Debates between Matt Rodda and Sarah Hall during the 2024 Parliament

Lobular Breast Cancer: Moon Shot Project

Debate between Matt Rodda and Sarah Hall
Thursday 9th July 2026

(3 weeks, 4 days ago)

Westminster Hall
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Sarah Hall Portrait Sarah Hall (Warrington South) (Lab/Co-op)
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It is a pleasure to serve under your chairship, Mrs Hobhouse. I thank the hon. Member for Horsham (John Milne) for securing this hugely important debate and for his powerful speech.

Just a few weeks ago, I stood outside Downing Street alongside women living with invasive lobular breast cancer, their families and campaigners for the Lobular Moon Shot Project’s 22-minute silence. Those 22 minutes represented the 22 women who lose their lives to lobular breast cancer every day. It was a deeply moving experience. Standing in silence with women who are living with the disease alongside those who have lost loved ones brought home why today’s debate really matters. They were not asking for sympathy; they were asking to be seen. They were asking for better research, earlier diagnosis and better outcomes for women diagnosed in the future.

Today, I want to share the story of my constituent, Trish. She has kindly given me permission to share her story because she hopes that by doing so, another woman may recognise the signs of lobular breast cancer sooner. Trish did everything that we ask women to do. Between 2014 and 2025, she attended six mammograms—six opportunities for cancer to be found, and six occasions when she believed that if something was wrong, it would be detected. But none of those mammograms picked up any signs.

Like many women, Trish believed that cancer meant finding a lump. It was not a lump that led to her diagnosis; it was a shadow. After getting out of the shower one morning, while putting her hair up, she noticed a shadow underneath her breast. She took a photograph and could clearly see dimpling in her skin. Thankfully, her GP listened and referred her urgently under the two-week-wait pathway. I place on the record my thanks to that GP, because despite there being no obvious lump, they recognised that something was not right.

At the breast clinic, Trish underwent mammograms, ultrasounds and biopsies. Initially, she was reassured that there was no lump to feel. She was then told that there was a small area of concern. The plan was for a lumpectomy and a short course of radiotherapy, and she recalls being told that she would likely be back at work in a month. She underwent an MRI, which is when everything changed. It showed that the tumour measured approximately 72 millimetres. Following surgery, it was confirmed to be 75 millimetres. Trish’s treatment changed completely: she needed a mastectomy with immediate reconstruction, followed by 15 rounds of radiotherapy. She is currently undergoing 10 years of hormone therapy. She certainly was not back at work after a month.

Trish’s experience raises important questions. Lobular breast cancer is the second most common type of breast cancer, yet many women have never even heard of it. Unlike the breast cancers many of us are more familiar with, lobular breast cancer often does not form a distinct lump. Instead, it grows in strand-like tumours, making it much harder to detect on mammograms and feel during examination. That is why women with lobular breast cancer are so often diagnosed later, when tumours are much larger and treatment becomes far more extensive. For Trish, six mammograms over more than a decade failed to detect her cancer.

That is why the work of the Lobular Moon Shot Project matters. Campaigners are not asking for special treatment; they are asking for research into lobular breast cancer that reflects the scale of the challenge. They are asking for earlier diagnosis, better understanding of how the disease behaves, improved imaging and more effective treatments. Above all, they are asking that women with lobular breast cancer are no longer overlooked because their cancer behaves differently. Awareness of lobular breast cancer must improve. For many years, the message has quite rightly been, “Check for lumps,” but breast cancer is not always a lump; women also need to know about dimpling, puckering, changes in breast shape, thickening of the breast tissue and changes to the skin. As Trish said to me,

“You should know your breasts as well as you know your face.”

I welcome the engagement that Ministers have already had with campaigners and researchers, and I hope that today’s debate marks another step forward.

Matt Rodda Portrait Matt Rodda (Reading Central) (Lab)
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My hon. Friend and other colleagues are making some very powerful points today. Is she going to come on to the important issue of medical training and education for doctors and other medical professionals, and the possible benefits of greater public awareness? The Department of Health and Social Care has historically done very important work leading on public awareness campaigns on illnesses and other issues in the health world. I hope that my hon. Friend will be able to highlight that as well.

Sarah Hall Portrait Sarah Hall
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Trish is a phenomenal campaigner—a lot like Susan—and she wants to work together to create an awareness campaign so that women understand that there is a difference between types of breast cancer. We are looking to establish a support group for women who have lobular breast cancer; that is in the works. On training, my hon. Friend is absolutely right: recognition and training forms part of research, understanding and detection—what it is and what causes it—but also what we need to do in the training required by people in the profession.

I hope that the Government will continue working with researchers, clinicians and the Lobular Moon Shot Project to improve understanding of lobular breast cancer, support further research and ensure that women receive the earliest and most accurate diagnosis possible. Behind every statistic is someone like Trish, a woman who did everything that she was supposed to and who wants her experience to help somebody else. Next week, many of the women I stood with outside Downing Street will gather once again. My hope is that one day, they will no longer need to, and that through better research, greater awareness and earlier diagnosis, fewer women will hear the words that Trish heard. I hope that colleagues from across will continue to stand with those women until that becomes a reality.