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Monday, April 11, 2016

Euthanasia and the Outlier Defence

In Lynn Smith's reasons for her declaratory orders, it would seem only a few would use assisted suicide or euthanasia per year. To me, that would mean one or two individuals.  It would only be used in exceptional circumstances;  Lynn said a means of last resort. However, I was wrong, it is more like one percent of all deaths. 

This is what I received from the euthanasia prevention people this morning April 16, 2016, in answer to how many are going to use MAD (medically assisted death) in Canada.

Probably less than 1% in the beginning but in 3 - 5 years there will be 4% of deaths.

There were 268,000 deaths in 2014. Therefore, there will be 10,000 or more deaths in 3 - 5 years and probably 20,000 deaths in 2025.

The medical vultures are already going in for the $kill. The first death in Canada per Carter  was done by Dr. Ellen Wiebe, she has already started a clinic, to much media applause, in Vancouver, being a good death clinic.

And since your family physician, if you are lucky enough to have one, will not want to get involved in any of this, he will refer you to Dr. Ellen, a stranger. And you will die in a sterile clinic. I wonder who funded her clinic.

There is no law yet and already there has been four individuals that have used the exemption clause: two died in BC and another approved in BC and another approved in Manitoba.  Three have died in Quebec under its own law to hasten death. There could be more but the white wall of silence prevents disclosure. The public might never know of  further deaths unless the Death with Dignity people leak out the information to the media as a good news story.

And who is paying the $10,000 or more to do the court applications and the costs of travel to the good death clinic in Vancouver to make these deaths a good news story.  Was it on the condition that the participants participate. When Bill C-14 passes, hopefully, it does not, there will be no legal fees as a doctor will make the order, not a judge.  This also means there will be no transparency.  No oversight; just the truth of health care professionals.

Bill C-14 has to be defeated.  Contact your MLA and MP and say you want to veto Bill C-14 and invoke the "notwithstanding clause". We have to study this further to make sure the safeguards are safe and cannot be circumvented.  Collateral deaths are not allowed: we are not at war.

We as a society did not contract for lethal injection at the HEMLOCK AID CLINIC.  Dr. Ellen could have come up with a less vomitoid name.  Hemlock is dark... very very dark.  Does anyone know how the very very very rich die, the 1%,  I have read that it is the 1% who want the rest of us to die as soon as we are not productive.





Friday, April 8, 2016

Non-ambivalent

I do not like the fact that the word non-ambivalent was taken out from Lynn Smith's declaratory order in 2012, see 2015 Appeal.

Thursday, April 7, 2016

You will never forget/forgive the doctor who euthanasized your loved one, with or without consent

April 4, 2016
Prime Minister Justin Trudeau
Office of the Prime Minister
80 Wellington Street
Ottawa, ON K1A 0A2
To the Honourable Prime Minister Trudeau,
I am writing to you out of deep concern for the legislation that will soon be drafted regarding physician assisted suicide. I am so concerned, that I produced videos on the websites, DearGodLetter.ca and CherDieuLettre.ca, in the hope that more Canadians would be informed about the potential ramifications of such legislation.
As a medical doctor, there are many arguments I could provide detailing why physician assisted suicide is wrong for Canada. But the one argument that many have overlooked is the very real likelihood that physician assisted suicide in Canada would actually lead to more pain and suffering in Canada—not less.
Let me explain:
As a pain specialist I have evaluated hundreds of car accident victims over the past several years.  Interestingly, the patient suffering chronic pain from injuries sustained in the crash is almost always the victim—rarely the individual(s) responsible for the crash. Many falsely believe these patients are just trying to scam the system. While this might be the case in rare circumstances, almost always these victims have legitimate chronic pain.
Research has demonstrated that when the mind is clouded by negative emotions, such as anger, hate, bitterness, or depression, the body is unable to properly “turn off” pain signals arising from lower in the body. Car accident victims are often angry at the individual(s) who hit them, and frequently develop low mood and/or anxiety. All these negative emotions play a role in the development of chronic pain by way of something pain specialists call, “Central sensitization.” Peripheral sensitization and maladaptive central nervous system (i.e. brain) neuronal plasticity are also factors in the genesis of chronic pain. 
How does this relate to physician assisted suicide? 
If the recommendations provided by the Special Joint Committee on Physician-Assisted Dying become law, there will be many teenagers, parents, and grandparents killed against the will of their family members (especially those suffering from depression). Prime Minister Trudeau, it won’t be long and your children will be teenagers. You wouldn’t want someone to kill your teenagers against your will.  Why then would you want to kill other teenagers against the will of their parents?

A family can eventually learn to forgive a member who rashly commits suicide on their own. However, it will be extremely hard—if not impossible—for Canadian families to forgive the doctors and politicians responsible for their loved one’s death. The same rage that the Goldman’s displayed against O. J. Simpson will be the same anger directed at you and many others by Canadian families. These angry family members will be at significantly greater risk of developing depression and anxiety, with a high likelihood of developing chronic pain from even minor injuries—and sometimes no injury at all. For every one person you kill against the will of the family, you run a very high risk of triggering a lifetime of mental and/or physical illness/pain in at least one family member—and possibly the entire family.
Furthermore, there are over 5,000 physicians across Canada in the Coalition for HealthCARE and Conscience, committed to protecting conscience rights for health practitioners and facilities. Many will refuse to kill their patients, and refuse to refer patients to be killed. For every doctor’s license you consequently take away, you will erase on average at least 2,000 patient encounters per doctor per year. Then there’s the doctors who will just quietly leave the country, and those who will refuse to move to Canada because of the hostile environment where doctors are forced to work against their consciences. Then add to this the number of healthcare professionals who will drop out of palliative care and Geriatrics for fear of losing their licenses. Do the math and the number of Canadians affected are staggering.
Will all this not result in even more pain and suffering for Canadians in the end?
Yes, there will always be individuals who want to kill themselves at the first diagnosis of a chronic disease. And there will always be arguments saying that not everyone has equal access to quality palliative care across Canada where adequate pain control is very often achieved. But what kind of country would rather kill its citizens than provide the necessary care and compassion they deserve?
Will the Liberal Party be popular with Canadians 1 year, 2 years, or 3 years from now? 
Will the Liberal Party be popular with the Person who created the teenagers, parents, and grandparents that you will kill? 
Thank you very much for your kind attention to this letter.
Sincerely,
Brad Burke, MD, FRCPC
Physical Medicine & Rehabilitation
Cc The Honourable Jody Wilson-Raybould, Minister of Justice







