(3 years, 6 months ago)
Lords ChamberMy Lords, it is a pleasure to follow the previous group. The noble Baroness, Lady Greengross, has had many decades of campaigning for older people. I know that she had a long-standing friendship with my father, both when he was a Member of this House and in his days in local authorities, and that it was of great benefit to him.
Amendment 171 looks at another group of people—those who suffer from some form of disability—who are also disproportionately affected by domestic abuse. The amendment would repeal what has been labelled by some as the “carer’s defence” under Section 76 of the 2015 Act. Domestic abuse of disabled people has not been discussed as part of the Bill so far, and it is not generally discussed.
When abuse against disabled people is discussed, it is usually in the context of safeguarding issues. The disabled people are labelled as vulnerable adults and the carer’s defence is that their behaviour is reasonable and justified, given the nature of their caring responsibilities. The defence in the carer’s defence is that there could be a wrongful conviction of a carer for coercive and controlling behaviour when the carer was acting in the disabled person’s best interests. They might say, “I did it for their own good”—an expression often used by abusers who are also carers, and the courts might let them off with that defence.
The statistics on the abuse of disabled people are frightening and grim, and I imagine that we will hear more of them from my co-signatory, the noble Baroness, Lady Grey-Thompson, but I will give a couple of statistics which have been brought to my attention.
Disabled adults are at least one and a half times more likely to be a victim of domestic abuse than non-disabled adults. Disabled women are up to three times more likely to experience domestic abuse from their family members. Some of these abusers will also be their carers. I believe it is highly likely that those figures are an underestimate, as disabled people often find reporting crime difficult, and DA survivors often find it more difficult to access the help that they need.
There is a proper place for a carer’s defence. Genuine carers must be able to protect themselves from malicious allegations, but I argue that other Acts do this better—namely, the Care Act 2014 and the Mental Capacity Act 2005. Both provide proper protection for genuine carers.
This Bill is about domestic abuse and how to tackle its many manifestations and protect victims. Too often, disabled victims are ignored. Through the Bill, the Government have an opportunity to show that they are listening to disabled victims, who can be fully acknowledged with this landmark legislation. With the carer’s defence being found in other legislation, my amendment would not dilute the central message of the Bill, which is that all forms of domestic abuse are unacceptable. Disabled victims, too, need to be fully reflected in the Bill. I beg to move.
My Lords, in speaking to this amendment, I draw your Lordships’ attention to my declaration of interests, and I am vice-chair of the Local Government Association.
I thank the noble Lord, Lord Ponsonby, for comprehensively covering the reason for tabling the amendment, and I am delighted that my name is added to it. It is a very difficult issue to raise. There are many, many kind carers out there, but we should recognise that some are not. I know that some people have difficulty with this being debated as part of a domestic abuse vehicle and question whether it is the right vehicle for raising the issues, but I argue that it is, because many cases of abuse occur in a domestic situation.
It is incredibly difficult for disabled people to raise these issues when not only personal care but control of transport and money and the ability to get out might be at stake. We know from various pieces of work that it is very difficult for disabled people to raise these issues. The Equality and Human Rights Commission, in its work from November 2020 entitled Survival, Recovery and Justice: Specialist Services for Survivors of Domestic Abuse, said that disabled women are already disproportionately impacted by domestic abuse. In its 2017 report, SafeLives says that they are
“twice as likely to experience domestic abuse as non-disabled women”
and
“four times more likely to report abuse from multiple perpetrators”.
The charity Stay Safe East, which supports disabled survivors of domestic abuse, considers that the defence has the potential to prolong the abuse of disabled victims, to prevent victims getting justice and to disadvantage disabled victims of coercive control. This is particularly concerning in a context where disabled survivors already experience abuse for longer before seeking help. According to the SafeLives work from 2017, called Disabled Survivors Too, on average disabled victims wait for 3.3 years before accessing support, compared with 2.3 years for non-disabled victims.
A statutory framework is already in place to involve professionals where a person might lack capacity and require medication or confinement—for example, the procedures under the Mental Capacity Act or the Mental Health Act—and there is protection from criminal liability for carers of people who lack capacity. Should a person not lack capacity, they have the right to refuse medication or other treatments or restraints. Nobody should be subject to coercive or controlling behaviour by a spouse or carer, and the law should not provide lesser protection just because somebody is disabled.
There is a high bar for the crime of coercive control. Behaviour must cause a victim serious alarm or distress and have a substantial adverse effect on their day-to-day activities. We should consider the best-interests defence and the risks of it, as it could enable potential abusers to justify that behaviour by claiming that they were acting in the disabled person’s best interests. It also risks feeding into the stereotypes of disabled people, which suggest that they lack autonomy.
We are living in an increasingly paternalistic and ableist world. I know from my personal experience of the pandemic, because I have not been out every day and carrying out my normal line of work, how much resilience disabled people need to deal with their day-to-day experiences, when they are not being believed or having their views accepted. This applies to simple things. Even before our first lockdown, when I was travelling on public transport people felt able to ask me whether I was able to make the right decision about whether to get on a bus or Tube in London, whether to wear my coat out or what I should do with my purse in a shop.