Wednesday, November 30, 2016

Bucket list

Preparing to "kick the bucket"

At this month’s Jewish Community Center of San Francisco’s 2nd Annual Embracing the Journey End of Life Resource Fair, attendees were presented with a bucket list kit—complete with bucket, pencil, mini-composition book and instructions to answer: What do you want to do before you “kick the bucket”?

I thought been there, done that.  Long before the Hollywood film The Bucket List (2007), I compiled a list of places to visit and pursued them all.  While I enjoyed the anonymity and stimulation from exposure to different cultural experiences during my world travels, however ephemeral, I felt world-weary after I became eligible to join Travelers Century Club.  Like Thomas Jefferson noted, travel makes one “wiser, but less happy.”  So I reduced my carbon footprint by staying home, content to put down roots while returning to my childhood pastime of gardening (being with nature).   

“…chasing bucket-list thrills ignores a deep psychological truth: You don’t need to make yourself happy in old age.  We get happier naturally as we grow older… The increased happiness doesn’t come through doing but simply through being.  It is the natural result of lower expectations and ambition, less emotional volatility, increased gratitude and acceptance and enhanced problem-solving skills.

In fact, the need for a bucket list goes against our deepest instincts as we age. Older brains are less influenced by novelty-seeking and more by conscientiousness; they are less impetuous and more emotionally stable.” 
– Marc E. Agronin, MD, geriatric psychiatrist, It's Time to Rethink the Bucket-List Retirement 

Stan Goldberg, cancer survivor, hospice volunteer and author of Lessons for the Living: Stories of Forgiveness, Gratitude, and Courage at the End of Life, presented, One Day to Live: What Would You Say and Do?
  1. focus on journey – makes it easier to accept losses and prepare for death; start with one simple, enjoyable activity
  2. ask for forgiveness – makes you more peaceful
  3. offer forgiveness – begins healing
  4. understand what/when you can’t forgive – work towards understanding
  5. let go of what you can’t change
  6. offer thanks for kindness shown – change relationship
  7. complete unfinished business
  8. create legacy – make a difference 
Therapeutic humor expert Allen Klein provided comic relief in his presentation, Seeing Demise Thru Humorous Eyes: How Cartoonists, Comedians and Cinematographers Help Us See Death as Less of a Grave Matter.   My favorites were clips from Woody Allen films like Hannah and Her Sisters (life affirmation after attempted suicide) and Love & Death (dance with death).

End of Life (EOL) Options (ways to "kick the bucket")

Matt Whitaker, Multi-State Implementation Manager at Compassion & Choices, provided an overview of authorized EOL options:
  1. refuse treatment
  2. discontinue treatment
  3. hospice – “gold standard” for last 6 mos. covered by Medicare, but average utilization only 20 days
  4. VSED (Voluntarily Stop Eating & Drinking) – death by dehydration
  5. palliative sedation – induce coma
  6. aid in dying – legal in 5 states, OR (since 1997), WA (2008), MT (2009), CA (2016) and CO (2017)
California’s End of Life Option Act requires self-ingestion of a lethal dose of 100 capsules of Seconal, produced by Valeant Pharmaceutical, at a cost of $4,000; in California, only 80% of private insurers and Medi-Cal cover this cost.  A 1997 federal law prohibits use of federal monies (Medicare, VA) to cover aid in dying costs. 
JFCS Seniors at Home hosted End of Life Option Act: Effects on our Practice panel presentation:
  • Linda Blum, GNP, Palliative Care Coordinator at California Pacific Medical Center: shared two cases when patients were not able to exercise EOL Option due to short time frame of patient with untreatable gastrointestinal bleeding who died in hospice at home before he was able to manage 2 requests to doctor, and another patient with ALS who was not able to self-administer aid-in-dying drug; in both cases, it was “care as usual, the old way.”
  • Maryellen Collamore, ASW, Oncology Clinical Social Worker at UCSF: talked about her role to provide educational materials on EOL Option and to conduct psychosocial assessment of patient (motivation for inquiry, understanding of diagnosis, social supports, defining quality of life, perception of dying process, exploring belief systems, etc.); patient also must obtain mental health evaluation by psychiatrist; easier to find consulting MD than to find MD who will actually prescribe aid-in-dying drug; patient’s initial inquiry opens door to conversation, and most patients go to hospice.
  • Lael Duncan, MD, Medical Director at Coalition for Compassionate Care California: opined that access remains an issue, given the length of the process (patient makes 2 oral requests > 15 days apart, patient attestation 48 hours prior to ingestion) and few participating providers. She described lethal prescriptions—traditional high dose barbiturate (100 capsules of Seconal used in Oregon) dissolved in 4 oz. water; cocktail mixtures (opiates, benzos, cardiac meds); complications can arise if patient has difficulty swallowing, digestive issues, insufficient absorption; time to death depends on underlying disease process and patient’s physiology, but usually deep coma within 10-15 min. after ingestion.
  • Redwing Keyssar, RN, Director of Palliative Care at JFCS Seniors at Home: shared two cases of patients who changed their minds about EOL due to different outlook and changed circumstances because pain and symptoms were better managed. 

