Jim Shannon

If I could ask for one thing in this debate, it would be that—it is important. I should have welcomed the hon. Member for Wellingborough and Rushden (Gen Kitchen) to her position; apologies for not doing that at the beginning of my speech. It is a real joy to see her there. It is better than whipping, I am sure she knows. This is two debates in two days running in which we have had Parliamentary Private Secretaries and, in this case, a Whip in the place of Ministers. I wish her well in her role today. Many of the people I meet every day have diabetes, dementia, Alzheimer’s, multiple sclerosis, Parkinson’s, osteoporosis or chronic obstructive pulmonary disease. COPD has been more prevalent this last while than it has been in the past. It is an accumulative disease, of course—it comes at the end of a person’s life, unfortunately —and it catches up with people, in many cases. It is not just about the long-term physical conditions; it is the depression, the anxiety and the mental health effects, as well as the pressure of life. The physical pressures are part of it, but the mental pressures come off the back that. Many of the people I speak to have complex needs, and might have one, two or perhaps three of those conditions, which adds to the issue. Ahead of the debate I met representatives from the Cystic Fibrosis Trust and spoke to them about the effect of cystic fibrosis on people. This week, I celebrate the people, like the trust, who have responded to cystic fibrosis by trying to find a cure. CF is a chronic, life-limiting genetic condition without a cure. It affects more than 11,000 people across the UK, with approximately 500 of those diagnosed back in Northern Ireland. I meet some of them regularly in my constituency. For those living with the condition, medication and general health must be considered when planning the simplest of projects or activities—even getting out of bed, for goodness’ sake, or going down the stairs or making breakfast. Going shopping is a no-no for most of them, and interaction with family is another issue. Being unwell can interfere with work and education every day. Research has highlighted the intense financial costs of the condition, which causes an average loss in income of nearly £6,800 a year. This is not a direct attack on the Minister, but I have to make a point about the potential changes to the guidance on welfare and personal independent payments. I have raised before how the changes will impact people with certain health conditions who are on benefits such as PIP. I know that the Government are trying to get people who want to work back into work. Some people with these conditions cannot work, of course, but for people with other conditions there are days that they feel good, and days that they do not. They cannot regulate themselves and say, “I’m going to work Monday, Tuesday and Wednesday of next week,” because the fact is that they do not know how they will feel next week. They may not be able to get out of bed. The Government need to look at flexibility in the PIP process. That probably means that a person cannot do every job that they would like to do, and is restricted. It might be that they have to do some of their work from home. When they look at changes, the Government need to consider that. The Government must commit—this is my absolute red line in the sand—to scrap the four-point rule for personal independence payments, which disproportionately harms people with conditions such as Parkinson’s and CF by failing to account for conditions that tend to fluctuate. That is the very issue I am trying to put forward. As I said, the cost of some of these conditions is financially challenging for many. Aside from the loss of PIP payments, it is also important that a safety net is provided by increasing the age of transition for young people who are currently eligible for disability living allowance but transferring to PIP. These are not issues that the acting Minister will understand, or respond to positively, in a focused way, but it is important to feed these issues into the process so that when Labour comes up with a way forward, it understands the issues. I wish to speak briefly about the Government’s national cancer plan, which is extremely important for people living with cancer and the care they receive. The plan states that more care will be shifted from hospitals to local communities. Earlier today, the hon. Member for Wokingham (Clive Jones) asked the Minister for Secondary Care a question on the health and social care statement, and expressed disappointment at not hearing anything about cancer in the statement. The Government need to focus on cancer, including the early diagnosis of the disease and how quickly the process can move forward to ensure that people get treatment. Back home in Northern Ireland, general practitioners are referring people for cancer treatment, and only 35% of those people have been seen. What a disappointment. That is not the Minister’s fault—it is a devolved matter, so it is the responsibility of the Minister back home—but if 65% of people who are diagnosed with cancer are not getting treatment, my goodness me! That comes to the point that the hon. Member for Eastbourne (Josh Babarinde) made about his constituent who had to wait two and a half years—how long are people waiting to get treated? Sometimes the delay in treatment means that the person does not survive and passes away. What a tragedy that they did not get the response they needed at the time that they needed it. We need to be ever mindful that the care of people who require long-term cancer care is tailored to them and structured in a way that suits them and makes them as comfortable as possible. It is wonderful how the NHS has advanced, and how the cures for cancer have advanced. Although 50% of the people in this room will get cancer, 70% of us will hopefully survive. Is it not marvellous how the NHS has progressed and how the research into finding the cure for diseases has marched on? One in two people with a serious disability or other long-term condition, such as diabetes or heart disease, say that it is now harder than ever to get a diagnosis, and some people may have the complex issues I referred to earlier as well as cancer. Too many opportunities to support people are being missed. I look to the Minister for a response, and for her to say that the Government will do what they can, through the legislature, to provide support for people with long-term health conditions. So many people across this nation are suffering and we must do more to ensure that their lives are made as easy as possible. I look to the Minister for a very positive answer. I hope that I have not given her a difficult time; that was not my intention. I try to do things in a respectful way, and hope my questions have not been too hard to answer. They are straight from the heart, and from the heart of us all, because we are here to work on behalf of our constituents. The stories that I bring to this Chamber are those of my constituents, and the hon. Member for Eastbourne brings the stories of his constituents. The hon. Member for Leicester South (Shockat Adam) told us three or four different stories about vision, which is not something we hear about often, but those are the true, everyday experiences of his constituents. We need something in response to that. When it comes to the answers, perhaps we could have a better working relationship with the devolved Administrations. I am ever mindful that health is devolved in all three of them, but there could be concerted plans. Whenever I first came to this place, we had a United Kingdom of Great Britain and Northern Ireland diabetes plan that was agreed by this Parliament and by all the regions and all the Administrations. Sometimes, we need to do things collectively. I always put forward the advantages, and this great nation—this United Kingdom of Great Britain and Northern Ireland—is great because of all the people who make up the component parts: the Scots, the Welsh, the Northern Irish and, of course, the English.