Artificial feeding-Terri Schiavo

Published

I posted this here becaue I think this subject is something that we as nurses deal with on a regular basis.....Many many people state that they have a big problem with the feeding being stopped "allowing her to starve to death" The Vatican says " To starve her to death is pitiless" Most everyone agrees that it is one's right to refuse to initiate artificial feeding but somehow this situation "is different" How? The patient "starves to death " in both cases-so why has this one galvanized the WORLD? My husband read me a quote from the Bible -forgive me because I can't remember it in detail-it was something along the lines that a woman marries and leaves her father's house and her husband becomes her family....My husband is my POA I hope no-one in my family questions his motives -He KNOWS exactly what I want....I can't question her husbands motives-I know that some suspect foul play and state the results of a bone scan support this...That bone scan was obtained 53 months after she went into her coma-after her body suffered the effects of her eating disorders for a number of years.... Her present level of responsiveness does not pertain to this matter IMHO-she CAN'T eat naturally--she did not ever want to "be kept alive like that " and she can't state otherwise at this point...So- #1 can someone PLEASE make me see why this case is" DIFFERENT" and #2 How do YOU support your patients and their loved ones when they are agonizing over this decision? ONe thing I always ask is "Did your loved one ever give you any idea of what they would want if something like this happened" and if they did then I advocate that stance for that pt as much possible.......I believe that death is the last great trip we'll go on and we should PLAN it as much as possible.The greatest GIFT we can give to our loved ones is an itinerary...........

Specializes in MICU, SICU, PACU, Travel nursing.
i think terri is like stuck in the middle of this, poor lady doesn't even know what's going on she's brain dead.they should make a law in every state,that says if I am put in to a life threatning situation let me die don't keep me alive for sake of loved ones.everyone should sign one when they turn 18.then the hospital will know what to do.cause I know if i was in her situation i'd wanna die right away,you know let me go.let her rest in peace now GOD wants to give her angel wings now in heaven.

amen. i hope that if something like that happened to me i could die quickly with some dignity. not on cnn for 14 years with politicians using me for political gain.

Specializes in MICU, SICU, PACU, Travel nursing.
_______________

she is NOT brain dead. Even her husband admits to that. She is brain damaged.

she has no cerebral cortex. there is just fluid where it was. it doesn't grow back. thats a little worse than being brain damaged

September 12, 2002

Re: Terri Schiavo

I was asked to examine Terri Schiavo per the request of the Second District Court of Appeal. They requested that current information about her present medical condition be obtained. They also requested that an evaluation be performed to ascertain treatment options.

HPI:

Ms Schiavo was in her usual state of good health until 2/25/90, when her

husband reported that he was awakened from sleep approximately 6 Am by her

falling. He reports that she was unresponsive.

Paramedics were called, and aggressive resuscitation was performed with 7

defibrillations en route.

In the Emergency Room, a possible diagnosis of heart attack was briefly

entertained, but then dismissed after blood chemistries and serial EKG's did not

show evidence of a heart attack. Similarly, a pulmonary or lung cause of the

disorder was ruled out in the Emergency Room after normal blood gases and Chest X-Rays were obtained. The possibility of toxic shock syndrome was also

entertained. The diagnosis of the cause of her condition was unknown. Her

admission laboratory studies showed low potassium level, markedly elevated

glucose level, and a normal toxic screen without evidence of diet pills or

amphetamines.

The abnormal potassium level and sugar level were found on admission to the

Emergency Room and were successfully corrected by the hospital staff over the next several days. The patient had a difficult hospital course with the development of poorly controlled seizures and prolonged coma state requiring, for a time, ventilator support. However, the staff noted improvement, and it was recommended by several physicians that she be discharged to an intensive rehabilitation center.

She was eventually transferred to Mediplex in Bradenton for intensive

rehabilitation. She was poorly responsive. However, after a brain stimulator was placed in 11/90, the staff started to report greater interactions of the patient with her environment, including intermittently apparently following commands, turning her head to voice, tracking visually, etc.

This pattern continued even after discharge to a nursing home, although her

course from that time on included multiple medical problems including recurrent

urinary tract infections and hospitalizations, at times with severely low episodes of blood pressure due to a lack of treatment of urinary tract infections ordered by the husband and subsequent urinary sepsis requiring hospitalization.

