Mental health
Study explores link between breast cancer treatment and fatigue

Researchers are probing why breast cancer patients face lasting fatigue after treatment, with exhaustion affecting up to 90 per cent during therapy.
Cancer-related fatigue (CRF) — persistent tiredness not eased by rest — can affect mood, activity and work life. Many survivors report symptoms for months or years after treatment.
A University of Brighton team is exploring whether cancer and its treatments alter how the brain reads body signals, potentially increasing exhaustion.
“Cancer-related fatigue is one of the most distressing, frustrating and least understood side effects of cancer treatment.” said Dr Jeanne Dekerle, principal investigator.
“We want to understand why it affects some patients more than others, and how this influences their ability to be active.”
“If we can understand the brain’s role in fatigue, we can help people recover faster, feel more energetic and live more fully after cancer.”
The study will recruit approximately 80 women aged 18 to 60, divided into groups of breast cancer survivors experiencing CRF and healthy women of similar ages.
Researchers aim to find out whether those with cancer-related exhaustion perceive body signals differently from healthy individuals.
The team hopes the findings will inform development of personalised treatments and exercise programmes tailored to patients’ needs.
Insight
Women’s mental health happens between appointments

By Ritika Sukhani – Psychologist, part of Véa’s Clinical Advisory Board
Women’s mental health often unfolds before, between and around appointments, long before it can be neatly explained in one conversation.
A woman arrives at a GP appointment with six months of feeling “off” behind her. Not acutely unwell. Not necessarily in crisis. Just not herself.
Poor sleep. Brain fog. Lower tolerance. Irritability before her period. Anxiety before meetings. A sense that her cycle, workload, relationships and energy are interacting – but not in a way she can neatly explain when the appointment begins.
She has tracked symptoms, Googled at midnight, screenshotted articles, made notes in her phone and tried to remember what changed, when it changed and what might have triggered it.
But when she finally gets the chance to talk, the task is not only to describe how she feels. It is to organise months of fluctuating experience into a story clear enough to communicate.
This is one of the most overlooked forms of labour in women’s mental health: not simply experiencing distress but having to make it coherent.
In the NHS, women’s mental health rarely arrives through one door. It may appear in primary care as exhaustion, poor sleep or “not feeling like myself”.
It may appear in NHS Talking Therapies as anxiety or low mood. It may sit beneath a menopause conversation, a fertility journey, chronic pain, trauma, caring responsibilities, burnout or the quiet work of holding everyone else together.
The NHS provides essential care.
NHS Talking Therapies received 1.81 million referrals in 2024/25, with 1.21 million referrals accessing services and 50.5 per cent of referrals moving to recovery after completing treatment.
But women’s lives do not unfold in pathway-shaped ways.
Their distress is often cumulative, contextual and relational. It is shaped not only by symptoms but by the conditions around those symptoms: work, debt, trauma, hormones, caregiving, discrimination, physical health, relationships, sleep and the pressure to keep functioning.
That is why women’s mental health needs more than access to services.
It needs continuity.
The work before the appointment
Women are often encouraged to advocate for themselves in healthcare. At its best, this is empowering. It supports agency, preparation and active participation in care.
But self-advocacy can also become another unpaid job.
It requires women to notice what is happening, remember when it started, connect it to context, decide what feels relevant, find the right words and communicate it clearly – often while already tired, anxious, in pain or emotionally overwhelmed.
In clinical care, distress is often the beginning of an assessment. Clinicians are trained to explore duration, severity, functioning, risk, context, history and meaning.
That process matters. It is how distress becomes understood with care.
The issue is broader than any single consultation.
Women’s mental health experiences often unfold over weeks, months and years, while healthcare conversations may happen in short, pressured windows.
Patterns form outside the appointment room: between cycle phases, work demands, caring responsibilities, relational stress, poor sleep and moments of emotional overload.
The UK Government’s Women’s Health Strategy survey found that 84 per cent of respondents said there had been times when they, or the woman they had in mind, were not listened to by healthcare professionals.
It points to something structural: the difficulty of making complex, fluctuating and context-dependent experiences legible inside systems that are often fragmented, time-limited and under pressure.
Endometriosis shows why continuity, language and recognition matter.
Research has found that delays in diagnosis can occur at both patient and medical levels, including when symptoms are normalised by women themselves and by doctors.
For many women, receiving a diagnosis did more than name pain; it provided language, reassurance and possible management strategies.
This is the point we should pay attention to.
Women do not always lack information. Often, they have fragments of it.
The challenge is how to preserve context, recognise recurrence and bring scattered experiences into a form that supports reflection, communication and earlier action.
Tracking captures moments. Continuity reveals patterns
We have made enormous progress in helping women track their bodies.
