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Remembering Terri Schiavo: A Five-Year Anniversary Marked By Cruel Bigotry
Townhall ^ | 3/31/10 | Bobby Schindler

Posted on 03/31/2010 5:10:34 AM PDT by wagglebee

March 31st will mark the five-year anniversary of the needless death of my sister, Terri Schiavo.

It is difficult to believe this much time has passed since that horrible event which will be forever seared into my memory.

I wish I could say things have changed for the better since my sister’s death or that people with cognitive disabilities are now better protected in response to the horror she had to endure.

Tragically, however, it seems the rights of the brain-injured, elderly and others are still being violated.

All one has to do is look at what happened just last week. On March 21st, Fox aired an episode of The Family Guy that featured a "sketch" called "Terri Schiavo: The Musical." I was astonished at the producer’s cruel bigotry directed towards my sister and all cognitively disabled people.

Sadly, although more offensive than what my family has seen in the past from the media since Terri died, the bald-faced ignorance expressed in that episode of The Family Guy was nothing new. In fact, all signs indicate that we have embarked on a very disturbing path.

There is no disputing that Terri’s life – and death – had an astonishing impact on our nation. Our family still receives letters, emails and phone calls almost every day from people who tell us how Terri’s story touched them in profound ways, particularly when they come to know the facts.

Indeed, it was because of my family’s experience trying to protect Terri that we realized how all persons with similar cognitive disabilities are completely vulnerable to state laws that currently make it “legal” to deny them the most basic care – food and water.

This horrifying realization was why we established Terri’s Foundation. In Terri’s name, my family now works to protect tens of thousands of people with similar brain-injuries from having their fundamental freedoms taken away by an aggressive anti-life movement hell-bent on portraying severely disabled and otherwise vulnerable human beings as nothing more than “useless eaters”.

If the amount of phone calls we receive is any indication, what happened to Terri has become common. I think most people have no idea how our individual rights to make decisions about basic care like food and water, antibiotics, etc., have been so dramatically eroded. This not only includes family members advocating for loved ones but also protecting oneself by medical directive.

We recently heard from a woman whose mother was being cared for at a hospice facility. The daughter was powerless to effectively advocate for her mother because she had no power of attorney.

Even though she was her mother’s next-of-kin, and despite the fact her mother was begging her for food, the daughter was not allowed to feed her. It had been determined the mother was no longer able to swallow. But the daughter said her mother was eating safely just prior to being sent to hospice and questioned whether she still could. The mother was not given a feeding tube, and died just a short time later.

Perhaps the “Death Panels” Sarah Palin spoke of sounded like bombastic language. Yet when Palin added this term into our nation’s debate on health care, I believe she did not realize that many hospitals and facilities already have something frighteningly similar. Ethics committees are making many life and death decisions about patients, including whether to withhold simple provisions.

In a seemingly clandestine way, these ethics committees – comprised of medical and legal professionals – are empowering facilities to make life and death decisions independent of the family or a person’s own wishes.

The chilling stories we receive make it clear few citizens have any idea how vulnerable they are when it comes to judgments left in the hands of these ethics committees and facilities. And with the federal government now controlling our health care, there is no reason not to believe that these types of committees won’t become nationalized. Particularly when a health care system has been sabotaged by cost factors and quality of life judgments.

When our office receives phone calls from people fighting for their loved ones, I cannot help but look back and reflect on the courage of many individuals and groups who advocated on behalf of my sister.

As time has passed, however, many of those people, organizations and politicians – even many of our own friends – have fallen silent. Many who once ardently supported Terri’s life no longer actively educate or advocate for vulnerable patients.

With each troubling phone call from a frantic family, I am reminded there are countless other Terris in desperate need of our voice. Terri’s Foundation has been successful helping to save some, but sadly so many others have fallen victim.

I understand our nation faces many challenges today that may threaten our very existence. But how can we claim to be a just and honorable society, deserving of any blessing at all, if we richly reward hateful bigots while refusing to protect our weakest citizens?

Moreover, how did the tremendous courage and kindness we saw when we were fighting for Terri’s life have faded? How can any of us abandon this issue when all signs are that things are getting worse?

There are still many who support our efforts, who recognize the erosion of the value and dignity of the medically weak and who believe in protecting the life and liberty of all human beings.

The problem is their voices are often drowned out by the din of the pro-death lobby that claims death is the only dignified answer to a complicated problem.

Meanwhile the pro-death movement has not fallen silent. Rather, it has grown more vocal. The issue for them did not die with Terri. Indeed, their success in killing her seems to have only bolstered their determination to gain wider acceptance among the American people.

There will always be people with needs, there will always be others who work tirelessly to help them, and there will always be those who turn the other way; or worse – sit behind their drawing tables, disseminating cruel bigotry and hatred toward the disabled and vulnerable.

Until we all recognize that our inherit worth doesn’t change because of life’s circumstances, illness, disability or other events, we will continue to rob our most vulnerable of their right to fairness, justice and the ability to guide their own course in life.


TOPICS: Culture/Society; Editorial; News/Current Events
KEYWORDS: bravery; braveryagainstevil; euthanasia; moralabsolutes; prolife; terridailies; terrischiavo; whiterose
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To: Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; angelwings49; ...
The biggest lie Zero has EVER told is that there won't be death panels that ration health care.

Thread by me.

ObamaCare and Britain's NHS Move Forward With Rationing of Health Care

LifeNews.com Note: Dr. David Prentice is Senior Fellow for Life Sciences at Family Research Council. Up to July 2004 he had spent almost 20 years as Professor of Life Sciences, Indiana State University, and Adjunct Professor of Medical and Molecular Genetics, Indiana University School of Medicine.

The U.K. is ramping up healthcare rationing under its National Health Service (NHS). According to The Sunday Telegraph, the NHS has drawn up plans for restrictions on the most basic treatments for the sick and injured. Operations including hip and knee replacements and cataract surgery will be rationed in a new attempt to save money.

According to the report, plans also include cuts for terminally ill patients (dying cancer patients will supposedly be sent home and told to manage their own symptoms), closure of nursing homes for the elderly, cost-cutting measures in pediatric and maternity services and care of the elderly.

Doctors have already been told that their patients can have some operations only if they are given “prior approval” by a “primary care trust”, with each authorization made on a “case by case” basis.

Why is this increase in healthcare rationing in the U.K. of concern for the U.S.? Because many of ObamaCare’s nationalized regulations for treatment will be designed by Dr. Donald Berwick. The President used a recess appointment to put Berwick in as Administrator of the Center for Medicare and Medicaid Services.

Berwick is an advocate for government rationing of health care and says “I am romantic about the NHS; I love it.” (pdf of Berwick backgrounder)

But the NHS in Britain is a failure.

A recent study found that under the British nationalized health care system, inequities in the mortality rate between rich and poor have increased, with the inequalities today worse than those during the 1930's economic depression (prior to the NHS). The British government is apparently moving to a decentralized system of healthcare management (opposite to what ObamaCare is doing), to put power in the hands of patients and clinicians and eliminate layers of bureaucracy.

Redistribution of Health

To pay for ObamaCare, almost a half trillion dollars will be cut from Medicare, including Medicare Advantage. According to the Wall Street Journal:

“The law will spend $938 billion over a decade, mostly to expand coverage to lower-income Americans. To finance that, there will be $455 billion coming from cuts in government payments to health-care providers that serve patients on Medicare and two other federal programs. The hardest hit—to the tune of $136 billion—will be private insurance companies that run Medicare Advantage plans.”

The article notes that ObamaCare presages a redistribution of funds from the old to the young. A redistribution of health, as well as wealth. Not surprisingly, this redistribution is also something that Dr. Berwick has expounded on, noting that:

“…any health care funding plan that is just, equitable, civilized and humane must, MUST redistribute wealth from the richer among us to the poorer and the less fortunate. Excellent health care is, by definition, redistributional.”

This same redistribution of health, from old to young, is also favored by another member of the ObamaCare team, Cass Sunstein, who has said:

“I urge that the government should indeed focus on life-years rather than lives. A program that saves young people produces more welfare than one that saves old people.”

Sunstein, the “Regulatory Czar”, will be helping Berwick develop those regulations on who gets healthcare in the U.S.


181 posted on 08/01/2010 10:10:03 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: NYer; Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; angelwings49; ...
Dr. Alveda King continues to carry on her uncle's dream of real human rights.

Thread by NYer.

Pro-Life Rally Disrupted: Alveda King: ‘I Dare You to Arrest Me on My Uncle’s Grave’

PriestforLife.org

SPEAKING UP. Alveda King said ‘This is a time for boldness’ after Freedom Riders were denied the right to gather at the tomb of Martin Luther King Jr.

ATLANTA — A pro-life event at the Martin Luther King Jr. historic site was disrupted by officials July 24.