Lonny Shavelson, MD, started Bay Area End of Life Options in Berkeley, to consult with physicians and patients who are deciding whether to participate in EOL Options Act. He sees writing the lethal prescription to a terminally ill patient as the last resort only after considering alternatives (hospice and palliative care approaches).  


Documenting life
At Rhoda Goldman Plaza, Gloria Hollander Lyon, who survived seven concentration camps during the Holocaust, read excerpts from her memoir, Mommy, What’s that Number on Your Arm? A-6374: failing Dr. Mengele’s inspection and then escaping the gas chamber by jumping off a truck at age 14; later living with a foster family in Sweden after liberation when she noticed she lost her sense of smell – perhaps her body’s defense mechanism to protect herself from the horrific stench of bodies burning in the gas chambers and crematoria; and then returning to visit Auschwitz in 1991 when she finally regained her sense of smell after 47 years. 
Addressing an intergenerational audience that included her son, Lyon said her father told her what is important: do not cry over what is lost if you have freedom for continued life, let it rest and start all over; those who survive are eager to tell the world that it’s worth surviving regardless of loss. 

Lisa Kokin’s Inventory, exhibited at From Generation to Generation: Inherited Memory and Contemporary Art at Contemporary Jewish Museum, is composed of over 1,000 pieces of objects representing the lives of those who endured the Holocaust.  Inventory was created in 1997 after the artist, whose own Jewish family left Europe before Hitler’s rise, visited Buchenwald concentration camp and confronted the piles of objects left behind.
At this month’s meeting of San Francisco Task Force on Hoarding, Carolyn Rodriguez, MD, PhD, Director of Stanford Hoarding Disorders Research Program, talked about her research combining Buried in Treasures (BIT) workshop support group with one-to-one home de-cluttering.  She viewed hoarders as “enthusiastic collectors” and talked about elevating ordinary objects into art by Marcel Duchamp’s Readymades and Andy Warhol’s Time Capsules.  She mentioned artist Song Dong’s Waste Not installation of over 10,000 everyday objects collected by his mother in their Beijing home over five decades that reflects on culture of frugality; in persuading his mother to make art out of her possessions, the artist showed respect while also improving the quality of home life by de-cluttering – more creative than the KonMari method

