Amicus Curiae Brief — Gonzales v. Oregon

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Supreme Court. US

a Tare

No. 04-623 OFFICE OF THE CLERK

————

IN THE

Supreme Court of the Anited States

October Term, 2004

ALBERTO R. GONZALES, ATTORNEY GENERAL, ef al.,

PETITIONERS,

v.

STATE OF OREGON, ef al.

RESPONDENTS.

On Writ of Certiorari to the

United States Court of Appeals for the Ninth Circuit

BRIEF OF AMICI CURIAE NOT DEAD YET, ADAPT,

CENTER ON DISABILITY STUDIES, LAW AND POLICY

AT SYRACUSE UNIVERSITY, CENTER FOR SELF-

DETERMINATION, HOSPICE PATIENTS ALLIANCE,

MOUTH MAGAZINE/FREEDOM CLEARINGHOUSE,

NATIONAL COUNCIL ON INDEPENDENT LIVING,

NATIONAL SPINAL CORD INJURY ASSOCIATION,

SELF-ADVOCATES BECOMING EMPOWERED,

SOCIETY FOR DISABILITY STUDIES, TASH AND THE

WORLD INSTITUTE ON DISABILITY

IN SUPPORT OF PETITIONERS

Max Lapertosa Walter J. Kendall Ill

Counsel of Record Professor of Law

Kenneth M. Walden THE JOHN MARSHALL LAW

Adrienne Detanico, Law Clerk SCHOOL

ACCESS LIVING 315 South Plymouth Court

614 West Roosevelt Road Chicago, IL 60604

Chicago, IL 60630

TABLE OF CONTENTS

TARE GS AEF CRIIE UTED cccccccesctnesesnssvesccsnsvvnssesscsccnceeees

INTEREST OF AMICI CURIAE .............sssscsssssssssssssssesseeee I

xf Center on Disability Studies, Law and Human

Policy at Syracuse University ...............::cscceeeee

ae

4

4

Hospice Patients Alliance........ssssssssssvscseseseseeeeeeee 4

Mouth Magazine/Freedom Clearinghouse........... 5

National Council on Independent Living............ 5

National Spinal Cord Injury Association ............ 5

Society for Disability Studies... ........cccccesee0000. 6

6

6

6

7

x

=

a

—

Self-Advocates Becoming Empowered ..............

I. Assisted Suicide Serves No Legitimate Medical

Purpose Because It Discriminates Against and

Degrades the Lives of People with Disabilities ........ 8

A. Laws, Programs and Services Operate to

B. The Oregon Assisted Suicide Law Denies

People with Disabilities the Benefits of _

C. Euthanasia and Assisted Suicide Are Part of

the Long and Tragic sn 5 of Discrimination

rox

‘

ii

D. Assisted Suicide Contravenes Medical Ethics

and Practice Because of the Abuse It Poses to

People with Disabilities..................cccsesseeseeeees 14

a The Uncertainty of Diagnosing a

TOSI GE ccccsncetitatucsmsiaamene 14

2. The Law’s False Assumption that

Suicide is “Rational” When Committed

By a Person with a Disability................ 16

3. The Law’s False Assumption that

Disability Intrinsically Deprives Life

of Dignity and Value..................:0000008 18

4. The Difficulty in Ensuring

Decisions to Die Are Not

Coerced or Made by Others .................. 22

Il. The Attorney General’s Determination that

Assisted Suicide is Not a “Legitimate Medical

Practice” is a Permissible Construction of the

Controlled Sebetemces A6t ...cccccccccccccccosesescsscsccossenes 23

A. The Attorney General’s

Interpretive Ruling is Entitled to Deference...... 23

B. The “Clear Statement” Rule Does Not Apply to

Regulation of the Practice of Medicine............. 25

CUINGLIBIIUIN ...000:cccssscecscaseceseseeessnsesnimansnnmmna 28

TABLE OF AUTHORITIES

CASES

Abbott v. Bragdon, 912 F. Supp. 580 (D. Me. 1995),

aff'd, 107 F.3d 934 (ist Cir. 1997),

vacated & remanded, 524 U.S. 624 (1998)... 28

ADAPT v. Philadelphia Hous. Auth.,

2000 U.S. Dist. LEXIS 5380 (E.D. Pa. Apr. 14, 2000)..... 3

ADAPT v. Skinner, 881 F.2d 1184 (3d Cir. 1989) ................ 3

ADAPT v. SkyWest Airlines,

SS MPU, GED IPUPE Paxsesnscscccncesessnncsensecsenenencesees 3

Atascadero State Hosp. v. Scanlon, 473 U.S. 234 (1985)... 27

Barnhart v. Walton, 535 U.S. 212 (2002) ........ccccccceeee 24, 25

Bragdon v. Abbott, 524 U.S. 624 (1998)............006 24, 27-28

Buck v. Bell, 274 U.S. 200 (1927) .......ccccccscsssenesseeesesrenseeees 12

Chevron U.S.A. v. Natural Resources Defense Council,

a 7, 23-25

City of Cleburne v. Cleburne Living Center,

ET CR 12, 26

Equal Employment Opportunity Comm'n v. Massachusetts,

III, ITI ccscennssncsenasennnsenessecsseusczecocesese 26

Gregory v. Ashcroft, 501 U.S. 452 (1991) ..........0.. 7-8, 25-26

Helen L. v. DiDario,

46 F.3d 325 (3d Cir.), cert. denied sub nom.,

Secretary of Publ. Welf. v. Ideil S.,

ee 3

In re Grand Jury | roceedings,

801 F.2d 1164 (9th Cir. 1986) 0... ccccccccecseeeeeeeeeenens 26

In re Kober’s Will, 285 P. 1032 (Or. 1930)..........cccccccccceeeees 9

In re Simpson,

180 N.E. 2d 206 (Ct. Common Pleas Oh. 1962)............. 12

McKay v. Bergstedt, 801 P.2d 617 (Nev. 1990)............. 21-22

Minor v. United States, 396 U.S. 87 (1969) ........cccccccceeeeees 26

Olmstead v. L.C., 527 U.S. 581 (1999) ......cccccccceeees 20, 24, 27

Oregon v. Ashcroft, 368 F.3d 1118 (9th Cir. 2004). ......25-26

Reina v. United States, 364 U.S. 507 (1960)... 26

iv

School Comm. of Burlington v.