We can now log cycles, sleep, mood, fertility windows, temperature, symptoms, recovery and heart rate variability with increasing precision. Period-tracking apps, for example, have been described as tools that can support body awareness and menstrual health literacy, while also introducing new forms of work, distress and privacy concern for some users.
That tension matters.
Tracking can help women notice what is happening. But noticing is not the same as understanding. And understanding is not the same as being able to explain.
A cycle tracker can show when a period started. A wearable can show disrupted sleep. A symptom log can hold isolated data points. A notes app can capture fragments of a difficult week.
But unless those pieces are brought together, the interpretive work still falls to the woman.
She is left asking: Is this hormonal? Is this stress? Is this burnout? Is this anxiety? Is this normal for me? Is this pattern important? Should I mention it? How do I explain it?
This is where the first wave begins to meet its limits.
The first wave helped women capture signals.
The next wave could help women interpret context.
The promise of patient-generated health data has always been that it could bridge the gap between everyday life and formal care. But reviews continue to highlight challenges around integration with electronic health records, trust, provenance, data quality and contextual information.
That matters because women’s health data does not become useful simply because it is collected. It becomes useful when it is contextualised.
A poor night’s sleep means something different after one stressful day than after six weeks of overextension.
A low mood entry means something different when it appears in isolation than when it appears repeatedly around a cycle phase, a work pattern or a relationship dynamic.
A spike in anxiety means something different when it is viewed alongside workload, recovery, conflict, hormonal change or self-critical thinking.
The value is not in turning every experience into a metric.
The value is in seeing what repeats, how it repeats and what else is happening around it.
Women’s mental health is systemic
The latest Adult Psychiatric Morbidity Survey found that one in five adults in England had a common mental health condition, with prevalence higher in women at 24.2 per cent compared with 15.4 per cent in men.
It also found a clear socioeconomic gradient, with common mental health conditions more prevalent in the most deprived areas and among people with problem debt.
These figures matter because they remind us that women’s mental health cannot be understood only at the level of individual coping.
Of course, individual support matters. Therapy matters. Medication may matter. Assessment, formulation, risk management and diagnosis all have their place.
But a systemic lens asks what else is happening around the woman.
Who is she caring for? What is she carrying at work? What has she had to normalise? What physical symptoms have been separated from her emotional life? What inequalities shape how quickly she is heard, referred or supported? What happens while she is waiting?
Women’s mental health is often partly biological, partly psychological, partly relational, partly occupational and partly social.
It may not fit neatly into one symptom box at first. It may need time, pattern and context before it becomes clear what kind of support is needed.
This is why the missing layer is not more monitoring – it is supported sense-making.
The need for supported sense-making
Supported sense-making means moving beyond isolated logs and dashboards towards tools that help women understand how different parts of their lives interact over time: body, mood, cycle, stress, relationships, work, recovery and self-talk.
It also means being clear about what technology should and should not do.
Technology should not replace clinical assessment. It should not diagnose from a journal entry.
It should not turn ordinary emotion into pathology or place yet another responsibility on women to optimise themselves.
At its best, it can support the wider ecosystem around care.
It can help women hold onto context before an appointment.
It can help them notice patterns while they are waiting. It can support reflection between sessions. It can help them arrive at conversations with more continuity, while respecting the clinical judgement, formulation and relational care that services provide.
This is where platforms like Véa point toward a thoughtful role for women’s health technology.
By treating reflection, emotion and language as part of women’s longitudinal health context, Véa supports the kind of pattern recognition that often gets lost in daily life. Through micro-check-ins, journalling and reflective prompts, it helps women notice shifts in their internal state over time – not to self-diagnose but to build a clearer relationship with their own patterns.
For some women, that may support a better conversation with a clinician.
For others, it may help them recognise early signs of burnout, understand cyclical changes or notice when work, relationships and recovery are interacting in ways they had not previously named.
At its best, this kind of technology reduced the burden of self-interpretation. It helps women hold onto the thread.
From more data to better continuity
The women’s health gap is often discussed as a research gap, a funding gap and a diagnostic gap.
It is all of those things. McKinsey Health Institute and the World Economic Forum estimate that closing the women’s health gap could add at least $1 trillion annually to the global economy by 2040.6
But there is another gap sitting underneath the others.
A continuity gap.
Women’s mental health experiences are often long, fluctuating and context-dependent. Healthcare systems often encounter them in snapshots. Workplaces may only notice them when performance drops. Women themselves may only recognise the pattern once they are already exhausted.
That gap between lived experience and later explanation is where too much meaning gets lost.
The next generation of women’s health technology should help preserve the story behind the symptom.
It should make room for emotional, cognitive, hormonal and social context without collapsing everything into diagnosis or optimisation. It should support better conversations without pretending to replace clinical care.
Women should not have to rely on memory alone to make sense of months of fluctuating emotional, cognitive and physical experience.
