Disability Living Allowance: Qualifying Period for Children

Michelle Welsh Excerpts

Wednesday 2nd September 2026 Westminster Hall

[Dawn Butler (in the Chair)]

I will call Michelle Welsh to move the motion; I will then call the Minister to respond. I remind other hon. Members that they may make a speech only with prior permission from the Member in charge of the debate and from the Minister. As is the convention for 30-minute debates, there will not be an opportunity for the Member in charge to wind up.

[Michelle Welsh (Sherwood Forest) (Lab)]

I beg to move,

That this House has considered the potential merits of removing the qualifying period for Disability Living Allowance for children.

It is a pleasure to serve under your chairmanship, Ms Butler. It is right and fitting that I start this debate where it all began for me, with dear Mabel—a brave, kind, clever, funny four-year-old girl who lives in my constituency—and her tenacious mum Rachael. When I was first elected to Parliament, I met with Rachael, my constituent, and she shared her experience with her daughter Mabel, who sadly had been diagnosed with cancer.

Aged four, Mabel was diagnosed with Wilms’, a form of kidney cancer. After a horrifying six months, including two major operations and a tough course of chemotherapy, the family received the news that Mabel was free of cancer. Now, aged six, Mabel attends her local school, where I was fortunate enough to meet her, and is enjoying her life as a young child should. I know that the House will join me in wishing Mabel well.

Following Mabel’s diagnosis, Rachael made an application for disability living allowance, which required completing a 40-page questionnaire that asks questions such as whether the four-year-old needs help monitoring their blood oxygen levels. Disability living allowance is supposed to support families of children with disabilities and serious conditions such as cancer. It can provide a lifeline of financial support at the time when it is most needed, yet the current system requires families to wait three months for the qualifying period. Let me be clear: the financial impact of cancer does not begin after three months. It is instant.

Rachael shared with me that Mabel being diagnosed with cancer was the toughest time of her family’s lives. Despite that, she felt that they were in a more fortunate position than many of the other families on the ward. Rachael’s employer gave her six months off work as sick leave and her partner was able to work flexibly so that they could both spend time with their daughter at hospital. That time allowed Mabel to have support and care from her loved ones, and it allowed support from their family. I cannot even begin to imagine the anguish that families face with such a diagnosis—all the more when it is their child. Unfortunately, not every employer is able or willing to offer that support. That disparity should leave us asking: if we cannot be there when a child is diagnosed with cancer, what are we doing?

[Jim Shannon (Strangford) (DUP)]

I congratulate the hon. Lady on securing the debate. It is debates such as this that remind us of our job as MPs. Does she agree that when a family receive a devastating diagnosis, whether that is of a terminal illness, a severe disability or an aggressive childhood cancer, the financial shock and caring responsibilities are felt immediately? In the three-month qualifying period, families can sometimes accumulate up to £5,000 in additional debt during the most agonising months of their lives, while—I say this respectfully—the Government drag their heels. Will the hon. Lady join me in pressing the Minister, in her compassionate and understanding way, to get Government to recognise that a child’s suffering does not wait 90 days to become real, and to ensure that crucial financial support is delivered from the very point of diagnosis?

[Michelle Welsh]

I absolutely agree. Too often, the financial impacts of a cancer diagnosis are forgotten. People think about the hospital visits, the sickness and the endless tablets, but a disability or serious condition such as cancer has an impact on every single part of someone’s life. Following a diagnosis, families immediately have to deal with the financial impact. It is a sad fact of life that bills do not care whether a child has cancer; they will still be due.

But we can care. Cross-party, we can care. We can unite and do the right thing. Families with children with a disability or serious condition have to wait seven months on average before receiving a single disability living allowance payment. That is months and months of rent, mortgage payments, electricity bills and council tax, and it is weeks and weeks of food shopping. It is compounded by the fact that household income drops by an average of £6,000 per year. For one in three, that can reach over £10,000. Sadly, it gets even worse: the delay in receiving DLA means that a parent’s ability to claim any carer’s allowance as an additional or an alternative has a further impact on the financial strain. It is also important to note that parents in work are unable to apply for universal credit, and that that cuts out other potential streams of support.