Massachusetts Dep't of Educ.,

I ls Se IED crnecenerersnniacenententenatininaniiainmninitiate 12

Solid Waste Agency v. Army Corps of Engineers,

Be Se GI a cctennennpnnemnnatanntaninninniinacanenitns 25

Tennessee v. Lane,

541 U.S. 509, 124 S. Ct. 1978 (2004) ooo ccccccccceeeeeees 26

United States v. Moore, 423 U.S. .22 (1975) ............... 24, 27

Vacco v. Quill, $21 U.S. 793 (1997) ..............ccccesseesssseeseees 14

Washington v. Glucksberg,

eee 2, 3, 8, 11, 14, 16

Wyckoff v. Mutual Life Ins. Co.,

Pe Ca I Ge cennnsnsntnenenennnitipnninicinninitienidiai 9

FEDERAL STATUTES

Americans with Disabilities Act,

ee l

Se lie Ob See cenrsereresnnrsensenncccomeenemnsneiiinainsianiinil 10

Controlled Substances Act, 21 U.S.C. §§ 801-971 ......... 7,24

ae ies SPIED counennmmnecincnsineanitanceniietniaapinaneaniendis 24

See les SD cxenecrnnveresenmneiannicnnnninetininneiininiannain 24

I 24

Be eee SP crinscennnennengeccninnsmnnneniaiiitaninmenaes 24

Food, Drug and Cosmetic Act, 21 U.S.C. §§ 301-397........ 27

Section 504 of the Rehabilitation Act,

ss 0 Penns 10

STATE STATUTES

Alaska Stat. §§ 44.29.300-44.29.390 0000ooooocccccceceeeeeeneeeeees 9

TR. TR, RD. Fa eerrteeenetarettcmenniviuntitiiiatiiitiatnniin 8

RED, GRR. GB, Bee nee 9

AGS. GEG GER: BEG Gennes 9

Ca Saat, Ga i eenemiemmmennennin 9

Cal. Welf. & Inst. Code §§ 4098 — 4098.5 0000.0 ccccceeeeees 9

a GR GRR, BS Pee eceerenenneneneteiainmeniiaites 9

ee GR GE. Fi ED encanta 8

Vv

Haw. Rev. Stat. § 703.308 .............ccscscscsssssssscsesseeseeseeseeeseseee 8

ee 9

La. Rev. Stat. Amn. § 17.282.4 .......ccccccsccscsesssessessesseesseesecsees 9

Mass. Ann. Laws ch. 40, § 36C ......ccccccsccssesssessesseeseessessnesees 9

Md. Code Ann., Health-General § 10-1403(a)(1)(iii)........... 9

NS ARI 9

NS Ee 9

oO Ear ee 8

INLD. Cant. Code § S7-40.6-10 .....c.ccescessccsccescesccsccecosscssecssee 9

DUBE. Reov. Stat. § 1OGG PO ccecacecnneccccscceccccccesccescccnsccscossscess 9

N.H. Rev. Stat. Ann. § 627.6.........ccccessesssessessessessecseesesseseeeees 8

a as: 8

N.J. Stat. Ann. §§ 30:9A-13 — 30:9A-27.......cccccccessessessveseeeees 9

et 8

Nev. Rev. Stat. §§ 439.511 — 439.513 .....ccccccccccccsessessesseeseeees 9

Okla. Stat. Ann. §§ 12-101 — 12-105 ........cccecccessecsesseeseeeneeees 9

The Oregon "Death with Dignity” Act,

Or. Rev. Stat. §§ 127.800 — 127.995 ......cccccccecesseesveees 1,10

icin i eeiinn 17

teen ae 8

RATS 8

Or. Rev. Stat. § 181.860(8)(a) .......c.ccccccccsessesseeseeseseesveseeeveens 9

SS | | eee 9

eS eS 9

ie, rh, Be I iiitisccticnnitmnctinientinmamedl 9

SEES 9

I I ac crcritinsesiinssinieiueitinthinbietiinadistias 8

24 P.R. Laws Ann. §§ 3241 — 3244 .....ccccccccsesceessecseeseeseeeveens 9

a, GR, BS BO rrcremneeeeeeememnen 9

CO 8

eS eee ees 9

ee 8

FEDERAL REGULATIONS

SORE. CUED. .xintntiidtiniondael 7,24

vi

OTHER AUTHORITIES

American Medical Association,

SII ceenenetuniantrarsenneninsmnmaninniinseniititiiin 2

Evelyn Hoover Barnett,

ls Mom Capable of Choosing to Die?

The Oregonian, Oct. 16, 1999, at G1 ooo... eee 2, 22

William Breitbart ef ai.,

Depression, Hopelessness and Desire for Hastened

Death in Terminally Ill Patients with Cancer,

284 JAMA 2907 (Dec. 13, 2000). ..0........cccecccceeeeeees 16, 18

Harvey Max Chochinov ef ai,

Dignity in the Terminally Ill:

A Cross-Sectional, Cohort Study,

360 The Lancet 2026 (Dec. 28, 2002) 20.........ccccccecceeeeeees 20

Kathleen M. Foley,

Competent Care for the Dying

Instead of Physician-Assisted Suicide,

336 New Eng. J. Med. 54 (Jan. 2, 1997) 200000 cccceecceeees 19

Linda Ganzini et al,

Evaluation of Competence to Consent to

Assisted Suicide: Views of Forensic Psychiatrists,

157 Am. J. Psychiatry 595 (Apr. 2000)..................... 17,21

Carol J. Gill, Suicidal Intervention for People with

Disabilities: A Lesson in Inequality,

8 Issues in L. & Med. 37 (1992) ...........::ccccsccceeeeeceeeeeeeees 1]

Herbert Hendin ef ai,

Physician-Assisted Suicide:

The Dangers of Legalization,

150 Am. J. Psychiatry 14 (Jan. 1993). 20.00.0000... 16, 18

Herbert Hendin,

Seduced by Death:

Doctors, Patients and the Dutch Cure (1997).............0..-+« 2

Herbert Hendin,

Seduced by Death:

Doctors, Patients and the Dutch Cure,

10 Issues in L. & Med. 123 (1994). 0... eeeecceecceeeeeeeeeees 15

vii

Stanley S. Herr,

No Place to Go: Refusal of Life-Sustaining

Treatment by Competent Persons with Physical

Disabilities,

eS 21

Brendan D. Kelly et al.,

Euthanasia, Assisted Suicide and Psychiatry:

A Pandora's Box,

181 British J. Psychiatry 278, 279 (2002)................. 17, 18

Evan J. Kemp, Could You Please Die Now?

UU UF UR 16

H. Laughlin,

Eugenic Sterilization in the United States (1922).......... 12

James V. Lavery et al.,

Origins of the Desire for Euthanasia and

Assisted Suicide in People with HIV-1 or AIDS:

A Qualitative Study,

358 The Lancet 362 (Aug. 4, 2001) ..........:.ccccceeeeeees 19, 21

Robert J. Lifton,

The Nazi Doctors: Medical Killing and

the Psychology of Genocide (1986) .............cceeseeeeeeenees 13

National Council on Disability,

Assisted Suicide: A Disability Perspective

OU 2, 15, 18

M. Louis Offen, Dealing with “Defectives”’:

Foster Kennedy and William Lenox on Eugenics,

61 Neurology 668 (Sept. 2003) ............ccccsecseereeeeeneeees 13

Oregon Department of Human Services,

Oregon's Death with Dignity Act:

Three Years of Physician-Assisted Suicide (2001)..... 19-20

Oregon Department of Human Services,

Seventh Annual Report on

Oregon's Death with Dignity Act (2005) ...........--+++ 15,17

Timothy E. Quill ef ai.,

Sounding Board: Care of the Hopelessly Ill,

327 New Eng. J. Med. 1380 (Nov. 5, 1992) ..........cc000000+ 14

Vili

Lori A. Roscoe et al,

Dr. Jack Kevorkian and Cases of Euthanasia

in Oakland County, Michigan, 1990-1998,

343 New Eng. J. Med. 1735 (Dec. 7, 2000)................ 2, 15

Peter Singer,

Rethinking Life and Death:

The Collapse of Our Traditional Ethics (1994).............. 13

The Right to Kill, Time, Nov. 18, 1935, at 53-54................ 13

The Surgeon General's

Call to Action to Prevent Suicide 1999 ..........cccccccccceeees 1,8

Peter Van der Maas ef al.,

Euthanasia and Other Medical

Decisions Concerning the End of Life,

338 The Lancet 669 (1991) .0........cccccccccceeceeeeeeees 15, 18, 22

World Health Organization,

World Report on Violence and Health (2002) ...............0... i)

l

INTEREST OF AMICi CURIAE

Amici are among the nation’s leading organizations

representing people with disabilities. Most are governed and

staffed by a majority of people with disabilities of all types.

