Well, I had a brother-in-law that functioned very much as Terry functions (assuming she's not already dead of dehydration as I type this). She was given very, very little physical therapy well over a decade ago (it halted after her husband won the multi-million dollar settlement and began insisting she should die). She would require highly intensive therapy in order to function beyond the level of a newborn. And, that is exactly the level she functions at - a newborn's. She is not brain-dead, she has severe brain damage due to oxygen being withheld from her brain (the exact same thing occurred in my bil and his brain scans looked VERY similar from his autopsy upon his death). I have heard that newborns only smile "reflexively" as well and, having had four now I know that that statement is absolute rubbish.
Terry tracks with her eyes, she responds to stimuli, her brain functions - simply not at the level you or I experience. Sure, we can claim she doesn't feel pain or hunger as she dies slowly - but there was a time until recently when many claimed a newborn could not feel any pain and they were denied anesthetics during surgeries. We now know that even fish can and do feel pain. Terry, who is not brain-dead, who can respond to stimuli and seems aware of her surroundings can respond to pain just as you and I can - just as a newborn can.
I consider this state-endorsed death. Terry's husband is already living with another woman. He will not divorce Terry because he cannot receive the balance of her settlement from the reportedly multi-million dollar malpractice suit upon her death in that case. He has denied her the physical therapy that the settlement was meant to pay for for well over a decade. If Terry were a death-row inmate the governor could halt her execution. But, since she is permanently disabled her death is sealed.
I faced the real possibility of having a child with severe brain damage when my oldest went in for his first neurosurgery as an infant. His second surgery as a toddler could've also resulted in life-long brain damage. Both times I had to decide if I was willing to take care of a child in essentially an infantile state for the rest of his life. The second surgery in particular could've resulted poorly with him specifically not being able to swallow due to the particular portion of the brain affected. Would I consider my son's life not worth living because he was infantile the remainder of his life? I knew then as I know now that an infantile state is still a state of life - of worthy life (although, Peter Singer would disagree as he believes an infant is not worthy to live if he/she is a "burden"). And, I would not have sought to end his life if all that was required was assistance in feeding him as a permanently brain damaged person - a disabled person. My children are all burdens upon me - all children are burdens upon their parents. The reasoning that one should never be a "burden" would negate the existence of every person on this earth (since we've all experienced infancy and childhood).
The following statement was issued by a national disability advocacy group The Arc of the United States:
"For people with disabilities and their families, the Schiavo case represents a slippery slope and raises the possibility that the right to life of people with significant intellectual and or physical disabilities might one day be questioned...
"... Today, there are thousands of people with various physical and cognitive disabilities who use feeding tubes as their normal means of getting food and water. For these people, a feeding tube is not life support or heroic intervention. It is a simple way of getting hydration and nourishment. When they are hospitalized for any reason – however minor – they risk having their normal means of eating and drinking be classified as as “extraordinary treatment” or “life support.”
"...The disability community has grappled with these issues in the past and has come to the conclusion that in such cases, it is best to assume that life is preferable over death. Is that not what the Schiavo case is all about? Laws governing surrogate decision-making vary among states and are often the result of well-funded advocacy from a narrow group of professionals. In most cases, disability organizations were not included in changes of statutes on the state level, and the drafters of those statues did not take into account the views of those with disabilities..."
"...Our society must stop using the term “persistent vegetative state.” Too many people with significant disabilities have been called “vegetables,” and this must stop. It is beyond demeaning; it is dehumanizing. In fact, some of the people who use the term most freely are doctors, and what comes next is a discussion of the death or warehousing of the individual labeled that way."
"...When a person has serious disabilities, the debate should not be about whether or not they are going to “get better” some day. For millions of Americans, disability is a fact of life,every day of our lives. People with disabilities have wonderful lives. And some have lousy lives. In that way, they are just like other Americans. Just because a person has a significant disability does not mean that they do not love their life. It does not mean that they should be assumed to be better off dead."
"...It is time for a call to conscience to both the Right and the Left. Guardianship should not be a death ship. People like Terri Schiavo are persons under the law, and they deserve constitutional protection."
"...The disability community is grateful that so many in Congress supported Terri Schiavo’s right to live, even though we are concerned about the precedent they set. We would like to see them follow up with the same level of concern for making sure we can provide care and support for the millions of Americans with disabilities by supporting Medicaid Community Attendant Services and Supports Act, which would allow people receiving Medicaid funding to have a life, not just stay to alive.– We call on them to ensure continued appropriate funding of Medicaid and other programs that people need..."
"...Terri Schiavo’s case is every family’s nightmare. Disability doesn’t have to be a nightmare. Even if our nation disagrees on how we define compassion, we must certainly agree that all lives are equal under the law."
