British Healthcare Policy: Killing Babies Slowly & Painfully

     The recent case out of the U.K. of a baby “to die like an abandoned animal” is not an isolated case.  As has been noted previously, socialized medicine often leads to the “weak” being removed from the population.  Sometimes it is based on some deluded idea of racial supremacy or eugenics, but the most pernicious is when a child’s life is considered less than zero simply it would tax the stretched and already heavily rationed socialized healthcare system.

     This has become even more clear with the revelation that it is the policy of the U.K.’s National Health Service to let “weak” babies die a prolonged and horrible death.  Cash incentives to doctors and hospitals may have been given to put ill babies on the “Liverpool Care Pathway,” which is nothing more than a sick and twisted euphemism for involuntary passive euthanasia that involved removal of all care, food, and water, as revealed in the British Medical Journal.

     Now, it has been revealed by the U.K.’s Daily Mail just how painful and inhuman this “care pathway” is.  Below is a letter from the Daily Mail.  It is being quoted as it appeared on the Mail Online because unless we sear this horror upon our souls as the horrors of the NAZI death camps were seared upon the liberators of those camps.

The voice on the other end of the phone describes a newborn baby and a lengthy list of unexpected congenital anomalies. I have a growing sense of dread as I listen.

The parents want ‘nothing done’ because they feel that these anomalies are not consistent with a basic human experience. I know that once decisions are made, life support will be withdrawn.

Assuming this baby survives, we will be unable to give feed, and the parents will not want us to use artificial means to do so.

Regrettably, my predictions are correct. I realise as I go to meet the parents that this will be the tenth child for whom I have cared after a decision has been made to forgo medically provided feeding.

The mother fidgets in her chair, unable to make eye contact. She dabs at angry tears, stricken. In a soft voice the father begins to tell me about their life, their other children, and their dashed hopes for this child.

He speculates that the list of proposed surgeries and treatments are unfair and will leave his baby facing a future too full of uncertainty.

Like other parents in this predicament, they are now plagued with a terrible type of wishful thinking that they could never have imagined. They wish for their child to die quickly once the feeding and fluids are stopped.

They wish for pneumonia. They wish for no suffering. They wish for no visible changes to their precious baby.

Their wishes, however, are not consistent with my experience. Survival is often much longer than most physicians think; reflecting on my previous patients, the median time from withdrawal of hydration to death was ten days.

Parents and care teams are unprepared for the sometimes severe changes that they will witness in the child’s physical appearance as severe dehydration ensues.

I try to make these matters clear from the outset so that these parents do not make a decision that they will come to regret. I try to prepare them for the coming collective agony that we will undoubtedly share, regardless of their certainty about their decision.

I know, as they cannot, the unique horror of witnessing a child become smaller and shrunken, as the only route out of a life that has become excruciating to the patient or to the parents who love their baby.

I reflect on how sanitised this experience seems within the literature about making this decision.

As a doctor, I struggle with the emotional burden of accompanying the patient and his or her family through this experience, as much as with the philosophical details of it.

Debate at the front lines of healthcare about the morality of taking this decision has remained heated, regardless of what ethical and legal guidelines have to offer.

The parents come to feel that the disaster of their situation is intolerable; they can no longer bear witness to the slow demise of their child.

This increases the burden on the care-givers, without parents at the bedside to direct their child’s care.

Despite involvement from the clinical ethics and spiritual care services, the vacuum of direction leads to divisions within the care team.

It is draining to be the most responsible physician. Everyone is looking to me to preside over and support this process.

I am honest with the nurse when I say it is getting more and more difficult to make my legs walk me on to this unit as the days elapse, that examining the baby is an indescribable mixture of compassion, revulsion, and pain.

Some say withdrawing medically provided hydration and nutrition is akin to withdrawing any other form of life support. Maybe, but that is not how it feels. The one thing that helps me a little is the realisation that this process is necessarily difficult. It needs to be.

To acknowledge that a child’s prospects are so dire, so limited, that we will not or cannot provide artificial nutrition is self selecting for the rarity of the situations in which parents and care teams would ever consider it.

     I encourage you all to visit the Mail Online article and express your outrage, and give them the web traffic they deserve for uncovering such unabashed evil.

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