They played a key role in enacting the nation’s civil rights

laws for people with disabilities, including the Americans

with Disabilities Act, 42 U.S.C. §§ 12101-12181. Based on

their shared experience as people with disabilities, including

conditions judged to be “terminal,” Amici strongly oppose

the legalization of assisted suicide. '

In the United States, as in most other nations, a

person who attempts or desires to commit suicide wili

typically be rushed to the nearest emergency room, as one-

half million Americans are each year. The Surgeon

General's Call to Action to Prevent Suicide 1999 1. The

person will be subject to numerous laws, programs, and

medical and therapeutic interventions designed to convince

him or her not to commit suicide, or to prevent him or her

from doing so. /d.

It seems axiomatic that society’s response to a person

who attempts suicide should not differ based on that person’s

race, ethnicity, gender, religion or disability. Yet Oregon’s

“Death with Dignity” Act, Or. Rev. Stat. §§ 127.800 -

127.995, encourages, rather than discourages, certain people

to die solely because of their disability. Indeed, the law

guarantees that the suicide attempts of the severely disabled

will succeed. Although the Surgeon General has stated that

suicide prevention policies “must recognize and affirm the

value, dignity and importance of each person,” Surgeon

General's Call to Action at 13, Oregon’s assisted suicide law

implicitly states that some people’s lives are worth saving

' The parties have consented to the filing of this brief. No

counsel for a party has authored this brief, in whole or in part, and no

person other than amici and their counsel has made any monetary

contribution for its preparation.

2

and others are not. For amici, this debate is not about the

“choice” of someone who is suicidal. Rather, it is about

demanding a uniform legal and societal response to those

who want to kill themselves. Amici’s experience as people

with disabilities is that the false assumption that suicide is a

rational solution to the barriers and discrimination they face

devalues them as human beings and sanctions their unequal

treatment under law.

Supporters of physician-assisted suicide laws such as

Oregon’s claim they are limited only to competent people

who face imminent death as a result of terminal illness. Yet

neither Oregon’s system of physician-assisted suicide nor

any other — whether de jure (the Netherlands)” or de facto

(Dr. Kevorkian)’ — has operated within these boundaries.

Physician-assisted suicide invites anyone involved in the

decision to die, including the physician, to make

monumental judgments on the relative value of a person’s

life — or, as one Oregon reporter noted, to act as “the

gatekeepers of death.” Evelyn Hoover Barnett, /s Mom

Capable of Choosing to Die? The Oregonian, Oct. 16, 1999,

at Gl. It is no coincidence, then, that this Court has refused

to recognize assisted suicide as a fundamental right, see

Washington v. Glucksberg, 521 U.S. 702, 735 (1997), the

medical profession has eschewed it as a legitimate practice,

see American Medical Association, Code of Ethics § 2.211,

and every other state besides Oregon has refused to allow it

shelter under their laws, Glucksberg, 521 U.S. at 710. And,

as Amici here submit, it is condemned by the vast majority of

people with disabilities. See National Council on Disability,

Assisted Suicide: A Disability Perspective (1997, re-released

2005).

? See Herbert Hendin, Seduced by Death: Doctors, Patients and

the Dutch Cure (1997), cited in Washington v. Glucksberg, 521 U.S. 702,

730 (1997).

> See Lori A. Roscoe et al, Dr. Jack Kevorkian and Cases of

Euthanasia in Oakland County, Michigan, 1990-1998, 343 New Eng. J.

Med. 1735 (Dec. 7, 2000).

A. Not Dead Yet

Not Dead Yet is a national grassroots organization of

people with disabilities formed in response to the movement

to permit physician-assisted suicide and euthanasia in the

United States and around the world. Not Dead Yet’s mission

is to protect the civil rights of people with disabilities by

advocating against discriminatory legalization of physician-

assisted suicide and euthanasia and to bring a disability-

rights perspective and awareness of the effects of

discrimination to the legal and _ sociological debate

surrounding these practices. Not Dead Yet has worked to

educate, support, coordinate and lead the disability

community's effort to stop the "right to die" from becoming a

duty to die or a right to kill. This Court cited Not Dead Yet’s

amicus brief in Washington v. Glucksberg, 521 U.S. 702,

733 n.23 (1997). Not Dead Yet has also testified before the

U.S. Congress three times on the subject of physician-

assisted suicide.

B. ADAPT

ADAPT is a national disability rights organization

comprised primarily of people with disabilities. ADAPT has

a long history and record of enforcing the civil rights of

people with disabilities. in addition to being one of the key

organizations that helped enact the Americans with

Disabilities Act, ADAPT has been a plaintiff in numerous

civil rights lawsuits. See e.g. ADAPT v. Skinner, 881 F.2d

1184 (3d Cir. 1989); Helen L. v. DiDario, 46 F.3d 325 (3d

Cir.), cert. denied sub nom., Secretary of Publ. Welf. v. Idell

S., 516 U.S. 813 (1995); ADAPT v. Philadelphia Hous.

Auth., 2000 U.S. Dist. LEXIS 5380 (E.D. Pa. Apr. 14, 2000);

ADAPT v. SkyWest Airlines, 762 F. Supp. 320 (D. Ut. 1991).

4

C. Center on Disability Studies, Law and Human

Policy at Syracuse University

The Center on Disability Studies, Law and Human

Policy is an interdisciplinary disability research and policy

institute at Syracuse University. Established in 1971, the

Center's work focuses on people with cognitive disabilities.

The Center's research has included studies of institutions,

schools, and community services, the history of the treatment

of people with disabilities in America, disability law and

policy, images of disability in the media and popular culture,

and the politics and ethics of treatment.

D. Center for Self-Determination

The Center for Self-Determination is a national

organization comprised of individuals with disabilities,

family members, and professionals committed to the

principles of self-determination: freedom to choose where

and with whom one wants to live, as well as what one will

do with one's life; authority and control over the dollars

necessary for long term supports; designing and providing

individual, community-based supports for people with

disabilities; and responsibility for both the wise use of public

dollars and for contributing to one's community.

E. Hospice Patients Alliance

The Hospice Patients Alliance, Inc. is a charitable

nonprofit patient advocacy organization that works to

promote excellence in end-of-life care and to protect the

rights of patients. It provides information about hospice

services, directly assists patients, families and caregivers in

resolving difficulties they have with current hospice services,

and promotes better quality hospice care.

5

F. Mouth Magazine/Freedom Clearinghouse

Mouth Magazine, published by Free Hand Press, Inc.,

is a magazine run by and dedicated to issues concerning

people with disabilities. Its mission is to promote the lives

and freedoms of all people with disabilities through

magazines, books, handbooks, speeches, pamphlets, and

electronic media. The mission statement of Freedom

Clearinghouse is to publicize and implement the right of

people with disabilities to live in the community.

G. National Council on Independent Living

The National Council on Independent Living (NCIL)

represents over 700 advocacy organizations and people with

disabilities of all types. The independent living philosophy,

which NCIL and its members advance, holds that people

with disabilities have the right to live with dignity and

appropriate supports in their own homes, participate in their

communities, and control and make decisions about their

lives, regardless of the degree of disability.

H. National Spinal Cord Injury Association

Founded in 1948, the National Spinal Cord Injury

Association (NSCIA) is the largest organization in the

United States dedicated to improving the quality of life of

persons with spinal cord injuries and diseases. The NSCIA's

mission is to enable people with spinal cord injuries to make

choices and take actions to achieve their highest level of

independence and personal fulfillment. Spinal cord injury

has been cited as the type of impairment warranting a desire

to hasten death. The NSCIA believes that expediting one’s

death because they have a disability is immoral and unwise,

both for society at large and members of the disability

community in particular.

6

I. Self-Advocates Becoming Empow ered

Self-Advocates Becoming Empowered is a national

organization comprised of and directed by people with

developmental disabilities, including intellectual disabilities

or mental retardation, cerebral palsy and autism. First

established in 1974, Self-Advocates Becoming Empowered

now has over 900 chapters in 46 states (known locally as

“People First” organizations), with an estimated 20,000

members. Many members have been unnecessarily

institutionalized and have experienced discrimination by

medical practitioners.