Participants in the “Freedom Rides for the Unborn” rally — more than 100 pro-life supporters — were kept from rallying on the federal park surrounding the gravesite of the black civil-rights activist even though they had a permit.

Meanwhile, pro-choice opponents who showed up without a permit were ushered onto the grounds for a counter rally.

Organized by Priests for Life and Martin Luther King’s pro-life niece Alveda King, who heads the organization’s African-American Outreach, the event brought several pro-life black pastors and a busload of supporters to the King Center in Atlanta in emulation of the civil-rights Freedom Rides of the 1960s.

The Martin Luther King Center for Nonviolent Social Change, an independent nonprofit founded by the King family, is part of a National Historic Site under the National Park Service, so both King Center staff and Park Service personnel were present at the event.

Free Speech Obstructed
When King and Father Frank Pavone, the national director of Priests for Life, arrived with the Freedom Riders, they were denied access to the King tomb by King Center staff.

When Park Service staff finally allowed King onto the federal property surrounding the center, she managed to get to the gravesite via a back way.

When she was stopped by the King Center’s CEO, John Mack, King was distressed enough by the obstruction that she climbed into a reflecting pool and reportedly said, “I dare you to arrest me on my uncle’s grave.”

Later she joined Father Pavone across the street from the center in front of a laundromat to deliver a speech calling for justice for the unborn.

Before the Freedom Riders arrived at the site, local pro-lifers were already running into trouble from the Park Service, according to Bridget Kurt, an Atlanta pro-lifer and event participant.

“When we got there, a rally of pro-choicers was already going on right on park property, chanting and using a bullhorn,” reports Kurt. “The park superintendent told us we couldn’t congregate on the sidewalk or go onto the grounds and that we couldn’t carry signs. She told us the pro-aborts had a permit but later changed that to say they had permission.”

Kurt was shocked by what transpired: “The Park Service and the King Center disrupted something that was to be very peaceful and prayerful. It all was totally contrary to the spirit of nonviolence that Martin Luther King stood for. I heard one park ranger joke about whether they should get their clubs out. It was a joke, but still, how nonviolent was that?”

Kurt published her version of events on the CNN iReport website under the headline “National Park Service violates free-speech rights of Alveda King and pro-lifers at MLK grave.”

For its part, the Park Service denies that remarks about clubs were made. Moreover, according to Marianne Mills, the public affairs spokeswoman for the National Park Service’s southeast region, any ordering about of pro-life supporters was intended to keep them and pro-choice demonstrators apart.

“The actions directed by Park Superintendent Judy Forte were focused on trying to separate the parties present as their conflict escalated, not show support for one group over another,” Mills told the Register in an e-mail.

Pro-Lifers Assert Rights
Some pro-lifers began turning their signs over to park staff, says Kurt, but she told Superintendent Forte, “We had every right to be on a city sidewalk. She told me to shut up and told a staff member to call 911. I said, ‘Fine, and I’ll call CNN.’”

Both followed through on their statements. However, neither CNN nor any local news agencies sent reporters. The Atlanta police did, however, eventually respond to Forte’s call.

“They told Forte,” says Kurt, “that we could use the sidewalks.”

According to Park Service spokeswoman Mills, Alveda King told Park Service southeast regional director David Vela in an e-mail exchange that the problems that day were with the King Center “and not the National Park Service.” Therefore, Mills told the Register, “the assertion that the ‘National Park Service violates free-speech rights of Alveda King and pro-lifers at MLK grave’ is incorrect.”

Not so, says Kurt. Egged on by King Center staff, Park Service officers did impede King initially, and before she arrived, they bullied and coerced pro-lifers into giving up their signs and tried to disperse them from city sidewalks.

“Park Service staff escalated a tense situation rather than calming it down,” Kurt says. “And it was quite apparent to me the superintendent did not understand free speech and the boundary between what was public and private property and that free speech is allowed on public property.”


182 posted on 08/01/2010 10:13:39 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: frithguild; Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; ...
The UK's health care system demonstrates EXACTLY what we can expect from Obamacare.

Threads by frithguild and me.

Girl texted pics of herself

A DESPERATE woman texted photos of herself slowly DYING to her mum as she lay suffering on a hospital bed - being ignored by NHS doctors. Tragic Jo Dowling, 25, sent over forty messages to her mother and best friend including pictures of a deadly rash spreading across her body as her life ebbed away.

The pretty youngster was diagnosed by her family GP with suspected Meningococcal Septicaemia after developing a purple skin rash and low blood pressure last November.

She was rushed to Milton Keynes Hospital where A&E doctors rejected the diagnosis believing instead her illness was a mild infection caused by her Cystic Fibrosis.

Doctors abandoned Jo on a observation ward and gave her headache tablets and fluids as they failed to spot the purple rash spread over her arms, hands and legs.

As the hours passed terrified Jo took photos of her rash on her mobile phone and sent them to her mum and best friend describing her condition as "getting worse".

The meningitis bug left her in septic shock choking and coughing as fluid filled her lungs and she died four hours after her last text message - just 14 hours after arriving at hospital.

Her family yesterday accused the hospital of "neglect" after an inquest at Milton Keynes Coroners' Court heard doctors failed to spot she was suffering 'blood poisoning shock'.

Coroner Tom Osborne criticised the hospital for a "communication breakdown" that led to her death as tragically a simple dose of penicillin and antibiotics would have saved Jo's life.

The inquest heard there were only two doctors on duty to cover the entire hospital the night Jo died.

Devastated mum Sue Christie, 48, of Milton Keynes, a distribution worker, said: "Our doctor knew it was meningitis but when we got to hospital all the care seemed to stop.

"They didn't seem to know what they were meant to do or what meningococcal septicaemia was.

"The hospital was saying it was just an infection. She had a lot of infections with Cystic Fibrosis but never a rash like this.

"I saw her picture messages and the rash was really bad. You couldn't miss them but the nurses did. I thought she was in hospital and with the best people.

"She wasn't given a chance and was left to die without being given any treatment.

"It is so sad as Jo had got through everything with her Cystic Fibrosis and was such a strong girl."

Jo was given penicillin and admitted to hospital at 3.25pm on November 23 last year with a letter from her GP Dr Nessan Carson diagnosing Meningococcal Septicaemia.

Dr Carson listed symptoms as low blood pressure, a raised pulse and a purple rash that would not disappear when pressed with a glass.

The inquest heard locum consultant Dr B. S. Khattak sent Jo for a CT Scan and lumber puncture and results were sent to micro-biology to determine which type of anti-biotics to use.

When the scans showed no traces of meningitis Dr Chris Akubuine, physician in general medicine, refused to continue treating Jo's symptoms with antibiotics.

Instead Dr Akubuine administered headache pills and fluids and left her in the Clinical Decision Unit (CDU) for overnight observations, the inquest heard.

Trainee GP Vivake Roddah failed to keep a written observation record but told the inquest he did not see Jo's purple rash on her hands, arms and legs.

Five nurses also told the two day hearing they did not spot any rash on Jo's body.

As her condition worsened Jo swapped 42 text messages with friends and her mum describing her illness and symptoms.

Just two hours after doctors ruled out meningitis she texted a friend to say "rash is getting worse".

She took around 10 photos of the purple rash on her legs, hands and arms and sent one to her mum complaining her condition was not improving.

Her death was pronounced at 5.20am on November 24 three hours after hospital logs show she was last checked on.

Dad Ivor Dowling, 52, a mechanic, said: "If she had been given antibiotics she would have survived. The hospital failed her.

"The first doctor who saw my daughter did everything he was supposed to do. But after that these doctors and nurses failed to spot her failing vital signs.

"They were obnoxious and arrogant. She was neglected."

Delivering a narrative verdict Deputy Coroner Tom Osborne ruled Jo died from a combination of Meningococcal Septicaemia and Cystic Fibrosis.

He criticised hospital doctors for failing to realise she was in 'blood poisoning shock'.

Mr Osborne said: "As a result of a breakdown in communication the antibiotics was not continued and resulted in lost opportunities to render further medical treatment."

Jo, who was on a waiting list for a lung transplant, occasionally needed a wheelchair to get around after she was diagnosed with Cystic Fibrosis as a baby.

She worked as a cashier at Great Mills and The Bag Shop, in Milton Keynes, and competed in junior cross country championships as a child.

Her best friend Jess Wales, 20, from Kent, who received the other messages also suffered from cystic fibrosis and died in January shortly after a lung transplant.

A spokesman for Milton Keynes Hospital said: "Following Joanne's unexpected death, the Trust conducted a comprehensive internal investigation to review her care and treatment.

"The findings of the investigation were presented in detail at the inquest today and the recommendations are already being implemented.

"The Trust fully accepts the verdict of the inquest."

Former director Maggie Southcote-Want, 48, revealed a series of shocking incidents at the hospital at an employment tribunal claiming unfair dismissal in May.

