Legalising assisted suicide would cement the belief that terminally ill
people are ‘a burden’, according to the chair of one of the UK’s leading
disability charities.
Dr Alice Maynard said that Lord Falconer’s Assisted Dying Bill could
lead people into making decisions they would regret.
The Private Members Bill, which Peers debated for ten hours inside the
House of Lords on July 18, would legalise assisted dying for some terminally
ill patients.
The Bill, which is based on Oregon’s Death with Dignity Act, would allow
people who have ‘a clear and settled intention to end his or her own life’ to
seek medical assistance if they are in a fit state of mind to make the
decision.
Dr Maynard sharply criticised the Bill. She said: “I think this Bill stems
from a deep-seated belief that the lives of sick and disabled people are not
worth as much as other people’s.
“I’ve met people who
have experienced very serious accidents, and who begged to be allowed to die
because their lives were changed beyond all recognition.
“Now they are really
glad to be here. I worry that a change in the law would lead to people making
the biggest decision they can make, when they aren’t in the right frame of
mind.”
Campaigners from
Dignity in Dying have rubbished these claims and highlighted the successes of
Oregon’s Act.
Chief Executive Sarah Wootton said: “an overwhelming
majority of the public has consistently supported change, and the traditional
opposition from faith leaders and medics is beginning to crumble.”
A joint statement from faith leaders
expressed concern about the Bill’s impact. Leaders from Christian, Jewish,
Muslim, Sikh, Hindu and Buddhist faiths said: “This bill would
have a serious detrimental effect on the wellbeing of individuals and on the
nature and shape of our society.
“Every human life is of intrinsic value and ought to be
affirmed and cherished. Being perceived as a burden or as a financial drain is
a terrible affliction to bear, leading in many cases to passivity, depression
and self-loathing.”
”The bill raises the issue of what sort of society we wish to
become: one in which life is to be understood primarily in terms of its
usefulness and individuals evaluated in terms of their utility or one in which
every person is supported, protected and cherished even if, at times, they fail
to cherish themselves.”
Suzanne Stevenson, Head of Press
at Help the Hospice, said that is was paramount that people received excellent
care before they made decisions about ending their life.
Ms Stevenson said: “Good hospice and palliative care can greatly improve
most people’s
experience of living with and dying from a terminal condition.
“Many people using hospice services find that they have a further
positive phase of life which they never expected to have – perhaps coming to
terms with their situation and experiencing a greater quality of life than they
had imagined possible during their final weeks or months.”
…………………………………………………………………………………………………………………………………………….
VIEWS
FROM THE PUBLIC:
“If an individual expresses
their wish to die due to agonising pain caused by an incurable illness it seems
to me that it is a moral obligation to relieve them of such suffering where we
can. We should have a right to die to without suffering and with dignity.”
(Emma Obertelli, 24, a teacher, from London)
“I
am in favour of it because I believe that everyone has the right to choose how
to end their lives. I think its absurd to assume that everyone would go out and
kill their rich relatives if euthanasia were legalized.”(Mary Davies, 71,
retired, from South East London)
“I don’t believe anyone should be
placed in a position where they take someone's life with or without their
consent.
We shouldn’t place people in a
position where they may feel pressure to end their lives if they perceive
themselves to be a drain on resources or a nuisance to society.” (Cathy Burke,
Nurse, 56, from Salisbury)
No comments:
Post a Comment