J. Society for Disability Studies

The Society for Disability Studies is an international

non-profit organization that promotes the exploration of

disability through research, artistic production, and teaching.

K. TASH

TASH (formerly the Association for Persons with

Severe Handicaps) is an international advocacy organization

of people with disabilities, their families, advocates and

professionals in the disability field. It has over 30 chapters

covering 37 states and members in 34 nations. TASH has

adopted a resolution opposing physician-assisted suicide.*

L. World Institute on Disability

The World Institute on Disability (WID) is a

nonprofit research, public policy and advocacy center

dedicated to promoting the civil rights and full societal

inclusion of people with disabilities. WID is governed and

staffed by a majority of people with disabilities.

: www .tash.org/resolutions/resO2assistedsuicide.htm.

7

SUMMARY OF ARGUMENT

Amici support the Attorney General’s interpretive

ruling that assisted suicide is not a “legitimate medical

practice” under the Controlled Substances Act, 21 U.S.C. §§

801-971, and its implementing regulations, 21 C.F.R. §

1306.04(a). When applied only to people with significant or

even “terminal” health impairments, Oregon’s assisted

suicide law encourages the disabled to end their lives — and

guarantees such efforts will be successful — while other state

laws concurrently discourage non-disabled persons from

doing so. Assisted suicide laws deny people with disabilities

the benefit of programs and laws that prevent suicide and are

the ultimate legal judgment that the life of a person with a

disability is not as worthwhile as that of a non-disabled

person.

Assisted suicide also raises serious ethical concerns

regarding the medical profession’s treatment of the disabled.

It requires doctors to make difficult, if not impossible,

determinations of a person’s competency and life

expectancy, the consequences of which are both ultimate and

irreversible. The availability of assisted suicide also distracts

from the determination whether a person’s desire to die

might be lifted with improved treatment, community-based

health care or other measures that improve a person’s

independence and dignity.

Thus, given the Attorney General’s latitude to

interpret federal statutes that Congress has authorized him to

enforce, see Chevron U.S.A. v. Natural Resources Defense

Council, 467 U.S. 837, 844 (1982), this difference in

treatment, based solely on the presence of a severe disability,

justifies the Attorney General’s action here. Additionally,

Congress and the Attorney General are not precluded from

acting to protect the rights of people with disabilities simply

because such protection regulates the practice of medicine.

The Court of Appeals’ erroneous reliance on Gregory v.

8

Ashcroft, 501 U.S. 452 (1991), and its imposition of the

“clear statement” rule to an area that is not a “fundamental”

state function, unduly impairs Congress’ ability to legislate

against state infringements on the civil rights of people with

disabilities.

ARGUMENT

I. Assisted Suicide Serves No Legitimate Medical

Purpose Because It Discriminates Against and

Degrades the Lives of People with Disabilities

A. Laws, Programs and Services Operate to

Prevent People from Committing Suicide

Suicide is a practice that American society

disapproves of and actively discourages through laws and

prevention programs. Washington v. Glucksberg, 521 U.S.

702, 711 (1997) (“[F]or over 700 years, the Anglo-American

common-law tradition has punished or otherwise

disapproved of both suicide and assisting suicide.”). The

U.S. Surgeon General has called suicide “a serious health

problem.” The Surgeon General’s Call to Action to Prevent

Suicide 1999 at 1. Every year, 500,000 people in the United

States use emergency room services as a result of suicide

attempts. /d In almost every state, helping someone

commit suicide is a crime. Glucksberg, 521 U.S. at 710-11.

In Oregon, intentionally causing or aiding another person to

commit suicide is second-degree manslaughter. Or. Rev.

Stat. § 163.125. Oregon law also authorizes physical force

to prevent someone from committing suicide. Or. Rev. Stat.

§ 161.205(4).° Additionally, many states statutorily mandate

* See also Ariz. Rev. Stat. § 13-403; Del. Code Ann. tit. 11, §

467; 9 Guam Code Ann. § 7.92; Haw. Rev. Stat. § 703.308; Neb. Rev.

Stat. § 28.1412; N.H. Rev. Stat. Ann. § 627.6; N.J. Stat. Ann. § 2C:3-7;

N.D. Cent. Code § 12.1-05; 18 Pa. Cons. Stat. § 508; Tenn. Code Ann. §

39-1 1-613; Wis. Stat. § 939.48.

9

suicide prevention plans, hotlines, or other intervention

programs.

According to the World Health Organization (WHO),

depression and anxiety are often associated with suicide and

over 80 percent of suicide victims had severe depression.

WHO, World Report on Violence and Health 192 (2002).

Oregon law reflects this assumption that persons who

commit suicide do not act rationally. For life insurance

purposes, Oregon law creates a presumption against suicide,

under the reasoning that “it is common knowledge that sane

persons do not ordinarily kill themselves.” Wyckoff v.

Mutual Life Ins. Co., 147 P.2d 227, 229 (Or. 1944); see also

Or. Rev. Stat. § 656.310 (for worker’s compensation claims,

worker’s death presumed not to be suicide). Oregon also

presumes that the will of one who commits suicide is invalid

and the product of a “deranged” mind. Jn re Kober’s Will,

285 P. 1032 (Or. 1930).’

® See e.g. Alaska Stat. S§ 44.29.300-44.29.390; Ariz. Rev. Stat.

§ 36.3415; Ark. Code Ann. § 6-18-1005; Cal. Gov. Code § 53110;

Cal.Welf. & Inst. Code §§ 4098 — 4098.5; Conn. Gen. Stat. § 7-294;

410 Ill. Comp. Stat. 53/5-15; La. Rev. Stat. Ann. § 17.282.4; Md. Code

Ann., Health-General § 10-1403(a\(1 iii); Mass. Ann. Laws ch. 40, §

36C; Minn. Stat. § 146.56; Mo. Rev. Stat. § 630.900; Nev. Rev. Stat. §§

439.511 — 439.513; N.H. Rev. Stat. § 186.67-a; N.J. Stat. Ann. §§ 30:9A-

13 — 30:9A-27; N.D. Cent. Code § 57-40.6-10; Okla. Stat. Ann. §§ 12-

101 — 12-105; 24 P.R. Laws Ann. §§ 3241 — 3244; R.I. Gen. Laws § 16-

22-14; Va. Code Ann. § 32.1-73.7.

” Other ways in which Oregon law discourages suicide include:

the exclusion of suicide threats from a state law mandating

confidentiality of statements made during counseling sessions, Or. Rev.

Stat. § 181.860(8)(a); establishing a statewide team to investigate youth

suicides, Or. Rev. Stat. § 418.748; establishing a Youth Suicide

Prevention Coordinator, Or. Rev. Stat. § 418.756; and mandating that

hospitals refer children who attempt suicide to crisis intervention

services, Or. Rev. Stat. § 441.750.

10

B. The Oregon Assisted Suicide Law Denies

People with Disabilities the Benefits of Suicide

Prevention Laws and Measures

The Oregon “Death with Dignity” Act, Or. Rev. Stat.

