Disability Living Allowance: Qualifying Period for Children

Jim Shannon Excerpts

Wednesday 2nd September 2026 Westminster Hall

[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.

--- Later in debate ---

[The Parliamentary Under-Secretary of State for Work and Pensions (Lilian Greenwood)]

I am delighted to serve under your chairship, Ms Butler. I congratulate my hon. Friend the Member for Sherwood Forest (Michelle Welsh) on securing this important debate. She has made a particularly valuable, thoughtful and passionate contribution this morning, and I join her in wishing Mabel, her mum Rachael and their whole family well.

My hon. Friend called this debate to discuss the qualifying period for disability living allowance for children. As we have heard, DLA contributes to the extra costs that may arise as a result of a disability or health condition. For some, it can provide a total of just over £10,000 a year. It is usually paid to the child’s parent or guardian; it can help with the overall family finances and can be used as they see fit to meet their needs. It continues to be paid in full to children and young people under the age of 18 when they are in hospital.

DLA is available if a child’s condition or illness is both of a long-term nature and one that gives rise to care or mobility needs. Payment begins once the three-month qualifying period has been satisfied. That helps to establish that the disability and resulting needs are of the long-standing nature for which this benefit is designed to offer support. The qualifying period provides a sensible division between short and long-term disability, but, importantly, it does not begin with the date of the claim; it starts with the beginning of the need for care and/or mobility that makes the child eligible for DLA. That period can start before the date of claim. The question as to when the need started will be taken into account by decision makers, meaning that consideration will always be given to whether the qualifying period has already been partly or fully completed prior to the date of claim.

[Jim Shannon]

If I have correctly understood what the Minister is saying, if a consultant, GP or other doctor sent a letter confirming that the condition started way before the application was made, that would be the qualifying period, and that would be done by a medical person. Am I reading it right?

[Lilian Greenwood]

It starts with the issue of need. The point at which the child became eligible for disability living allowance marks the start of the qualifying period, even if that precedes the point at which parents make a claim. Understandably, when parents are in very difficult circumstances, their first thought is probably not about applying for disability living allowance. For children who are severely disabled at birth, the qualifying period can start at birth.

The date of claim is usually the date the request for a claim pack is received. Provided that the customer returns the claim form within six weeks, the date of claim will be treated as the date that the claim form was requested. The Secretary of State also has the discretion to extend that period beyond six weeks if the delay is considered reasonable. In the sort of circumstances that my hon. Friend the Member for Sherwood Forest has described, we can understand how those issues can arise.

If a child sadly has an end-of-life diagnosis, special rules are rightly in place. Those claims are always fast-tracked and the three-month qualifying period does not apply. The highest rate of the DLA care component will be paid from the date of the claim. My officials are currently exploring options to enhance bereavement support for parents through the social security system, and we will continue to engage with stakeholders as that work develops.

Given that this debate stems from concerns about how quickly families get the support they need, it is worth highlighting that we have recently made significant improvements to waiting times for new child DLA claims. People are not waiting nearly as long as they did for their claim to be processed. My hon. Friend rightly highlighted the need to address long waits.