My husband's family made the correct choice in taking care of a child brain damaged in infancy when told by physicians he would be a vegetable for the remainder of his life and that life was not worth living. That child, with intense physical therapy lasting over the course of 15 years, was able to progress to the estimated level of a toddler/preschooler. Perhaps that was exceptional and Terry would never progress with the same intense treatment over the same period of time to a level beyond, say, a one or two year old. I fail to see how that would make her life more worthy of execution.
Jennifer
Terry tracks with her eyes, she responds to stimuli, her brain functions - simply not at the level you or I experience. Sure, we can claim she doesn't feel pain or hunger as she dies slowly - but there was a time until recently when many claimed a newborn could not feel any pain and they were denied anesthetics during surgeries. We now know that even fish can and do feel pain. Terry, who is not brain-dead, who can respond to stimuli and seems aware of her surroundings can respond to pain just as you and I can - just as a newborn can.
I consider this state-endorsed death. Terry's husband is already living with another woman. He will not divorce Terry because he cannot receive the balance of her settlement from the reportedly multi-million dollar malpractice suit upon her death in that case. He has denied her the physical therapy that the settlement was meant to pay for for well over a decade. If Terry were a death-row inmate the governor could halt her execution. But, since she is permanently disabled her death is sealed.
I faced the real possibility of having a child with severe brain damage when my oldest went in for his first neurosurgery as an infant. His second surgery as a toddler could've also resulted in life-long brain damage. Both times I had to decide if I was willing to take care of a child in essentially an infantile state for the rest of his life. The second surgery in particular could've resulted poorly with him specifically not being able to swallow due to the particular portion of the brain affected. Would I consider my son's life not worth living because he was infantile the remainder of his life? I knew then as I know now that an infantile state is still a state of life - of worthy life (although, Peter Singer would disagree as he believes an infant is not worthy to live if he/she is a "burden"). And, I would not have sought to end his life if all that was required was assistance in feeding him as a permanently brain damaged person - a disabled person. My children are all burdens upon me - all children are burdens upon their parents. The reasoning that one should never be a "burden" would negate the existence of every person on this earth (since we've all experienced infancy and childhood).
The following statement was issued by a national disability advocacy group The Arc of the United States:
"For people with disabilities and their families, the Schiavo case represents a slippery slope and raises the possibility that the right to life of people with significant intellectual and or physical disabilities might one day be questioned...
"... Today, there are thousands of people with various physical and cognitive disabilities who use feeding tubes as their normal means of getting food and water. For these people, a feeding tube is not life support or heroic intervention. It is a simple way of getting hydration and nourishment. When they are hospitalized for any reason – however minor – they risk having their normal means of eating and drinking be classified as as “extraordinary treatment” or “life support.”
"...The disability community has grappled with these issues in the past and has come to the conclusion that in such cases, it is best to assume that life is preferable over death. Is that not what the Schiavo case is all about? Laws governing surrogate decision-making vary among states and are often the result of well-funded advocacy from a narrow group of professionals. In most cases, disability organizations were not included in changes of statutes on the state level, and the drafters of those statues did not take into account the views of those with disabilities..."
"...Our society must stop using the term “persistent vegetative state.” Too many people with significant disabilities have been called “vegetables,” and this must stop. It is beyond demeaning; it is dehumanizing. In fact, some of the people who use the term most freely are doctors, and what comes next is a discussion of the death or warehousing of the individual labeled that way."
"...When a person has serious disabilities, the debate should not be about whether or not they are going to “get better” some day. For millions of Americans, disability is a fact of life,every day of our lives. People with disabilities have wonderful lives. And some have lousy lives. In that way, they are just like other Americans. Just because a person has a significant disability does not mean that they do not love their life. It does not mean that they should be assumed to be better off dead."
"...It is time for a call to conscience to both the Right and the Left. Guardianship should not be a death ship. People like Terri Schiavo are persons under the law, and they deserve constitutional protection."
"...The disability community is grateful that so many in Congress supported Terri Schiavo’s right to live, even though we are concerned about the precedent they set. We would like to see them follow up with the same level of concern for making sure we can provide care and support for the millions of Americans with disabilities by supporting Medicaid Community Attendant Services and Supports Act, which would allow people receiving Medicaid funding to have a life, not just stay to alive.– We call on them to ensure continued appropriate funding of Medicaid and other programs that people need..."
"...Terri Schiavo’s case is every family’s nightmare. Disability doesn’t have to be a nightmare. Even if our nation disagrees on how we define compassion, we must certainly agree that all lives are equal under the law."
My husband's family made the correct choice in taking care of a child brain damaged in infancy when told by physicians he would be a vegetable for the remainder of his life and that life was not worth living. That child, with intense physical therapy lasting over the course of 15 years, was able to progress to the estimated level of a toddler/preschooler. Perhaps that was exceptional and Terry would never progress with the same intense treatment over the same period of time to a level beyond, say, a one or two year old. I fail to see how that would make her life more worthy of execution.
Jennifer
Comment