§§ 127.800 — 127.995, modifies the assumption that suicide

is irrational and undesirable — but only as to persons with

“terminal” disabilities or conditions. For these people,

Oregon law does not assume that suicide is irrational or a

practice that should be discouraged. Rather, the law allows

doctors and others to facilitate suicide, an act that would be a

crime but for the person’s disability. Persons with severe

health impairments are therefore denied the benefit of

suicide prevention laws and programs. Indeed, state law

guarantees their suicide attempts will succeed — unlike those

of other persons with suicidal ideations. A practice that the

State would otherwise expend public health resources to

prevent is instead allowed to occur. This differing response

is based solely on a person’s disability.*

If a state overtly excluded people with “terminal”

disabilities from suicide prevention laws and programs, it

would undoubtedly violate federal civil rights laws such as

the Americans with Disabilities Act, 42 U.S.C. §§ 12132,

and Section 504 of the Rehabilitation Act, 29 U.S.C. §

794(a). Yet that is precisely the design and effect of the

Oregon assisted-suicide law. A more devastating form of

discrimination would be difficult to imagine. By assuming

that it is irrational for a non-disabled person to end his or her

life, but rational for a disabled person to do so, the law

assumes that the non-disabled person’s life is intrinsically

more valuable and worthwhile than that of a disabled person.

* Amici do not advocate here for forced treatment or against the

right of people with disabilities to refuse treatment. Amici include

persons with psychiatric disabilities who have been subject to unwanted

treatment. Amici are concerned solely with the Oregon assisted suicide

law’s unequal treatment of the disabled. See www.mindfreedom.com.

11

For amici, perhaps no other attitude strikes closer to

the heart of the disability civil rights movement to which

they have dedicated themselves for the past three decades.

Central to this movement is the idea that a disabling

condition does not inherently diminish one’s life; rather,

surrounding barriers and prejudices do so. Assisted suicide

takes the opposite approach — it gives official sanction to the

idea that life with a disabling condition is not worth living.’

As this Court has recognized:

The State’s interest here [in prohibiting

assisted suicide] goes beyond protecting the

vulnerable from coercion; it extends to

protecting disabled and terminally ill people

from prejudice, negative and inaccurate

stereotypes, and “societal indifference ...”

The State’s assisted-suicide ban reflects and

reinforces its policy that the lives of

terminally ill, disabled and elderly people

must be no less valued than the lives of the

young and healthy, and that a seriously

disabled person’s suicidal impulses should be

interpreted and treated the same as everyone

else’s.

Glucksberg, 521 U.S. at 732.

Cc. Euthanasia and Assisted Suicide Are Part of

the Long and Tragic History of Discrimination

Against People with Disabilities_

Assisted suicide must be seen against the background

of the United States’ long and tragic history of state-

* See Carol J. Gill, Suicidal Intervention for People with

Disabilities: A Lesson in Inequality, 8 \ssues in L. & Med. 37 (1992)

(“When a culture values human life conditionally, suicide intervention

becomes selective. Devalued populations fail to receive rigorous

protection. assessment and treatment.)

12

sanctioned discrimination against the disabled, which five

members of the Supreme Court have called “grotesque.”

City of Cleburne v. Cleburne Living Center, 473 U.S. 432,

454-55 & 461 (1985). Amici’s experience is that this history

continues to haunt the everyday lives and realities of people

with disabilities, particularly when making so-called “end-

of-life” decisions.

Throughout history, state officials, with the support

of the medical community, have authorized the sterilization

of people with disabilities. Buck v. Bell, 274 U.S. 200, 207

(1927) (“It is better for all the world, if ... society can prevent

those who are manifestly unfit from continuing their kind ...

Three generations of imbeciles are enough”).'” People with

disabilities were placed in “massive custodial institutions ...

built to warehouse the retarded for life; the aim was to halt

reproduction of the retarded and ‘nearly extinguish their

race.” City of Cleburne, 473 U.S. at 461-62 (Marshall, J.,

concurring & dissenting) (citations omitted). The disabled

were deemed “uneducable” and excluded en masse from

public schools. See School Comm. of Burlington v.

Massachusetts Dep't of Educ., 471 U.S. 359, 373 (1985).

These practices, like Jim Crow laws in the south, were

carried out by elected officials with the support of the voters.

This did not make them any more legitimate or

constitutional.

Euthanasia played a key role in this history. In the

1940s, medical professionals sought the involuntary

euthanasia of the severely disabled. In a 1941 presentation

to the American Psychiatric Association, which was later

° See also In re Simpson, 180 N.E. 2d 206 (Ct. Common Pleas

Oh. 1962) (ordering sterilization of woman with retardation because of

“probability that [her] offspring will be mental'y deficient and become a

public charge for most of their lives.”); H. Laughlin, Eugenic

Sterilization in the United States 369 (1922) (“(Djefectives who are

practically certain to breed principally defectives, owe a debt to the

community that can be discharged only by an adequate guarantee that

they shall not contribute to the next generation.”).

13

published in the Association’s journal, Dr. Foster Kennedy,

the President of the American Neurological Association,

stated:

[T]he place for euthanasia, I believe, is for the

completely hopeless defective: nature’s

mistake; something we hustle out of sight,

which should never have been seen at all.

These should be relieved of the burden of

living ... to allow them to continue such a

living is sheer sentimentality, and cruel too;

we deny them as much solace as we give our

stricken horse. Here we may most kindly kill.

M. Louis Offen, Dealing with “Defectives”: Foster

Kennedy and William Lenox on Eugenics, 61 Neurology 668

(Sept. 2003) (quoting Foster Kennedy, The Problem of

Social Control of the Congenital Defective, 99 Am. J.

Psychiatry 13, 16 (1942)). In 1935, a Nobel Prize-winning

fellow at the Rockefeller Institute similarly urged that

“sentimental prejudice ... not obstruct the quiet and painless

disposition of incurable ... and hopeless lunatics.” The Right

to Kill, Time, Nov. 18, 1935, at 53-54."

Such attitudes, unfortunately, are not completely in

the past. Prominent ethicists such as Peter Singer of

Princeton University have sanctioned the killing of infants

with severe disabilities based on a belief that they will not

lead a “good” life and will burden their parents and society.

Peter Singer, Rethinking Life and Death: The Collapse of

Our Traditional Ethics 197-98 (1994). Professor Singer has

also written that it is impossible to kill people with severe

cognitive disabilities “against their will” “because they are

not capable of having a will on such a matter.” /d.

' See also Robert J. Lifton, The Nazi Doctors: Medical Killing

and the Psychology of Genocide (1986).

14

Amici do not claim that Oregon’s assisted suicide law

was intended to “extinguish” the disabled. Nevertheless,

given this history and the slippery slope it exemplifies,

federal safeguards are appropriate and necessary to ensure

that euthanasia against the disabled is not, once again,

sanctioned as a “legitimate medical practice” as it was for so

many years.

D. Assisted Suicide Contravenes Medica! Ethics

and Practice Because of the Abuse It Poses to

People with Disabilities

As this Court has recognized, assisted suicide is

contrary to well-established medical ethics. Glucksberg, 521

U.S. at 731 (quoting American Medical Association, Code of

Ethics § 2.211 (1994)); see also Vacco v. Quill, 521 U.S.

793, 801 n.6 (1997) (discussing medical profession’s

distinction between withholding treatment and assisted

suicide). This rejection is firmly grounded in the potential

harm the Oregon assisted suicide law poses to the lives of

people with disabilities.

1. The Uncertainty of Diagnosing a

“Terminal Illness”

First, the diagnosis and prognosis of a “terminal

condition” — defined under the Oregon law as a condition

likely to cause death within the next six months — is

inherently uncertain. Timothy E. Quill ef al., Sounding

Board: Care of the Hopelessly Ill, 327 New Eng. J. Med.

1380, 1381 (Nov. 5, 1992) (“[W]Je acknowledge the

inexactness of such prognosis [of imminent death]”).