Ms Southcote-Want claimed bodies were routinely dumped on the floor of the mortuary fridge and photographs of a car crash victim uploaded to websites, prompting a police inquiry.

She also claimed a locum doctor wrongly analysed dozens of breast cancer biopsies, a leading consultant was suspended for surgical blunders and two employees were caught having sex in the pharmacy during working hours.

The hospital denied the claims.

___________________________________________________

Malnutrition of elderly Scots is 'euthanasia'

WASHINGTON (BP)--Government-run hospitals in Scotland are guilty of a "form of euthanasia" by malnutrition, a patients' organization leader has charged.

Jean Turner, executive director of the Scotland Patients Association (SPA), said hundreds of patients, especially the elderly, are undernourished in National Health Service (NHS) hospitals because of a lack of assistance from staff members, according to The Herald of Glasgow, Scotland.

About 50,000 patients die in a state of malnutrition each year at NHS facilities, according to one recent report.

"The SPA would call this a form of euthanasia to allow dehydration and malnutrition to develop due to lack of awareness, lack of staffing or carelessness," Turner said, according to The Herald's July 4 story.

The patients' organization has urged the Scottish government to urgently tackle the problem of malnutrition of the elderly in the nation's hospitals. Turner indicated the problem stems from staff who do not help patients who cannot feed themselves.

One woman died of kidney failure, The Herald said, after 14 weeks in a hospital, and her family believes poor standards of care, particularly in nutrition, contributed to her death.

"Staff would tell me, 'It takes an hour to feed your mother and we don't have an hour,'" one family member told the newspaper, adding, "We believe that the care she received in that hospital is the reason she is not here today."

Turner said the case is one of many.

"If patients do not manage to swallow food, nutritious or otherwise, and drink then they will not heal, their general health will deteriorate and death may be an outcome, sooner or later," Turner said.

"... Whatever happened to measuring input and output and keeping charts to prevent this? We are in no doubt many wards short-staffed and staff do not have the time that they know is needed to provide the best care, but SPA would say it is down to all staff to be accountable and raise their issues of concern."

When the hospital staff is aware that a patient has difficulty eating, the patients' organization said it expects them to help the patient eat, The Herald reported.


183 posted on 08/01/2010 10:18:13 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; angelwings49; ...
The death mongers must be defeated.

Thread by me.

Selling Assisted Suicide, State by State

REUTERS/Staff

Wheelchair-bound disabled protesters against physician-assisted suicide are silhouetted as they hold up a banner outside the U.S. Supreme Court in 2005 on the day of the Gonzales v. Oregon case. The Supreme Court revisited the emotionally charged issue of physician-assisted suicide in a test of the federal government's power to block doctors from helping terminally ill patients and end their lives.

DENVER — Kathryn Tucker has been busy the past few years. As director of legal affairs for Compassion & Choices, she peruses state constitutions and laws to see if they address assisted suicide, which she refers to euphemistically as “aid in dying.”

So far, Washington and Oregon are the only states that have legalized assisted suicide in this country. Some believe that Montana has also, but a legal analysis of two court decisions which supposedly legalize assisted suicide in the state questions that assumption.

For all its efforts, Compassion & Choices, which was once known as the Hemlock Society, has seen more setbacks than successes. But that hasn’t stopped its latest campaign from revving up in Idaho.

It started in the local press with a column Tucker wrote in the June 25 issue of the Coeur d’Alene Press.

Tucker writes that “Idaho does not have a statute specifically addressing aid in dying, either to permit or prohibit the practice. It does not have [a statute making it] a crime of assisting another to ‘commit suicide.’ Accordingly, in Idaho, physicians can provide aid in dying.”

Margaret Dore, an attorney in Seattle who specializes in elder law, wrote a rebuttal to Tucker’s column for the Idaho Medical Association.

Dore stated that Tucker’s claim that there were no statutes dealing with assisted suicide “is untrue.”

“Idaho does have a statute prohibiting assisted suicide. Moreover, it has been in effect since 1994. Prior to that time, assisted suicide was prohibited solely by common law,” Dore emphasized.

“With assisted suicide prohibited by common law and not subsequently made legal, a doctor who causes a suicide with ‘deliberate intention’ is guilty of an unlawful killing … [and] can be statutorily charged with murder,” Dore explained.

Dr. Robert Ancker, an Idaho physician, board certified in hospice and palliative medicine, wrote a response to Tucker’s column as well.

He attacked her “factually untrue” reading of Idaho statutory law, which states that it “does not make legal, and in no way condones, euthanasia, mercy killing or assisted suicide or permit an affirmative or deliberate act or omission to end life, other than to allow the natural process of dying.”

“Any coroner in Idaho will classify any ‘aid in dying’ death as an assisted suicide, thus making it illegal [according to] Idaho code,” Ancker emphasized.

He concluded that this is “a dangerous game that Ms. Tucker is playing with Idaho citizens. Worst of all, it takes away from meaningful conversations regarding death, dying, advanced directives, and comfort, palliative and hospice care.”

Ancker gave a rebuttal of Tucker’s comments July 17 at an event sponsored by the Idaho Medical Association. Margaret Keeler, a nurse who was present at the event, recalled that Tucker started her talk “by showing statistics about how many people have significant pain at the end of life and stressing a person’s right to have pain and symptom relief.” Ironically, later in her talk, Tucker gave a slide presentation on why people chose assisted suicide. The statistics showed that “91% of those surveyed gave ‘a loss of autonomy’” as their reason for asking for a lethal overdose, followed by “the patients’ inability to engage in life fully,” Keeler remembered.

She added: “Far down on the list was the issue of ‘unrelieved pain.’”  In other words, Keeler noted, “pain was not the chief reason, or even the more prominent reason, that people asked for help in dying.”

Keeler mentioned that Tucker was trying to convince attendees that “because they had three adjoining states [with] legalized assisted suicide [Oregon, Washington and Montana ], it lent support to a standard of care [for legalizing] the practice in Idaho.”

At one point in his rebuttal, Ancker asked the medical professionals in the room how many supported assisted suicide. No hands went up, Keeler recalled.

Connecticut Case

Tucker’s attempt to switch terminology in a Connecticut case last year failed as well. The murder-suicide of an elderly couple in North Haven, Conn., led to a lawsuit filed last October, Blick v. Connecticut, which was represented by local counsel and lawyers from Compassion & Choices.

Dr. Gary Blick, an HIV/AIDS specialist in Norwalk, Conn., and Dr. Ronald Levine, an internist in Greenwich, Conn., filed a legal challenge to the state’s assisted-suicide statute, saying that the threat of punishment prevents them from prescribing lethal doses of medication for their patients.

But in June, a Superior Court judge said that the lawyers failed to make their case by insisting that the issue was a case of “aid in dying” rather than “assisted suicide.” The judge ruled that the change in terminology would make no difference in prosecuting the plaintiffs.

Unbowed, Tucker said she would not rule out lobbying the Connecticut Legislature to take up the issue of legalizing assisted suicide.

Meanwhile, in Montana, there has been a groundswell of activity to fight assisted suicide in the state, according to Mo Wosepka, executive director of the Montana Catholic Conference. He spoke to the Register in July about the formation of a broad-based coalition to stop legalized assisted suicide following last year’s State Supreme Court ruling in Baxter v. Montana: that nothing in state law or the court’s precedent indicated assisted suicide was against public policy. The court did not determine whether the Montana Constitution guarantees a right to assisted suicide.

Montanans United consists of “physicians, health-care professionals, disability-rights advocates, faith communities, seniors, people who are seriously ill and their caregivers, and many other Montanans in communities across the state.” He is confident, he says, that this group will be successful in “getting the truth out” on assisted suicide and the proposed legislation. “With good information, people can make good decisions,” he said.

On May 30, state Sen. Greg Hinkle introduced “the Montana Patient Protection Act, prohibiting physician-homicide and physician-assisted suicide, based on Montana’s public policy to prevent elder abuse and to value all citizens.”

State Rep. Dick Barrett issued a formal request for a draft bill in favor of physician-assisted suicide, ensuring that terminally ill patients in Montana can elect to choose assisted suicide, while providing physicians protection from civil liability.

As Sen. Hinkle recently said, “[Compassion & Choices talks] about choice, but in many cases, there is no choice made. … They put the decision in the hands of other people — the doctor and the family.”

Legalizing physician-assisted suicide “opens a Pandora’s box,” Hinkle said. “I don’t believe the people of Montana want to go there.”

Disability

Bob Liston is disabled and has problems with the idea that those advocating for assisted suicide are really doing so out of a true concern for the suffering.

Liston is an organizer for Not Dead Yet in Montana, a group officially opposed to assisted suicide and euthanasia, and works for Adapt, a national disability-rights organization. He told the Register, “I think that in Montana it is unnecessary for an assisted suicide law to be written because we already have laws on the books that allow a physician to provide palliative care up to and including efforts that might hasten death.” He added: “So, I have a really hard time seeing why we need to go beyond this.”

