“This option will allow P the opportunity to develop her independence and have the chance to start forming sexual relationships. This option is seen as the least restrictive whilst ensuring risks are minimised. It is felt that the IUD has not had a negative impact on P’s well-being as advised by the medical professionals. The IUD remaining mitigates the risk of further pregnancies. A decreasing care would enable P to take more control of her daily routines and promote the chance of forming meaningful relationships. This will be done under subterfuge as it was highlighted within the medical expert reports (Dr D) that informing P would be detrimental to her well-being and impact on her relationship with family and professionals.”
“Developments in the case law both of the European Court of Human Rights and domestic courts have highlighted the importance of ensuring that P takes an appropriate part in the proceedings and that the court is properly informed about P; and the difficulties of securing this in a way which is proportionate to the issues involved and the nature of the decisions which need to be taken and avoids excessive delay and cost.”
“capacity to consent to sexual relations is … a question directed to the nature of the activity rather than to the identity of the sexual partner.”
“ … capacity to consent to sexual intercourse depends upon a person having sufficient knowledge and understanding of the nature and character – the sexual nature and character – of the act of sexual intercourse, and of the reasonably foreseeable consequences of sexual intercourse, to have the capacity to choose whether or not to engage in it, the capacity to decide whether to give or withhold consent to sexual intercourse. It does not depend upon an understanding of the consequences of sexual intercourse with a particular person. Put shortly, capacity to consent to sexual relations is issue specific; it is not person (partner) specific.”
“24. I adopt and follow the approach of Munby J in MM, namely that capacity to consent to sexual relations is act specific and has to be assessed in relation to the particular kind of sexual activity in question. 25. In passing, I observe that there may be cases where, having held that P has the capacity to consent to sexual relations, the Court of Protection subsequently holds that P lacks the capacity to make decisions as to contact, either generally or with one or more named individuals. There may therefore be circumstances in which P’s sexual relationship with a specific person may be curtailed by the court notwithstanding the fact that he has capacity to have sexual relations.”
“if P lacks capacity to make decisions regarding contact (in particular of people who may cause a risk to her) how on earth can she have capacity in respect of sexual relations? A decision just to have sex with a person surely needs to include a decision based on STDs and other risks involved. Such a decision in my view is narrow-minded and does not include any thought of consequences for care, accommodation, family etc.”
“P is able to understand some basic information regarding sexual activity and retain that information, although at times the information that she retains is inaccurate and unfounded. However, at the present time, P does not appear able to use that information appropriately at the time that she needs to be able to make the decision. She appears, due to her vulnerability, to allow herself to get into situations where inappropriate, exploitative and possibly non-consenting sexual activity occurs. It is my opinion that with further sexual education she would gain greater knowledge about sexual activity. What is unclear, however, in view of her … history … is whether she is able to use the information at the time it is required in order to make herself safe and clearly state whether she is consenting or not consenting to sexual activity. Ongoing sex education, coupled with consistent advice and boundaries from a family and those professionals involved in her care may enable her to gain further knowledge and be facilitated to act in a way that reduces the significant risk that she currently places herself at.”
“At interview, P could give me a basic but reasonable description of the physical mechanics of sexual intercourse and also understood the potential consequences were pregnancy. She has a reasonable understanding of sexually transmitted infections and the potential impact on her own physical health should she contract an infection. P could tell me that she knows she could say ‘no” to a man who asked for sex if she did not want it to go ahead and she understood that forcing a woman into sex was a criminal offence. Given the current case law regarding sexual relationships, it is my opinion that P has capacity to consent to sexual relations. However, I would state that, in my opinion, P has limited insight into her own vulnerability and could not make a judgement as to whether an individual was a potential risk to her or understand the motives of a potential partner in wanting to have sex with her.”
“It is my opinion that P is unable to recognise those who may be a risk to her. I believe she overestimates her ability to keep herself safe in relationships and struggles to understand the motivation of others. I believe that P lacks capacity to make decisions regarding contact with others, particularly potential sexual partners.”
“The most that can be said, therefore, is that in considering the best interests of this particular patient at this particular time, decision-makers must look at his welfare in the widest sense, not just medical but social and psychological; they must consider the nature of the medical treatment in question, what it involves and its prospects of success; they must consider what the outcome of that treatment for the patient is likely to be; they must try and put themselves in the place of the individual patient and ask what his attitude to the treatment is or would be likely to be; and they must consult others who are looking after him or interested in his welfare, in particular for their view of what his attitude would be.”