As in Roz Chast’s Can’t We Talk About Something More Pleasant? discussing hoarding and even the inevitable like end of life can be uncomfortable for some.  Yet, the wisdom of Ecclesiastes chapter 3 reminds us: “there is a time for everything … a time to be born and a time to die … all come from dust, and to dust all return.”
With Howard Levy, Executive Director at Legal Assistance to the Elderly (LAE) for 28 years until his retirement today, all discussions are possible! (Though professionally, Howard is probably not as candid as his high school classmate Pepper Schwartz, AARP’s Sex and Relationship Expert and author of the sizzling erotic memoir, Prime: Adventures and Advice on Sex, Love and the Sensual Years.)  At weekly case acceptance meetings deftly facilitated by Howard, all staff and volunteers present contributed to the lively, often passionate, discussions for each client intake after hearing the facts.  Occasionally tired of the faux (steamed, not authentically boiled) bagels brought in by Howard, staff and volunteers turned the weekly meetings into potluck affairs.  Howard and the mostly senior staff at LAE remind me of The Supremely Old, Supremely Sharp, Supreme Court, with their wit and crystallized intelligence, which gets better with age. 

Inspired to create my own art, here’s collage of Howard's greatest hits at LAE’s office and fundraising events!

6 comments:

  1. Telling Their Life Stories, Older Adults Find Peace in Looking Back
    Retiring
    By SUSAN B. GARLAND DEC. 9, 2016
    …Like many older people who write their life stories, Ms. Bick found some peace in looking back. “Writing is painful because it brings back memories,” …she recognized “that there was this joyous little girl” whom she could finally “reclaim.” And she described “an awe that I survived some of the things I went through.”
    Ms. Bick…considers her stories a gift to future generations — and to past ones. “I am keeping my parents and grandparents alive,” she said. “And, as an egotist, I am keeping myself alive. I am remembered.”
    Whether they are writing full-blown memoirs or more modest sketches or vignettes, many older people like Ms. Bick are telling their life stories. Some are taking life-story writing classes …, while others are hiring “personal historians” to record oral histories or to produce videos that combine interviews, home movies and family photos. Some opt to write a “legacy letter,” which imparts values to the next generations. New websites enable families to create digital personal histories that can be preserved for their descendants.
    Ms. Bick took a course called Guided Autobiography, in which a trained instructor draws out students’ memories and helps them channel their thoughts and recollections into essays…
    …getting feedback from a supportive group “gives you a perspective on your life.”
    …Research by many gerontologists — including James E. Birren, who created the discipline of guided autobiography — has found that reminiscing can improve the confidence of older adults. By recalling how they overcame past struggles, they are better able to confront new challenges, doctors say, and they may be able to forgive themselves for their mistakes. Moreover, a life review can help with grieving, research has found.
    Armed with this knowledge, many nursing homes and assisted living facilities are offering storytelling programs. Bonita Heilman …life enrichment coordinator, uses a program called Life Reflection Story, developed by Celebrations of Life, a company in Minneapolis.
    Ms. Heilman will ask questions on topics like childhood and parents. She then compiles each resident’s life story, and family photographs, into a bound book of about 30 pages.
    Most Harbor residents were farmers. “They tell stories about when they were productive citizens working toward the greater good,” Ms. Heilman said. “Remembering gives them self-esteem at a time when they can no longer do the things they once could do.”
    …Sylvia Kuenzel, 88, said …writing her story…helped her see that she had dealt well with the hardships and created a good life for her four children. “I made it, so I guess I was O.K.,” …She also “realized what is most important” — and it was a comfort to share those lessons with her children, six grandchildren and one great-grandchild. Among those lessons: the importance of focusing on the positive, hard work and treating people right.
    Storytelling also can benefit terminally ill patients by addressing their need to feel that life has purpose. One end-of-life treatment is called Dignity Therapy, which was developed by Dr. Harvey Max Chochinov, a professor of psychiatry at the University of Manitoba. During a 30- to 60-minute audiotaped session, a therapist will ask patients questions about their most important accomplishments, the experiences that made them feel most alive and their hopes for loved ones. Patients can give the transcribed interview to friends and family.
    …In several studies of dignity therapy, patients reported an increased sense of purpose and meaning. A study of family members of patients who had died said the transcripts consoled them while they grieved…
    http://www.nytimes.com/2016/12/09/your-money/telling-their-life-stories-older-adults-find-peace-in-looking-back.html

