The Disability Rights Education & Defense Fund (DREDF), which worked in partnership with NCD on the series of reports, summarizes this groundbreaking work:
Despite the growing consensus that
disability is a normal part of the human experience, the lives of people
with disabilities are routinely devalued in medical decision-making.
Negative biases and inaccurate assumptions about disabled people
persist. In medical situations, these biases can have serious and even
deadly consequences.
Beginning on September 25, the National
Council on Disability (NCD) is releasing a series of reports on
bioethics and disability. The five reports were developed through a
cooperative agreement with the Disability Rights Education & Defense
Fund (DREDF), which appreciates and acknowledges the valued work of our
partners, the Autistic Self Advocacy Network, the Bazelon Center for
Mental Health Law and Not Dead Yet, in creating the series.
Each report examines the status and
future of how a variety of key issue areas – including organ donation,
assisted suicide laws, genetic testing, systems such as Quality Adjusted
Life Years, and assumptions about medical futility – are developing due
to technological and scientific advances as well as legal changes and
healthcare delivery. A combination of original research, stakeholder and
scholar interviews, literature reviews, reviews of media reports, and
legal analysis is used to examine each topic. Each report includes
findings and makes recommendations to lawmakers and policymakers that we
hope will ensure that the lives of people with disabilities are valued
on an equal and nondiscriminatory basis with all others.
NCD’s release on today’s assisted suicide report includes the following details, and an example of a seriously mistaken cancer prognosis personally experienced by the NCD Chairman, Neil Romano:
Despite the belief that pain relief is the primary motivation for seeking assisted suicide, in Assisted Suicide Laws and their Danger to People with Disabilities, NCD
found that the most prevalent reasons offered by someone requesting
assisted suicide are directly related to unmet service and support
needs, which NCD urges policy makers respond to through legislative
changes and funding.
“Assisted suicide laws are premised on
the notion of additional choice for people at the end of their lives,
however in practice, they often remove choices when the low-cost option
is ending one’s life versus providing treatments to lengthen it or
services and supports to improve it,” said NCD Chairman Neil Romano.
Closely examining the experience in
Oregon, where the practice has been legal for 20 years, NCD found that
the list of conditions eligible for assisted suicide has expanded
considerably over time, including many disabilities that, when properly
treated, do not result in death, including arthritis, diabetes, and
kidney failure.
Assisted Suicide Laws and their Danger to People with Disabilities also
notes suicide contagion in states where assisted suicide is legal; as
well as a loosening of existing safeguards both in states with legalized
assisted suicide and states considering bills to legalize.
In the report, NCD details limitations of purported safeguards of assisted suicide laws, finding:
- Insurers have denied expensive, life-sustaining medical treatment, but offered to subsidize lethal drugs, potentially leading patients to hasten their own deaths;
- Misdiagnoses of terminal disease can cause frightened patients to hasten their deaths;
- Though fear and depression often drive requests for assisted suicide, referral for psychological evaluation is extremely rare prior to doctors writing lethal prescriptions;
- Financial and emotional pressures can distort patient choice;
- Patients may “doctor shop” limitlessly to find a physician who will obtain a colleague’s concurrence and prescribe a lethal dose
“As someone who has battled cancer and
been given weeks to live and am still thriving years later, I know
firsthand that well-intending doctors are often wrong,” said Mr. Romano.
“If assisted suicide is legal, lives will be lost due to mistakes,
abuse, lack of information, or a lack of better options; no current or
proposed safeguards can change that.”
NCD concludes its research with recommendations, including highlighting the need for:
- Federal research on disability-related risk factors in suicide prevention, as well as on people with disabilities who request assisted suicide and euthanasia;
- Federal regulation requiring non-discrimination in suicide prevention services; and
- Greater federal investment in long-term services and supports.
Full Article & Source:
Federal study finds assisted suicide laws rife with dangers to people with disabilities
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