Slippery Slope is happening


OPINIONEND OF LIFEThu May 21, 2015 - 4:38 pm EST

Dutch court acquits man who euthanized his mother after doctor refused

May 21, 2015 (LifeSiteNews.com) -- A Dutch appeals court acquitted a 74-year-old man earlier this month of the murder of his mother in 2008, because he acted in an “emergency situation”: the woman wanted euthanasia and had not obtained it from her family doctor.
The decision is a surprising one, even in the Netherlands, and will probably be followed by an appeal from the public prosecutor, who has already published a communiqué reminding the public that euthanasia and assisted suicide “are and remain, in the eyes of the prosecutor, exclusively to be performed by a doctor.”
As it stands, the decision marks a new step down the slippery slope of euthanasia. The decision justifies an act of euthanasia contrary to the letter of the law on the grounds that the accused, Albert Heringa, was careful to act in compliance with the law’s provisions.
Albert Heringa acted in accordance with his conscience of his own duty and he was right to do so, ruled the Arnhem-Leeuwarden appeals court, because his sense of duty “justly” carried more weight than the legal prohibition of the act, which in theory can only be decriminalized when performed by a medical doctor under strict conditions.
The accused said he was “very happy” about the decision. The Netherlands Right to Die Society (NVVE) hailed it as “a step in the direction we want to follow.” “Many people who consider their life complete wish to be helped by loved ones,” said its spokeswoman, Fiona Zonneveld.
The judges did not take into account the fact that Albert Heringa’s mother, “Moek,” was deemed ineligible for euthanasia by her doctor.
In 2008, Moek was 99. She had no grave illness; she was just old and blind and did not feel like living any longer, calling her suffering “unbearable” and “without hope of improvement.” When her doctor refused euthanasia on those grounds, she turned to her son who decided to help his mother die.
He was later to explain that his mother started hoarding her medication in order to kill herself through an overdose. The pills she was taking would not have been able to bring about her death, he argued, but would have made her health much worse. This was confirmed during the subsequent judicial enquiry.
Heringa decided to go to work “transparently,” filming his every gesture in view of the killing of his mother. He used an overdose of his own malaria pills together with sleeping pills and anti-emetics to poison her. The films were later used to illustrate a documentary on “Moek’s last wish,” which was aired in 2010 on Dutch TV. The appeals court judges took this “transparency” into account in their decision to acquit him.
The public prosecution was not so lax. Despite the “rectitude” of Heringa’s intention, it accused the man of not having acted in compliance with the law. In 2013, he was judged guilty but exempted from punishment. The prosecution appealed that decision, demanding a three months suspended prison sentence in order to underscore the illegality of his actions. But the Arnhem-Leeuwarden appeals court went even further than the first judges in exonerating him completely.
They invoked the euthanasia law, which decriminalizes euthanasia when no other “reasonable solution” is available to alleviate a patient’s suffering and thus avoid euthanasia, but in this case they equated the potential “reasonable solution” with the ability to find a doctor who would be willing to perform the act, as if euthanasia were a patient right. Heringa could not find one, therefore he was justified in taking the law in his own hands, the judgment says in substance.
This marks a double revolution. Firstly, the court overlooked the legal requirement that a doctor should perform euthanasia, and no one else. Secondly, it justified euthanasia on a woman who was simply “tired of living,” a situation for which the euthanasia law definitely does not provide.
But this is just another element of the Pandora’s box that was opened when the Netherlands legalized euthanasia in 2002. Increasingly, regional control commissions, which verify all declared acts of euthanasia retrospectively, have cleared “mercy-killings” of elderly people who had multiple complaints but no single life-threatening disease. “Intolerable suffering” is being interpreted more and more widely. In Heringa’s case, it is simply his mother’s plea for euthanasia that justified the act in the eyes of the court.
The court even went so far as to say that Heringa would have had to live with a “sense of guilt until the end of his life” had he not taken measures to end his mother’s life.
In 2011, the Dutch medical association KNMG changed its position on “intolerable suffering,” declaring that “unbearable and hopeless” suffering can result from other causes than physical illness. Also, the End of Life Clinic founded in 2012 caters to euthanasia requests that have been refused by patients’ family doctors on conscientious or medical grounds. Would Heringa have found a doctor willing to perform euthanasia on his mother in this new situation?
Whatever the answer to that question – and no one will ever know – the fact of his acquittal is a definite sign that euthanasia is being treated more and more as a right and an acceptable option in the Netherlands. It is also good news for unscrupulous family members who might find it expedient to push their relatives towards the grave.
.
 


Sunday, April 3, 2016

Safeguards

Sunday, April 3, 2016 (updated April 27, 2016)
 
  
I have not been doing much on my blog. I have been in severe bereavement for the longest time.

I am seeing the parallel between DNR and Euthanasia.   If Bill C-14 becomes law leaving the safeguards in the hands of the medical regulators it will cause collateral damage (deaths). Canada does not allow capital punishment and yet when it comes to euthanasia the courts have decided it is okay to make mistakes that will result in collateral deaths. We are not at war. If a DNR can be unauthorized, then it can be argued that Euthanasia can also be unauthorized. All safeguards so far mentioned in the proposed Bill can be circumvented.

No one believes this but it is true.  If a patient wants medical aid in dying, neither family nor best friend has to be consulted. It could be devastating not knowing for sure. The family might never know as the death certificate will say a natural death . All assessments for such deaths should be made public, so anyone can voice his concern as to possible coercion.

We have to demand that the government invoke the notwithstanding clause to gain time so safeguards are designed to be true safeguards.

I am of the view that consent should be videotaped as it is done in Switzerland.  Not once, but during the whole process.

Was Brittany Maynard forced to end her life on November 1 2014.  She had changed her mind on October 31 2014.  If her husband truly loved her, he would have stopped it as she was ambivalent.

She was locked in the process and could not change her mind. And so was Gloria Taylor.

The word "non-ambivalent" is the word that is missing in the Supreme Court of Canada’s Declaratory Order [para. 127] in 2015. Justice Smith’s Declaratory Orders in 2012 [para. 1393] contained it. Why was it taken out?  Ambivalent means “not sure.”  
 

-------------------------------------------------------------------------------------------------------------------------
 

I was just told from an insider that letters to members of parliament are read if not by the member then by his staff.  Just say something from your heart and you will be heard and it will get to the member of parliament. It is important.It will be archived forever.

Send an email to Prime Minister Trudeau : justin.trudeau@parl.gc.ca; and/or write Justin Trudeau, House of Commons, Ottawa, Canada, K1A 0A6.(postage is free).

Send an email or a letter to your Member of Parliament: House of Commons, Ottawa, Ontario, K1A 0A6 (postage is free). Or go see him in his local office.


Send an email to the Senators c/o Denise Batters, denise.batters@sen.parl.gc.ca; and/or send an email or write to a senator who you might know at The Senate of Canada, Ottawa, Ontario, K1A OA6 (postage is free).



