That it is not in his best interests to continue to receive life sustaining treatment including ventilation;

It is in his best interests and lawful for such treatment to be withdrawn;

In the event of a deterioration in his condition, it is not in his best interests to receive bag and mask ventilation, cardiac massage (with or without adrenaline), endo-tracheal reintubation, invasive or non-invasive ventilation, antibiotics (save in order to provide pain relief) or inotropic support;

In the event of a serious deterioration in his condition, it is lawful for the treatment set out in (d) to be withheld.

The application is supported by the Children’s Guardian. It is opposed by S’s parents.

S was born in June 2020, so he is almost nine months old. His parents told the Guardian that the pregnancy was uneventful and when the mother went into spontaneous labour at 40 weeks they had every reason to expect a healthy full term baby boy, a sibling for the father’s older son who is 9 years old. Soon they were confronted with the unimaginably harrowing circumstances that something was wrong given the immediate and intensive response of the medical professionals following the birth. S was born without any heart rate, breathing movement, spontaneous movement of his limbs and with very poor colour and abnormal cord blood gas result. He required active resuscitation including intubation and ventilation, external cardiac massage, medications and blood transfusion. After about 30 minutes of resuscitation his heart rate achieved a normal level, but it took some 18 hours for him to have a sustained respiratory effort, even with ventilator support.

As a result of his severe lack of oxygen and blood supply to vital organs around delivery, S sustained a severe brain injury, diagnosed as severe perinatal hypoxic ischaemic encephalopathy. He was also born with an infection and was treated with antibiotics.

S has remained on the neonatal intensive care unit (NICU) since he was born. He has been ventilated since his birth and is fed by a nasogastric tube. He also suffers from seizures and is treated with anticonvulsants.

The law in relation to the withdrawing of life-sustaining treatment is clear and well established. The welfare of the child is paramount. In Re NHS Trust v MB and Others

The decision must be objective; not what the judge might make for him or herself, or a child;

Best interests considerations cannot be mathematically weighed and include all considerations, which include (non-exhaustively), medical, emotional, sensory, (pleasure, pain and suffering) and instinctive (the human instinct to survive) considerations;

In Re A (A Child) [2016] EWCA Civ 759 King LJ stated at paragraph 31: “Whilst its application requires sensitivity and care of the highest order, the law relating to applications to withdraw life-sustaining treatment is now clear and well-established. It can be summed up with economy by reference to two paragraphs from the speech of Baroness Hale in what is generally regarded as the leading case on the topic, notwithstanding that it related to an adult, against the backdrop of the Mental Capacity Act 2005. In Aintree University Hospital NHS Foundation Trust v James [2013] UKSC 67; [2014] AC 591, Baroness Hale said at paragraph 22:-

No single factor determines the outcome; it is important that the court takes an overarching view of the child’s best interests. I have also read and take into account the Royal College of Paediatrics and Child Health Guidance on “Decisions to Limit Treatment in Life-limiting and Life-threatening Conditions in Children: A framework for practice”.

I have read all the documents in the bundle, including three reports by Dr. C, an independent report prepared by Dr. Simon Hannam, Consultant Neonatologist and Head of Neonatal Services at Great Ormond Street Hospital. I have also read the Guardian’s report and the statement of the parents. I heard oral evidence from Dr. C and the parents. The mother provided me with a photograph of S, and four video clips of him. In addition the Trust set up a video link so that I could see S in hospital, and have a brief look around the ward he is in.

Dr. C became involved in S’s care when he was about two weeks old. He remains on the NICU. His condition appears to be stable with minimal breathing help on the ventilator and is tolerating nasogastric tube feeding.

MRI scans performed after his birth are consistent with severe neonatal hypoxia.

There have been numerous multi-disciplinary meetings concerning S, attended by neonatal consultants and other neonatal professionals (nurses, therapists) and consultant meetings. On 14^th October all the professionals present agreed that a withdrawal of life supporting treatment and a transfer to palliative care was in S’s best interests.

When S was about 7 months old an attempt was made to assess him using the Bayley III Scales of Infant Development. Due to his abnormal neurology, it was not possible to score him on any items on the scales.

During his oral evidence Dr. C explained that it was the view of the entire team that the movements in S’s limbs were reflex rather than purposeful, and that the same applies when he opens his eyes. Although Dr. C respected and understood the position of the parents he could not agree with them that S responded to touch.

The fact that S needs lower concentrations of oxygen now than he did at birth is explained by the fact that at birth he was extremely unwell with an infection and as a consequence of the hypoxia, not, very sadly because his overall condition is getting better. There is nothing very wrong with his lungs themselves, the problem is that the damage to his brain is such that he is unable to sustain respiratory effort. It is right that at one stage he managed to survive for 10 days with the assistance of CPAP (which supports respiratory effort as opposed to providing all of it) but his oxygen

Dr. C was absolutely clear that there is no prospect of any improvement in S’s condition, which is underpinned by permanent and irreversible brain damage. In order to survive he will require the current care regime to continue, and as time goes on, there will be more and more complications. Questioned about the possibility of S being able to be cared for at home, he said that such could only be achieved if he had a tracheostomy and PEG feeding (which both require surgery) and 24 hour nursing care. If S was allowed to go home, Dr. C said it was a ‘certainty’ that he would be readmitted to hospital within days or weeks.