It is the faulty assumptions about those whose lives it will affect that he finds upsetting. “Compassion & Choices … seems to think that taking one’s own life is dignified, often using the example of [a disabled person’s need for assistance with personal care and hygiene] as a reason to not go on living.” But he adds that some disabled people need this kind of total assistance on a daily basis “and are grateful for it.”

Compassion & Choices “puts forth the argument that so few people in Oregon have chosen assisted suicide [because] the guidelines are so strict. Nothing could be further from the truth,” he insisted, adding: “We have no idea what is really going on in Oregon because recordkeeping is not required.”

Liston stated: “As a person with a disability, I would say that not only is this the wrong law [favoring assisted suicide] to pass — it is definitely the wrong message.”

“If [the citizens of Montana] put as much effort into suicide prevention for people wanting this, or services for people with disabilities to live in their communities, not just have a life in a nursing home,” Liston concludes, “we would be a much greater nation.”


184 posted on 08/01/2010 10:21:33 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: All; wagglebee

“hundreds of patients, especially the elderly, are undernourished in National Health Service (NHS) hospitals because of a lack of assistance from staff members, “

Even in a good hospital, we had to feed my dad, because it took him almost an hour to eat, and the hospitals just don’t have enough staff. They would only spend ten minutes, or so, and maybe figure the slow-eating patients just aren’t hungry (or they don’t want to lose their job because they have other duties).

Anybody who can, volunteer to feed patients at a hospital or nursing home, even if you can only do it once in awhile.


185 posted on 08/01/2010 10:40:07 AM PDT by Sun (Pray that God sends us good leaders. Please say a prayer now.)
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To: wagglebee

Thanks for the ping!


186 posted on 08/01/2010 10:40:56 AM PDT by Alamo-Girl
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To: All; wagglebee
There's been another mysterious death at Michael Schiavo's job.

Where was Michael Schiavo? What did he know, and when did he know it?

-


News Release

Public Information Office:
(727) 582-6221

Marianne Pasha:
mpasha@pcsonet.com

Media News Line:
(727) 582-6495

Cecilia Barreda:
cbarreda@pcsonet.com

Fax:
(727) 582-5911

Sgt. Thomas Nestor:
tnestor@pcsonet.com

Inmate Found Unresponsive In His Bunk Is Later Pronounced Dead At Local Hospital - Investigation Is Underway

Release Number: 10-182

Who:
Inmate:

Kyle Donald Howard
DOB: 3/6/86
Address: 1310 Bayview Drive - Clearwater

Arrested on July 24, 2010
Transported to Northside Hospital on July 26, 2010

What: Sheriff's homicide detectives are conducting a death investigation involving Pinellas County Jail inmate Kyle Howard, who was found unresponsive on his bunk Monday in the Health Care Facility, and transported to Northside Hospital. He was pronounced dead at 4:45 p.m., Monday evening.

Where: The Inmate Health Care Facility is located at the Pinellas County Jail on 49th Street in Clearwater.

When: Howard was discovered unresponsive in his bunk in the Inmate Healthcare Facility just after 3:30 p.m., Monday, July 26, 2010.

How/Why: Kyle Howard was booked into the Pinellas County Jail in the early morning hours of Friday, July 24, 2010. He was arrested on a series of probation violations.

He was eventually housed in the Jail's Inmate Health Care Facility due to reported substance abuse issues. According to detectives, the inmate reportedly had not been feeling well and went to rest on his bunk. Another inmate attempted to rouse Howard for dinner just after 3:30, when Howard was found unresponsive.

The medical staff responded and CPR was initiated. Howard was transported out of the Jail by ambulance to Northside Hospital where he was pronounced dead at around 4:45 p.m.

Sheriff's homicide detectives routinely investigate these cases.

The autopsy was conducted this morning. According to detectives, there was no obvious cause, and that the determination is pending other test results.

The investigation continues.


187 posted on 08/07/2010 1:11:52 PM PDT by BykrBayb (Somewhere, my flower is there. ~ Þ)
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To: All; wagglebee
Patient dehydrated to death by jail workers at Michael Schiavo's workplace. No word on whether or not he was directly involved.

Pinellas County Jail death from negligence, attorney says

LARGO — Negligence by several Pinellas County Sheriff's Office employees caused the death of a 50-year-old woman with a history of mental health issues, according to an attorney representing the dead woman's husband.

Jennifer DeGraw of St. Petersburg was found unresponsive on the floor of her jail cell on March 24, 2009, eight days after Pinellas deputies arrested her on a charge of battery of a law enforcement officer.

In a notice of intent to sue that was sent to Sheriff Jim Coats last month, the attorney representing DeGraw's husband Michael said the preventable chain of events that led to the woman's death began when a deputy decided to jail DeGraw instead of committing her under the state's Baker Act.

~ snip ~

DeGraw was taken to the county jail and assigned to the medical wing. But the medical staff there failed to give her the medications she needed for the bipolar disorder as well as other health ailments, including seizures and hypertension, Laporte said.

~ snip ~

Laporte said Michael DeGraw called the jail several times to try to speak with his wife, but was never allowed.

"You've got a caring husband who calls the Sheriff's Office to help, and they essentially kill his wife," Laporte said.

DeGraw was revived in her cell, then taken to Northside Hospital and Heart Institute, where she was pronounced dead. Laporte said the cause of death was determined to be fluid and electrolyte imbalance.


188 posted on 08/07/2010 6:43:51 PM PDT by BykrBayb (Somewhere, my flower is there. ~ Þ)
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To: topher; Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; angelwings49; ..
It's taken a long time, but people are finally starting to see the truth about stem cells.

Thread by topher.

Mainstream Media Recognizes Adult Stem Cell Research Far Ahead Of Embryonic

WASHINGTON, DC, August 3, 2010 (LifeSiteNews.com) - Following an announcement on Friday by U.S. biotech firm Geron Corp. that it received clearance from the Food and Drug Administration to carry out clinical trials using stem cells derived from human embryos, the mainstream media has been awash in stories that acknowledge the success of adult stem cell treatments, and the absence of any positive results from embryonic stem cell research.

AP reported the fact that adult stem cells have the ability not only to differentiate into bone, cartilage and blood vessels, but have also been shown to stimulate tissue repair.

"That gives adult stem cells really a very interesting and potent quality that embryonic stem cells don't have," Rocky Tuan of the University of Pittsburgh told AP.

Harvard University’s Dr. David Scaden, on the other hand, told CBS News of adult stem cells: “That’s really one of the great success stories of stem cell biology that gives us all hope. If we can recreate that success in other tissues, what can we possibly imagine for other people?”

In one prominent case that is being cited by the mainstream press, a patient had a broken ankle that would not heal, despite multiple surgeries. Dr. Thomas Einhorn, Chairman of Orthopedic Surgery at Boston University Medical Centre, drew bone marrow from the man’s pelvic bone, and condensing it he then injected the four teaspoons of rich red liquid into his patient’s ankle.

Four months later, the man’s broken ankle had healed, which Einhorn credits to the adult stem cells in the marrow injection. Einhorn said he tried the procedure based on published research from France.

"Adult stem cells are being studied in people who suffer from multiple sclerosis, heart attacks and diabetes. Some early results suggest (adult) stem cells can help some patients avoid leg amputation. Recently, researchers reported that they restored vision to patients whose eyes were damaged by chemicals," AP reported, adding that adult stem cell treatments "have become a standard lifesaving therapy for perhaps hundreds of thousands of people with leukemia, lymphoma and other blood diseases."

According to CBS news, U.S. scientists at biotech companies and at the Pentagon are devising potential treatments that use adult stem cells rather than embryonic stem cells, news that is being welcomed by those who oppose the destruction of human embryos, both for moral reasons and based on the fact that embryo research has not resulted in a single positive outcome.

Stories of "catastrophic" results from the experimental use of fetal stem cells abound.

Last year a report by Israel's Public Library of Science journal said that a young Israeli boy suffering from a fatal genetic disease was injected with fetal stem cells that resulted in the development of brain and spinal cord tumors. Tests revealed that the tumor tissue was composed of fetal cells.

A study published in the March 2001 issue of the New England Journal of Medicine describing the use of fetal tissue to treat Parkinson's disease, said that the treatment resulted in what the researchers themselves described as "disastrous side effects."

The study said the treatment caused patients to "chew constantly" and "writhe and twist, jerk their heads, fling their arms about."

Dr. Paul Greene, a neurologist at the Columbia University College of Physicians and Surgeons, said that the results of the experiment were "absolutely devastating ... It was tragic, catastrophic. It's a real nightmare. And we can't selectively turn it off."

