Tag: Vikki Slade

The speech made by Vikki Slade, the Liberal Democrat MP for Mid Dorset and North Poole, in Westminster Hall on 6 January 2026.

I thank the hon. Member for Southport (Patrick Hurley) for that really moving account. We know that cancer affects us all. In my family it claimed my mum Lin; my sister-in-law Lisa and my stepmum Sally have both beaten it, and now my dad Ray is living with terminal cancer. One of my team is also undergoing treatment for cancer, so we know that it is prevalent among all our lives. All of them were fit, healthy people who did everything right, as are so many others each year who get the horrible news or—worse—turn up in A&E after becoming suddenly unwell. According to a Cancer Research study, many of those patients had visited their GP but had not been referred for tests, either because they did not meet the thresholds or because they had been missed altogether. This is not a criticism of our GPs, who are working in highly difficult situations. Indeed, when I shadowed Dr Wright from Walford Mill surgery in Wimborne, he had the sober task of sharing a diagnosis and undertaking a very personal test during his appointment, which he let me witness.

If diagnosis doubled across the six least survivable cancers alone, an additional 7,500 lives a year would be saved. Each year in my constituency of Mid Dorset and North Poole, there are 540 diagnoses of cancer and 300 cancer deaths. Although 85% of them should be starting treatment within 62 days, the number is actually only 60%. What is the Minister doing to bridge that gap? If we met the target in my constituency, 70 additional people would be getting on with their lives. Across the country, 45,000 additional people would be given a greater chance of not just surviving but having a life shared with those they love.

Furthermore, once they get to hospital, patients are faced with out-of-date machinery and not enough specialist nurses. Macmillan Cancer Support says there is an acute shortage and calls for a cancer nurse fund to increase the numbers by 3,700. Will the future cancer strategy include such funding?

I want to speak briefly about pancreatic cancer, which claimed the life of my cousin Colin, a super-fit former Welsh Commonwealth games cyclist who died in his 50s despite the best care available. Many other constituents have written to me about poor prognosis for this treatment. They have flagged that the NHS has approved selective internal radiation therapy, but only for colorectal and liver cancers—not those whose primary cancer was in the pancreas and then spread to the liver. These families are keen for urgent trials to be undertaken to allow the treatment to be used, given the incredibly short life expectancy faced by patients. Will the Minister consider that?

We have been waiting such a long time for this cancer strategy. We need the workforce plan and the road map for the NHS plan. Nine hundred and fifty people will be diagnosed with cancer today, and those people need hope.

The speech made by Vikki Slade, the Liberal Democrat MP for Mid Dorset and North Poole, in the House of Commons on 29 November 2024.

We do not need to choose between palliative care and supporting those who want to make their deaths better. It is so fantastic to hear Members from every part of the Chamber with a shared commitment to funding more palliative care, and I hope that the Secretary of State and his team hear that and will go further, knowing that they have our support in investing more. But until they do, we cannot condemn those who are at the end of life to terror, loneliness and being forced into horrible circumstances.

I have been concerned by some of the comments in the debate, so I re-read the Bill as I sat here. It has been suggested that mental health conditions would be included, but they would not—under clause 2(3). It was also suggested that people might not be offered surgery or other treatment, but they must, under clause 4(4). It is also worth noting the suggestion that a person being coerced could be protected by disclosing to the very family that might be coercing them. The provision for a witness in clause 5(2)(c)(ii) and the period of reflection would allow the independent person to be present at the appropriate time.

I have already shared publicly my own family’s death journeys—and I wear them on my jacket—but today is not about them. Today is about all those people who need this Bill. Last night I read the book “Die Smiling”, about Nigel’s journey to Dignitas. It ends with his final journey and a Facebook post, prepared before he made that agonising 20-hour journey to Switzerland with his wife and children. It moved me to tears. However, most people cannot afford that option. Most do not want to put their families at risk of prosecution; they want death on their own terms.

Gary lives in my constituency, and he asked me to tell the House his story of dying with liver cancer. He knows that the end stages will be brutal, and he wants to decide when enough is enough. He me:

“Death does not worry me at all. Dying a slow death with my dignity stripped away terrifies me. So when my time is right I will kill myself—alone and afraid. My sick dog will not have to die alone and afraid, but I am forced to do so. I want to die on my terms. How can this be right?”

Tracie, who was a palliative care nurse, told me:

“I’ve witnessed many end of life patients and I cannot say hand on heart that many of those patients had a peaceful death. I left palliative nursing as the emotional trauma became too much. There are neither the range of medication or symptom relief treatments available for many of the harrowing things people are forced to go through in their last days and weeks of their life.”

This Bill is about compassion and humanity, and we must listen to the voices of dying people.