During 1998, she was evaluated by Dr. James Barnhill, neurologist, who

testified that he examined her for ten minutes and determined that she had no

chance for recovery, and was in a persistent vegetative state. He also identified that her skull was filled with spinal fluid; there was no brain present on the scans. All responses he identified were reported as "reflexes." He obtained no blood pressure nor did anyone else, apparently, on the day of his exam, the closest documented blood pressures being obtained two days earlier and five days later. No tests including Urinary Tract infection evaluations, blood tests, EEGs, evoked potentials, or new CT/MRI exams were ordered.

One year later he again reconfirmed his earlier diagnosis. He felt no tests of

any sort were needed for evaluation.

In the spring of 2000, three physicians, including Dr. Jay Carpenter, who is a

former Chief of Medicine at Morton Plant Hospital, filed affidavits after observing Ms. Schiavo. All three physicians stated that it is visually apparent that Ms Schiavo is able to swallow and, in fact, does swallow her own saliva.

The patient continued with no physical therapy, communication or speech

therapy, or routine medical screening evaluations and treatment such as dental care, mammography, gynecological exams or pap smears during this time.

In May 2002, access to the patient was allowed for two physicians appointed

by the family. At that time, my observation of Terri Schiavo in person occurred, having previously viewed videotape that was first shown at her first trial.

The examination

Medical examination and evaluations were performed on Ms Schiavo on

September 3 and 4 with videographers present.

Medical reviews of the charts provided were carried out, from which the

above history is obtained.

On September 3, I spent from approximately 11AM until 4PM with Ms.

Schiavo, returning the next day to also observe Dr. Maxfield and complete my

portion of the exam (which duplicated that of Dr. Maxfield, so I observed without myself specifically repeating that part of the exam that same day).

The exam was videotaped at my request.

The exam started with the setting up of the video camera by the

videographers, with Mr. Michael Schiavo present. I then came into the room and introduced myself to Ms. Schiavo. The patient was looking at the ceiling in a chair.

She had a wide-eyed look to her. She appeared to be aware of my presence with slight facial changes and tone changes in her body, She did not look at me, or turn to look in the direction of my voice, continuing instead to look directly forward.

Her mother then entered the room, coming toward her and speaking her name. The daughter immediately showed awareness of the presence of her mother, looking for her, then finding her visually when the mother was approximately 8 inches from her face. She then smiled and made sounds. Her father also entered the room with further apparent recognition by the daughter.

The first part of this exam included observing her interactions with her

mother and her father. Here she clearly was aware of them and attempted to

interact with them: the sounds, facial expressions, and searching out and tracking them. There are several previous reports by medical personnel and others of her responding to live piano music. Accordingly, I asked the mother to bring a tape of piano music. Two separate pieces were listened to. The first she appeared aware of the sound, but would not sing or interact significantly. The second she did interact making sounds with the music. She stopped making these sounds, when the music stopped.

During this time, she would move her head and track her head and eyes to

the sound of music, or her mother's voice.

I started my exam first on her right side, introducing myself and then

examined her contracted right arm, the goal being to get a blood pressure, as

neurological abilities are very sensitive to blood pressure. She looked at me and would track me with voluntary facial and upper torso movements.

I later moved to the left arm and attempted to release contractures there. In

order to get significant relaxation of the arm to a degree necessary to obtain a blood pressure, I worked for approximately 35 minutes to release the contractures enough to get arm extension to approximately 140 degrees. During this time, the patient would track the mother or the father, depending on who was interacting with her.

Interestingly, she appeared to respond to her mother or father by tone of voice. At one time, after working on her arm for approximately 20 minutes, and no further extension of the elbow was to be had, the father walked up and started speaking reassuringly to his daughter. The elbow immediately extended approximately another 20 degrees. This was during a time period that I had been talking with Ms. Schiavo, and the music was also running. Yet with neither the addition of the music nor my voice did the elbow extend. With the father coming to his daughter and speaking, she immediately extended the arm further. At other times, he would speak more sharply to her, and she would immediately tighten, and appear to lose her spot of visual focusing, and her expressions would change. At times during and immediately after this part of the exam, she would also appear to voluntarily move

her right upper extremity.

