Hospice stages of death patients

Common Questions and Answers about Hospice stages of death patients

death

In the last stages of my daughters illness she had hospice in KC Mo the first bunch started when she was in hosp, and they called me, and i heard one of them yell at her and say tell your mother that you only have six weeks to live they did not know i was on the phone yet as i lived in ok my daughter beleived in God and was a woderfull person, ans she said maybe i will get better dont you beleive in miricles, and the one said this is ewality tell you mom what i said when one got on the phone i t
The patients ARE close to death when a doctor orders Hospice and Hospice is there to help the patient and to also give support to the patients loved ones. They are a wonderful Organization and I thank God for them. They are like ministering Angels as far as I am concerned.
I thought hospice care did not allow hospitalizations or active treatments for a disease. Only pain control and comfort measures.
A very wise Chaplin, told a class of young nurses one time, when asked about how to deal with death of their patients. He said God gave some people a warning that they were facing death, others he said had no warning, like in an accident. He asked us which we would prefer, This idea of that choice has followed me since then, as a young nurse I decided I would want to go with no warning.
Palliative care is very important and is not limited just to hospice patients who are in the final stages of living. If her doctors can't recommend someone, make some phone calls to your local hospice organizations and ask for their assistance. This is a loving, supportive community and I hope you will feel comfortable to ask specific questions as you think of them. We do have people here who live with PPMS and its devastating effects.
as a Hospice nurse I have always talked my patients and their familys through the stages of death and dying. Denial Anger Bargaining Depression Acceptance I realized this past weekend as I helped my 7 year old with the worst flu I have ever seen a child suffer from. That my own pain and discomfort was nothing to keep me from caring for her. I realized I was suffering but i didn't care.
Death has never crossed my mind at anytime. A friend of mine here died a couple of weeks ago from Ovca... and her death was very peaceful, and quite quick. The Hospice nurses do a wonderful job, and it's not like it was years ago apparently, so I don't think your Mum will suffer. Your Mum is way too young to go, so I'm hoping that the Gemzar will slow the cancer down, and your Mum will have more time of life with you and your family.
I knew what my mom wanted and I did everything I could to make sure she was well taken care of. At Hospice I overheard my 2 sisters talking about me and the middle one said that in the future when someone askes her how many sisters and brothers she had she was only going to mention the other 2 and not me. Some other hurtful things were also said about me and my husband. Needless to say that now my mom is gone I no longer have a family and that will never change.
When my husband died of cancer three years ago I took care of him at home with the help of Hospice and his last breaths were like a fish out of water. I wondered why God put me on this journey and I still have to remind myself that God's ways are always right. They may not make sense. They may be mysterious, inexplicable, difficult and even painful. But they are right. My mother received tainted blood years ago and now she is in her final days of liver cirrhosis.
however, the disease is slowly progressing and it eventually will be the cause of death. Anne, As I said, I am on a liver transplant list. MY LIVER FUNCTION TESTS ARE NORMAL !!!! The symptoms you described are those that I had when I was in a decompensating crisis (the swollen abdomen is called ascites and is abdominal fluid from portal hypertension). The only way to determine the degree of damage to the liver is by biopsy; the LFTs may or may not reflect damage.
it would also allow a recovery of an average of 60-65 percent of the HCV work force that we currently will otherwise all pay for as they deteriorate to catastrophic stages of disease. Some will lose 20 plus productive years otherwise. And, Either way, whether people are insured or not, most will end up in a system, be it state/university or private health care, that we all end up paying for in the end anyway.
org/wiki/Hepatic_encephalopathy “Hepatic encephalopathy (also known as portosystemic encephalopathy) is the occurrence of confusion, altered level of consciousness and coma as a result of liver failure. In the advanced stages it is called hepatic coma or coma hepaticum. It may ultimately lead to death.[1] It is caused by accumulation in the bloodstream of toxic substances that are normally removed by the liver.
for a patient to be placed on hospice is that the doctor has given them a prognosis of 6 months or less to live. Patients are referred to hospice when all measures to cure them has been exhausted and there is nothing left to do. It then becomes about pain and symptom management. At this point there are so many changes that are occuring within the body to prepare for the final stages of life.
I am David aged 55 and employed as a postman/driver/sorter, well up until 38 months ago I had never been into hospital,well boy was that about to change.
* Patients with ascites who are thought to have an alcohol component to their liver injury should abstain from alcohol consumption. * First-line treatment of patients with cirrhosis and ascites consists of sodium restriction (2000 mg/day) and diuretics (oral spironolactone with or without oral furosemide). * Fluid restriction is not necessary unless serum sodium is less than 120-125 mmol/L.