Send a letter to the media.  Just do something. We must invoke the notwithstanding clause.
Copy this and give it to your neighbours.

Audrey Jane Laferriere,
5976 Cambie Street,
Vancouver, B.C.
V5Z 4X3     604-321-2276
blog: http://voiceofgoneballistic.blogspot.com, to read my story.

Back to Reality as I know it.

I have not been doing much on the blog about Randy because I could not.  But I have decided to start again.  I am seventy-one years old and do not have much life left and I must focus and what is important.  And what is important is Randy's story.  The medical system is broken.  The medical system is for patients and not doctors.

Thursday, March 17, 2016

CBS and assisted suicide.

http://www.cbsnews.com/news/60-minutes-aid-in-dying-lapook/

The above is a must see link.

The following is some insight by Nancy Valko to the above link.


CBS’s “60 Minutes” and the Selling of Physician-assisted Suicide

In the March 13, 2016 TV “60 Minutes” segment titled “Aid in Dying” (retitled “Should the terminally ill control how they die?” in the online transcript, the vaunted investigative news show crossed the line from presenting facts to enthusiastic advocacy.
The stage was set when medical correspondent Dr. John LaPook, an internist and son-in-law of liberal activist Norman Lear, opened the segment by stating:
This is not euthanasia, when a doctor gives a patient a lethal injection. That’s illegal in all 50 states. Aid-in-dying, or what opponents call “assisted suicide” and supporters call “death with dignity,” relies on people taking the medication themselves. Oregon became the first state to legalize it 18 years ago, but because a nurse or doctor is rarely present, it’s remained mostly a private affair, practiced behind closed doors. We wanted to hear from patients and family members who’ve experienced it and are fighting to make it legal nationwide. (Emphasis added.)
If you go to the link for the transcript, you will also see “related videos” with segment extras not included on the TV show.
One titled “ethical concerns” is an interview with Dr. Katrina Hedberg, state epidemiologist of the Oregon Public Health Division, to discuss “ethical concerns raised by her state sanctioning aid-in-dying”. Not surprisingly, Dr. Hedberg strenuously denies that assisted suicide is a danger for the “disenfranchised” or for medical economic or family burden reasons. Instead, she says “the opposite has happened” despite cases like Barbara Wagner’s.
In the segment extra “How does the medicine work?”, the assisted suicide doctor explains that the medicine simply just “shuts off the brain” starting “at the top” where consciousness is and then goes to “the bottom” of the brain where heartbeat and breathing occur. Not a very accurate or scientific explanation but designed to reassure the public.
In the televised segment, there was only a very short interview with Dr. William Toffler, National Director of Physicians for Compassionate Care  but only identified by Dr. LaPook as a doctor “who’s taken care of terminally ill patients for 40 years” and whose wife died of cancer in comfort and without physician-assisted suicide. Dr. Toffler’s practical and ethical concerns were ignored or dismissed by Dr. LaPook.
The rest of the segment involved interviews with people fighting for physician-assisted suicide for themselves or a relative and an assisted suicide doctor. The usual lethal overdose drug and the method for using it for suicide were described in detail.
A major portion of the segment were interviews with Brittany Maynard’s husband and Dr. Eric Walsh, the Oregon physician who prescribed the overdose for the 29 year old woman with a gliobastoma brain tumor whose countdown to assisted suicide became a media sensation in October, 2014.  Brittany’s suicide was described by her husband as Brittany just going to sleep and slowly stopping to breathe.  Not surprisingly, it was after Brittany’s suicide that most mainstream media then changed the usual term “physician-assisted suicide” to softer terms like “aid in dying” or “physician-assisted death”.
Ironically, 60 Minutes aired a segment on March 29, 2015-just 5 months after Brittany Maynard took her lethal overdose-titled “Killing Cancer  The segment followed patients in a year long clinical trial who had gliobastoma brain cancers like Brittany’s. Many of these patients saw their cancers disappear after being treated with a reengineered polio virus. This was touted as a great breakthrough by “60 Minutes” but went unmentioned in this segment.
Another interview was with a man in hospice who was being seen by Dr. Walsh but, as the segment stated:
Though usually extremely effective at keeping people comfortable, in rare instances, standard hospice care doesn’t work well enough. In those cases, Dr. Walsh says, one option is something called palliative sedation.
Dr. Eric Walsh: When the physician decides that suffering is intolerable, the physician prescribes a medication which puts the patient in a coma…The nurse administers it. It’s given until the person is asleep. The person sleeps for three days, five days. I’ve had someone live 10 days, still excreting, still breathing, with the family at the bedside wondering, “When is this going to end?”
When an assisted suicide doctor himself “decides that suffering is intolerable”, prescribes a intravenous continuous medication to be administered by a nurse to speed a patient’s death, how is that NOT euthanasia?
Sadly, the last interview with a woman dying of colon cancer illustrates the dangers of assisted suicide for so-called “altruistic” reasons that would also appeal to many non-terminally ill but debilitated or suicidal people:
Dr. Jon LaPook: And it sounds like from what you’re saying your decision to
perhaps take the medication will be a final act—
Elizabeth Wallner: Absolutely.
Dr. Jon LaPook: –of protecting your son.
Elizabeth Wallner: Absolutely. I just want him to remember me laughing and, you know, giving him a hard time, and telling him to brush his teeth, and knowing that I would– I would, you know, walk across the sun for him. (Emphasis added)
The public deserves a better and more comprehensive discussion about physician-assisted suicide. Such discussions have been occurring in state legislatures where physician-assisted suicide groups like Compassion and Choices relentlessly push for legalization and medical, disability, pro-life and other groups testify to the real facts and dangers.
There must be something to this opposition since so far this year 8 states have rejected physician-assisted suicide bills.




Saturday, March 5, 2016

www.alexschadenberg.blogspot.ca

There are daily reports about euthanasia on the blog www.alexschadenberg.blogspot.ca, go to it. This is important so you can understand all the issues.  At my age, replicating this information limits my life experience.

My fear is about the dangers of euthanasia evidenced by my experience with DNRs without full informed consent or any consent. Randy would have died if I did not intervene on November 18 2013 and call 911 as GPC (VCH) would not because Dr. Dunn had a DNR on Randy. It was Randy's DNR not Dr. Dunn's. Dr. Dunn was told earlier (7:00 pm) to take off the DNR and he said he would consider it after he returned from Prince George.  So much for CHANGING YOUR MIND and who owns your body.  DNRs are no different than euthanasia, in reality, will you be able to change your mind? Each year DNRs cause more deaths than euthanasia ever will. A DNR tells staff not to give aggressive treatment to a patient.