Multiple takes of her blood pressure were taken, and there were several

readings of "error." During the reading of her blood pressure, I also palpated the median artery at the wrist. In general, the systolic readings on the blood pressure cuff correlated well with the wrist palpations. Thus, the systolic readings are probably fairly accurate, although the diastolic readings cannot be independently confirmed. Three readings were successfully obtained 96/65 pulses of 70, 107/78 pulse of 72, and 101/71 pulse of 70. The pulse was erratic by both machine and palpation. The blood pressure errors occurred due to spasticity in the arm being evaluated.

A general physical exam was also performed, although pelvic, breast, rectal,

fundoscopic, sinus and ear exams were not performed. Technical difficulties

prevented the fundoscopic exam from being performed.

The general physical examination and the neurological examination tended to

be performed in an extremity-by-extremity fashion, as her cooperation was best by focusing on specific regions, and then not coming back to those regions at a later time. Moving rapidly and from side to side tended to result in apparent confusion and stress in the patient, manifested by increased tone and less facial interactions, eye contact, and less accessibility to her limbs due to the increased tone causing contractures to redevelop.

The general facial exam was significant for acne, probably due to a chronic

stress induced steroid responses. No bruits were identified. Cranial nerves were intact, and the patient was able to swallow and handle all secretions.

The neck exam was abnormal. She had severe limitation of range of motion

in the flexion, and to a lesser degree in extension. Indeed, I was able to pick up her entire torso and head and neck area with pressure on the back of her neck in the suboccipital region. These findings of cervical spasm and limitation of range of motion are consistent with a neck injury. No bruits were identified.

Lung exam showed scattered wheezes in the right lung fields. No rhonchi or

rales were identified. Cardiac exam was normal to my exam. Interestingly, the

significant arrhythmias identified by the electronic cuff, as well as my palpation of her wrist exam was not identified during this cardiac portion of the exam, suggesting the arrhythmia is intermittent.

Abdominal exam showed good GI sounds throughout, and was non-tender.

No masses or aneurysms were palpated.

Extremities exam showed severe contractures in all four extremities. On the

left upper extremity, she initially showed 4/4 on the Allen's spasticity scale about the wrist, fingers, and the elbow. However, with approximately 40 minutes of massage and release, the exam in this upper extremity showed spasticity on the Allen's scale, and at times, later in the exam, would show 2/4 on the Allen's exam.

The right upper extremity also showed 4/4 on the Allen's scale, and also improved with efforts at muscular tension release. However, time did not allow me the same degree of effort on her right upper extremity, and thus I am unsure of the degree of relaxation available in this area.

In the lower extremities, she has 2/4 about the hips and the knees, meaning

full range of motion, but spasticity still present. However, about the ankles, she is 4/4 and I could obtain no improvement in the range of motion.

With levels of 3/4 and 4/4 spasticity, it is frequently difficult to determine

the degree of voluntary control if any a patient has over an extremity. The internal spasticity and stiffness of the limb, makes gauging voluntary efforts very difficult.

Efforts that may be easily seen or felt in a patient with no spasticity may be

completely missed or only able to be identified from sophisticated testing in a

patient with 3/4 or 4/4 levels of spasticity.

Spasticity generally is due to neurological injuries, and is aggravated by lack

of physical therapy and muscle stretching. To understand spasticity, it is important to understand what is normal with muscle activity

(His explanation of muscles and spasticity deleted here for space purposes)

The Allen's scale is a 0-4 scale with 0 as normal or no spasticity. The scale

is as follows:

0 Normal, no spasticity

1 Slight spasticity, palpated by the physician, but full range of motion of a joint

2 Moderate spasticity, but full range of motion. Here the examiner may

be allowed to use a great deal of his own muscle contraction to straighten a joint. If the joint can be straightened to its full range of motion, this is a 2.

3 Severe spasticity, but some motion can be identified. Full range of

motion does not exist.

4 Severe spasticity, no range of motion.

Pulses in these extremities were symmetrical. Skin was intact in these areas.

The patient wore a diaper, and this was not removed for the exam.

Back exam was carried out and there were no evident areas of tenderness,

masses, or other abnormalities seen.

The first two hours of the exam, focusing on cognitive awareness of her

surroundings, was carried out in a chair. The last one hour on videotape was

carried out in her bed. In neither position did she have difficulty handling any

saliva or secretions. Only briefly, for a few minutes at a time, did she appear to tire and lose the ability to respond, track or interact with her surroundings.

She had no tube feedings or water during the entire time of the exam.

Alertness: The patient was alert throughout essentially the entire exam.

