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That's right Barbara, soft and easy, as that's certainly how I would want it! Know that I am thinking of you during this very emotional time!

My FIL is doing well on Hospice in my home. He loves all "his girls", and they make a fuss over him.

We are keeping him comfortable and now he is even asking for the medications, something that I thought he would never do, Stuborn Norwegian! Lol!

He's got plenty of visitors in our kids, my sisters, the Hospice team, and every day is busy, and we are pooped out at the end of every day.

He is beginning to sleep much more during the day, and is eating less and less, and the Nurses say to not force him to eat if he doesn't want to.

This is a very difficult journey, but it's our job to make it as peaceful and comfortable as possible, and that's what we are doing.

Thankfully it's a quiet day today, so we are ALL resting up!

Take care Barbara, and God speed to your lovely Mam!
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Barb, I'm sorry it's come to that point, but in 100% of cases of life, there is an end. You have been through so much- I know you must be relieved a little bit to know that end is near. You all have a good handle on this.

I love the imagery of "letting (mom) down easy like she has a parachute." Happy landings to your mom!
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We put mom on hospice yesterday. I didn't think she was going to make it through the night without hospice. She's on a low dose of morphine, her regular psych drugs and is comfortable. Hospice gave us a choice of just PRN morphine or scheduled doses with prn as well. We opted for the scheduled doses because in the past, the nh has not covered her pain as well as they needed to. Just texted with SIL, she is getting both schedule and prn, that is what it's taking to keep her comfortable. We've turned down the Ativan so far because mom is on another Benzo med and I don't want to change too much at once.

So no, they are not rushing anything. We are letting her down easy as though she has a parachute.  And we had a long conversation yesterday about our wishes.
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My sister had stage 4 breast cancer and she just died last night, and she was under hospice care. I'm saddened because several months prior to being placed in hospice she had gone to an in home natural treatment place. She had after 24 hrs there with cleansing and healthy, vital juicing, had no more need of morphine since her pain was gone. And in a few days, she had an appetite and could eat healthy meals. However, it is important (if experiencing high anxiety) to continue to use the anxiety medicine so there are no withdrawal symptoms.
In my sister's case, she was taken from there by another family member and by not staying with the strict health program, her pain returned in about 1 month. And by June, family members placed her in hospice.
I think she felt abandoned and experienced the same treatment...heavy dosages (enough to make her unresponsive, so much so that she didn't even know yesterday morning, that my other sister was there). I believe in the body's God given ability to eliminate toxins and with divine help and proper cleansing and nutrition, the quality of life can be dramatically improved and possibly fully healed.
I'm still in shock...I know there are nurses with compassion (my sister was an RN) but, she was realizing that with natural healing methods, divine intervention and prayer, that you can get amazing results. I live almost a 20 hour drive from her and I wonder if I was closer, if I could have convinced her to try another natural healing place, especially since she saw some amazing, miraculous results...I feel that being in hospice care rushed her death along too...
I feel and can relate to your pain.
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Shattered heart try and think of it from your point of view. Would you want to spend your last days with pain and overwhelming anxiety. I know I would quickly be asking for the drugs. Sedated and sleepy that is what I would want so rest assured you are doing the right thing.
So sad for you that he is only 62 but it is what it is so take good care of yourself so you can be strong enough to take care of him till the end.
Make use of all that hospice has to offer. Try and make some time for yourself and don't feel guilty about leaving him in someone else's care while you go out and have lunch with a friend, go shopping or have your hair done.
Don't concern yourself that something happens while you are out of the house. It may have been what he wanted. Many people wait till their dearest loved one is not present to pass. You might feel bad that you were not home but immediately get rid of the guilt, that is not what your husband would have wanted.
My mother passed away one afternoon after a couple she had been friends with for many years had stopped by and enjoyed a cup of tea with her. Later they said if they had known it was going to happen they would have stayed longer. The truth is she probably had no idea either as she was found by another friend shortly thereafter on the floor by the kitchen sink. I am sure she was washing the dishes that had been used for tea. She had experienced a second heart attack about a week earlier and seemed to be recovering well. So as life is unpredictible so is death.
Blessings to you and your husband.
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shatteredheart,
I, too, am so sorry for you and your husband.
Yes, you are doing the right thing. These are drugs that Palliative Care and Hospice use to keep people comfortable.
If your husband is suffering from pain, Morphine will handle that. If he is agitated or having anxiety, the Ativan will help that.
A few people think that drugs shouldn't be given because it makes the person sleepy. But why would you want to have your loved one in pain or agitation when you could relieve it?
If you have a belief in a Higher Being hang on to it. Try to get some time away from care-taking to keep you going.
You sound like a caring wife. You are doing the best you can.
Please keep in touch.
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This is not coming to my e-mail anymore. Had to look it up.
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Shattered, I'm so sorry! How tragic that your husband developed dementia at such a young Age!