Dr. Hannam was contacted to provide a second opinion at the request of the parents.

Dr. Hannam concluded that S has no prospect of having a meaningful quality of life in the future, and that he would need round the clock nursing. He would not be able to experience pleasure in terms of feeding, will have severe cognitive impairment, and he is unlikely to be able to see or hear. Although he said it was ‘impossible to prove’ he was concerned S was experiencing discomfort during the cares needed to keep him alive, having noted that his response to oral suctioning with movements of the jaw suggested that he reacted in some way to stimulation. He concluded ‘To my mind, this means that continuing him on a ventilator would result in him having an unbearable existence as he is suffering’.

S’s parents are utterly dedicated to him and have shown him nothing but love and care throughout his short life. He was a much wanted child. The mother visits him every day, and the father several times a week. The parents are able to lift S onto their lap to hold and cuddle him.

The parents and Dr. C have had a very good relationship throughout the period S has been cared for by him. Indeed their relationships with all the staff are very good and appreciative. The parents have a great respect for the opinion of the doctors and the work of the team in caring for S; it is simply the case that they disagree as to what is in S’s best interests.

Until the day of the hearing, the parents had no legal representation. Parents whose children are the subject of an application by the local authority to take them into care receive full non means and non-merits tested public funding but parents who face an application for the withdrawal of treatment from their child do not, despite the enormous significance of the decision to be made. Not only are these cases medically complex, but emotionally they are as hard as is possible to imagine for the parents. In this case, the father works and his wages mean that the family are over the limit for assistance with representation. Unsurprisingly, they could not afford to pay for a lawyer themselves. Upon hearing of their plight through counsel for the Hospital Trust, Mr. Mylonas QC, Mr. Thomas, counsel from Serjeants Inn Chambers stepped in to help and represent them for free. He assimilated all the documents and spent time discussing the case with the parents. He has represented them with the greatest of skill and care, ensuring that their case was properly put before the court and taking the burden from them of having to do it all by themselves. I am extremely grateful to him, and wish to commend him for what he has done.

The parents have spoken to various professionals, including Dr. C, Dr. Hannam and the Guardian. They also prepared a short statement for the court. In this they ask the court to take into consideration their request to take their son S home to continue to care for him. They state that they understand that he will need full time care and that they are ‘committed to fulfil that role with love and happiness’. They state that they hope to see more progress in their son’s state, and protect his right to live whatever his condition is. They state that he is a lovely fighting boy, and that at the beginning he needed the maximum amount of oxygen and was not responding to touch. Now he needs only the minimum setting and responds to touch as well as sometimes opening his eyes. They point to the fact that he managed to breathe for 10 days with the help of CPAP, which was a big surprise.

What the parents say in their statement mirrors what they have said to the other professionals. The mother told the Guardian that whilst they accepted the opinion of the doctors she held onto her dream that ‘everything will be ok’ and spoke of her conviction that S can recover. The mother also told the Guardian that S has moved in response to a cold wet wipe when having his nappy changed.

The parents also told the Guardian that they hoped S could go home on a ventilator and feel able to rise to the challenge of 24 hour care. They would like him to meet his brother and other family members. This has not been possible in lockdown in the NICU.

The mother gave oral evidence on behalf of both of the parents. She has visited their son every day, usually for two hours or so, and has been able to do such things as hold him, dress him, change his nappy, and sometimes to suction him. She said that S moves when he is touched, and indeed the videos do seem to demonstrate that. She said that when she touches or tickles his right leg he responds with the same leg that

When she was asked about S being able to feel discomfort and pain she acknowledged this, but drew an analogy with people who have to undergo painful or uncomfortable medical treatment for illnesses such as cancer. When S was not having any procedures done to him he is comfortable and stable. She said that whilst understanding that S will always have disabilities and complications she wished for him to be given a chance to survive, for he does things at his own pace and makes gradual progress. She believes that if he wished to give up the fight for life he would do so despite being on the ventilator, and explained that there was another mother on the unit who said that her baby had done this.

Movingly she told me that his life was precious and that he needed to be given the chance to show his progress and wake up, or to give up if he wished to do so. The mother told me that if S himself gave up she would rest more easily because it would be his choice, as opposed to treatment being denied to him.

The mother would like to be able to care for S at home if possible.

The parents have also explained that as people of faith they cannot relinquish their hope that S will make some sort of improvement, and believe it would be wrong for them to agree to the withdrawal of treatment.