Responsiveness: The patient would immediately respond to sound, tone of voice and to touch and pain. With respect to responding to those around her, she had limited responsiveness to me personally until approximately 45 minutes into the exam. She started to look at me, against her traditional right gaze preference, about the same time that we started getting significant relaxation in her contracted left arm (the arm that had been contracted for several years.) She appeared to identify the sound of my voice, with the relaxation of the arm. From that point, she would generally look toward the sound of my voice when heard, attempt to find me

visually, then track the sound of my voice in its movements, or track me if I was within approximately one foot of her eyes. Prior to that time, she did not track me, or try to locate me visually. When playing music, she had a clear preference to the specific sound track played, and would listen to piano music, but change levels of listening depending on the track played. Her attention to the music would not wander during the track she preferred. She would pick out her mother's voice or her father's voice separate from the music or other voices or sounds in the room, and re-fix her gaze to those people. She would tend not to blink when watching those people. She ignored her husband's loud foot-tapping that went on for approximately five minutes at one point. She also ignored his voice and did not try to seek him out visually when he would at times interject comments during the exam or immediately afterwards.

During various portions of the exam, she would be moved or have her position readjusted. She continued to handle her saliva during this time, never

being observed to choke on her saliva.

Following Commands: At various times during the exam, I asked her to close her eyes, or open her eyes widely, look towards her mother, or look towards

me. At times, she appeared to properly follow these commands. Interestingly,

some of the commands, such as close your eyes, open your eyes, etc. she tended to do several minutes after I gave her the command to do so. She had a delay in her processing of the action. However, when praised for the action, she would then continue to do the action repetitively for up to approximately 5 minutes. As we had moved on to other areas of the exam, at times she was continuing to do the previous command, then at inappropriate times since the focus of the exam had changed.

During different portions of the exam, I would ask her to squeeze my hand on

command, or, in the lower extremities, to pick up her right lower leg to command.

The upper extremities are contracted and weak. She appeared to squeeze my hand, and then relax her grip, in the upper right extremity, possibly in the upper left extremity. I am unsure if she was doing it to verbal command, or in response to body language; however, it was voluntary activity and not reflex. In the lower extremities, she showed these same abilities, marked on the right and to a lesser degree on the left (voluntary control over the ankles could not be determined due to the severity of the contractures there). However, in the right lower extremity, I again gave verbal commands, but also noted that she would oppose activity voluntarily. Thus, moving a hand against a thigh would elicit an equal and opposite reaction from her. She would gauge the degree of pressure, and counteract it equally. This is not a reflexive movement. With respect to her lower leg, we were able to clearly show that on videotape. I had her push her lower leg against my hand; my hand was on the top of her leg. Removing my hand suddenly, allowed her leg to suddenly continue voluntarily rising up and be seen on videotape. We

had her do this repetitively on videotape.

Her right lower leg is quite strong. Other areas are either not as strong, or

have such high spasticity brought on by neglect that voluntary activities are able to be felt, but difficult to show large degree of motion that are represented on videotape so well.The voluntary control is there, but does not show up well on videotape, as the range that the motion goes through is less.

Cranial Nerve Exam: Cranial nerve function is present and appears normal

in all groups tested. The fundoscopic exam and ophthalmic nerve function could not be tested directly. She tracks well and voluntarily. She does not exhibit "Doll's Eye" motion, an abnormality seen in coma patients whose eyes move back and forth like a doll's when their head is moved.

Coma patients cannot direct their gaze to specific things and maintain their

gaze on those things regardless of head motion or motion of the object.

She can do these things. She appears to see things best at approximately the

8-12 inch area. She was best able to track large reflective objects like aluminum balloons or sparkling lights (for which a focal length limitation is not an issue.)

This is a patient who has very poor language abilities. Her interactions with the world, as well as her ability to convey thought will depend in large part on her visual abilities and limitations. Thus a complete opthamological exam and evoked potential exam needs to be performed. This needs to be performed in comfortable situation and the patient needs to be comfortable with the examiner and the examinations. I would estimate that at least one day should be allotted for the exam and should be carried out her in room.

Sensory Exam: The patient was tested to light touch, pressure, and sharp

touch and pain in all four extremities and on her face. The pain portion in the

extremities was conducted by pinching the nail beds of her hands and feet. She clearly feels pain as the videotapes show.