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  2. SF establishing local policy to align with new ‘aid in dying’ state law
    By Laura Dudnick on January 29, 2017 1:00 am
    San Francisco health officials are developing a city policy to comply with a new state law that allows terminally ill patients to legally end their lives, shedding light on how the quality of life for a patient in his or her final days might be improved because of the law.
    … “When patients ask about this, I think about what’s leading to their request,” said Dr. Kara Bischoff, an assistant professor at UC San Francisco and a palliative care physician, noting patients typically are “motivated by fears of dying [and] discomfort.”
    In September 2015, California became the fifth state in the U.S. to allow doctors to prescribe life-ending medication after Gov. Jerry Brown signed into law the California End of Life Option Act.
    The process, known as “aid in dying,” was formally enacted on June 9, 2016, following the highly publicized case of Brittany Maynard, a 29-year-old woman diagnosed with a brain tumor who moved from California to Oregon to legally end her life.
    The City’s Department of Public Health has since tasked its Office of Policy and Planning with establishing a policy for patients and doctors in the San Francisco Health Network who wish to opt in to the voluntary program.
    Health officials earlier this month presented a draft of the policy to the Health Commission. A final draft of the policy is slated to be approved by July.
    To opt in to the program, a patient must be at least 18 year old, reside in California, have been diagnosed with a terminal illness with a prognosis of less than six months to live and be able to make medical decisions and self-administer the medication, which is usually Seconal.
    OPTING IN
    As soon as the law was passed, Bischoff said she knew she wanted to provide the right to die for her terminally ill patients.
    The life-ending medication, she explained, is “just one more tool in a very large tool belt of ways to provide patients care at the end of their lives.”
    …In fact, just one of her patients has followed the exhaustive process through to the point the patient ingested the life-ending medication. Bischoff couldn’t release many details about that case, but said the patient was experiencing “absolutely tremendous, excruciating physical symptoms.”
    …“Being able to have the option of life-ending medication in and of itself has provided comfort and peace of mind, even if the medication itself isn’t more accessed,” Bischoff said.
    LOCAL POLICY
    When the law took effect last summer, the California Hospital Association recommended that hospitals develop a local policy to comply with the End of Life Option Act.
    …Dr. Alice Chen, chief medical officer for the San Francisco Health Network, said there’s no formal list of physicians who have opted in to the program, but an internal survey indicated there are enough physicians willing to participate to warrant a city policy.
    …As of mid-January, Chen was aware of one patient in The City’s Health Network who had been prescribed the medication, but had not yet taken it. She didn’t know of any patients who had taken the medication.
    “The number is going to be very small, is our expectation,” said Dr. Anne Kinderman, director of Supportive and Palliative Care at Zuckerberg San Francisco General Hospital.
    This is also somewhat the case in states that also legally allow patients the right to end their lives: In 2015, of the 218 patients in Oregon who requested the medication 132 — 60 percent — ingested it. Of the 213 patients in Washington who requested it that same year, 166 — 77.9 percent — took the medication.
    …“California and San Francisco are so unique in its diversity that I think it merits watching how it unfolds,” Chen said. “When you look at the data from other states where this type of law has been implemented, it’s typically white, college-educated” patients who opt in…
    http://www.sfexaminer.com/sf-establishing-local-policy-align-new-aid-dying-state-law/