Is he agitated? I believe that is what the Ativan helps with; morphine is for pain.

If you have questions, is there a 24 hour nursing line you can call?
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Is atavan and morphine good for someone with advanced dementia due to several cardiac arrests they suffered 2 years ago? My husband is home from a week in the hospital. Palliative care. Am I doing the right thing? I just want no pain for him and he is only 62 years old.
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Wish we had a time machine. Would turn it back to 2012
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Glad, good point about wanting and wishing things could have been different. So many of us go through the "what ifs" stage... oh why didn't I do this, or do that.

And some people need to blame someone or some thing for a death that was going to happen anyway. My sig other is one who points fingers at others whenever there was a death in his family.

This finger pointing goes on for many years. I keep telling him that that relative would be really upset if he/she knew that all you could think about regarding their whole life was the day they died and whom you want to blame..... [sigh]
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Myth, I really do not think that is what it is. I think that the accusations by family members after a loved one has passed, are coming from a place of grief. Wanting and wishing things could have been different. Maybe some guilt for having made the decision to choose hospice, and wishing they as family members had taken more time to provide care, support for the family member.

My mom was on hospice for eight months before she passed. She had a fall three weeks before passing and hospice has dealt with these issues many, many times. They were successful at making her comfortable to ease her passing. And now, after all, she is reunited with her beloved family members (that she talked and wondered about often).
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So many times in this thread, it sounds like family members believe and expect that their LO's on Hospice are going to get better! That is never the objective, or the plan. Quality of life and Comfort are the goal, and a calm and peaceful death.

I've been through Hospice care with my own Mother, and am currently Caregiving for my FIL in my home on Hospice. We were lucky to have been given the option of using the same Hospice care organization as we had with Mom so many years ago, as they were tremendous, and are now working with us caring for my FIL.

They are an amazing group of Nurses, Social Workers, and aides! They have such a great way of putting my FIL at ease, and the SW is currently putting together a plan, to have my FIL honored by the Veterans of Foreign War, to acknowledge him and his Naval service to our country, she's such a Sweetie!

While they have made every medication option available to him, I've yet to see them push any medication or sedation upon him. Although when I've asked for a calming agent, so that he can rest comfortable in the afternoons and not be so agitated (so that I can get some rest too!) and at nighttime for good sleep, they haven't hesitated to make it available to him. His pain is well controlled, and should his needs increase, they told me there is much, much higher doses that he can be prescribed without worry of overdose. Again, comfort is the key. Never do they euthanize a patient, that is a Myth! Do they make patient comfortable enough to to the point of sleep, certainly, and sometimes just being relieved of the horrific pain, and made comfortable, is exactly what it takes to allow the patient to give in, let down, and let go.

Imagine yourself being in that insanely heightened and prolonged agitated feeling of severe pain, your body is naturally pumping out those "Fight or Flight" endorphins to the point that it cannot sleep, let alone relax. Now be given a nice relaxant and something for that severe pain, and ahhh, relaxed, less pain, and either sleep or hopefully even death, as when that pain control wears off, it all starts over and over again. No thank you, give me a calm and peaceful death any day!