On the face, noxious stimulation including cotton swab up the nose and gag

sensation and papillary touch with cotton evidenced a pain response. These were more than just reflexes, as she appeared to be annoyed by these painful responses long after they had stopped, and would not smile at me again for the rest of the day.

She certainly feels pressure, as was discussed earlier, and opposes pressure with voluntary motor activity. When using a sharp piece of wood, which she found uncomfortable, and going over her entire body (except diapered areas and breast areas), we found that sensation is present everywhere. Sensation on the right side as evidenced by moaning or tightening up muscles or withdrawal and was more prevalent than on the left.

We found that she had two sensory levels. The first is the side-to-side

asymmetry, where she feels more on the right than the left. The second is a major increase in pain approximately C4 and cephalic to the head. This is consistent with a spinal injury and spinal cord injury near this level.

Motor Exam: As discussed earlier, it is difficult to measure motor strength

on the classical scales. The classical motor strength scale is a 0-5 scale and is described as patient's voluntary motor strength score /normal which is represented as a 5. Thus a person with no voluntary motion would be 0/5 and a person with normal voluntary motion is a 5/5. Normal motor strength requires relaxation of the muscles around the muscle being tested. Thus, if grip squeeze is being tested, the muscles that straighten the fingers must relax in order to have a good squeeze. If those muscles don't relax, they tend to keep the fingers straight, and thus give a weaker squeeze than if they did relax. When the muscles near the area being tested don't relax, that is called spasticity, and makes the exam less accurate. At times the spasticity is so severe that a muscle tested may not be strong enough to

overcome the opposing muscles, and no evidence of voluntary muscle movement is seen even though there is in fact voluntary control over those muscles. This is the problem that we have with Ms. Schiavo. She clearly has voluntary control that is good control over her facial musculature. Formal testing of those cranial nerves showed no weakness or facial asymmetry.

In the upper and lower arms, however, the spasticity is severe. She at times

would voluntarily move her right arm/ hand complex against gravity, which is

considered a strength of 3/5 or greater by convention. When squeezing my hand and relaxing on the right side, she had approximately a 2-3 (-)/5 but range of activity was severely limited by spasticity. On the left side, it appeared weaker. In the upper extremities, she would oppose pressure on her, or try to move her arms with approximately 3/5, but not to command (probably due to the aphasia). The right side was stronger than the left.

The leg motion on the right was generally approximately 2-3/5 in all groups

except around the ankle. However, when opposing my hand in the lower leg, she was 3+ -4-/5 and the voluntary action caught on videotape was clearly a strong 3/5 or better. On the left side the strength appeared to be more of a 2/5 range in all groups, but due to the difficulty of the exam, may actually have been stronger than this.

The convention of the 0-5 scales for testing voluntary motor strength is as

follows:

0 No voluntary movement

1 Trace movement able to be felt

2 Movement of an extremity if gravity is removed. Thus if

movement of a leg occurs in a bed while a patient is lying down,

but he cannot move that same area up off of the bed, this is

considered 2/5.

3 Movement against gravity

4 Movements against examiner's actively resisting the patient's

muscular activity

5 Normal

The scale has some additional aspects, in that a - or + sign may further

allow an examiner to delineate a specific number into sub-gradations.

Reflexes: Were 2+ throughout on the left side, and slightly brisker on the right side. The reflexes to my exam were slightly brisker in the upper extremities than in the lower extremities. These reflex findings may be related in part to differing level of tone due to spasticity. No clonus was identified. The reflexes at the pectoralis muscles were 2++ and symmetrical. Reflexes at the ankles could not be obtained due to the severe contractures. Babinski exam did not show abnormal reflexes, probably due to the severity of the contractures in the feet. Both glabellar and palmomental reflexes were mildly abnormal.

Impression:

The patient is not in coma.

She is alert and responsive to her environment. She responds to specific

people best. She tries to please others by doing activities for which she gets verbal praise. She responds negatively to poor tone of voice. She responds to music.

She differentiates sounds from voices.

She differentiates specific people's voices from others.

She differentiates music from stray sound.

She attempts to verbalize.

She has voluntary control over multiple extremities

She can swallow.

She is partially blind

She is probably aphasic and has a degree of receptive aphasia.

She can feel pain.

On this last point, it is interesting to observe that the records from Hospice

show frequent medication administered for pain by staff.