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  3. How To Spend Your Final Months At Home, Sweet Home
    By Judith Graham
    November 10, 2016
    …What’s needed to make care at home possible during the last six months of life? …
    Reallocating resources. “We have to reallocate resources within the healthcare system to the home setting,” said Dr. Diane Meier, a geriatrician and director of the Center to Advance Palliative Care in New York City.
    …Medicare is testing the feasibility of bringing comprehensive medical services directly to frail, ill seniors through its Independence at Home demonstration project, now in 14 locations.
    And house call programs that send physicians into seniors’ homes are beginning to expand across the country. To find a program near you, check this website sponsored by the American Academy of Home Care Medicine.
    Clarifying priorities. If staying at home at the end of life is a priority, this has to be communicated — clearly and frequently — to your family, caregivers, and physicians, said Dr. Thomas Lee, co-author of the New England Journal study and chief medical officer at Press Ganey, a firm that tracks patients’ experiences with care.
    Tradeoffs have to be part of this discussion.
    Lee gives the example of his 89-year-old mother, who lives by herself in a condominium in Boston’s Beacon Hill neighborhood. Though she’s fallen several times, she’s refused to consider moving to assisted living or having a paid caregiver come in to help.
    Being safe isn’t his mother’s foremost goal, independence is, Lee said. And that means accepting the risk that she could fall again or hurt herself.
    Every time he sees a frail elderly patient, Dr. Thomas Cornwell asks “do you want to go to the hospital if you get sicker or do you want to stay at home?”…
    Making medical decisions. Take advantage of services designed for people with serious illnesses who need help at home.
    One is home-based palliative care, which addresses worrisome symptoms such as pain or nausea that otherwise could send a vulnerable older adult to a hospital. In this model, a doctor, nurse and social worker join together to address a patient’s needs after a comprehensive assessment.
    … To learn more about programs in your area, go to www.getpalliativecare.org. Contact a few and ask if they offer these services or know of another organization that does.
    Hospice care is similar in its approach, but only for people expected to live six months or less. The vast majority receive care in their homes. Unfortunately, most adults wait to sign up for hospice services until the last several weeks of life, missing out on potentially valuable assistance.
    Getting needed help. Meier worries that an emphasis on home-based care for people with terminal illness could translate into more work for family caregivers who shoulder the burden of this care, not more support.
    Currently, caregivers patch together services as best they can. Medicare doesn’t pay for aides who help frail, ill seniors bathe, dress, toilet, take their medications, keep their homes clean, and prepare breakfast, lunch, or dinner. Low-income seniors can qualify for help from Medicaid, but the amount of assistance available is limited and varies by state.
    There’s no easy solution to this “how can I get the help I’ll need?” dilemma. Be realistic about the cost of care …and the resources you have available. …skills that will be required and whether the environment can support this challenge.
    “Are the bedroom, the bathroom, and the kitchen on the same floor?” asked Cornwell. “If not, you’re going to have a problem.”
    Building community. “You’re going to need support” from family, friends or other social contacts if you’re trying to manage a serious illness at home, said Laura Connors, executive director of Beacon Hill Village in Boston.
    …As with children, it “takes a community” to care for vulnerable older adults, Connors said, and you need to know “who’s going to be there for you.”
    http://californiahealthline.org/news/how-to-spend-your-final-months-at-home-sweet-home/

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  4. Stop accepting death: A doctor rejects medicine’s ‘self-righteous’ approach with patients
    BOB TEDESCHI @BOBTEDESCHI
    MARCH 13, 2017
    PHOENIX — Dr. Diane Meier won a MacArthur Foundation “genius” grant in 2008 for her pioneering work in palliative medicine, which seeks to optimize patients’ quality of life by preventing or reducing their suffering.
    That journey, she said, started on the first morning of her internship — during which she assisted in an hour-long, fruitless effort to resuscitate an 89-year-old man with end-stage heart disease — and culminated in 1999 with her cofounding of the Center to Advance Palliative Care.
    Meier is vice chair for public policy and professor of palliative medicine at the Icahn School of Medicine at Mount Sinai. When she spoke here on a recent day at the annual meeting of hospice and palliative care specialists, there wasn’t a single empty chair in the room.
    STAT caught up with Meier for an interview later.