Earlier this year California's Institute for Regenerative Medicine quietly changed its focus, after years of fruitless work and the expenditure of billions of dollars, from embryonic stem cell research to adult stem cell research. The institute cited adult stem cell treatment as responsible for dozens of positive results and all-out cures for maladies ranging from spinal cord injury, to Alzheimer's, to type I diabetes.

Los Angeles-based Investor's Business Daily magazine commented that, "Five years after a budget-busting $3 billion was allocated to embryonic stem cell research, there have been no cures, no therapies and little progress. We are pleased to see California researchers beginning to put science in its rightful place."

The Vatican responded on Saturday to the U.S. Food and Drug Administration's approval of Geron Corp.'s clinical trials using embryonic stem cells.

Elio Sgreccia, emeritus head of the Pontifical Academy for Life, told Radio Vatican, "Despite the efforts that are made to deny it, science continues to show us that the embryo is a human being in the making" and condemned the move as "unacceptable."


189 posted on 08/08/2010 11:33:00 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: markomalley; Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; ...
It's clear that Pelosi and her ilk don't believe that ANYONE has the right to life.

Thread by markomalley.

Pelosi Won’t Say When Jesus Got the Right to Life

(CNSNews.com) – House Speaker Nancy Pelosi (D-Calif.), a Catholic, publicly stated earlier this year that she had a duty to pursue policies “in keeping with the values” of Jesus Christ, the “Word made Flesh.” But at a press briefing last week, when reminded of this statement, Pelosi declined to say when Jesus got the right to life.

“Whenever it was,” said Pelosi, “we bow our heads when we talk about it in church, and that’s where I’d like to talk about that.”

Later, when asked in writing through her press secretary whether the speaker believed Jesus had a right to life from the moment of conception, the press secretary responded: “The speaker answered the question. Thanks.”

Pelosi, who favors legalized abortion, voted against the ban on partial-birth abortion that was enacted in 2003.

On May 6 of this year, at a Catholic Community Conference on Capitol Hill, Pelosi said: “They ask me all the time, ‘What is your favorite this? What is your favorite that? What is your favorite that?’ And one time, ‘What is your favorite word?’ And I said, ‘My favorite word? That is really easy. My favorite word is the Word, is the Word. And that is everything. It says it all for us. And you know the biblical reference, you know the Gospel reference of the Word.”

“And that Word," Pelosi said, "is, we have to give voice to what that means in terms of public policy that would be in keeping with the values of the Word. The Word. Isn’t it a beautiful word when you think of it? It just covers everything. The Word.”

“Fill it in with anything you want,” she said. “But, of course, we know it means: ‘The Word was made flesh and dwelt amongst us.’ And that’s the great mystery of our faith. He will come again. He will come again. So, we have to make sure we’re prepared to answer in this life, or otherwise, as to how we have measured up.”

In the New Testament, John 1:14 states, “And the Word was made flesh, and dwelt among us, (and we saw His glory, the glory as it were of the only begotten of the Father) full of grace and truth.”

The Apostle’s Creed says: “He was conceived by the power of the Holy Spirit and born of the Virgin Mary.”

At her July 29 press briefing, CNSNews.com asked Speaker Pelosi: “You said at a recent Catholic Community Conference that your favorite word was ‘The Word, as in the word made flesh,’ and that we need to quote, ‘give voice to what that means in terms of public policy that would be in keeping with the Word.’ So, when was the Word made flesh? Was it at the Annunciation, when Jesus was conceived by the power of the Holy Sprit, as the Creed says, or was it at the Nativity when he was born of the Virgin Mary? And when did the Word get the right to life?”

Speaker Pelosi responded: “Whenever it was, we bow our heads when we talk about it in church, and that’s where I’d like to talk about that.”

CNSNews.com then sent an e-mail to the speaker’s press secretary, Nadeam Elshami, seeking to clarify the speaker’s answer. The e-mail said:

“Speaker Pelosi said at a Catholic Community Conference that her favorite word was ‘the Word’ as in ‘the Word made flesh’ and that we ‘need to [give] voice to what that means in terms of public policy.’ We’d like to clarify the speaker’s position on this: Did Jesus have the right to life from the moment of conception?”

In an e-mailed response, the press secretary wrote: “The speaker answered the question. Thanks.”

The Catechism of the Catholic Church discusses Christ’s divinity from His conception. It states, “Christ's humanity has no other subject than the divine person of the Son of God, who assumed it and made it his own, from his conception.” (466)

The Catechism also states, “From its conception, the child has the right to life.” (2322)


190 posted on 08/08/2010 11:37:25 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; angelwings49; ...
Two threads by me on the evilness of the death mongers.

The legalisation of assisted suicide

The arguments for legalising assisted suicide and euthanasia are in the process of imperceptibly changing from a duty of compassion towards the suffering, into the right of self-destruction for the hopeless.

They are predicated on a potent individualistic delusion of isolated autonomous choice, a refusal to acknowledge the reality of our mutual interconnectedness and interdependence as human beings in society.

The principled opposition of our current law to homicide and assisted suicide provides an essential safeguard for carers, for the medical profession and for the elderly and vulnerable who may fear that their lives have become burdensome and valueless.

In our latest Cambridge Paper, Professor John Wyatt argues that the increasing public support for the legalisation of assisted suicide provides an urgent challenge to the medical and legal professions and to the Christian community as a whole.

Many people have a fear of inappropriate and burdensome medical over-treatment at the end of life, and this drives the demand for assisted suicide.

The provision of skilled palliative care is inadequate, few doctors receive detailed training in palliative techniques, and tragically, many people in the UK still die with inadequate pain and symptom relief.

Vastly more resources are spent by Government and medical charities alike on researching treatments for life-threatening illness, than are devoted to improving the quality and availability of end of life care.

As a community we need to insist on a reorientation of priorities so that care for the elderly, the chronically disabled and the terminally ill receives the focus that it deserves.

The growing focus on personal autonomy and self determination provides a challenge to the Christian community to demonstrate a countercultural and alternative understanding of the sanctity of human life and the nature of human interdependence and interconnectedness.

In a society where millions of elderly suffer isolation, abandonment and the silent horror of abuse, can the Christian community provide a resource of compassionate and sacrificial caring?

The arguments for legalising assisted suicide and euthanasia are in the process of imperceptibly changing from a duty of compassion towards the suffering, into the right of self-destruction for the hopeless.

They are predicated on a potent individualistic delusion of isolated autonomous choice, a refusal to acknowledge the reality of our mutual interconnectedness and interdependence as human beings in society.

The principled opposition of our current law to homicide and assisted suicide provides an essential safeguard for carers, for the medical profession and for the elderly and vulnerable who may fear that their lives have become burdensome and valueless.

In our latest Cambridge Paper, Professor John Wyatt argues that the increasing public support for the legalisation of assisted suicide provides an urgent challenge to the medical and legal professions and to the Christian community as a whole.

Many people have a fear of inappropriate and burdensome medical over-treatment at the end of life, and this drives the demand for assisted suicide.

The provision of skilled palliative care is inadequate, few doctors receive detailed training in palliative techniques, and tragically, many people in the UK still die with inadequate pain and symptom relief.

Vastly more resources are spent by Government and medical charities alike on researching treatments for life-threatening illness, than are devoted to improving the quality and availability of end of life care.

As a community we need to insist on a reorientation of priorities so that care for the elderly, the chronically disabled and the terminally ill receives the focus that it deserves.

The growing focus on personal autonomy and self determination provides a challenge to the Christian community to demonstrate a countercultural and alternative understanding of the sanctity of human life and the nature of human interdependence and interconnectedness.

In a society where millions of elderly suffer isolation, abandonment and the silent horror of abuse, can the Christian community provide a resource of compassionate and sacrificial caring?

__________________________________________________

Wesley J. Smith: The Selfishness of Assisted Suicide Advocacy/Ideology–Murder/Suicide

I make it a point of not criticizing people who commit suicide.  None of us knows what might cause such despair that we decide to terminate ourselves.  Indeed, my focus is on how a loving community responds to the suicidal despair of our brothers and sisters, not on judging people who have died.

But I am going to make an exception in this particular story.  Over the years, I have noticed an utterly “it’s all about me” orientation among the more doctrinaire assisted suicide types–not people who may support legalization in limited cases (not knowing it is a false premise)–but the committed activists, the kind who pour over stories of assisted suicides, attend how-to-commit-suicide seminars, and get the vapors at suicide machine conventions.  Not only are such assisted suicide fanatics disturbed, but often their actions cause great harm, not only to themselves but to society itself, e.g.,  the Final Exit Network members who helped a mentally ill woman kill herself in Phoenix.