With respect to specifics and specific recommendations in order to carry out

the instructions of the Second District Court of Appeal:

From a neurological standpoint: The patient appears to be partially blind.

She needs a full opthamological evaluation and visual evoked potentials done to

flash and checkerboard patters. The opthamological examination is to evaluate her

retina and her ophthalmic nerve to try to determine the cause of her visual

limitations and if any treatment exists. The evoked potentials looks at the nerve

between the eye and the visual centers in the brain, to see if there is treatable

damage and the type of damage, if any in these areas. This is important, as for

individuals to interact with her, and possibly teach her better ways of

communicating with others, they must know what sort of limitations she has. This

even extends to whether she can see people or objects in specific areas of her

vision, and what size objects need to be to be accurately seen. Additionally, if one

were to properly examine her, it would help if one knew the full extent of these test

results.

Communication: She can communicate. She needs a Speech Therapist,

Speech Pathologist, and a communications expert to evaluate how to best

communicate with her and to allow her to communicate and for others to

communicate with her. Also, a treatment plan for how to develop better

communication needs to be done.

Rehabilitation Medicine: The patient has severe contractures. She needs a

specialist to evaluate these and develop a treatment plan.

Endocrine: The patient has clinical evidence of an abnormally functioning

endocrine system. Her blood pressure is abnormally low. Many patients with

severe neurological injury have low blood pressure due to an abnormally

functioning endocrine system. The reason for this should be determined and

corrected, as with a more normal blood pressure, she is likely to have even better

neurological functioning. She has facial acne consistent with hormonal

abnormalities.

ENT: The patient can clearly swallow, and is able to swallow approximately

2 liters of water per day (the daily amount of saliva generated). Water is one of the

most difficult things for people to swallow. It is unlikely that she currently needs

the feeding tube. She should be evaluated by an Ear Nose and Throat specialist,

and have a new swallowing exam.

Mammography needs to be performed.

Spinal Exam: The patient's exam from a spinal perspective is abnormal.

The degree of limitation of range of motion, and of spasms in her neck, is consistent with a neck injury. The abnormal sensory exam, that shows evidence of her hypoxic encephalopathic strokes (right side sensory responses are different from left) also suggests a spinal cord injury at around the level of C4. Her physical exam and videotapes also suggest a spinal cord injury is also present, as she has much better control over he face, head, and neck, than over her arms and legs. This reminds one of a person with a spinal cord injury who has good facial control, but poor use of arms and legs. It is possible that a correctable spinal abnormality such as a herniated disk may be found that could be treated and result in better neurological functioning. This should be looked for, as may be treatable. Thus,there may be an injured disk or spinal cord; the disk injury is more treatable, the spinal cord injury, if present without a disk injury, may be more difficult to treat. A person with a spinal cord injury and hypoxic encephalopathy will need different treatment and rehab recommendations than one who just has a hypoxic encephalopathic.

Interestingly, I have seen this pattern of mixed brain (cerebral) and spinal cord

findings in a patient once before, a patient who was asphyxiated.

____________________________

William M. Hammesfahr, M.D.

(I couldn't fit the rest of his report here, it consists of his recommendations to the court.. you can find his report and the affadavits of more than 30 docs, very well known, at Terrisfight.org )

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How about giving a website that is neither influenced by Terri's family or by her husband.?

I found this site http://abstractappeal.com/schiavo/infopage.html#timeline

It gives a up to date timeline of what has happened with the Schiavo case and is a factual site not one based on feelings of one side or the other. It also has copies of actual court documents in pdf form to read as well.

I found it informative and interesting to read a unbiased site.

Now for my own opinion.. :-)

For me personally... I'd never want to be kept alive as Terri is.. my freinds and family all know my wishes should i ever become in a state that i can not make my own decisions.

I also think that the government and religion have NO place in a families PERSONAL decision about such matters and should NEVER have gotten involved.I also feel that both sides are being used as pawns in a political game and that saddens me.

None of us truly knows what state Terri is in unless we can see with our own two eyes and decide for ourselves. Anything else is going to be pure conjecture based on two very opposing viewpoints each with their own agendas. Again this is just MY opinion and i realise that everyone else's will vary. :-)

Thanks for letting me get my opinion out..

Kaylesh

I also think that the government and religion have NO place in a families PERSONAL decision about such matters and should NEVER have gotten involved.I also feel that both sides are being used as pawns in a political game and that saddens me.