Euthanasia is quick and painless while a DNR can dictate a death that can be long, very painful and terrifying.  A DNR is a red flag saying to staff not to treat you aggressively. Why would anyone want to look forward to a heart attack or torture by waterboard (unable to breathe) when euthanasia is much more inviting.

And guess what, you the consumer are blamed as you are the ultimate decision maker.

Randys anniversary of his death is rapidly approaching.  Every where I go and I see him.  I am not crying as  much but the pain is so regretful. I could have done more I keep telling myself.  .  But the circumstances of his death is causing me flashbacks and I cannot do very much. If I was not banned from seeing him by VCH.  VCH caused Randy and me irreparable and unforgivable pain.

Randy had a green burial under trees and a mountain cliff.  The day I buried him was cold but beautiful.  The trip home on the ferry from Victoria was fitting as it was a cold but a beautiful day.
I want to demonstrate downtown with my sign and little Owen, but I cannot.  I feel paralysed by grief.  I only want to stay home.  Perhaps, when spring comes, I will feel better.  The sign says:  If you cannot trust doctors to do a DNR, how can you trust doctors to do euthanasia.






Thursday, March 3, 2016

Andrew Coyne: Society has lost its way

February 29, 2016

Canada is making suicide a public service. Have we lost our way as a society?

By Andrew Coyne

Assisted suicide has gone, in the space of a year, from a crime, to something to be tolerated in exceptional circumstances, to a public service

When the Supreme Court, overturning Section 241(b) of the Criminal Code, several votes of the House of Commons and its own previous ruling, legalized assisted suicide last year, it did so on a particular understanding of to whom and under what circumstances the new regime would apply.
It would permit a physician, normally obliged by the code of his profession to save life, to take a life instead, at the request of 1, an adult who is 2, mentally competent and 3, clearly consents, in cases of 4, a "grievous and irremediable" medical condition that imposes 5, suffering that is "intolerable to the individual."
On its own, this made it legal to assist in suicide in a much broader set of circumstances than had previously been contemplated. The emphasis in all previous discussion - the basis of the apparent widespread public support for legalization - had been on persons who suffered, not just from an irremediable, but a terminal condition, such that suicide would merely hasten the inevitable; who were in acute physical pain, rather than enduring subjectively "intolerable" suffering, which the court was clear could be physical or psychological; and who were, or feared they might become, physically unable to kill themselves on their own.
Assisted suicide was presented, paradoxically, as a way of extending life
Assisted suicide was thus presented, paradoxically, as a way of extending life, rather than shortening it, sparing patients from what the court called the "cruel choice" to which they would otherwise be subject: kill themselves while they were able, at the cost perhaps of several years of life, rather than endure the pain and indignity that might come with waiting for nature to take its course. Yet the court's decision did not depend upon this dilemma being present. It was enough that a competent adult was suffering, intolerably and irremediably, and wanted help killing himself. The necessity of the assistance was not at issue.
So the court not only opened the door to assisted suicide, but opened it a little wider than it had been asked to. Nonetheless, it remained confident that the door would open no further. Indeed, the ruling arguably depended on it. The Crown's case for retaining the prohibition, after all, had rested on the concern that the logic of assisted suicide would not permit it to be limited to the sort of narrow circumstances the court had in mind. Expert testimony was called on the experience in Belgium and other countries, where eligibility for assisted suicide has been extended to children, the mentally incompetent, and others.
The court found this sort of "anecdotal" evidence unpersuasive. These countries, it said, had a very different "medico-legal culture" than ours. In Canada, the "risks" of legalized killing could be limited "through a carefully designed and monitored system of safeguards."
That was a year ago. The court's ruling has not yet taken effect, and already we have the report of an all-party joint committee on "physician-assisted dying" recommending legislation that would go far beyond what the court prescribed.
To be sure, the report builds on the court's foundations. It would apply to both terminal and non-terminal conditions, physical and psychological, debilitating or otherwise. But its definition of a competent adult would not exclude people with mental illnesses - which is to say virtually all current suicides - nor people who had previously expressed the wish to be killed in the event they should later become mentally incompetent. Moreover, after a three-year trial period, it recommends extending the practice to what it calls "mature minors," a term left undefined.
Not only would "assisted dying" be legalized, under the committee's recommendation, it would be publicly funded.
Fred Dufour/Getty Images An all-party committee on assisted dying is recommending that it be publicly funded.
Not only would doctors be permitted to kill their patients on request, they would be obliged to, or provide "effective referral" to others who will. And while the committee suggests that those seeking assistance in killing themselves should be required to get two doctors to certify they met the criteria, the criteria are so open-ended it is hard to see in what circumstances they could say no. In any event: the consent of two doctors? Where have we heard that before? What if none are available? How long could it be before the Supreme Court rules on the inequity of denying "access" on these grounds?
Indeed, no sooner had the report been released than advocates were pushing to expand its bounds. For example, should eligibility be restricted to "mature" minors? Could it, in law or conscience? As Dr. Derrick Smith, chair of the physicians' advisory council of Dying with Dignity Canada, told the CBC, "obviously a five-year-old is not going to be able to give consent for something like that, but should we allow a substitute decision maker like the parent to say, 'Johnny's had enough suffering. I think it's time that we assist him to terminate the suffering.' "
Well, of course. Once you have normalized suicide, from a tragedy we should seek to prevent to a release from suffering we should seek to assist, it is logically incoherent - indeed, it is morally intolerable - to restrict its benefits to some, while condemning others to suffer interminably, merely on the grounds that they are incapable of giving consent. So it is that assisted suicide has gone, in the space of a year, from a crime, to something to be tolerated in exceptional circumstances, to a public service. Perhaps you see this as progress. But I cannot help feeling that a society that can contemplate putting children to death has somehow lost its way.

Tuesday, March 1, 2016

1.7% of doctors

How can we trust doctors when they refused to fill out a survey on medical assisted death.  Only 1.7% of doctors in Canada filled out the Canadian Medical Association's survey.  Every single doctor should have filled out the survey with comments. Maybe then they would know what is going on.  I spoke to a doctor three weeks ago and he did not even know that euthanasia was on the table. 

Earlier this year, the CMA invited its 80,000 members to participate in an online survey about assisted death. Of the 1,407 members who responded, 29 per cent said they would consider providing assisted dying, while 63 per cent said they would not, the CMA reported.
With a report by CTV’s medical specialist Avis Favaro

Friday, February 26, 2016

EPC Response to Recommendations for Euthanasia

Canadian government Assisted Dying recommendations will not protect people.

For Immediate Release - February 25, 2016

The Euthanasia Prevention Coalition (EPC) is a national organization representing groups and individuals representing medical, personal and disability perspectives since 1999 with the purpose of protecting people from euthanasia and assisted suicide.