In determining what is in S’s best interests, I look at his welfare in the widest sense, including medical, emotional, sensory and instinctive matters. I also bear in mind the strong presumption for the prolongation of life. As the mother says of S, his life is precious.

The benefits to S of continuing treatment would be that he would be alive, and he could continue to experience the care and love each of his parents have for him. The doctors do not believe he is able to feel any pleasure or comfort, but if he is able to feel discomfort it seems likely that in some intangible way he must be able to feel the soothing touch of his mother (and father too) as he is held and cuddled.

It is not hard to understand the parents’ fervent hope that S will defy expectations and show some improvement in his condition. The medical evidence is, however, that the brain damage that he has suffered is permanent and irreversible. There is therefore no realistic prospect of S ever being able to breathe without a ventilator, to feed or be fed orally, or do anything for himself at all. He cannot and will not ever be able to see or hear. I can see why the parents believe that S’s limb movements are more than reflex ones, but I accept, sadly, the medical evidence that this is not so. Although the mother in particular has been able to spend considerable periods of time with S in hospital, I believe that her longing to see a reaction in her son is likely to have coloured her observations. In all the circumstances the continuing artificial ventilation cannot, in my view, offer S the benefit of any chance of an improvement in his condition.

On the other side of the balance I must consider the burdens to S of continuing life sustaining treatment. The medical professionals are concerned that the measures required to keep him alive cause him discomfort and even pain. S has deep suctioning every two or three hours every day, his nasogastric tube is replaced every three days, and his NETT tube is replaced every three weeks. Replacement of each of these tubes needs to be followed by abdominal or chest x-rays to ensure they are properly sited. The fact that S moves his jaw in response to being suctioned suggests he does react and therefore in turn that he might well be able to experience pain and discomfort. S could have a tracheostomy and/or surgery to have a PEG tube inserted, but each of these require surgery which brings with it risks and the possibility of more pain and discomfort. The tubes would still need to be regularly cleaned and replaced and there is an ongoing risk of infection in any of these scenarios. In addition to the procedures I have set out above, S also has heel prick tests every two days and his body position changed regularly. He is on a variety of medication.

Beyond this, S faces longer term problems as he grows older. Getting larger he will be harder to move. He will be susceptible to contractures – spasms in the muscles which might lead to his suffering from dislocations or fractures, all of which are capable of being very uncomfortable and/or painful. As time goes by he will become more susceptible to suffering from epilepsy. He is likely to developing chest infections (aspiration pneumonia), and there is a risk of his suffering uncontrollable fits, apnoea and sudden cardiac arrest. Any of these could lead to his death, including his sudden death.

There are five options put forward by Dr. C on behalf of the hospital trust which range from continuing the current regime to cessation of artificial ventilation and palliative care. If I approve the plan put forward by the hospital trust (Option 5), it will enable high quality palliative care to be provided to S, including every treatment to try and reduce pain and distress when dying.

The parents argue that the court should endorse Option 2, and do not argue for Option 1. Option 2 would mean continuing with intensive ventilation and support care but not escalating treatment if S deteriorates further. They believe that this will give S the chance to carry on living, but also to relinquish life if he becomes sicker.

Option 3 would be for S to be extubated but re-intubated if he cannot manage. Option 4 would be to extubate him and give him Vapotherm or CPAP if he cannot manage, rather than re-intubating him.

Whilst Option 2 would relieve S of an escalation of treatment if he were to deteriorate, whilst he remains stable (which could be for a considerable period of time) things will continue as they are at the moment. Option 3 is much the same again. Option 4 would relieve S of invasive ventilation, but even if it was successful (which is highly unlikely) the other burdens in being kept alive would remain. The parents have said they would like S to be able to go home, but given the need for surgery and all the other risks, this is not a realistic option.

My heart goes out to these parents, who have to bear the pain and grief of what has happened to their beloved son. Hard though it is, however, I am clear that the only

This is a case where the burdens and possible suffering that continuing treatment brings with it outweigh the benefits of prolonging life. In my judgment the treatment cannot bring about any real improvement in his overall condition. Although the preservation of life is a very important consideration, continued living means S being exposed to repeated medical procedures that may well be uncomfortable or even painful. If he lives long enough his condition may worsen, and either way he may die suddenly from apnoea or heart failure without time to administer palliative care to relieve any possible distress. I understand and respect the parents’ views, including their religious views (which no doubt S would share) but it is not in his best interests to put him through so much simply to keep him alive even if he is able to experience some comfort from being looked after by his parents. If he were able to express any wishes about this it is difficult to believe he would choose this sort of existence for himself.

It speaks volumes about the parents and the medical team who have treated S that they have worked so well together and continue to do so despite the different views they hold. The care S has received in the Neonatal Intensive Care Unit has been of the highest quality. It is also right, as Mr. Thomas has said, that there is one area of his life in which S has been fortunate, and that is in having the unstinting love and devotion of his mother and father.

In all the circumstances I will make the declarations sought.