All this leaves parents with an impossible choice, a cruel choice that no parent should have to make: do they leave their child alone in hospital to face this battle by themselves, or do they not go to work? Do they skip bills? Do they run the risk of losing their home? Do they not eat? Do they turn the heating off? This is the reality. These are decisions that families should never have to make, yet they happen daily for families up and down this country.

During my meeting with Rachael, she told me about a young boy of just six years old who was also on the ward. His parents were left with no option but to carry on working. As the nurses were unable to provide round-the-clock care, Rachael helped him to use the toilet, helped to dress him and helped him to eat. It is heartbreaking to think of the many children who have no one beside them—not just for the children, but for the mothers and fathers being left with no choice. I missed my son’s first day back at school today and have cried about it, but that is nothing in comparison with having to leave a child who is suffering from cancer in a hospital bed. Let me be clear: DLA is not designed to act as a source of income. It is there to help with the extra costs of looking after a child with a health condition.

[Rachael Maskell (York Central) (Lab/Co-op)]

I am grateful to my hon. Friend for her incredibly powerful speech. She is right that this is not a necessity; it can be addressed. Does she agree that the Department for Work and Pensions needs to ensure that parents get support from day one so that they can address the increased financial costs that they face from the beginning of a diagnosis, and the real need for parents to be present to support their child?

[Michelle Welsh]

I absolutely agree. Cancer is actually one of the clearest diagnoses that someone can get from day one.

Cancer does not wait, yet families have to. The three-month qualifying period does not reflect the realities that families face. In Mabel’s case, the family were informed that they would not qualify for any support, as Mabel’s condition had not lasted for more than six months. In other words, she had not had cancer for long enough. That is despite her having undergone multiple operations and chemotherapy; to this day, she must still attend regular hospital appointments. It is my understanding that the qualifying period is meant to establish that a health condition is long-standing in nature, but with a diagnosis of cancer surely support should be given from the outset.

[Alex Easton (North Down) (Ind)]

I congratulate the hon. Member on securing this debate. Does she agree that there is a strong case for greater flexibility in rapidly diagnosed cases where a clinician has already identified a severe, serious and long-lasting condition, and that in such cases a qualifying period can be unnecessary, bureaucratic and indeed insensitive?

[Michelle Welsh]

Absolutely. The bureaucratic system is failing families, but these issues could easily be resolved if medical evidence could be used instead of the qualifying period. I urge the Minister to look at ways in which medical evidence and research can be used in DLA to make the system better for those who rely on it. There are already provisions that allow the use of medical evidence to bypass the qualifying period, such as the special rules cases where someone is approaching the end of life. The qualifying period is outdated and does not reflect the complexities of lifelong conditions. I am aware that the Government do not know the cost of removing the qualifying period, but I do not think that any cost is worth more than parents’ ability to be there for their child when they have cancer.

As it stands, we cannot cure childhood cancer. We cannot spare families the fear, the sleepless nights or the heartbreak of watching a child undergo surgery and chemotherapy. But we can ensure that when the worst happens, the Government stand beside them rather than placing further barriers in their way. Families should not have to prove their desperation for three months before receiving support. They should not have to navigate mountains of paperwork while sitting beside a hospital bed. They should never be forced to choose between earning a wage and being there for their child.

Mabel’s story is one of hope. Today, she is back at school, enjoying the childhood that every parent wishes for their son or daughter. But her family’s experience has exposed a system that is failing too many in this country. The question before us is a simple one: when a child is diagnosed with cancer or another serious condition, do we respond with bureaucracy or with compassion? I believe we should choose compassion. I therefore urge the Minister to work with families, clinicians and charities to remove the three-month qualifying period and replace it with a system that recognises medical evidence at the outset. Let us ensure that no parent is forced to leave a child alone on a hospital ward because they cannot afford to be there. Let us build a system worthy of the families who rely on it—and let us act now, because cancer does not wait.