    …I think the job of health professionals is to help our patients and their families live as well and as fully as possible while they are alive.
    We in medicine should not be in the business trying to sell people the idea that death is OK. Death is never going to be OK. And it feels a bit self-righteous to me — as if we are saying it’s a moral obligation for people to prepare for their own death. It makes me very uncomfortable, because that impulse is more about us than about the people we’re trying to serve.
    The people we’re trying to serve have serious illnesses, and they’re trying to live as well as they can for as long as they can. This notion that somehow you’re braver or smarter or wiser if you confront your death and accept it and plan for it — this is not what most patients and families are seeking. It’s not what most people care about. And it actually can get in the way of people having a good life.
    …Because quite naturally, all living things try to avoid death, and are afraid of death. And by focusing on that inevitable event, you’re not living in the present. You’re letting your life be defined by the fear of death.
    …as a physician, I have a much greater appreciation for the value of present moment, because I’ve taken care of so many people who had fewer moments than they wanted. But I don’t feel like it’s my job to impose that awareness or approach to life on my patients.
    …achieving the good death — where death is not full of pain or shortness of breath, or fear, or families falling apart — I think that’s a societal good. But I don’t think you get there by forcing people to face the fact of their mortality.
    And it’s not our job as health professionals to be convincing people that it’s OK to die, and that death is natural and death is good. It flies in the face of millions of years of human evolution. It’s not OK to die. Very few people want to die, particularly if they have a quality of life that’s acceptable to them. Life is precious, and sweet, and my job as a physician is to help my patients get as much of that good quality life as they can.
    …patients are mostly afraid of what might happen before they die. Will they be short of breath? In pain? And it’s amazing how reassured people are to know that for the great majority of people death is very peaceful. And in the unusual instances where there are symptoms like pain and shortness of breath or confusion or restlessness, we have very effective medicines for those things.
    …I think the question is not one of forcing people to look in the mirror and say, “You’re going to die.” The right question is, “What’s a good life for you? How can I as a clinician wrestle the resources and capacities of the health care system into something that’ll serve what matters most to you?”
    https://www.statnews.com/2017/03/13/death-patients-diane-meier/

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  5. 'Death Cleaning' Is the Newest Way to Declutter. Here's What to Know
    By Amanda MacMillan
    October 17, 2017
    …In the past 12 months, two of my grandparents have passed away, and since then, my mom and dad have spent a huge chunk of their time combing through and cleaning out their own parents’ homes, discarding and donating their possessions to anyone who would take them.
    It’s been a wake-up call for my dad, especially, who is suddenly encouraging me to take the items from their basement I’ve been eyeing for my own place. “You’re going to get it eventually, so you might as well take it now,” he joked.
    There’s a Swedish word for my dad’s newfound willingness to unload and declutter:dostadning, a hybrid of the words for death and cleaning. And as morbid as it sounds, that’s exactly what death cleaning is: the process of cleaning house before you die, rather then leaving it up to your loved ones to do after you’re gone.
    A new book called The Gentle Art of Swedish Death Cleaning makes the case that the task isn’t morbid at all. Author Margareta Magnusson—a Swedish artist who describes herself as somewhere between age 80 and 100—says it’s “more like a relief,” and that it has benefits you can enjoy while you’re still very much alive.
    …Magnusson says people should start thinking about death cleaning as soon as they’re old enough to start thinking about their own mortality. “Don’t collect things you don’t want,” she says. “One day when you’re not around anymore, your family would have to take care of all that stuff, and I don’t think that’s fair.”
    The Death Cleaning method bears similarities to that of the tidying-up guru Marie Kondo: Keep what you love and get rid of what you don’t. But while Kondo tells people to trash, recycle or donate what they discard, Magnusson recommends giving things you no longer want to family and friends “whenever they come over for dinner, or whenever you catch up with them,” reports the Australian website Whimn.
    However, Magnusson does advocate for keeping sentimental objects like old letters and photographs. She keeps a “throw-away box,” which she describes as things that are “just for me.” When she dies, her children know they can simply throw that box away, without even looking through its contents.
    The Gentle Art of Swedish Death Cleaning is slated for U.S. publication in January. If the trend catches on stateside, it could be a good way for families to discuss sensitive issues that might otherwise be hard to bring up, says Kate Goldhaber, a family therapist and assistant professor of psychiatry and behavioral neurosciences at Loyola Medicine.
    ... “There can also be something very empowering and healthy about taking care of your own space and making it more organized while you’re still around.”
    ... Some research suggests that clutter in the home can raise stress levels and reduce productivity. As adults get older, having a house full of stuff may also raise their risk for falls and create other health and safety hazards.
    Goldhaber points out that many people may engage in a type of death cleaning without calling it that—when they downsize from a large house to a small apartment as they get older, for instance. “It’s a new way of thinking about the grunt work that comes along with those transitions, which can be really stressful,” she says.
    ... “If you present it as, ‘Let’s organize the house so it’s a more enjoyable place for you to live and for us to have holidays,’ it might be better received than ‘Let’s throw away your stuff now so we don’t have to sort through it later,’” she says. “It can be fun, even late in life, to redecorate and declutter, and it can be a great thing for families to do together.”
    Magnusson says that death cleaning is an ongoing process that’s never truly finished. “You don’t know when you are going to die, so it goes on and on,” she says in the video.
    Her daughter chimes in, stating the obvious: Death cleaning ends with death…
    http://time.com/4985533/death-cleaning-declutter/