Research proves that the misuse of Assisted Dying in jurisdictions where it is legal has resulted in deaths without an explicit request, assisted deaths of people with a wrong diagnosis, the under reporting of assisted deaths, and assisted death of people with treatable psychiatric conditions including depression.

EPC urges the federal government to:
  • devise guidelines with clear oversight that cannot be abused.
  • reject the concept that assisted dying is a form of medical treatment.
  • reject assisted death for people who are incompetent to make decisions.
  • devise clear guidelines to ensure that people, who are experiencing a vulnerable time of their life, will not die an assisted death, based on situational depression.
  • protect the conscience rights of healthcare institutions.
  • protect the conscience rights of medical professionals who reject that killing patients is an acceptable medical act. Medical professionals must not be forced, in any manner to participate in killing their patients.
  • increase support for palliative care, home care for people with disabilities, mental health services and suicide prevention.
For interviews contact:

Alex Schadenberg (London ON) EPC Executive Director, (519) 851-1434 (cell) info@epcc.ca

Hugh Scher (Toronto ON) EPC Legal Counsel, (416) 816-6115 (cell) hugh@sdlaw.ca

Amy Hasbrouck (Montreal QC) Toujours Vivant Not Dead Yet, (450) 921-3057, tigrlily61@gmail.com

Dr. Will Johnston (Vancouver BC) EPC – BC Chair, (604) 220-2042.

Euthanasia Prevention Coalition, 1-877-439-3348, info@epcc.ca, www.epcc.ca

Saturday, February 20, 2016

Flashbacks

I haven't been posting to this blog as I have not been feeling well.  Mostly attributable to flashbacks of how Randy died and how Vancouver Coastal Health treated us.  VCH knew Randy was dying and yet it banned me from seeing him before he died based on false information.  I was a victim of its psychological abuse.  It was designed. 

Thursday, February 11, 2016

Canada's euthanasia lobby pushes euthanasia for people who cannot consent.


Sounds familiar.  A senior gives power of attorney to her niece and the next day the niece finds a doctor who certifies the senior is incapable and the senior loses all her legal rights.  She becomes a non-person. This is even better, the senior is euthanized.

Will a NHL hockey player who has a concussion and cannot remember your name will he be classified as dementia and his consent will not be necessary to be euthanized..

 Call you MP (Member of Parliament and MLA) and say you are opposed to euthanasia except with court oversight. Busy doctors and social workers are not to be trusted. Doctors put DNRs on patients without consent so it would be equally easy for a doctor to put an euthanasia Order on a patient as well.  

 Like in Belgium, forget about hospice and palliative care, Belgium got euthanasia. 

Justice Lynn Smith said that it was okay based on questionable statistics provided to the Court that it is alright for a few people to be wrongly euthanized as their lives could be written off as collateral damage.`


Canada's euthanasia lobby pushes euthanasia for people who cannot consent.

By Alex Schadenberg
Executive Director - Euthanasia Prevention Coalition


A recent poll commissioned by the euthanasia lobby was designed to pressure Canada's parliament to approve euthanasia for incompetent people with advanced dementia.

The Supreme Court February 2015 Carter decision permitted euthanasia for:

“a competent adult person who
(1) clearly consents to the termination of life and
(2) has a grievous and irremediable medical condition (including an illness, disease or disability) that causes enduring suffering that is intolerable to the individual in the circumstances of his or her condition.”
The Supreme Court decision stated that the person must clearly consent, but the euthanasia lobby is not satisfied with limiting euthanasia to consenting adults so they designed a poll to suggest that 80 per cent of Canadians agree that individuals with a terminal medical condition like dementia should be permitted to consent to assisted death in advance. 

According to a recent study from Belgium, where assisted death was legalized for competent adults in 2002, there were more than 1000 assisted deaths without explicit request in 2013.

The euthanasia lobby wants you to believe that they only support euthanasia for people who are competent, terminally ill and suffering, but in reality they also want euthanasia without an explicit consent for incompetent people. 

If this is about "freedom of choice," as the euthanasia lobby claims, how can it be assured that the person with dementia is freely choosing to be killed? 

The euthanasia lobby is not satisfied with the Supreme Court decision to limit killing to people who clearly consent, they also want death for people who they define as better off dead and who cannot consent. Another soon to be constitutional issue: fFor equality under the Constitution anyone can ask to be dead without even being ill:  everyone is entitled to a safe and painless death.
CARP wants euthanasia on demand (searchh Susan Eng)
The Humanists want euthanasia on demand.
Dying with Dignity want euthanasia on demand.



 

Tuesday, February 9, 2016

Alex Schadenberg, Euthanasia Prevention Coalition: Native leader: Assisted suicide is not part of our...

Alex Schadenberg, Euthanasia Prevention Coalition: Native leader: Assisted suicide is not part of our...: By Alex Schadenberg Executive Director - Euthanasia Prevention Coalition Francois Paulette Francois Paulette, the Dene Nation Elders ...

Monday, February 8, 2016

Native leader: Assisted suicide is not part of our system of life.

By Alex Schadenberg
Executive Director - Euthanasia Prevention Coalition

Francois Paulette
Francois Paulette, the Dene Nation Elders Council Chair told Rachel Zeiniker from CBC news that:
"Traditionally, that (assusted death) is not part of our system of life," 
"We have a very high standard of looking after our people that are sick."
Paulette said that the indigenous perspective has been left out of the assisted death debate. He told CBC:
I think the leadership really needs to get on top of this and find a way for indigenous people to have a seat at the table so legislation respects and honours the UN Declaration of Indigenous People's Rights and treaty rights. 
I hope either the federal or territorial government provides assistance and money to bring leaders together.
Paulette hopes that the guidelines will be "respectful of traditional values and principles." 

The concerns of the native community, the disability community and minority communities have so far been ignored in the quest to impose euthanasia and assisted suicide upon Canadia.
The N.W.T. government has begun to solicit opinions from people in the territory. It has sent letters to stakeholders, and is accepting public feedback on its website until Monday, Feb. 15.

Alex Schadenberg, Euthanasia Prevention Coalition: Assisted Death: I never thought this day would com...

Alex Schadenberg, Euthanasia Prevention Coalition: Assisted Death: I never thought this day would com...: This article was published as a CMAJ blog on Feb 3, 2016 and republished with permission. Diane Kelsall By Diane Kelsall,  Deput...