An Arizona murder/suicide “death with dignity” shows what happens when one commits oneself wholeheartedly to  ideological hemlock. From the story:

An Arizona couple followed through with a decades-long plan to end their lives before the ravages of old age took their toll. Lansing C. Holden, 83, and his wife, Carol, 78, were found shot to death July 26 in a remote cabin south of Pagosa Springs in Archuleta County. Archuleta County Coroner Carl Macht on Wednesday said the deaths had been classified as a murder-suicide…The Holdens were members of the Final Exit Network, a nonprofit that promotes “the right of every adult to a peaceful, dignified death,” according to its website. Members receive consultations and advice about suicide methods. She wore an orange plastic bracelet that read, “Do not resuscitate” from the Hemlock Society, a national right-to-die organization. Such groups typically recommend less-violent means of death, like a lethal dose of medication, rather than a gunshot…

The Holdens were in fairly good condition considering their age, Macht said. Mr. Holden had the beginnings of heart disease and she had digestive issues…They left behind a suicide note signed by both participants and notarized March 3, 2010, in Arizona. The letter read: “Many years ago we decided to be in charge of the timing of our own death. Hopefully it would be when the lines of normal aging, health problems and finances all crossed. “It is our intention to avoid the indignities of prolonged nursing home care or terminal hospitalization. Unfortunately, there is little chance of ‘death with dignity’ under present laws which do not recognize our right to die a peaceful and painless death at the time and place of our own choosing. “We have concentrated on the quality rather than the quantity of our lives together, and now it is time to move on while we are still in control. We want our bodies to be cremated directly and no religious or memorial services.”

Oh, and get this bit of utter selfishness–making a cleaning woman find their bodies:

The couple e-mailed the homeowner before the shooting and asked that a cleaning lady be sent by. She discovered the bodies July 26 – about a day after they had been shot. “She was really shaken up,” Macht said.

This is no different than the double assisted suicide committed at Dignitas in Switzerland (more planned), or the recent well publicized double suicide in Wisconsin. And it is fully in keeping with Canadian assisted suicide advocate Ruth Von Fuchs who, for example, lauds suicide as a prophylactic against future suffering.  And indeed, it is just like the suicide of my friend Frances, who killed herself o her 76th birthday under the influence of  Hemlock Society literature–which is what dragged me into this field of advocacy in the first place.  Here’s what I wrote about that pointless death in my first anti assisted suicide piece in Newsweek, published June 28, 1993.  From my column, “The Whispers of Strangers:”

Frances once told me that through her death she would be advancing a cause. It is a cause I now deeply despise. Not only did it take Frances, but it rejects all that I hold sacred and true: that the preservation of human life is our highest moral ideal; that a principal purpose of government is as a protector of life; that those who fight to stay alive in the face of terminal disease are powerful uplifters of the human experience.

Of greater concern to me is the moral trickledown effect that could result should society ever come to agree with Frances. Life is action and reaction, the proverbial pebble thrown into the pond. We don’t get to the Brave New World in one giant leap. Rather, the descent to depravity is reached by small steps. First, suicide is promoted as a virtue. Vulnerable people like Frances become early casualties. Then follows mercy killing of the terminally ill. From there, it’s a hop, skip and a jump to killing people who don’t have a good “quality” of life, perhaps with the prospect of organ harvesting thrown in as a plum to society.

And that is precisely what is happening.

This couple didn’t just kill themselves, they did it in a way to create a public controversy.  That means we have a right to comment about what they did and what they believed.  They didn’t just devastate their family, they hurt society.  That makes what they did triply wrong.


191 posted on 08/08/2010 11:41:52 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; angelwings49; ...
I cannot help but wonder what Terri was thinking as she was being murdered.

Thread by me.

Former ‘locked-in’ patient speaks of her will to live

A mother of two has revealed how she never lost her will to live after an illness left her paralysed and unable to speak for 18 months.

Kerry Pink was left suffering from a condition known as ‘locked-in syndrome’ by an undiagnosed neurological illness when she was just 35.

Mrs Pink, writing in the Daily Mail, said: “My memories are blurred. But some things remain absolutely certain. I know that however dark the twilight world I inhabited, I never lost my will to live.

Determined

“I was always determined to come back home. And it was my absolute faith in my husband Greg’s love that propelled me on – that and, of course, the knowledge that my two beloved children needed me there to care for them.”

Her comments come in the wake of a legal challenge by Tony Nicklinson, who also suffers from ‘locked-in syndrome’, to force the Director of Public Prosecutions to issue guidance clarifying whether his wife would be prosecuted for murder if she kills him.

Mrs Pink, whose determination is likely to strengthen calls for the law on assisted suicide and euthanasia to remain firm, also recalled how at one point during her illness she heard her doctors advising her husband that she wouldn’t make it through.

Terror

Describing the moment she said: “I remember a flash of abject terror, then anger. I clearly recall thinking: ‘How dare they say I’m not going to pull through.’

“I don’t ever recall being worried that the doctors would allow me to die. I always had absolute faith that Greg would not let them.”

And she also recalls how her family kept her going by talking to her and telling her to keep fighting.

Love

She says she remebers her children saying to her: “Mummy we love you. Come home soon.”

And while many people may have given up on her at one time, Mrs Pink is now able to walk a few steps and has recovered all of her speech.

And, with the help of her family or a carer, she is able to socialise and visit shops, pubs and restaurants.

Her comments come after Richard Rudd, who currently suffers from ‘locked-in syndrome’, used eye movements to signal to doctors that he wanted to live as they were about to switch off his life support machine.

Overjoyed

Mrs Pink said that she wanted to show Mr Rudd that it “is worth battling on”.

She added: “When the day of my home-coming finally arrived I was overjoyed. AJ, then 12, yelled, ‘Mummy’ and raced down the ramp they’d put in for my wheelchair.

“Georgie, ten, peeped shyly round the door and as Greg wheeled me into the house there were tears of happiness in all our eyes.

Laughter

“Today my life is rich in love and laughter and I revel in my children’s achievements. AJ, now 20, is a mechanical engineer and Georgie, 18, is training in childcare.”

Last month a severely disabled woman urged other disabled people who may feel like ending their lives not to abandon hope for the future.

Marini McNeilly, who also suffers from ‘locked-in syndrome’, is paralysed and can only move her face, head and, very slightly, her fingers.

But in an interview with The Times newspaper she called for other sufferers not to give up hope, saying: “Hope is the last thing you should lose.”

"We will not be silent.
We are your bad conscience.
The White Rose will give you no rest."

192 posted on 08/08/2010 11:45:48 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: wagglebee

Thanks for the ping!


193 posted on 08/09/2010 6:55:33 AM PDT by Alamo-Girl
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To: markomalley; Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; ...
The culture of death has long sought to change the meaning of words to advance their agenda.

Thread by markomalley.

“Get a Life!”

“Get a life!”  An angry shout from a passing care reached our ears.  And again, a little later, came the same cry from another car: “Get a life!”

Irony of ironies.

For this is exactly what we hope to do: get a life (saved).

Now “Get a life!” is certainly not the worst thing that someone hears as they pray in front of a Planned Parenthood or abortion mill.  Much worse remarks are flung at us. Yet I am struck by this irony.  Can it be that they do not realize that these places deal in death?  Some have said we are ‘blocking freedom’. Freedom from what?  Is freedom the same as liberty?  Can we have liberty without life?  Isn’t life the first right of an American?  Is there a difference between freedom and license?  Does anyone know this?

“It’s not your body”, is hollered at us. No, it is not. Nor is it the body of the woman that is being sacrificed on the altar of abortion.  It is not her body either.  She may well, in most cases, have had a choice prior to this moment. But now there should be no “choice” which is a word perverted to mean abortion.

“Reproductive Health” is the innocuous term used to cover up the abomination of abortion.  Some even claim a religious veil on this intrinsic evil with some clergy and others promoting the decimation of peoples.  Or there are the countless others who remain silent or “neutral” in the face of the greatest evil of our age.  They might say, “I am personally opposed, but…” ; they look the other way while millions of unborn children die.

Get a life!  Yes, I have a life. But the child dismembered in the abortion clinic will not “get a life”. The mother will go on doing whatever she is doing but the little soul is returned to God before drawing breath. And the mother’s soul dies.  Get a life!  The life of God in the souls of those who promote, provide, and procure abortion dies.  For them we pray that reconciliation and repentance be found.

Get a life!  God is the Author of life.  It is the devil who deals in death. Demonic is the institution that deals death.  The devil, that “liar and the father of lies…a murderer from the beginning” as Jesus states in the 8th chapter of the Gospel of St. John, is the one behind “reproductive choice”.  Ultimately it must be realized that “we are not contending against flesh and blood, but against the principalities, against the powers, against the world rulers of this present darkness, against the spiritual hosts of wickedness” (Eph 6:12). This is a spiritual battle.  We must call on our spiritual weapons to fight it.  This combat is one done on our knees. The legal system will not bring about the changes needed in hearts and souls. We beg the Author of Life for the graces needed to touch hearts and souls to embrace life, to “get a life”.