Oregon’s own reports on the implementation of its assisted

suicide law confirm this uncertainty. In 2004, 60 patients

were determined “terminally ill” and prescribed lethal

medication, but only 35 ingested the medication. Of the 25

who did not, 12 — almost half — were still alive at the end of

2004. One patient who was prescribed medication in 2003,

15

and thus determined to have less than six months to live, did

not ingest the medication and was nevertheless still alive by

the end of 2004. Oregon Department of Human Services,

Seventh Annual Report on Oregon's Death with Dignity Act

12 (2005).

Assisted suicide has not been limited to persons

facing imminent death. In the Netherlands, whose assisted

suicide law was a model for Oregon, a governmental report

confirmed that many people have been killed who did not

have a “terminal” illness. Peter Van der Maas ef al,

Euthanasia and Other Medical Decisions Concerning the

End of Life, 338 The Lancet 669, 672 (1991).'? Similarly,

only one in four of the people whom Dr. Jack Kevorkian

helped commit suicide had a terminal illness; others simply

had physical or neurological disabilities. Lori A. Roscoe ef

al., Dr. Jack Kevorkian and Cases of Euthanasia in Oakland

County, Michigan, 1990-1998, 343 New Eng. J. Med. 1735,

1736 (Dec. 7, 2000).

The medical profession’s predictions of the

capabilities and life spans of people with disabilities have

been historically unreliable. As the National Council on

Disability has reported, “people with disabilities are aware of

enough instances of dramatic mistakes that many of them

have a healthy skepticism of medical predictions,

particularly as it relates to future life quality.” Assisted

Suicide: A Disability Perspective at 27-28. Evan Kemp,

Director of the Equal Employment Opportunity Commission

under President George H.W. Bush, wrote:

'? Not all such cases involve unintentional misdiagnosis. In one

Dutch case, a court acquitted a psychiatrist who helped a physically

healthy 50-year old womar — who was unquestionably not terminally ill

~ commit suicide. The woman had been diagnosed with leukemia and

had a history of depression. Herbert Hendin, Seduced by Death:

Doctors, Patients and the Dutch Cure, \0 Issues in L. & Med. 123, 123-

26 (1994).

16

As a disabled person, I am_ especially

sensitive to the “quality of life” rationale that

is frequently introduced in the debate [over

assisted suicide]. For the past 47 years I have

lived with a progressive neuromuscular

disease that first began to manifest itself when

I was 12. My disease, Kugelberg Weylander

Syndrome, has no known cure, and I have no

hope for “recovery.” Upon diagnosis, my

parents were informed by the physicians

treating me that I would die within two years.

Later, another group of physicians was certain

that I would live only to the age of 18. Yet

here I am at 59, continuing to have an

extraordinarily high quality of life.

Evan J. Kemp, Could You Please Die Now? Wash. Post,

Jan. 5, 1997, at C1.

2. The Law’s False Assumption that Suicide

is “Rational” When Committed by a

Person with a Disability

As the Glucksberg Court recognized, “those who

attempt suicide — terminally ill or not — often suffer from

depression or other mental disorders.” 521 U.S. at 730.'°

The Court continued, “Research indicates ... that many

people who request physician-assisted suicide withdraw that

request if their depression and pain are treated.” Jd For

example, a study of cancer patients showed that those with

depression were four times more likely to want to die.

William Breitbart ef al, Depression, Hopelessness and

Desire for Hastened Death in Terminally Ill Patients with

Cancer, 284 JAMA 2907, 2909 (Dec. 13, 2000).

'? Ninety-five percent of those who commit suicide have been

found to have a diagnosable psychiatric illness in the months preceding

suicide. Herbert Hendin et al/., Physician-Assisted Suicide: The Dangers

of Legalization, 150 Am. J. Psychiatry 14 (Jan. 1993).

17

Although the Oregon law mandates that doctors must

determine that patients are “not suffering from a psychiatric

or psychological disorder or depression causing impaired

judgment” before prescribing lethal drugs, and must refer

such patients for counseling, see Or. Rev. Stat. § 127.825, in

practice such determinations are extremely problematic. In a

survey of Oregon psychiatrists, over half were “not at all

confident” they could assess in a single consultation whether

a psychiatric condition impaired a person’s judgment; only

six percent were “very confident.” Linda Ganzini ef al.,

Evaluation of Competence to Consent to Assisted Suicide:

Views of Forensic Psychiatrists, 157 Am. J. Psychiatry 595

(Apr. 2000). This is because such assessments are inherently

subjective and unreliable. As one research analysis

concluded:

There is a marked lack of clarity about the

. goals of mandatory psychiatric assessment in

all patients requesting PAS _ [physician-

assisted suicide]. More worryingly, there are

no clinical criteria to guide such an

assessment — just as there are no criteria to

assess the rationality of any person’s decision

to commit suicide.

Brendan D. Kelly ef al., Euthanasia, Assisted Suicide and

Psychiatry: A Pandora’s Box, 181 British J. Psychiatry 278,

279 (2002).

Perhaps for these reasons, counseling referrals in

assisted suicide cases under the Oregon law are alarmingly

rare. In 2004, only five percent of patients seeking assisted

suicide were referred for a psychiatric evaluation. Seventh

Annual Report on Oregon's Death with Dignity Act at 24. In

the Netherlands, whose assisted suicide law similarly asks

doctors to determine whether a person’s judgment is

impaired by a psychiatric disability, only three percent of

18

assisted suicide patients were so referred. Kelly, supra at

278. .

3. The Law’s False Assumption that

Disability Intrinsically Deprives Life of

Dignity and Value

Many people identified as candidates for assisted

suicide could benefit from supportive care or treatment, such

as counseling, pain medication, or in-home personal

assistance. These measures lessen their pain and suffering,

their perceived burden on family members, or their lack of

independence and choice. The National Council on

Disability has found that “improving laws, policies,

programs and services for people with disabilities ... would

go a long way toward assuring that any self-assessment or

decision about the quality of life of an individual with a

disability would be made in an optimal context of

independence, equality of opportunity, full participation, and

empowerment.” Assisted Suicide: A Disability Perspective

at 13.

Research demonstrates the lack of this type of

assistance and support, rather than any intrinsic aspect of a

person’s disability, is the primary motivation for suicide.

For example, one study found that people who experience

serious pain are no more likely to want to kill themselves

than those who do not. This finding was attributed to “the

quality of pain management” provided to terminal patients in

the study. Breitbart, supra at 2910. In a study of euthanasia

in the Netherlands, only ten of 187 patients listed pain as the

reason they wanted to die. Van der Maas, supra at 672.

Depression is also a condition that can be treated with

therapy or counseling, which often leads the patient to

withdraw his or her request to die. Kelly, supra at 279;

Herbert Hendin et al., Physician-Assisted Suicide: The

Dangers of Legalization, 150 Am. J. Psychiatry 14, 15 (Jan.

1993).

19

Assisted suicide, however, assumes that a disability

or medical condition inherently makes life unworthy of

continuation. Its availability causes medical practitioners to

ignore other measures, services and modifications that might

cause someone to reconsider their desire to die. As a doctor

at New York’s Memorial Sloan-Kettering Cancer Center has

observed, assisted suicide “runs the risk of further devaluing

the lives of terminally ill patients and may provide the

excuse for society to abrogate its responsibility for their

care.” Kathleen M. Foley, Competent Care for the Dying

Instead of Physician-Assisted Suicide, 336 New Eng. J. Med.

54 (Jan. 2, 1997).