Sunday, February 7, 2016

Simon’s Law: “To Be Heard”

Simon’s Law: “To Be Heard”

Read this.  Baby's death hastened because of an unauthorized DNR.  Illegal DNRs are very common in my experience in British Columbia.  DNRs (MOSTs) do not require the signature of the patient.  How easy it is for a doctor for whatever reason, perhaps, in the best interest of the patient, to put a DNR on a patient.  No oversight safeguard is necessary;  just the word of a doctor. Doctors justify illegal DNRs since a patient is going to die anyways.

Friday, January 29, 2016

Alex Schadenberg, Euthanasia Prevention Coalition: CARP is now a pro-euthanasia advocacy group.

CARP speaks for 300,000 plus members without consulting each member on this most important issue. Susan Eng from CARP said CARP wants euthanasia on demand.  According to the Carter decison, it is up to the patient to ask for euthanasia if the patient is suffering or thinks he is suffering.   It is not up to a doctor.

Alex Schadenberg, Euthanasia Prevention Coalition: CARP is now a pro-euthanasia advocacy group.:


Thursday, January 28, 2016

Euthanasia on Demand v. Free Trade (no regulations)

From Globe and Mail January 27 2016 CARP exec says she was fired over neutral approach to assisted dying.

Slippery Slope is already here.

CARP speaks for 300,000 Canadians, really (did 300,000 members vote on this issue)


Susan Eng was told on Tuesday that she was no longer needed as the executive vice-president of advocacy at CARP Canada. She then learned on Wednesday that she was being replaced by Wanda Morris, the head of Dying with Dignity Canada, which advocates for access to physician-assisted dying and against unnecessary barriers when safeguards are being imposed to protect the vulnerable.

The dismissal by Mr. Znaimer occurred as the federal government is preparing to change the law around assisted dying. Parliamentary hearings have already begun on the matter. "The only reason he fired me was so that they can put out an official position for CARP saying that they want to insist on assisted dying on demand," said Ms. Eng, a Toronto lawyer and former chair of the city's police services board.



Wednesday, January 27, 2016

the Noval case and how the medical system and his family hastened his death

The following article is from: http://www.courthousenews.com/2012/02/06/43641.htm
A copy of the actual filing may be viewed here:
http://www.courthousenews.com/2012/02/06/Kaiser.pdf
and at
http://legalstuff.kaiserpapers.org/pdfs/victorino-noval.pdf

         
Grim Complaint Against Kaiser Hospital - Victorino Noval Kaiser victim and Hector A. Noval his Personal Representative
By WILLIAM DOTINGA
RIVERSIDE, Calif. (CN) -

     A son claims a Kaiser hospital ignored his wealthy father's power of attorney so the plaintiff's greedy siblings could collect multimillion-dollar inheritances.

     Hector Noval sued Kaiser Foundation Hospitals and affiliates, a doctor and two social workers on behalf of his father, Victorino Noval, who died in May 2010 after a "terminal extubation." Noval says his father had been involuntarily admitted to Kaiser's intensive care unit for pneumonia on April 28, 2010, while suffering from early-stage of Parkinson's and chronic obstructive pulmonary disease.

     Before being hospitalized, Noval, 78, "lived in his own home, drove his own vehicle, and performed his own activities of daily living," according to the Superior Court complaint. "He was worth $60 million and had annual income of $3 million. He made investments and controlled his finances. He suffered from no neurological deficiencies. He did not have dementia or diminished capacity, He functioned independent of others. He was in no way nearing death, an irreversible coma, or a persistent vegetative state. Upon hospitalization, he only required temporary oxygen support while the pneumonia infection in his lungs cleared and he regained his strength. His condition was no more serious than that."

     However, Hector Noval says, two of his sisters, Lourdes Frost and Tania Noval, told Kaiser doctors, "falsely and fraudulently," that their father had "'advanced' Parkinson's disease" and had been declining for 6 months before his hospitalization.

     He claims that his siblings' false and fraudulent statements included "that he 'would not want to be hooked to a machine like a ventilator,' even if just temporarily, and that 'he had expressed this to [his] daughter both when he is well, and when not so well.' Frost and Noval told defendants that decedent 'would not [have] wanted to be resuscitated if he is to pass away ... he would want to die peacefully if that was to happen.' Each of these statements were untrue. Defendants performed no diligence into their veracity and accepted them as true."

     Neither sister is named as a defendant.

     Plaintiff Noval claims that on the day his father was admitted, April 28, 2010, he "expressed his desire that decedent be transported to Cedar Sinai in Beverly Hills, California for treatment and that he not be treated at Kaiser. Defendants acknowledged these desires but refused to honor them." (Emphasis in complaint.)

     Noval says he has three adult siblings. He says his sisters Lourdes Frost and Tania Noval "desired decedent's death to collect their multimillion-dollar inheritances." He claims that Tania Noval "had a pre-existing relationship with [defendant social worker Anthony] Tapia.

     Hector Noval claims that after his father was "sedated for comfort," Frost filed with Kaiser a copy of their father's durable power of attorney for health care, dating from July 1999. He says the power of attorney named him and Frost as their father's attorney in fact, and that California law required the defendants to get consent from both of them to make health care decisions for their father.

     But he says, "Defendants did not of this. They never disclosed the DPOA [durable power of attorney] to plaintiff or advised him of his rights or responsibilities therein. Neither did Frost or [defendant] Noval. Plaintiff was never made aware of the DPOA or his rights and responsibilities therein."

     In the days that followed, Hector Noval says, his father's doctor, defendant Richard Bradburne, and social worker Tapia met with his sisters and discussed their father's condition, medical outlook and quality of life.

     On May 3, he says, Dr. Bradburne prescribed "1-2 more weeks of continued aggressive treatment for the decedent. Plaintiff was at Kaiser at the time and again requested that defendants transport decedent to Cedar Sinai or a like facility. Defendants refused. They never disclosed the DPOA or discussed it with plaintiff, and plaintiff went unaware of his rights in the matter."

     Hector Noval claims that on May 4 his sisters "met with Tapia and told him that 'the entire family' desired terminal extubation, i.e. the withdrawal of treatment and death. 'The entire family' did not desire terminal extubation. Frost and [Tania] Noval instructed Tapia to contact a Catholic priest to visit [Victorino] Noval and read his last rites. Tapia did so. Tapia then communicated to defendants that the 'family' desired terminal extubation. No one contacted plaintiff or informed him that any of this was taking place. "Plaintiff was unaware of all of this," according to the complaint.

     Hector Noval claims that when he entered the Kaiser hospital on May 5, "Tapia appeared with security at the entrance and had plaintiff searched by security for weapons. No explanation was given. Tapia then took plaintiff to a conference room and told him that decedent was going to be terminally extubated the following day. He gave plaintiff no explanation for the change in treatment and didn't discuss the DPOA with plaintiff or advise plaintiff that he was a 'joint agent' for health care decisions and had the authority to prevent, delay, or postpone it."

