Vikki Slade

My hon. Friend is absolutely right. People have to pay extra to be part of the update system. Why would anyone pay extra to put themselves under additional scrutiny? Why is that not automatic? The other option, which has been suggested by some, is that the Government could consider a right to ask/right to know process for family members. That would ensure that the public could not have free and easy access to information that could be risky, but if they had a concern, there would be a route for them to find out. We were simply stonewalled every time that we tried to find out whether this teacher had been registered and whether those allegations had been made. Let me turn to another situation, which has come up on a number of occasions, relating to people who are caring for family members. DBS checks currently have to be undertaken by an employer, a registered organisation or an umbrella organisation. That increases costs, adds delays and makes it more complex for families using direct payments for the care of disabled children and for those starting the journey of caring for an elderly relative. Laura contacted me about the direct payments that she receives to fund the care of her son, noting that she cannot directly access DBS checks. She said that “my very vulnerable son, quadriplegic with cerebral palsy and profound multiple learning disabilities has a team of 15 carers none of whom have DBS checks.” She asks why the law does not allow parents to carry out DBS checks on carers, who are “working often alone in our home”. Another constituent, Sandra, is in a similar position. She said: “We had a carer a few years ago, who had been lone working with our daughter at night for over a year, with a current DBS check. We had a call from Child Protective Services—the carer had tried to smother her own child”. They later discovered that the reason why the carer’s other child lived with grandparents was because she had tried to smother the older child, and they had been removed from her care. The man from the child protection services said, “It probably should have been on her DBS,” but it was not. As a result, Sandra said, “What is the point? There is no reason for me to get a DBS check—it would not have protected my child.” I have also been contacted by Louise, from another part of Dorset, who approached me due to my dementia champion work. After her husband Richard was diagnosed with dementia, she decided to try to care for him at home. Her job meant that she went away for a few days at a time, and she felt that the best option was to find a carer to stay in her home with Richard. My colleagues in Somerset may remember this story, as it was in the local paper. Louise’s experience led to her starting a campaign for Richard’s law, which I said that I would take up. The law has three simple pillars—so simple that I was shocked they were not already in place. Those three pillars are mandatory registration of all care workers; mandatory enhanced DBS checks, with all carers required to join the update service; and mandatory, nationally recognised training for care staff in first aid, medication compliance, manual handling, dementia awareness and safeguarding. I find it hard to believe that a person can be a carer without all of those things being in place.