The desire to die of people with disabilities is often

driven by a temporal or situational depression that arises

from the perception that their lives lack value or that they are

a burden on their loved ones. In a study of HIV and AIDS

patients, one participant said, “I’m still inconveniencing

other people who look after me and stuff like that ... No, I'd

rather die.” Another described himself as “a bag of potatoes

to be moved from spot to spot ...” James V. Lavery et al.,

Origins of the Desire for Euthanasia and Assisted Suicide in

People with HIV-1 or AIDS: A Qualitative Study, 358 The

Lancet 362, 364-64 (Aug. 4, 2001).'*

'* Oregon’s experience also confirms these findings. Physicians

who administered assisted suicide under the Oregon law were asked

whether “end of life concerns” contributed to the patient’s desire to die:

In all cases, physicians reported multiple concerns

contributing to the request. Eleven (41%) patients

included at least four specific concerns: becoming a

burden, losing autonomy, decreasing ability to

participate in activities that make life enjoyable, and

losing control of bodily functions. Another 15 (56%)

patients included at least two or three of these

concerns. Most frequently noted across all three years

were loss of autonomy ... and participation in activities

that make life enjoyable ... Patients have increasingly

20

Another study linked suicidal ideation to unnecessary

institutionalization. It found that most terminally ill patients

who have a sense of “fractured dignity” were inpatients,

“suggesting that the degree of autonomy and independence

that can be maintained in a home setting with community

based care, as opposed to care enabled by an institution, is an

important mediator of one’s sense of dignity.” This loss of

dignity, and the corresponding feelings of depression and

hopelessness, are “strong predictors of desire for death and

suicidal ideation ...” Harvey Max Chochinov et al., Dignity

in the Terminally Ill: A Cross-Sectional, Cohort Study, 360

The Lancet 2026 (Dec. 28, 2002).

These medical findings mirror this Court’s

recognition of the deleterious effects of institutionalization.

In Olmstead v. L.C., 527 U.S. 581 (1999), the Court held that

unjustified institutionalization was a form of discrimination

under the Americans with Disabilities Act because it

“perpetuates unwarranted assumptions that persons so

isolated are incapable or unworthy of participating in

community life” and “severely diminishes the everyday life

activities of individuals, including family relations, social

contacts, work options, economic independence, educational

advancement, and cultural enrichment.” /d. at 600.

The question how to address the needs that underlie

the desire to die, however, is typically lost in the wake of the

law’s “competency” determination. As one Oregon

psychiatrist stated:

The focus of competence may distract from

adequate attention and resources on the

expressed concern about becoming a burden to family,

friends or caregivers.

Oregon Department of Human Services, Oregon's Death with Dignity

Act: Three Years of Legalized Physician-Assisted Suicide 11-12 (2001).

21

person and their circumstances ... we may

spend thousands of dollars on assessing

competence and little in care directed to the

day-to-day life and morale of the person.

Ganzini, supra at 600. Another study concluded that the

Oregon law’s competency determination “do[es] not provide

a framework to address social circumstances that contribute

to the desire for euthanasia or assisted suicide.” Lavery,

supra at 366.

The case of Kenneth Bergstedt exemplifies how

external concerns that could be remedied drive the desire to

die for people with disabilities. Mr. Bergstedt, a 30-year old

Nevada man with quadriplegia, wanted to die because his

father, who cared for him, was himself dying of cancer. Mr.

Bergstedt, though not in physical pain, feared he would be

institutionalized without his father’s support. See McKay v.

Bergstedt, 801 P.2d 617, 628, 637 (Nev. 1990); Stanley S.

Herr, No Place to Go: Refusal of Life-Sustaining Treatment

by Competent Persons with Physical Disabilities, 8 Issues in

L. & Med. 3, 10-13 (1992).

A psychiatric evaluation submitted to the trial court

found that Mr. Bergstedt was depressed, but that this was

irrelevant because “the quality of life for this man is ..

forever profaned by a future which offers no relief and only

the possibility of worsening.” Herr, supra at 12. Based on

his poor “quality of life,” the Nevada Supreme Court upheld

his decision to die. Bergstedt, 801 P.2d at 824-25. No

consideration was given to measures that might have helped

Mr. Bergstedt restore his sense of dignity and independence,

such as non-institutional, in-home health care.

A dissenting Nevada Supreme Court Justice observed

that “[w]ith this kind of support it is no wonder that he

decided to do himself in.” Bergstedt, 801 P.2d at 637

(Springer, J., dissenting). He added, presciently:

22

It is critical that the court not put its judicial

stamp of approval on negative stereotypes

about disability. This would result if it were

to allow the state to assist an individual to die

only because he or she had a disability.

Judicial decisions which are based on societal

prejudices merely reinforce those prejudices,

making them even more difficult to eradicate.

Id. at 836.

Because it rests on false assumptions and stereotypes

of the disabled, Oregon’s assisted suicide law enshrines these

debilitating attitudes under the protection of state law.

4. The Difficulty in Ensuring Decisions to Die

Are Not Coerced or Made By Others

Finally, evidence exists that some persons killed

under assisted suicide laws may “choose” suicide under

pressure from others. In the case of Kate Cheney, an 85-year

old woman with cancer, her psychologist was concerned that

Ms. Cheney was not competent to make the decision to die

and that her daughter was unduly pressuring her to choose

assisted suicide. The daughter simply obtained an opinion

from a second psychologist, who determined Ms. Cheney

was competent. Ms. Cheney was accordingly prescribed

lethal medication and died on August 29, 1999. Evelyn

Hoover Barnett, Js Mom Capable of Choosing to Die? The

Oregonian, Oct. 16, 1999, at Gl-2. A Dutch study

confirmed that some people administered lethal drugs in that

country did not ask to die. Van der Maas, supra at 672.

23

Il. The Attorney General’s Determination that

Assisted Suicide is Not a “Legitimate Medical

Practice” is a Permissible Construction of the

Controlled Substances Act

A. The Attorney General’s Interpretive Ruling is

Entitled to Deference

In Chevron U.S.A. v. Natural Resources Defense

Council, 467 U.S. 837 (1982), this Court set forth the

standard under which courts must defer to an Executive

Branch agency’s interpretation of a statute. When Congress

has authorized the agency to enforce the statute, the court

must make a twofold inquiry:

First ... whether Congress has directly spoken

to the precise question at issue. If the intent

of Congress is clear, that is the end of the

matter ... If, however, the court determines

Congress has not directly addressed the

precise question at issue, the court does not

simply impose its own construction of the

statute, as would be necessary in the absence

of administrative interpretation. Rather, if a

statute is silent or ambiguous with respect to a

specific issue, the question for the court is

whether the agency’s answer is based on a

permissible construction of the statute.

Id. at 842-43.

The Court clarified that “permissible construction”

was not “the only one [the agency] permissibly could have

adopted ... or even the reading the court would have reached

if the question initially had arisen in a judicial proceeding.”

Id. at 843 n.11.

24

Under this standard, an agency’s interpretative

rulings “are given controlling weight unless they are

arbitrary, capricious or manifestly contrary to the statute.”

Id.; see also Barnhart v. Walton, 535 U.S. 212, 218 (2002).

Even when this standard has not been applied, this Court has

nevertheless relied on “the well-reasoned views of the

agencies implementing a statute,” which “constitute a body

of experience and informed judgment to which courts and

litigants may properly resort for guidance.” Bragdon v.

Abbott, 524 U.S. 624, 642 (1998) (quoting Skidmore v. Swift

& Co., 323 U.S. 134, 139-40 (1944)); see also Olmstead v.

L.C., 527 U.S. 581, 598 (1999).

Under the Controlled Substances Act, 21 U.S.C. §§

801 — 971, Congress authorized the Attorney General to

register medical practitioners to dispense controlled

substances, 21 U.S.C. § 822(b), and designated the Attorney

General as the officer responsible for the Act’s enforcement.

21 U.S.C. § 871(a). The Attorney General may revoke such

registration if he “determines that the issuance of such

registration would be inconsistent with the public interest.”

21 U.S.C. § 823(f). In making this determination, the

Attorney General may consider, among other factors, “any

conduct which may threaten the public health and safety.”

