http://www.philly.com/philly/health/20130802_Judge_upholds_count_of_assisted_suicide.html#hLRSrC4PBjvmaCti.99
POTTSVILLE, Pa. - A judge on Thursday upheld charges against a Philadelphia woman accused of helping her 93-year-old father commit suicide through a morphine overdose at his home here, where he was in hospice.
Prosecutors in Schuylkill County charged Barbara Mancini, 57, with aiding suicide. The judge refused to drop the charges after a preliminary hearing.
Pottsville police say Mancini handed Joseph Yourshaw a bottle of liquid morphine at his home in February, leading to his death four days later. The death certificate, which listed the immediate cause as "morphine toxicity" that complicated high blood pressure and heart disease, was issued in June.
Mancini, who was trained as a nurse, remains free on bail. Her lawyer could not be reached for comment Thursday evening. The local district attorney's office asked the state to prosecute the case due to a conflict of interest.
An end-of-life advocacy group called for the charges to be dropped, saying the U.S. Supreme Court allows dying patients to receive adequate pain relief, even if it hastens their death. "Attorney General [Kathleen] Kane should leave Barbara and her family alone so they can grieve over their loss," Barbara Coombs Lee, president of Denver-based Compassion and Choices, said in a statement.*
*Compassion & Choices is the former Hemlock Society. To learn more about C & C, read: and Theresa Schrempp, Esq., "Compassion & Choices is a Successor to the Hemlock Society" and Senator Jennifer Fielder on Compassion & Choices: "Beware of Vultures."
Or, go to these links: http://www.montanansagainstassistedsuicide.org/2012/12/compassion-choices-is-successor.html and http://www.montanansagainstassistedsuicide.org/2013/06/beware-of-vultures-senator-jennifer.html
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Friday, August 2, 2013
Wednesday, July 17, 2013
Texas Women Underwent Chemo After False Diagnosis
http://news.yahoo.com/texas-woman-underwent-chemo-after-false-diagnosis-132745549.html
William Holt
5 hours ago
Health
A woman from Victoria, Texas, underwent several rounds of
chemotherapy, only to find out that she never had cancer to begin with,
reports CBS’s Houston affiliate, KHOU.
Herlinda Garcia, 54, was diagnosed with stage 4 terminal breast cancer after she had a benign tumor removed from her left breast. Through the next seven months and eight rounds of chemotherapy, she felt her body and mind deteriorating.
“Everything was swollen,” Garcia told KHOU. “I lost my eyebrows, my eyelashes. It’s really hard. I can’t explain how I felt. It’s like I was in a dream.”
Certain that her life was coming to an end, the part-time civil process worker gave away most of her belongings and wrote a bucket list.
"I just wanted to give up on everything," Garcia said.
But when she decided to seek help for her growing anxiety at Citizens Medical Center, a series of scans revealed a new reality: Garcia never had cancer.
At MD Anderson Cancer Center in Houston, a second opinion confirmed what doctors at Citizens Medical Center had discovered.
“I was happy, but at the same time, I had anger,” Garcia said. “The damage had been done.”
For her pain and suffering, a Victoria County jury awarded Garcia $367,000. Garcia said she hopes her experience will lead others to always seek a second opinion.
“I know I’m never going to feel the same because of what I went through,” she said. “It changed my life.”
Herlinda Garcia, 54, was diagnosed with stage 4 terminal breast cancer after she had a benign tumor removed from her left breast. Through the next seven months and eight rounds of chemotherapy, she felt her body and mind deteriorating.
“Everything was swollen,” Garcia told KHOU. “I lost my eyebrows, my eyelashes. It’s really hard. I can’t explain how I felt. It’s like I was in a dream.”
Certain that her life was coming to an end, the part-time civil process worker gave away most of her belongings and wrote a bucket list.
"I just wanted to give up on everything," Garcia said.
But when she decided to seek help for her growing anxiety at Citizens Medical Center, a series of scans revealed a new reality: Garcia never had cancer.
At MD Anderson Cancer Center in Houston, a second opinion confirmed what doctors at Citizens Medical Center had discovered.
“I was happy, but at the same time, I had anger,” Garcia said. “The damage had been done.”
For her pain and suffering, a Victoria County jury awarded Garcia $367,000. Garcia said she hopes her experience will lead others to always seek a second opinion.
“I know I’m never going to feel the same because of what I went through,” she said. “It changed my life.”
Sunday, July 14, 2013
The "Liverpool Care Pathway," Hospice and Palliative Care Abuse
The "Liverpool Care Pathway" (LCP) is a system of hospice/palliative care in the UK. In the last few years, the system has come under fire as "stealth euthanasia" in which patients are put on the LCP "without consent" and without "being allowed, food, fluids and medication." See the BBC article set forth below: “Liverpool Care Pathway: Your experiences.”
I periodically receive similar complaints from people in the US and Canada. Consider, for example, this letter by an elder care facility owner in Washington State where assisted suicide is legal:
Consider also, this letter published in a Montana newspaper:
Margaret Dore, Attorney at Law
President, Choice is an Illusion, a nonprofit corporation
___
"Liverpool Care Pathway: Your Experiences"
http://www.bbc.co.uk/news/health-23301360
The system was designed to allow terminally-ill patients to die peacefully and with dignity.
However, the LCP has come under criticism with some believe it is being used to speed up the process of dying. There have been some reports of patients being put on it without consent and not being allowed, food, fluids and medication.
Here, [three] family members of those who have been on the Liverpool Care Pathway, share their experiences of the programme. [There are two unfavorable views and one favorable view of the LCP]
During the six months from her diagnosis in January 2012 until her death, she was unknowingly to us put on the LCP. She was deprived of fluids and any source of nutritional supplement without even the slightest consent or conversation with me or my family.