The future of women’s mental health will not be built by asking women to monitor themselves more closely.
It will be built by helping them understand themselves sooner – and arrive at conversations about their health with more continuity, context and clarity.
Learn more about Véa at veajournal.app
Motherhood
Natural birth pressure harming new mothers’ mental health, research finds

Pressure to have a natural birth can cause lasting psychological harm when labour does not go to plan, new research shows.
The study found that the messages women receive during pregnancy are directly linked to the shame and self-blame many feel when those expectations are not met.
For the first time, the research provides an explanation for why unmet birth expectations contribute to psychological harm.
Several women involved in the research said they felt they had not given birth “properly”, even when medical intervention had saved their lives.
Rebecca Matthews, lead author and PhD researcher at the University of Reading, said: “These women were not failed by their bodies, they were failed by the messages they were given.
“Birth trauma does not begin with birth. It begins in the ideology sold to women throughout pregnancy.
“For the first time we can explain precisely how, by showing how birth culture creates a moral standard for women that defines what a good mother does and then leaves them to blame themselves when birth does not match that.
“Until we reform the way we prepare women for birth, we will keep seeing the same devastating consequences for mothers and their babies.”
The researchers interviewed 21 first-time mothers in the UK whose births did not go as planned.
From NCT and hypnobirthing classes, to social media to midwives, the researchers heard how women are surrounded by messaging that frames natural, unmedicated vaginal birth as the “gold standard”, not just medically preferable, but as a mark of being a good mother and the first test of maternal worth.
Research shows around half of women report their birth differed significantly from their expectations, and for the women in this study, all of whom experienced exactly that, the psychological consequences were profound.
Women judged themselves against the internalised moral standard that this ideology had created.
The researchers are calling for antenatal education to stop treating one kind of birth as the goal and to present all birth outcomes as equally valid routes to motherhood.
They also call for better postnatal screening for women whose births did not go as expected, specifically targeting the shame, self-blame and identity disruption that this research identifies as mechanisms underlying birth trauma.
The findings align with and extend the conclusions of the Kirkup, Ockenden and Birth Trauma Inquiry reports, all of which documented how the institutional pursuit of “normal birth” contributed to preventable harm.
This research provides the first theoretical explanation of how that ideology generates individual psychological harm and points to antenatal messaging as the primary site of such preventable harm.
Mental health
Dr-Julian helps deliver breakthrough mental health support for Black and ethnically minoritised mothers

A groundbreaking digital perinatal mental health pilot for Black and ethnically minoritised women has helped women access support faster, complete therapy at higher rates, and recover more successfully than national averages.
The partnership between digital tech company Dr-Julian and The Essential Baby Company Ltd within a new model of mental health care named haPPIE SHE Cares – who offer personalised support for women sharing their healthcare experiences, showed results well above NHS benchmarks for Black and ethnically minoritised women.
The pilot was created to help women who are less likely to use traditional mental health services during pregnancy and in the first year after giving birth.
By combining trusted community referrals, culturally aware support, and fast access to therapy through Dr-Julian’s online and virtual care platform, the programme delivered standout results.
Every woman who joined the pilot started therapy, 90 per cent completed treatment, and 74 per cent recovered; well above the NHS benchmark of around 52 per cent.
Women referred through community organisations accessed support in just one day on average, compared with around 21 days through many standard services.
Even the programme’s regular referral route reduced waits to 13 days.
The findings come as NHS leaders continue to focus on maternity inequalities and unequal access to mental health care.
Black and ethnically minoritised women can face barriers including stigma, language needs, lack of trust in services, childcare pressures, and difficulty navigating complex systems.
The haPPIE SHE Cares model was designed to break down those barriers by working with trusted community groups, offering culturally informed support, and where possible matching women with therapists who understood their background or language.
Gemma Poole for The Essential Baby Company said: “Too many women who need help feel unseen, unheard or unable to get support when they need it most.
“This project shows that when services are built around trust, culture and community, women engage, recover and thrive.
“This early success could provide a blueprint for reducing inequalities in maternal mental health care across the UK. Behind every statistic is a mother who felt supported, a family that benefited and a woman who found her voice.
“Mental healthcare must work for every community. This partnership shows that when high-quality therapy is combined with culturally responsive support, outcomes improve and women get help faster.
We are proud to have provided the therapists, virtual care systems and digital pathways behind this programme. We believe this model could help NHS organisations nationwide cut waiting times and improve recovery rates.”
Women who took part described the programme as life-changing, saying it reduced isolation, gave them confidence speaking with healthcare professionals, and made them more willing to seek help.
With growing pressure on maternity and mental health services, leaders behind the project say the pilot offers a practical solution that improves care while helping cut long waiting lists.
Plans are now being explored to expand the model through training, regional partnerships, and future funding.
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