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  6. State to defend California law allowing life-ending drugs
    Don Thompson, Associated Press
    Updated 2:23 pm, Wednesday, May 16, 2018
    SACRAMENTO, Calif. (AP) — Betsy Davis threw herself a party before becoming one of the first people to use a California law allowing her to take her own life in 2016.
    Her sister and other advocates fear others won't have the same choice after a Riverside County judge threw out the law Tuesday because he said it was unconstitutionally approved by the Legislature.
    Superior Court Judge Daniel Ottolia ruled lawmakers illegally passed the law during a special session devoted to other topics.
    Attorney General Xavier Becerra said in a one-sentence statement Wednesday that "we strongly disagree with this ruling" and that he will seek an expedited appeal.
    The law allows adults to obtain a prescription for life-ending drugs if a doctor determines they have six months or less to live, but plaintiffs say it lacks safeguards to protect against abuse.
    Davis would have been devastated by Ottolia's decision, said her sister, Kelly Davis.
    "It gave her back control of her life, it let her die on her own terms," she said.
    Betsy Davis was 41 when she took a fatal dose of morphine, pentobarbital and chloral hydrate prescribed by her doctor. She'd been diagnosed three years earlier with ALS, commonly known as Lou Gehrig's disease, which slowly robbed her of her ability to use her muscles.
    She celebrated the end of her life with more than two-dozen friends during a two-day party in Ojai, California, giving away her possessions and ordering her favorite foods.
    "I keep thinking of all the people who are facing a terminal illness and they're considering the use of this law, and they're in limbo right now and this right might be taken away from them," her sister said.
    Alexandra Snyder, an attorney and executive director of Life Legal Defense Foundation, one of the plaintiffs, said Ottolia properly ruled that lawmakers effectively "hijacked" a special legislative session that was called to address access to medical care.
    "Access to health care has no relationship to assisted suicide," she said, saying passing the law set a dangerous precedent that undermines the legislative process.
    Opponents have argued hastening death is morally wrong, puts terminally ill patients at risk for coerced death by loved ones and could become a way out for people who are uninsured or fearful of high medical bills.
    Democratic Sen. Bill Monning of Carmel, who carried the original legislation, argued the bill was properly considered, but said lawmakers could try to pass it again if the law ultimately is rejected by the courts.
    So far, he said, there has been "not a single report of malfeasance or problems."
    California health officials reported that 111 terminally ill people took drugs to end their lives in the first six months after the law went into effect June 9, 2016, and made the option legal in the nation's most populous state.
    Compassion & Choices, a national organization that advocated for the law, estimated that in its first year, 504 Californians requested prescriptions for medical aid in dying.
    "Our supporters, they've frankly expressed shock at this outcome. They're disappointed that this end of life option could be taken away," John Kappos said, an attorney representing the organization.
    https://www.sfgate.com/news/medical/article/Judge-tosses-California-law-allowing-life-ending-12918125.php

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