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In this episode of the LSTM in Conversation podcast, Dr. Tom Wingfield sits down with Fatima Karmadwala, a multidrug-resistant tuberculosis (MDR-TB) survivor and passionate advocate for person-centred care.

Fatima shares her deeply personal journey of navigating the UK healthcare system, enduring a four-month delay in diagnosis. Her story highlights a critical challenge: in low-incidence settings like the UK, TB symptoms can be difficult to recognise, sometimes leading to profound isolation and stigma when patients finally enter care. She recounts the fear and anxiety of being treated as a "walking disease" in an NHS hospital room, detailing experiences where medical professionals avoided her and left her meals on a clinical waste bin.

However, Fatima’s story is also one of incredible resilience. After transferring her care to Liverpool, she experienced the transformative impact of empathy, respect, and truly person-centred care from her medical team. Together, Dr. Wingfield and Fatima discuss why ending TB requires us to look beyond just the clinical science to address the deep social, economic, and psychological realities of the disease.

Released ahead of World TB Day on March 24, 2026, this episode is a reminder that TB cases are rising in England, and caring for those affected goes far beyond pills and tests.

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In this episode of LSTM In Conversation, Professor Russell Stothard speaks with PhD candidate Ayesha Bell-Gamwoto about female genital schistosomiasis (FGS), a neglected disease with serious consequences for women’s sexual and reproductive health.

Drawing on Ayesha’s research in Liberia, they explore the realities of conducting surveillance in post-conflict settings, the links between FGS, infertility, HIV risk, and cervical cancer, and why gender-responsive, context-appropriate health systems are essential. The conversation also highlights how locally led research can inform national policy and help close long-standing gaps in women’s healthcare.

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In this episode of In Conversation with LSTM, alumnus Dr Motto Nganda is joined by Ayo Akinmolayan, who brings lived experience of sickle cell disease, and Evelyn Matongo, a psychologist leading participatory research in Zambia, to explore what truly person-centred sickle cell care looks like in practice.

They discuss the physical, emotional, and social realities of living with sickle cell disease, the importance of mental health and psychosocial support, and how lived experience should shape both research and health systems. The conversation also highlights how participatory approaches are bringing patients, caregivers, communities, and clinicians together to address stigma, improve care, and co-create locally relevant solutions across sub-Saharan Africa and beyond.