194 posted on 08/15/2010 10:18:45 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; angelwings49; ...
The death mongers are dropping all pretenses that they just want "dignity" for the terminally ill.

Thread by me.

Wesley J. Smith: Dutch Culture of Death - Now, Proposed All Comers Suicide Clinics

There is no denying the evidence that euthanasia consciousness leads to a broader culture of death that eventually accepts all comers.  Latest examples from the Netherlands, which probably has the most liberal legalized euthanasia law in the world:

The Dutch pressure group Right to Die NL (NVVE) is investigating the feasibility of setting up a clinic for suicide and euthanasia. It would help people who sincerely wish to die and have nowhere else to turn. The NVVE says the clinic could assist people with chronic psychiatric problems, with Alzheimer’s or dementia and people who feel they have “completed” their life. These categories of people do not meet the requirements of hospices, which specialise in terminal care. Euthanasia is available in most Dutch hospices. The NVVE would like to see the “life’s end” clinic made part of an ordinary hospital or nursing home.

Perhaps they are trying to catch up with Switzerland’s suicide clinics.  Regardless, their logic is impecable. Once killing is considered an acceptable answer to human suffering, nihilism is unleashed and the “what” that causes “suffering” ceases to matter. Culture of death, Wesley?  What culture of death?


195 posted on 08/15/2010 10:22:05 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; angelwings49; ...
CBS can hardly contain their enthusiasm for Zero's death panels.

Thread by me.

The Cost of Dying: End-of-Life Care (CBS Pro-Death Panel Propaganda)

(CBS) This story was originally published on Nov. 22, 2009. It was updated on Aug. 6, 2010.

Every medical study ever conducted has concluded that 100 percent of all Americans will eventually die. This comes as no great surprise, but the amount of money being spent at the very end of people's lives probably will.

Last year, Medicare paid $55 billion just for doctor and hospital bills during the last two months of patients' lives. That's more than the budget for the Department of Homeland Security, or the Department of Education. And it has been estimated that 20 to 30 percent of these medical expenses may have had no meaningful impact. Most of the bills are paid for by the federal government with few or no questions asked.

Now you might think this would have been an obvious thing for Congress to address when it passed health care reform, but as we reported last November in the midst of the debate, what use to be a bipartisan issue has become a politically explosive one - a perfect example of the rising costs that threaten to bankrupt the country and how hard it is to rein them in.

Marcia Klish is either being saved by medical technology or being prevented from dying a natural death.

She is 71 years old and suffering from the complications of colon surgery and a hospital-acquired infection. She has been unconscious in the intensive care unit at Dartmouth-Hitchcock Medical Center in Lebanon, N.H., for the better part of a week.

One of her doctors, Ira Byock, told "60 Minutes" correspondent Steve Kroft it costs up to $10,000 a day to maintain someone in the intensive care unit. Some patients remain here for weeks or even months; one has been there for six months.

"This is the way so many Americans die. Something like 18 to 20 percent of Americans spend their last days in an ICU," Byock told Kroft. "And, you know, it's extremely expensive. It's uncomfortable. Many times they have to be sedated so that they don't reflexively pull out a tube, or sometimes their hands are restrained. This is not the way most people would want to spend their last days of life. And yet this has become almost the medical last rites for people as they die."

Dr. Byock leads a team that treats and counsels patients with advanced illnesses.

He says modern medicine has become so good at keeping the terminally ill alive by treating the complications of underlying disease that the inevitable process of dying has become much harder and is often prolonged unnecessarily.

"Families cannot imagine there could be anything worse than their loved one dying. But in fact, there are things worse. Most generally, it's having someone you love die badly," Byock said.

Asked what he means by "die badly," Byock told Kroft, "Dying suffering. Dying connected to machines. I mean, denial of death at some point becomes a delusion, and we start acting in ways that make no sense whatsoever. And I think that's collectively what we're doing."

A vast majority of Americans say they want to die at home, but 75 percent die in a hospital or a nursing home.

"How do so many people end up in the hospital?" Kroft asked Dr. Elliott Fisher, a researcher at the Dartmouth Institute for Health Policy.

"It's the path of least resistance," Fisher said.

The institute did a detailed analysis of Medicare records for patients in the last two years of their lives. Fisher says it is more efficient for doctors to manage patients who are seriously ill in a hospital situation, and there are other incentives that affect the cost and the care patients receive. Among them: the fact that most doctors get paid based on the number of patients that they see, and most hospitals get paid for the patients they admit.

"The way we set up the system right now, primary care physicians don't have time to spend an hour with you, see how you respond, if they wanted to adjust your medication," Fisher said. "So, the easiest thing for everybody up the stream is to admit you to the hospital. I think 30 percent of hospital stays in the United States are probably unnecessary given what our research looks like."

And once someone is admitted to the hospital, Fisher says, they're likely to be seen by a dozen or more specialists who will conduct all kinds of tests, whether they're absolutely essential or not.

Meredith Snedeker's 85-year-old mother spent her last two months shuttling between a nursing home and community hospital in New Jersey, suffering from advanced heart and liver disease.

Dorothy Glas was a former nurse who had signed a living will expressing her wishes that no extraordinary measures be taken to keep her alive. But that didn't stop a legion of doctors from conducting batteries of tests.

"I can't tell you all the tests they took. But I do know that she saw over 13 specialists," Snedeker told Kroft.

Asked what kind of specialists, Snedeker said, "Neurological, gastroenterologists. She even saw a psychiatrist because they said she was depressed. And she told the psychiatrist, 'Of course, I'm depressed. I'm dying.'"

When we reviewed the medical records, we discovered that there weren't 13 specialists who attended to her mother: there were 25, each of whom billed Medicare separately.

The hospital told 60 Minutes that all the tests were appropriate, and an independent physician said this case was fairly typical.

Among the tests conducted was a pap smear, which is generally only recommended for much younger women, not an octogenarian who was already dying of liver and heart disease.

"In medicine we have turned the laws of supply and demand upside down," Elliot Fisher said. "Supply drives its own demand. If you're running a hospital, you have to keep that hospital full of paying patients. In order to, you know, to meet your payroll. In order to pay off your bonds."

"So, the more M.R.I. machines you have, the more people are gonna get M.R.I. tests?" Kroft asked.

"Absolutely," Fisher said.

"There are people that would argue this is great medicine. You get tested for every conceivable, possible malady you might have," Kroft pointed out.

"Often the best care is saying 'Let's see how you do on this particular treatment for a couple of days. And see if you respond.' Not necessarily doing a lot of tests," Fisher said. "The best care may well be staying home with a trial of a new medication, rather than being admitted to a hospital where you can be exposed to a hospital-acquired infection. We have a system that rewards much, much more care."

In almost every business, cost-conscious customers and consumers help keep prices down. But not with health care. That's because the customers and consumers who are receiving the care aren't the ones paying the bill.

"The perverse incentives that exist in our system are magnified at end of life," David Walker, who used to be the government's former top accountant, told Kroft.

Walker used to be the head of the Government Accountability Office. He now heads the Peter G. Peterson Foundation, which is a strong advocate for reducing government debt. He says that 85 percent of the health care bills are paid by the government or private insurers, not by patients themselves. In fact most patients don't even look at the bills.

"Does that make any sense to have, I mean, most things you buy, the customer has some impact," Kroft remarked.

"We have a system where everybody wants as much as they can get, and they don't understand the true cost of what they're getting. The one thing that could bankrupt America is out of control health care costs. And if we don't get them under control, that's where we're headed," Walker said.

With end-of-life care, there are also delicate cultural and political considerations.

Patients, with their families' support, want to cling to life, and it is often easier to hope for a medical miracle than to discuss how they want to die.

When we met Charlie Haggart, he was 68 years old and suffering from liver and kidney failure. He wanted a double transplant, which would cost about $450,000. But doctors have told him he's currently too weak to be a candidate for the procedure.

At a meeting with Haggart's family and his doctors, Dr. Byock raised the awkward question of what should be done if he got worse and his heart or lungs failed.

Byock told him that resuscitation rarely works on someone in Haggart's condition, and that it could lead to a drawn out death in the ICU.

"Either way you decide, we will honor your choice, and that's the truth," Byock reassured Haggart. "Should we do CPR if your heart were to suddenly stop?"

"Yes," he replied.

"You'd be okay with being in the ICU again?" Byock asked.

"Yes," Haggart said.

"I know it's an awkward conversation," Byock said.

"It beats second place," Haggart joked, laughing.

"You don't think it makes any sense?" Kroft asked the doctor.

"It wouldn't be my choice. It's not what I advise people. At the present time, it's their right to request it. And Medicare pays for it," Byock said.

Haggart died a few months later. A family member told us that his condition deteriorated so much they decided to let him go peacefully.