It was only after my absolute insistence and persistence that my mother received fluids and that was after over 36 hours without any.
It scares me that people who do not have bossy and demanding families, like me and mine, to fight for them will be left or even encouraged to die via the LCP.
My mother survived another three months. We got to hear her laugh and joke again and importantly my mother got to say her goodbyes. Had the enforced LCP been allowed to continue, those few important months of time with my mother would have without a doubt been taken away from me and my family.
I can't stress how important me and my family feel about the process of the LCP. It needs to be readdressed - the memories it could have deprived me of are invaluable. She wrote me a letter that I will have forever and it will always be the most treasured item I possess.
Towards the end, my mother couldn't swallow and didn't want
food - this was her body getting ready to die. It was slow and peaceful,
and she was my mother until about the day before when we all knew she
was leaving.
There was no prolonging of life. She was ready to go and the Liverpool Care Pathway aided her in a gentle and thoughtful way. It wasn't the refusal to give her food and drink; she no longer wanted it.
She had as natural an early death as can be and I am thankful as it helped me and my family cope as we saw her slip away. This is something that should be offered and explained to patients and family and I have nothing but support for it.
I was assured by the staff at the hospital that would happen, that he would have died a dignified death. He didn't. He was sedated, unconscious and died within three days looking like something from Belsen concentration camp.
He was not given water or food but instead put on a driver syringe containing diamorphine, midazolam and cyclizine. The first two of those drugs would down a horse. . .
Sadly there is no going back. I didn't know that once started, it's irreversible.
No one makes this clear. This is the main part, if not for some the final part, of the LCP.
In the new scheme when that comes out, if they allow these two drugs to be continued to be used, it is euthanasia, plain and simple.
I periodically receive similar complaints from people in the US and Canada. Consider, for example, this letter by an elder care facility owner in Washington State where assisted suicide is legal:
"Since the [assisted suicide] act passed, we have . . . noticed that some members of the medical profession are quick to bring out the morphine to begin comfort care without considering treatment. Sometimes they do this on their own without telling the client and/or the family member in charge of the client's care."http://www.montanansagainstassistedsuicide.org/2012/07/dear-montana-board-of-medical-examiners.html
Consider also, this letter published in a Montana newspaper:
“If these terrible deaths happen when aid in dying (assisted suicide and euthanasia) is not legal, what will happen if these practices are made legal? Doctors will have even more power to take away patient choice."http://www.montanansagainstassistedsuicide.org/2013/04/dont-give-doctors-more-power-to-abuse.html
Margaret Dore, Attorney at Law
President, Choice is an Illusion, a nonprofit corporation
___
"Liverpool Care Pathway: Your Experiences"
http://www.bbc.co.uk/news/health-23301360
The LCP was developed to support dying patients
The Liverpool Care Pathway (LCP) should be phased out, an independent review is expected to say.
However, the LCP has come under criticism with some believe it is being used to speed up the process of dying. There have been some reports of patients being put on it without consent and not being allowed, food, fluids and medication.
Here, [three] family members of those who have been on the Liverpool Care Pathway, share their experiences of the programme. [There are two unfavorable views and one favorable view of the LCP]
Kayleigh Hollobone
Two years ago, when I was 22, I lost my 56-year-old mother to cancer.During the six months from her diagnosis in January 2012 until her death, she was unknowingly to us put on the LCP. She was deprived of fluids and any source of nutritional supplement without even the slightest consent or conversation with me or my family.
It was only after my absolute insistence and persistence that my mother received fluids and that was after over 36 hours without any.
It scares me that people who do not have bossy and demanding families, like me and mine, to fight for them will be left or even encouraged to die via the LCP.
My mother survived another three months. We got to hear her laugh and joke again and importantly my mother got to say her goodbyes. Had the enforced LCP been allowed to continue, those few important months of time with my mother would have without a doubt been taken away from me and my family.
I can't stress how important me and my family feel about the process of the LCP. It needs to be readdressed - the memories it could have deprived me of are invaluable. She wrote me a letter that I will have forever and it will always be the most treasured item I possess.
Helen Redshaw
"The Liverpool Care Pathway aided her in a gentle and thoughtful way”
My mother passed away from
cancer just three months ago. The Liverpool Care Pathway was used and I
have nothing but praise for it. We had help from night nurses through
the NHS Beacon program, Marie Curie and Macmillan, all of which gave
exemplary care. Leaflets on the LCP were given to us and time was taken
by all to fully explain why and how it would work.
There was no prolonging of life. She was ready to go and the Liverpool Care Pathway aided her in a gentle and thoughtful way. It wasn't the refusal to give her food and drink; she no longer wanted it.
She had as natural an early death as can be and I am thankful as it helped me and my family cope as we saw her slip away. This is something that should be offered and explained to patients and family and I have nothing but support for it.
William Hughes
My father Professor Robert Hughes was subjected to this technique without my or his consent. When it became clear that his cancer of the prostrate became untreatable I was asked what I wanted to do and I told them clearly that I wanted him to die with dignity.I was assured by the staff at the hospital that would happen, that he would have died a dignified death. He didn't. He was sedated, unconscious and died within three days looking like something from Belsen concentration camp.
He was not given water or food but instead put on a driver syringe containing diamorphine, midazolam and cyclizine. The first two of those drugs would down a horse. . .
No one makes this clear. This is the main part, if not for some the final part, of the LCP.
In the new scheme when that comes out, if they allow these two drugs to be continued to be used, it is euthanasia, plain and simple.
Wednesday, July 10, 2013
Excuse the mess!
If the website "looks funny," it's because we're doing some updates.
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Thank you so much!
Choice is an Illusion
Thank you for your patience and please consider making a donation to keep this website alive.
Thank you so much!
Choice is an Illusion
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