None of us truly knows what state Terri is in unless we can see with our own two eyes and decide for ourselves. Anything else is going to be pure conjecture based on two very opposing viewpoints each with their own agendas. Again this is just MY opinion and i realise that everyone else's will vary. :-)

Thanks for letting me get my opinion out..

Kaylesh

The problem here is that we have defined this as being merely a family's personal decision. However, decisions involving life and death are NEVER simply family decisions. And in the absence of clearly defined directives from Ms. Schiavo, starving her to death on orders from a husband who has clearly shown that he merely wants her to die, has forbidden simple, ordinary nursing and medical interventions, and has refused to allow impartial medical evaluations -- well, that's the reason the government is involved in this.

If someone decides to starve their dog, they can be arrested for abuse. Even the way we treat an animal is never just a "family's personal decision."

Why should we allow Ms. Schiavo to be treated worse than an animal?

Jim Huffman, RN

Well, here goes....I understand the differences between her parents and her husband.....I also understand that her parents did once try to care for Terri.

My problem is this.....surely starving someone to death is euthanasia/murder.

Why has no-one suggested that Terri not receive further active treatment (maybe they have, feel free to correct me on this one). No more antibiotics for infections etc. Could this not have been a compromise between the two sides?

_______________

You know, if Terri had committed murder she would be treated better.

If the courts were to say that Scott Peterson was to die of starvation and dehydration (even if he were given painkillers for a "painless death"), how many organizations would come out saying it was cruel and unusual?? Tons.

she has no cerebral cortex. there is just fluid where it was. it doesn't grow back. thats a little worse than being brain damaged

______________

She has had no MRI. Wouldnt the husband want the most up to date information?

And so what if it was.

You know, I am a nursing student. I am a high 4.0.

Since this case, I am questioning whether I need to be a nurse because I dont believe in the murder of he handicapped. Nothing that I read about nursing told me that I needed to be pro-euthanasia.

Yest. I talked with my favorite teacher about changing my major to chemistry. At least I can make drugs to help people live.

Patients in PVS have no perception of pain/hunger etc...therefore it's a lot different than "starving" a conscious person like Scott Peterson or a dog for that matter.

This is an article that ran today from a mother whose daughter is on a feeding tube (with a flat eeg) and whose own mother is on a feeding tube;

_____________

Sandwiched between feeding tubes: The lessons

By Marianne M. Jennings

Our daughter, Claire, has had a feeding tube for 10 years, and my mother is closing in on one year with hers. I am generationally sandwiched between feeding tube patients.

Like Terri Schiavo, no one is really sure how much breaks through my daughter's or mother's neurological remnants. Also like Mrs. Schiavo, neither needs a respirator.

To the clinical, the three are in a "vegetative state." The inexperienced callously refer to them as clumps of flesh that hover in a puzzling state for inexplicable reasons.

But those of us who live with and care for these magnificent souls question the analyses hurled about as cherished life hangs in the balance. I offer my lessons from a decade of exposure to the "vegetative state."

Doctors are almost always wrong. While I have the highest respect for the physicians who have treated our daughter and my mother and will be forever grateful for their selfless efforts and care, I know, and perhaps they do too, that these patients are unique.

Doctors are inevitably taken aback at some point by Claire and patients like her who fight for their lives. If I had dug my daughter's grave each time a doctor told me she wouldn't live, I'd be in China by now.

Their first death prediction was six months, then it was three years. When Claire turned 10, the good docs called her an outlier and threw in the towel on death predictions.

Claire turned 18 two months ago. Doctors read CAT scans, MRIs, and EEGs, and conclude that, clinically, there ain't nothin' there. But doctors are not with these patients 24-7. Our Claire has a perfectly flat EEG.

From what I can determine, Terri Schiavo is higher functioning than our Claire. Yet each morning when we touch the bottom of her shirt to prepare for her shower, she closes her eyes in anticipation of that shirt coming over her face.

She clinches her teeth if you put a washcloth to her face because washcloths mean a good mouth cleaning and she, like all 3-6-month infants (Claire's developmental age) wants no part of that. She turns her head when you say her name. Claire's smiles come mostly in response to her mother's and her father's voices.

They feel, they flinch, they startle, they turn, they moan, they react, they have some memory, and no one truly knows how much gets through, what is serendipitous, and what is a real response. When in doubt, doubt the doctors.