i have googled for any information to tell me what the stages are for her since death is unavoidable but i can't find anything anywhere, i know that all patients cancer and stages before death will differ but i am just looking for someone that can give some sort of information so i can understand what is going on and as the disease progresses i might not be as shocked when it does change and progress.
In the case of my father in law who was in his final days with cancer of the esophagus his hospice care takers were in direct contact with his physician and knew all the details of his condition and were able to call his doctor as needed. The hospice person maybe able to answer many of your questions. Hope some of this helps.
If you are looking to get some help coming off Tramadol, this is a good place for you. People here are in all stages of beating this terrible drug. I know you can do it! I believe in you!
I have yet to find a definite answer, though I have had my hormones tested and discovered all of my hormones are out of balance. I'm in the process of trying bioidentical hormone replacement to see if that helps. Hope you find some answers.
i wonder if your father has a liver doc who might be able to help you through this? hospice is wonderful and they might be able to connect you with professionals to clear some of your concerns. hospice is very good at managing pain but they usually work in conjunction with the family physician. this is a very difficult time but there are ways to make it less painful and hospice personnel are trained to assist not just the patient but the family.
Too often she saw people that were in the final stages of death, whatever the cause, and family couldn't be there or due to some falling out, didn't want to be there. She knew how important it was to have someone near because a dying patient can often still hear and think and be afraid. She started the program, enlisted the help of volunteers and when a patient was in the final few days, she would call a volunteer to come and sit.
I just wondered if this is part of the personality or personality and the end stages of this disease? Thank you ahead of time, even a small amount of opinions might help.
The level and quality of care directly effects someones longevity. To the best of my knowledge, MS by itself is not a cause of death. Last I heard, the average life expectancy of an individual with MS is about 7 years less than the average life expectancy. The average woman should expect to live to about 71.81 Years based on the US Census Life expectation for women being 78.81 years.
Mum has been an alcoholic for all of my life. She has progressed through the stages of liver disease like a text book, she has had many a chance to stop drinking but was unable to fight the demons I guess. A quick history of the last 2 years. Went into complete liver failure in October 2012 was hospitalised for 46 days and after we were told that she wouldn't make it, some how, she got through it and was able to come home. After 4 weeks she began drinking again and has never stopped.
I am a newly graduated RN, but have seen enough to know that you should not hesitate to give pain medications to terminal cancer patients.... sometimes it is unbearable. But Hospice can advise you of the proper use. Often more meds are needed than for other patients, due to the intensity of pain. Dad has been "given" 2 months to live, but one never knows. His attitude remains positive and he spends his days doing things he likes, as much as his energy allows.
They can make this transition a significant experience for all involved and provide you with much needed medical information on the end of life. A wonderful psychologist wrote several books on death and dying(Kubler-Ross) when you feel strong enough to read them.
I want to turn mine off when I get in my laast stages of CHF. It has went off a few times and each time is like being electrocuted. A pacemaker don't hurt, but a ICD is pure torture and besides that, each time it goes off it damages more heart muscle-may make you stay alive from irregular heart beat though. I have had CHF for 12 or so years and it went off about 3 time, twice in one row. It was horrible, terrible, like a mule kicking you with 700 jotes of electricity.
My Husband is in Hospice care at home with the final stages of Hep C. He is my 3rd Hospice patient in 9 years that I have cared for. I've lost both parents and now my Husband. When chemo does not work, please consider Hospice. My Husband was given 2 years maximum, but his disease is progressing much faster. He was only in remission 6 weeks, then went straight to 20% mortality rate. Now, he is on 3 kinds of Morphine round the clock. Hep C is one of the most painful diseases I have seen.
The problem is, none of get out of this world alive. caregiver222,I know you must know this, but hospice is a program that is provided to allow you to be able to hold a dying one's hand. They will pay for the program, but not the family's involvement. families can be involved as much or as little as they want to be. it is sad that you had such a terrible experience with your aunt that resulted in signing her out AMA.
Hi Kaysgirl, I'm so sorry to learn what you're going through. I went through this with my 74 year old mom in August 2007. It was a difficult time and it's still so hard to believe that my mom is no longer here. Yes, you need to get hospice in as soon as possible so that your mom doesn't need to deal with pain.
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