“The purpose of the best interests test is to consider matters from the patient's point of view. That is not to say that his wishes must prevail, any more than those of a fully capable patient must prevail. We cannot always have what we want. Nor will it always be possible to ascertain what an incapable patient's wishes are. …. But insofar as it is possible to ascertain the patient's wishes and feelings, his beliefs and values or the things which were important to him, it is those which should be taken into account because they are a component in making the choice which is right for him as an individual human being.”
“10. Where a patient lacks capacity it is accordingly of great importance to give proper weight to his wishes and feelings and to his beliefs and values. On behalf of the Trust in this case, Mr Sachdeva QC submitted that the views expressed by a person lacking capacity were in principle entitled to less weight than those of a person with capacity. This is in my view true only to the limited extent that the views of a capacitous person are by definition decisive in relation to any treatment that is being offered to him so that the question of best interests does not arise. However, once incapacity is established so that a best interests decision must be made, there is no theoretical limit to the weight or lack of weight that should be given to the person’s wishes and feelings, beliefs and values. In some cases, the conclusion will be that little weight or no weight can be given; in others, very significant weight will be due. 11. This is not an academic issue, but a necessary protection for the rights of people with disabilities. As the Act and the European Convention make clear, a conclusion that a person lacks decision-making capacity is not an “off-switch” for his rights and freedoms. To state the obvious, the wishes and feelings, beliefs and values of people with a mental disability are as important to them as they are to anyone else, and may even be more important. It would therefore be wrong in principle to apply any automatic discount to their point of view. 12 …. It is, I think, important to ensure that people with a disability are not – by the very fact of their disability – deprived of the range of reasonable outcomes that are available to others. For people with disabilities, the removal of such freedom of action as they have to control their own lives may be experienced as an even greater affront than it would be by others who are more fortunate.”
“A great judge once said, ‘all life is an experiment’, adding that ‘every year if not every day we have to wager our salvation upon some prophecy based upon imperfect knowledge’ (see Holmes J in Abrams v United States (1919) 250 US 616 at 630). The fact is that all life involves risk, and the young, the elderly and the vulnerable are exposed to additional risks and to risks they are less well equipped than others to cope with. But just as wise parents resist the temptation to keep their children metaphorically wrapped up in cotton wool, so too we must avoid the temptation always to put the physical health and safety of the elderly and the vulnerable before everything else. Often it will be appropriate to do so, but not always. Physical health and safety can sometimes be brought at too high a price in happiness and emotional welfare. The emphasis must be on sensible risk appraisal, not striving to avoid all risk, whatever the price, but instead seeking a proper balance and being willing to tolerate manageable or acceptable risks as the price appropriately to be paid in order to achieve some other good – in particular to achieve the vital good of the elderly or vulnerable person’s happiness. What good is it making someone safer if it merely makes them miserable?”
“My own view is that even in the case of incapacitous or very incapacitous patients (leaving aside those who lack consciousness), it remains extremely important in any civilised society that they are not subjected to anaesthesia or invasive surgery without, as a minimum, being informed in sensitive and appropriate language as to what is about to be done to them before it is done.”
“Covert medication is a serious interference with a person’s autonomy and the right to self-determination under Article 8. It is likely to be a contributory factor giving rise to the existing DOL [deprivation on liberty] Safeguards by way of review are essential.”
“(i) if a person lacks capacity and is unable to understand the risks to their health if they do not take their prescribed medication and the person is refusing to take the medication, then it should only be administered covertly in exceptional circumstances; (ii) before the medication is administered covertly, there must be a best interests decision which includes the relevant health professionals and the person’s family members; (iii) if it is agreed that the administration of covert medication is in their best interests, then this must be recorded and placed in the person’s medical records/care home records and there must be an agreed management plan including details of how it is to be reviewed; and (iv) all of the above documentation must be easily accessible on any viewing of the person’s records within the care/nursing home; (v) If there is no agreement, then there should be an immediate application to the court.”
“ … the negatives of telling P that she has an intrauterine device in place are significant. I believe that she would lose trust in her carers and professionals who support her, in addition to her family members. I believe that P would become distressed at the thought that something had been done to her without her knowledge and consent. This may make it significantly more difficult for her to trust those around her in the future, leading to potential breakdowns in relationships, which would have a negative impact on P’s emotional well-being. I also believe that it will be more likely that she may engage in sexual relationships, if she believed that she had a form of contraception, placing her at risk of sexually transmitted infections if she did not use condoms.”
“the applicant reserving for future decision / submission whether a new Care Act assessment might lead to changes in the support available to the first respondent which it would submit were not matters to be determined in best interests proceedings”