Spirituality engulfs the vegetative. Be afraid. The life that exists in these struggling frames has had the judicial imprimatur of "So not worth it" placed upon it and the plug (tube) pulled. Yet the life that resides in these bodies so ravaged by immobility scares the livin' daylights out of me.

If you already believe in a g-d, these souls will confirm your faith. If you don't believe, well, I have seen atheists and agnostics humbled, silenced, and in tears as they stumbled upon a spiritual experience that caught them unawares. These are the very elect of beings.

Those who allow these lives to be taken, especially in reliance upon clinical reports, engage in the sentencing of innocents. Leo the Dog, hurled to his death in a California road rage case, engendered more outrage and due process.

These souls should have the rights and respect of cats, dogs, ANWR moose, and death row inmates. If I turned our cat loose on the streets and refused her daily Little Sheba rations, I'd be charged with misdemeanors galore and sentenced to community service at the pound. And our cat has no cognitive skills, save for the ability to sniff bumpers.

Scott Peterson will enjoy hearings and representation over the next decade as he sits on death row, where he will die a natural death. Where is Terri Schiavo's lawyer? Who does indeed speak for her? When our Claire turned 18, my husband and I had to petition to become her guardians. We were investigated, went to court, and paid for a lawyer for Claire so that the state of Arizona could be assured that Claire was in the right home with decent folk.

There was no clamoring at the court house for custody of Claire, and the hearing was mercifully short. Three months and $972 later, not including copying costs, we were appointed guardians of our own child. How do Florida courts get away with less, not for just guardianship, but for the life of the ward herself? If Congress can dictate disability benefits, medical privacy, and any number of long-term care issues, it should make public policy on euthanasia for the disabled who have no living will.

We are not here for them. They are here for us. I don't know why my mother has had to suffer physically at the end of her life.

I have never understood why our Claire has had a life filled with illness, epilepsy, and deformity, or why we have a child who will never utter her first words. But my family and I have learned more from these two non-speaking souls than in any of our many studies for degrees. We have had our priorities shaped and our characters molded through their stoic presence. Eliminating them would mean no more diaper changes, no more feeding bags, and no more "1 - 2 -3 lift!" as we struggle to rotate their positions.

But if I lost my Claire or my mother, I would spend a lifetime longing to be of service again, to have just one more time to feel the warmth of those neurologically curled fingers.

I fear for the clinical callousness of this tube removal. We turn our backs on the closest thing this world has to offer when it comes to angels. This removal is a giant leap backwards as mankind denies its spirituality and harms the helpless. I worry about the precedent for our Claire and my mom, but I fear for us

Patients in PVS have no perception of pain/hunger etc...therefore it's a lot different than "starving" a conscious person like Scott Peterson or a dog for that matter.

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You could always give him enough narcotics to make him have no pain or consciousness.

And still...you would have people climbing the walls because it would be cruel of it all.

The "experts" can say all they want to about PVS...they dont feel anything, they are just a blob..but I am NOT willing to gamble with my soul on the unknown.

What I do know is that I was on full life support 12 years ago (feeding tube & vent along with other various other things). My parents were told there was no hope for me.

And if I did recover, I would be in a wheechair & retarded. The hospital tried in ernest to have my vent turned off. My parents refused and the Dr.s rolled their eyes at the silliness of my parents holding out hope.

Forms were pushed in front of my family with pens ready to give away my organs as soon as the vent was turned off and I came to my end.

But I was "in there" trying in earnest to communicate. I went thru the burn "baths" with possibly the staff not being as careful because some of them thinking I could feel nothing. But I did.

Give Terri the benefit of the doubt. I dont care what the "experts" say. We do not know enough about the brain to determine exactly what is going on.

Patients in PVS have no perception of pain/hunger etc...therefore it's a lot different than "starving" a conscious person like Scott Peterson or a dog for that matter.

1. There is difference of opinion with those who have examined Ms. Schiavo as to whether she is in PVS.

2. Even given that, at our stage of knowledge, we simply don't know enough about the perceptions of those in PVS. I am unwilling to risk someone's pain and suffering from dying of starvation on uncertain knowledge.

3. It's still "starving" someone, whether Scott Peterson or Ms. Schiavo.

4. Let's remember that there's a certain dignity involved here. Ms. Schiavo is not a dog. No matter what her state of living might currently be.

Jim Huffman, RN

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