     Hector Noval says he asked that terminal extubation be delayed and asked again that he father be sent to Cedars Sinai. The complaint states: "Tapia tried convincing plaintiff otherwise but ultimately agreed to communicate his request to delay extubation and said he would 'continue to follow up' with plaintiff and have 'continued conversations' with him 'regarding treatment and terminal extubation.' This was plaintiff's only conversation with Tapia regarding treatment and extubation. They never spoke again despite Tapia's promise.

     "Plaintiff left and retained counsel.

     "Tapia recorded in decedent's medical file that 'the entire family is in agreement with the terminal extubation except now [plaintiff] showed up today and is causing conflict.' He also recorded that plaintiff 'had history of substance abuse and paranoid personality.' Neither statement was true, and neither was discussed with plaintiff. Tapia wrote them in the record after hearing them from Frost and {Tania} Noval and without performing any diligence or due care into their veracity." (Brackets, but not braces, as in complaint.)

     Noval says Tapia "spread these misstatements to defendants, including Bradburne, who wrote in decedent's medical record: 'family discussion, all siblings except one son [plaintiff] and wife are in agreement [regarding terminal extubation] ... the son in disagreement [plaintiff] is a habitual drug user/addict and his judgments and motives are likely not sound in the context of acting as a surrogate decision maker.'" (Brackets as in complaint.)

     Hector Noval adds: "One single telephone call to plaintiff or related effort would have cleared the matter. Yet no defendant sought to communicate directly with plaintiff. He was unaware these allegations were being made about him."

     The complaint continues: "Bradburne has since apologized for the medical record, stating that Tapia 'had informed me at some point that this information [about plaintiff] had been alleged.' 'That is not a fair statement actually [about plaintiff].' 'I'm making a statement of fact there and that's not true.' 'The keyword that's left out of that sentence is "alleged."' ... He said 'frankly, I regret writing that way.'" (Brackets, but not ellipsis, as in complaint.)

     Hector Noval claims that he called a meeting with the sisters on the evening of May 5. He says his sisters produced a will and a trust, and told him to "stop complaining about decedent's death because he'd inherit millions of dollars."

     At the meeting, Hector Noval says, he and his lawyer demanded that no terminal extubation take place without his knowledge and consent and that when reasonable, their father be taken off sedation so he could communicate his wishes and direct his own care. He claims that both sisters "agreed to honor these demands. This was plaintiff's and counsel's last communication with Frost and/or Noval before decedent's death."

     Hector claims that on May 6, his two sisters met with Kaiser, and said "that plaintiff had 'threatened violence' the evening before and that they were 'afraid' of him. These were false and fraudulent misrepresentations designed solely to discredit and disparage plaintiff and convince defendants to terminally extubate pursuant to their instructions."

     He claims that had any of the defendants "made one single telephone call to plaintiff or related effort, they would have discovered the allegations of violence were untrue, that plaintiff had retained counsel, and that Frost and Noval were committing egregious fraud and fraudulent concealment to accomplish their father's death."

     On May 6, Hector says, the defendants referred this "true conflict" to defendant Dan Wilson, "a 'bioethics director' and/or on the 'bioethics committee' at Kaiser, to perform an analysis into how to handle decedent's health care going forward."

     Hector claims Wilson interviewed his sisters - but not him - "and concluded plaintiff was in a 'clearly impaired condition' and that Kaiser should proceed with terminal extubation at the desires of 'joint agent [Frost] and the remaining family members.'" (Brackets in complaint.)

     Hector says that Wilson never met with him, never communicated with him, and that no one at the hospital ever informed him of Wilson's involvement or conclusions.

     "Plaintiff believed, instead, from his discussion with Tapia on May 5 that Kaiser would communicate with him before terminal extubation, and from his discussion with Frost and [Tania] Noval on the evening of May 5, that Frost and Noval would not seek terminal extubation without obtaining plaintiff's expressed consent beforehand," the complaint states. (Brackets not in complaint.)

     Hector claims that on May 6, "Frost told Tapia that she was traveling to a meeting with plaintiff and his counsel and that the family 'plans to move forward with the extubation [the next day].' This was a false and fraudulent misrepresentation. There was no such meeting ever scheduled with plaintiff and his counsel, and plaintiff was never in agreement with extubation." (Brackets in complaint.)

     Hector claims that by then his father had shown "material improvement in his health condition," which Dr. Bradburne noted. He claims Bradburne noted, "'currently, [he] does not meet the ordinary criteria for extubation.'" (Brackets in complaint.)

     Hector adds: "Bradburne never communicated any of this to plaintiff."

     He claims that in a sworn deposition Bradburne was asked if extubation could have been postponed. "He said 'Absolutely,'" the complaint states. "He said that if anyone, including plaintiff, sought postponement, he would have done so. When asked how long he would have postponed extubation, he said 'Now till the cows come home.'" Hector claims that on May 7, moments before his father's terminal extubation, Bradburne told his sisters that their father's condition had further improved: that the pneumonia was clearing, his temperature had returned to normal, the ventilator had been replaced with a CPAP [continuous positive airway pressure] mask, "which meant there were no tubes, just a mask over his mouth and nose", that his father was "in no distress," with normal heart rate, stable blood pressure, and that he was "'awake to voice with eye opening and eye contact for more than 10 seconds.'"

     He says Bradburne gave his sisters "the opportunity to postpone extubation at that moment. They declined."

     Hector says Bradburne tasked Wilson with ensuring that he, Hector Noval, was aware of his father's terminal extubation and that he was still in favor of it. Hector says that Wilson never contacted him; he simply asked Frost.

     "(A)ccording to his note in decedent's medical file, '[Frost] confirmed that her brother Hector has agreed to follow family wishes regarding extubation and has decided not to be present at actual event,'" the complaint states. (Brackets in complaint.)

     Hector says that after his father's breathing tube was removed, Victorino Noval "maintained spontaneous breathing and satisfactory oxygen saturation (93-97%) on this 'simple mask.'" He says Bradburne again gave his sisters the opportunity to postpone their father's death. He says both sisters declined, and Bradburne quadrupled Noval's morphine "to quicken his death" and "effectively ended oxygen support".

     Hector says his father died 4 hours and 40 minutes after being extubated, "after 85 minutes fighting to survive with effectively no oxygen and heavily sedated."

     Hector says he learned his father had died when he arrived at the hospital for a visit that evening. He says his sisters told him that Kaiser "had done all they could and that the decedent had passed away in spite of active treatment, not because of any withdrawal of treatment or terminal extubation."

