strategies used to manage cyberharassment. Notably, participants
described unique coping methods, such as seeking reconciliation with perpetrators and deriving meaning from public service
through investigative journalism. These findings contribute to a more nuanced understanding of the challenges faced by male
public figures in the digital sphere. A series of individual and structural strategies are recommended to support individuals
experiencing online harassment. Further research is needed to explore intersectional factors and to inform policy and practice
recommendations for safeguarding the wellbeing of public figures against online harassment.2025-01-01T00:00:00ZProcedural ethics for participatory research : field-specific dilemmas and recommendations from researchers, co-researching community partners and the rec overseeing a community-academic ADHD research projectCilia Vincenti, SarahGrech, PaulannGalea, MichaelBriffa, VinceBorg Spiteri, SarahCachia, MariaDel Bene, SharonBriffa Desjardins, JenniferGalea McKay, NaomiMcElhatton, MelPrivitera Brightwell, HermaSaliba, Marie ClaireSchembri, EricaSpiteri, Rachel/library/oar/handle/123456789/1395432025-10-03T08:42:37Z2025-01-01T00:00:00ZTitle: Procedural ethics for participatory research : field-specific dilemmas and recommendations from researchers, co-researching community partners and the rec overseeing a community-academic ADHD research project
Authors: Cilia Vincenti, Sarah; Grech, Paulann; Galea, Michael; Briffa, Vince; Borg Spiteri, Sarah; Cachia, Maria; Del Bene, Sharon; Briffa Desjardins, Jennifer; Galea McKay, Naomi; McElhatton, Mel; Privitera Brightwell, Herma; Saliba, Marie Claire; Schembri, Erica; Spiteri, Rachel
Abstract: Philosophical assumptions of the participatory worldview collide with the biomedical framework on which procedural ethics have been grounded. Consequently, obtaining or approving ethical clearance for participatory research can be challenging. Researchers may resent being pressed to water down participatory features to suit institutional requirements. Co-researching community partners’ trust towards academia may be compromised at the outset if the REC comes across unappreciative of their tacit knowledge or is insensitive to their self-determination appeals. REC members may be conflicted over unfamiliar dilemmas. A report detailing effective collaboration during design and approval of a protocol for a photovoice study aimed to empower ADHD women is provided. This collaboration culminated in study plans which satisfied one and all’s requirements. In an attempt to include co-researcher voice in publications and promote more positive perceptions of REC oversight in participatory scholarship, recommendations by academic and community partners and the REC chair who is overseeing this project are advanced. Many lessons were drawn from this positive experience by those who engaged in it. Ethicality, in the context of participatory research is certainly not straightforward, but its pursuit need not be a battlefield. It requires the mobilization of values embedded in the participatory worldview and, akin to the research itself, holds transformative potential.2025-01-01T00:00:00ZEmergence of a new me : experiences of women diagnosed with HER2-positive breast cancerScerri, JosianneAgius, JaniceGalea, Michael/library/oar/handle/123456789/1371802025-07-14T10:48:02Z2025-01-01T00:00:00ZTitle: Emergence of a new me : experiences of women diagnosed with HER2-positive breast cancer
Authors: Scerri, Josianne; Agius, Janice; Galea, Michael
Abstract: Breast cancer subtypes vary in prevalence, prognosis, treatment protocols, and
side-effect profiles, that may impact patients’ lived experiences. Despite this, studies
often group the experiences of persons with breast cancer together. The aim of this
study was to explore the lived experiences of non-metastatic women diagnosed with
Herceptin2-positive breast cancer, from diagnosis to the completion of treatment.
Semi-structured interviews were conducted with 13 women who had undergone treatment
for HER2 + breast cancer within the past two years. Their ages ranged between
32–79 years. Data collected were analysed using interpretative phenomenological
analysis. Four experiential themes emerged: ‘My world came crashing down,’ ‘The
countdown,’ ‘To do or not to do, that is the question,’ and ‘Nearing the end of my journey.’
These themes correspond to four phases of the participants’ experiences: (i) the
diagnostic phase, (ii) the neoadjuvant chemotherapy phase, (iii) the surgical phase,
and (iv) the post-surgery adjuvant phase. The diagnosis elicited strong emotional
reactions due the particularly aggressive nature of this type of cancer. However, the
availability of targeted treatment and having a relatively common subtype of breast
cancer provided hope for recovery. Throughout the neoadjuvant phase, participants
experienced a range of emotions, including anxiety over missing any treatment,
distress about changes in body-image, and concerns for their families. As treatment
approached its end, they felt relieved but also anxious about the possibility of a recurrence.
Understanding the narratives of women having Herceptin2-positive breast
cancer, allows health professionals to better address their unique needs, concerns,
and values, leading to the development of personalised care plans that target their
lived experiences.2025-01-01T00:00:00ZTargeting the beast along my illness trajectory : a qualitative study of females with triple-negative breast cancerScerri, JosianneAgius, JaniceGalea, Michael/library/oar/handle/123456789/1360742025-06-04T07:17:12Z2025-01-01T00:00:00ZTitle: Targeting the beast along my illness trajectory : a qualitative study of females with triple-negative breast cancer
Authors: Scerri, Josianne; Agius, Janice; Galea, Michael
Abstract: Breast cancer subtypes differ in prevalence, aggressiveness, and availability of targeted therapies. However, research often
examines the lived experiences of individuals with breast cancer collectively. One subtype, Triple-Negative Breast Cancer
(TNBC) is an aggressive form of cancer that lacks targeted therapy and has higher recurrence and mortality rates. This
study aims to explore the lived experiences of individuals diagnosed with TNBC, from diagnosis through active treatment.
Audio-recorded interviews were conducted with 11 women who had completed treatment for TNBC. Ages ranged between
26 and 63 years. Data collected were analyzed using interpretative phenomenological analysis. Four group experiential themes
were extracted: “Living in shellshock,” “Fighting the aggressive beast,” “Pulling out the beast,” and “Facing the unknown.”
Participants described substantial emotional distress stemming from the aggressive progression of TNBC and its earlier
onset. The rarity of TNBC further intensified perceptions of reduced survival odds. This study underscores the importance
of comprehensive care for TNBC patients, incorporating ongoing engagement with TNBC survivors, access to mental health
services, and inclusive screening that includes younger women.2025-01-01T00:00:00Z