Id. Although preventing drug abuse is one of Congress’

goals under the Act, its plain language does not limit itself to

that goal; rather, the Act seeks to prohibit any use of

prescription drugs that may have a “detrimental effect on the

health and general welfare of the American people.” 21

U.S.C. § 801(2).

In 1971, the Attorney General promulgated a

regulation under the Act that states that prescriptions for

controlled substances are valid only if issued for a

“legitimate medical purpose” as part of “professional

treatment.” 2! C.F.R. § 1306.04(a). This Court has affirmed

the validity of this regulation. United States v. Moore, 423

U.S. 122, 140 (1975).

25

Under this regulation, the Attorney General issued an

interpretive ruling that assisted suicide is not a “legitimate

medical practice” for “treatment” within the meaning of this

regulation, thereby rendering any prescriptions made for this

purpose invalid. Given the well-documented medical

concerns over the harm and invidious discrimination the

Oregon assisted suicide law poses to people with disabilities,

see Sec. I, supra, the Attorney General’s ruling is

undoubtedly a valid interpretation of the Act, which does not

specifically foreclose this interpretation. Chevron, 467 U.S.

at 843; Barnhart, 535 U.S. at 218.

B. The “Clear Statement” Rule Does Not Apply

to Regulation of the Practice of Medicine _

The Court of Appeals avoided this analysis by

holding that the Attorney General’s directive on

prescriptions for assisted suicide “interferes with Oregon’s

authority to regulate medical care within its borders...”

Oregon v. Ashcroft, 368 F.3d 1118, 1124 (9th Cir. 2004).

Relying on Gregory v. Ashcroft, 501 U.S. 452 (1990), the

Appeals Court held the Attorney General had infringed on an

area of law “traditionally reserved for state authority, such as

regulation of medical care.” /d. at 1125. Thus, the Court of

Appeals turned the usual test for deference to agency

interpretations of federal law on its head: Congress had to

make a “clear statement” that it was prohibiting assisted

suicide to authorize the Attorney General to act. Because it

had not, the Appeals Court held, the Attorney General’s

ruling was invalid. /d. at 1125-26.

Under Solid Waste Agency v. Army Corps of

Engineers, 531 U.S. 159 (2001), the “clear statement rule” is

applied only when “an administrative interpretation of a

statute invokes the outer limits of Congress’ power ...” /d. at

172. It is clear that prohibiting prescriptions made for the

purpose of assisted suicide does not place the Controlled

26

Substances Act outside the boundaries of Congress’

Constitutional authority. Congress has always had the

power, under the Commerce Clause, to regulate medication

prescribed by doctors. See Minor v. United States, 396 U.S.

87, 98 n.13 (1969); Reina v. United States, 364 U.S. 507,

511 (1960); In re Grand Jury Proceedings, 801 F.2d 1164,

1169 (9th Cir. 1986) (“{[T]he Commerce Clause empowers

the federal government to regulate prescription drugs”).

Indeed, given the magnitude of the discrimination posed by

Oregon’s assisted suicide law, Amici here submit that the

Fourteenth Amendment, as well as the Commerce Clause,

provides a basis for the Attorney General’s interpretive

ruling. Cf Tennessee v. Lane, 541 U.S. 509, 124 S. Ct.

1978, 1989-93 (2004); City of Cleburne, 473 U.S. at 461

(striking down, on rational-basis grounds, law that prohibited

home for people with disabilities).

The Appeals Court’s underlying reasoning that

regulation of the practice of medical infringes upon “a

decision of the most fundamental sort for a sovereign entity,”

as establishing qualifications for state judges was held to be

in Gregory, 501 U.S. at 460, is patently flawed. There is no

support, legal or otherwise, for the Appeals Court’s

conclusion that regulating the practice of medicine “go[es] to

the heart of representative government.” /d. at 461 (quoting

Sugarman v. Dougall, 413 U.S. 634, 647 (1973)). See e.g.

Equal Employment Opportunity Comm'n v. Massachusetts,

987 F.2d 64, 67 (ist Cir. 1993) (distinguishing Gregory

because “[t]he Missouri constitutional provision was

concerned, not with regulating health care, but with ensuring

the qualifications of the highest state officials.”) (emphasis

added).

If any federal restriction on the practice of medicine

infringed upon a “fundamental” state function, it would call

into question Congress’ entire regulatory scheme for

prescription medication, which has been in effect for three

decades and has been repeatedly upheld and enforced. See

27

Moore, 423 U.S. at 139. Indeed, it is difficult to understand

how the practice of medicine could be considered solely a

state function, given that the federal government has

regulated in this area for at least the past 67 years. See e.g.

Food, Drug and Cosmetic Act, 21 U.S.C. §§ 301-397.

The Court of Appeal’s holding is of significant

concern to amici beyond its implications for assisted suicide.

Congress and federal agencies often regulate “medical care”

to prevent abuse of or discrimination against people with

disabilities. If every decision affecting the medical practice

were within a state’s sovereign power and subject to the

“clear statement” rule, Congress’ ability to prohibit states

from sanctioning disability discrimination in the medical

field would be severely undermined.

For example, in Olmstead, this Court held that the

unnecessary institutionalization of people with disabilities by

states was discrimination under Title II of the Americans

with Disabilities Act (ADA). Although Title II’s definition

of discrimination did not explicitly identify unnecessary

institutionalization, the Court relied in part upon the

Attorney General’s regulations and interpretztions of the Act

in discerning Congress’ intent. 527 U.S. at 598. Although

this interfered with a “medical” decision approved under

state law (and carried out by the State itself), it was

nevertheless understood as appropriate federal action. Jd. '°

Similarly, in Bragdon, this Court ruled that a patient

with HIV could bring a claim under Title III of the ADA

against a dentist who refused to serve him because of his

disability. 524 U.S. at 647. The Court relied on agency

determinations that Congress had intended to cover persons

'S Atascadero State Hosp. v. Scanlon, 473 U.S. 234 (1985),

while involving the rights of institutionalized people with disabilities, is

distinguishable because it involved a state’s waiver of sovereign

immunity under the Eleventh Amendment, not the underlying challenged

practices in the institution. /d at 242.

28

with HIV under Title Ill, which applied to medical

practitioners. Although this decision involved Congressional

regulation of the practice of dentistry, this Court did not

invoke the “clear statement” rule or find that Title IIl

encroached upon a “fundamental” state function. /d. at 642."

CONCLUSION

For the foregoing reasons, amici respectfully urge

this Court to reverse the Court of Appeals’ decision and

affirm the Attorney General’s interpretive ruling.

Respectfully submitted,

Walter J. Kendall Ill Max Lapertosa

Professor of Law Counsel of Record

THE JOHN MARSHALL LAW__ Kenneth M. Walden

SCHOOL Adrienne Detanico, Law Clerk

315 South Plymouth Court ACCESS LIVING

Chicago, IL 60604 614 West Roosevelt Road

(312) 987-2377 Chicago, IL 60630

(312) 253-7000

Counsel for amici curiae

May 9, 2005.

'© In the District Court below, the defendant dentist challenged

application of Title II] to him on grounds that “the practice of dental

medicine is an area of law reserved to the states, and thus beyond the

scope of Congress’ Commerce Clause authority.” Abbott v. Bragdon,

912 F. Supp. 580, 592 (D. Me. 1995), aff'd, 107 F.3d 934 (Ist Cir.

1997), vacated & remanded on other grounds, 524 U.S. 624 (1998). The

Court rejected this proposition and held Congress could regulate

defendant's dental practice because it was “an economic enterprise”. /d.

at 593-94 & n.15.

This is a copy of a public record, reproduced as it was published. It is not legal advice, and it may not be the version a court would rely on. Check the official source before you cite it.

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