But when it comes to expensive, hi-tech treatments with some potential to extend life, there are few restrictions.

By law, Medicare cannot reject any treatment based upon cost. It will pay $55,000 for patients with advanced breast cancer to receive the chemotherapy drug Avastin, even though it extends life only an average of a month and a half; it will pay $40,000 for a 93-year-old man with terminal cancer to get a surgically implanted defibrillator if he happens to have heart problems too.

"I think you cannot make these decisions on a case-by-case basis," Byock said. "It would be much easier for us to say 'We simply do not put defibrillators into people in this condition.' Meaning your age, your functional status, the ability to make full benefit of the defibrillator. Now that's going to outrage a lot of people."

"But you think that should happen?" Kroft asked.

"I think at some point it has to happen," Byock said.

"Well, this is a version then of pulling Grandma off the machine?" Kroft asked.

"You know, I have to say, I think that's offensive. I spend my life in the service of affirming life. I really do. To say we're gonna pull Grandma off the machine by not offering her liver transplant or her fourth cardiac bypass surgery or something is really just scurrilous. And it's certainly scurrilous when we have 46 million Americans who are uninsured," Byock said.

"Every other major industrialized nation but the United States has a budget for how much taxpayer funds are allocated to health care, because they've all recognized that you could bankrupt your country without it," David Walker told Kroft.

Asked if he is talking about rationing, Walker said, "Listen, we ration now. We just don't ration rationally. There's no question that there's gonna have to be some form of rationing. Let me be clear: Individuals and employers ought to be able to spend as much money as they want to have things done. But when you're talking about taxpayer resources, there's a limit as to how much resources we have."

But if recent history is any guide, rationing has become the third rail of American politics, even though Elliot Fisher says we already limit health care based on income and whether people have insurance.

After analyzing Medicare records for end-of-life treatment, Fisher is convinced that there is so much waste in the present system that if it were eliminated there would be no need to ration beneficial care to anyone.

Multiple studies have concluded that most patients and their families are not even familiar with end-of-life options and things like living wills, home hospice and pain management.

"The real problem is that many of the patients that are being treated aggressively, if you ask them, they would prefer less aggressive care. They would prefer to be cared for at home. They'd prefer to go to hospice. If they were given a choice. But we don't adequately give them a choice," Fisher said.

"At some point, most doctors know that a patient's not likely to get better," Kroft remarked.

"Absolutely," Fisher agreed. "Sometimes there's a good conversation. Often there's not. You know, patients are left alone to sort of figure it out themselves."

That's what Meredith Snedeker says happened to her mother. Though she received $40,000 worth of care in her last two months of life, not one of her 25 doctors sat down with Dorothy Glas and her family and discussed how she wanted to die.

Marcia Klish might have lingered for quite some time in the intensive care unit at Dartmouth-Hitchcock Medical Center. But Dr. Byock and his team had a number of meetings with her closest friend, Barbara Menchin. She said Klish would not want to be kept alive on machines if there was no meaningful hope of recovery.

It was decided the doctors would not try to resuscitate her if her condition worsened, which it soon did.

"Her heart has just flipped into a rhythm that doesn't allow it to beat effectively," Byock told Menchin.

Klish died a few moments later.

"This is a hard time in human life. But it's just a part of life," Byock said.

"Collectively, as a culture, we really have to acknowledge that we're mortal," he said. "Get over it. And start looking at what a healthy, morally robust way for people to die looks like."

If you are wondering whether the health care reform legislation passed in March addressed any of the end-of-life issues raised in our story, the short answer is no.

The new law is designed to slow the growth of Medicare expenses, and includes a pilot program to reward doctors for the quality of care they provide rather than the quantity. But it also reduces Medicare payments for hospice programs that studies have shown to be very cost efficient.


196 posted on 08/15/2010 10:24:53 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: wagglebee

Thanks for the ping!


197 posted on 08/15/2010 10:25:59 AM PDT by Alamo-Girl
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To: markomalley; Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; ...
Over-the-counter abortions are soon to be a reality.

Thread by markomalley.

FDA approves ella as 5-day-after emergency contraceptive (a/k/a abortion pill)

The Food and Drug Administration approved a controversial new form of emergency contraception Friday that can prevent a pregnancy as many as five days after sex.

The decision to allow the sale of the pill, which will be marketed under the brand name "ella," was welcomed by family-planning proponents as a crucial new option to prevent unwanted pregnancies. But critics condemned the decision, arguing that it was misleading to approve ella as a contraceptive because the drug could also be used to induce an abortion.

(snip)

Supporters and opponents both said the decision marked the clearest evidence of a shift in the influence of political ideology at the FDA. The last time the FDA considered an emergency contraceptive -- making Plan B available without a prescription -- the decision was mired in controversy amid similar concerns voiced by antiabortion activists. After repeated delays, Plan B was approved for sale to women 17 and older without a prescription.

Ella, which was approved in Europe last year and is available in at least 22 countries, was unanimously endorsed by an FDA advisory committee less than two months ago. Women will need a prescription but could keep a supply at home.

"Women's health advocates appreciate that the review process for ella was consistent with standard FDA procedure and based on scientific evidence, not politics," said Kirsten Moore, president of the Reproductive Health Technologies Project. "Approval of ella is further evidence that the FDA is committed to restoring scientific integrity in its decisions."

For their part, critics said the decision reflected the abortion-rights stance of the Obama administration.

(Excerpt) Read more at washingtonpost.com ...


198 posted on 08/15/2010 10:27:58 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: Ohioan from Florida; Goodgirlinred; Miss Behave; cyn; AlwaysFree; amdgmary; angelwings49; ...
Another group in Canada has decided to fight back.

Thread by me.

'Living with dignity' is group's message

MONTREAL - According to surveys, 80 per cent of Quebecers, including doctors, say they are in favour of "dying with dignity," but a new grassroots group is quietly building opposition to the campaign to legalize euthanasia.

"Our biggest concern -and what's at stake here -is that we don't want the practice of euthanasia smuggled into the public health care system under the guise of medical treatment," said Linda Couture, director of Living With Dignity, a nonpartisan, nonreligious group focused on end-of-life issues.

Couture's group has started an online campaign calling on Quebecers to say "no" to euthanasia and assisted suicide.

A separate group of about 50 McGill University professors, including several from faculties of medicine and pharmacy, recently warned that Quebec risks making doctors "society's executioners" by attempting to decriminalize euthanasia and assisted suicide.

Both groups submitted briefs to the National Assembly committee that is to hold public hearings on the issue in September.

"We want to make sure people know what's involved and what their rights are," said Couture, whose group sees itself as the "voice of the silent and vulnerable," including the elderly, the sick and the handicapped.

As soon as its English-language website went live last week (the French site was up in June), signatures on the manifesto jumped to more than 1,000, Couture said.

The group is concerned that the Quebec College of Physicians, the province's medical regulatory body, last year came out in favour of euthanasia as appropriate care under certain circumstances when death is imminent and inevitable.

A debate on end-of-life issues is a good thing but Quebecers are being asked to give their opinions on a topic few know much about, Couture said.

There's a lot of confusion with definition of terms in end-of-life care, Couture added -for example, between palliative sedation and euthanasia.

Few people want to suffer but there's no need to kill the patient to kill the pain, she said.

"We have a lot of unanswered questions: How much will it cost in Quebec? Who will pay for that? Who will practise (euthanasia) and where? How will that change the relationship between doctor and patient?"

Her concerns about terminology echo the Canadian Medical Association Journal position that confusion over euthanasia burdens the end-of-life debate. "Opposing sides use it to further their ideological views: murder vs. mercy; the right to live vs. the right to die with dignity; selfishness vs. compassion," Ken Flegel and Paul Hebert (senior editor and editor-in-chief) wrote in an editorial titled Time to Move on From the Euthanasia Debate.

They called on doctors to promote honest dialogue. For example, adding enough sedation to relieve pain and agitation and improve comfort in a cancer patient may increase the probability of death -but that's not euthanasia.

Those who oppose euthanasia are easy to mobilize, fanned by religion or ideology, said Helene Bolduc of the Association quebecoise pour le droit de mourir dans la dignite.

"It's not that we're fanatic about euthanasia. We want choice for those who are sick and suffering and can't go on anymore."

For information about the Living With Dignity manifesto, go to www.vivredignite.com/en/welcome.html

"We will not be silent.
We are your bad conscience.
The White Rose will give you no rest."

199 posted on 08/15/2010 10:31:06 AM PDT by wagglebee ("A political party cannot be all things to all people." -- Ronald Reagan, 3/1/75)
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To: wagglebee
I recall some posters stating when we discussed Terri's death, "Get over it" as if it were something like spilling coffee or breaking a plate.

A particularly offensive statement - to me - is their twisted use of the phrase "death with dignity."

200 posted on 08/15/2010 10:32:00 AM PDT by Dante3
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