     "At that point there was no reason to believe any wrongdoing had taken place," the complaint states. "Plaintiff had no knowledge of DPOA, no knowledge of the allegations of Frost and [Tania] Noval to defendants, and no knowledge of defendants' withdrawal of treatment and terminal extubation. He wasn't even aware of decedent's material improvement over the final days of his hospitalization. No one had communicated any of this to him. The only communications he received were from Frost and [Tania] Noval representing that decedent was gravely and terminally ill, that he was in agony, and that there was no likelihood of survival." (Brackets not in complaint.)

     Hector says he learned of the durable power of attorney after his sisters' attorneys produced it with other estate planning documents they had been concealing. Only then, he says did he order his father's medical records from Kaiser and discover the facts.

     Hector claims that in sworn depositions, both Bradburne and Tapia stated that Kaiser's policy is "to do all that is necessary to inform healthcare agents of their rights and responsibilities under a DPOA. They described past incidents wherein they would even search distant states and foreign countries for health-care agents and would even reach out to health-care agents through intermediaries and agents-of-the-agent. They testified with no doubt that defendants would go to great lengths to communicate with healthcare agents about their rights and responsibilities under a DPOA. It's that critical to a patient's care. Yet in this instant matter, defendants knew plaintiff, had his contact information, spoke to him and/or his family members multiple times, and had every opportunity to communicate with plaintiff about the DPOA and his rights and responsibilities therein, and they failed to perform even minimal diligence and due care in doing so. They undoubtedly wanted to believe Frost and [Tania] Noval and 'buried their heads in the sand.' This directly and legally caused the death of a relatively healthy, wealthy man with many more years left to live and love." (Brackets not in complaint.)

     Hector Noval seeks damages and punitive from all the defendants on claims of willful misconduct, negligence, elder abuse, fraudulent concealment, constructive fraud, breach of fiduciary duty and wrongful death.

     He seeks damages from Kaiser and Tapia for fraud and false promise; and damages from Kaiser and Bradburne for medical battery and lack of informed consent.

     The corporate defendants are Kaiser Foundation Health Plant, Kaiser Foundation Hospitals, and Southern California Permanente Medical Group.

     Hector Noval is represented by Casey Young of Newport Beach.


KAISERPAPERS.ORG
legalstuff.kaiserpapers.org

Tuesday, January 26, 2016

Cauliflower

Cauliflower is now $11.00 a head.  I never particularly liked cauliflower and now I want it.  Why.   I do not know why. Price creaets a demand.


Thursday, January 21, 2016

Euthanasia and the Canadian Medical Association

Today being Thursday January 21 2016, the Canadian Medical Association is presenting its Principles-based Recommendations for a Canadian Approach to Assisted Dying. What a joke.

The Recommendations (if the government accepts the recommendations) will be stealth law giving 99.9% power to doctors to do euthanasia when they want.  There is a window, so it will be opened.  The window is ...a standard waiting period is not appropriate for all requests ...this could be shorter ...the attending physician must wait no longer than 48 hours, or as soon as is practicable, after the written request is received.

Think about it why have a waiting period as each day costs $big, so why wait. More importantly, the patient may change her mind and all the preparation are for naught.  Doctors do not like patients who change their minds. This is what Ro Ang, the manager of GPC, told me. So was Randy declared incompetent because he might change his mind.  Is this one of the reasons used to justify his incompetence. 

Like the young woman (Brittany Maynard) in Oregon, she changed her mind against assisted suicide as it was too soon, she said (there was a video), and the next day she was dead. Was she forced to follow through with her original date to commit suicide. Also, Gloria Taylor, who was happy with all the attention she was getting.  She must have had a DNR on her and emergency refused to agressively treat her.  She did not want to die from an infection.

The first few of those who will be euthanized will have perfect oversight to satisfy the public as to  safe safeguards but after that what: confidentiality; and a death certificate, not mentioning euthanasia so an insurance company (I think that is criminal fraud) will never know.  

CORRECTION; Quebec is already euthanizing patients against federal law and details (the process) is confidential.  We live in Dodge City.

The CMA recommendations are not even dated. Trust doctors, you cannot even trust them to date a document recommending how they are going to euthanize patients. What an oversight.

Listen to this: http://rewardsradiotv.com/AUDIO/vickie-t/index2.htm.  This is also what is happening in Canada not only to the elderly but to anyone the system targets as not having a meaningful quality of life.  This parallels what happened to Randy and I.  The legislators in the US and also in Canada know that this is happening but do nothing except to maintain the status quo thus creating a culture of death.











Wednesday, January 13, 2016

BC's Health Authorities on how to effectively communicate with the public

A You Tube video.

 If the video does not show up on the blog page, please click the title below.

BC's Health Authorities on how to effectively communicate with the public, 



1.  delay
2,  deny
3.  divide
4,  discredit
5.  demoralize

The menu/recipe did not mention the 6th "d" being death.  Death is the result leaving the victim traumatized and scared of the health authorities, horrified that she was part of the premeditated menu and unable to do anything.

I was expected to become stockholmed in which the abused identify positively with the abusers (and in my case Vancouver Coastal Health) and all would be forgiven.

Below explanation from Wikipedia.

Stockholm syndrome can be seen as a form of traumatic bonding, which does not necessarily require a hostage scenario, but which describes "strong emotional ties that develop between two persons where one person intermittently harasses, beats, threatens, abuses, or intimidates the other."[4] One commonly used hypothesis to explain the effect of Stockholm syndrome is based on Freudian theory. It suggests that the bonding is the individual's response to trauma in becoming a victim. Identifying with the aggressor is one way that the ego defends itself. When a victim believes the same values as the aggressor, they cease to be perceived as a threat.
 

"Of all forms of inequality, injustice in health care is the most shocking and inhuman."
Martin Luther King, Jr. (1966)



740 views on You Tube jan03/16




Saturday, January 9, 2016

The Red Cross, it is corrupt

I did not know that the Red Cross was corrupt.  So if I did not know this I assume 99.9% of the population out there is not aware of what is happening.

I am sure that the Red Cross is like the Vancouver Food Bank that it has no members from the public.  Do not give any money to any charitable cause unless you can be an active members i.e. access to detailed financial records ,membership lists, attending board meetings, all that should be transparent, ability to become a director.

http://www.huffingtonpost.com/2015/06/04/red-cross-haiti-report_n_7511080.html

Years ago I was part of a conversation and I was told that well-educated parents were directing their children to enter the non-profit sector rather than public service as the non-profit sector is where the money is with job security and very little accountability.  Governments are downloading their social responsibilities to non-profits.

When there is an environmental disaster the military should be sent in to reconstruct.  Roosevelt got tired of the prima donnas that were constructing the Hoover Dam so he sent in the military to finish its construction: those who had to followed orders and could not quit.
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