And Chemist, I agree, dehydration in the End Stages of the dying process works wonders too! It was explained by our Mom's Hospice Dr/team that
patients incapable of drinking and swallowing enter into a state of ketosis, where the nervous system is
dulled and the patient rarely feels pain, hunger or thirst. Being dehydrated causes a feeling of welbeing, euphoria, and in this stage, the last stage, we do our best to keep our Loved Ones mouth moist and comfortable, using those spongettes. There are other routes of pain meds used at this point to keep the patient as calm and pain free as possible, either sublingual or injectable, and allow them NATURAL yet calm and painfree death.

Some states do have Death with Dignity laws (here in Washington state we do), but that is not the role of Hospice. In fact Hospice does not participate in the DWD organization. They do not admonish them, but will only come afterwards, after the DWD take care of the patients wishes and the patient has passed, to aid and assist the family in contacting the funeral home, and prepare the deceased for transport to the mortuary. I know this because I had a Nephew who went this route just this past February. He was was on Hospice, chose DWD, and ended his own suffering. The 2 agencies work separately, but in conjunction with one another, but "nary the 2 shall mix", as they say. It was a wonderful thing, but the decision was not taken lightly! A lot of discussion, planning and execution went into it. He is finally at peace.
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Honestly I don't know I feel by reading most of your comments I think mate it depends on workers or hospice your loved ones attended I didn't feel so angry with hospice until my dad passed away after my mother both at same hospice and wierd how there rooms were beside each other my mom and dad passed away two years apart due to lung cancer that spread through moms body and dad had cancer as well they both passed away three days after being brought in from being at hospital my mom seemed more cared for and passed peacfuly she was in hospital for three mths was given like two weeks and lasted that long she was reaponcive on and off at hospital some days she seemed fine and talked fine others shed lay there like she was already gone or sometimes she would try to talk and she couldn't but with my dad when he went in hospice u have sign the papers for them have oxygen tank and so I did but they like lowered his oxygen and wouldn't give him more he needed more I was getting soooo angry at that point I new once my dad was there he didn't like the nurses he was a grumpy man at times tho but I new he had reasons why he didn't like them and took same as my mom three days for him to pass I felt like they only keep drugging them and drugging them until they die so they can get next patients in the nurses don't get paid it all vulinteer work and the hospice is rubbed by donations that what I was told by hospice after my mom passed from hospice in Guelph Ontario I would never put anyone in hospice after seeing my parents go like that it just make me hurt and angry
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Chemist,
Hospice does not euthanize anyone.
What you experienced was the use of a medication to ease your mother's suffering which allowed her to pass peacefully.

The remarks about giving her the Pentobarbitol the previous Tuesday meant they were assuming you wished her to be kept alert for whatever reason, and there are many. For example, waiting for a relative to arrive, the birth of a new baby, a legal matter to be completed, tax returns to be signed, a service person to arrive from overseas.

As to the questions about your return plane ticket they were trying to remind you that it might need to be changed and the financial implications of that. None of these things are sinister, just misunderstandings between a stressed relative and a busy nurse who perhaps has poor communication skills or is totally exhausted.

Hospice nurses become very stressed at times especially when dealing with the death of someone young who is maybe going to leave young children or perhaps a tiny baby sent home to die within days of birth. There is no way you would know what else was happening with the nurse's patient load.

Many nurses burn out very quickly and leave this specialty because of the emotional stress it produces which they were far from prepared for. It is not a career path that is encouraged and other nurses seem to think that a hospice nurse has entered that field because they are too dumb to practice main stream acute nursing. This is far from the truth as a hospice nurse needs to be very experienced in many aspects of diseases and able to guide the patient and family in their correct course of action.

They are frequently the only course of communication between patient and Dr who rely on them for assessing conditions and medication requirements. Many Drs feel that loosing a patient is a failure on their part and therefor loose interest in the care. During ten years as a hospice nurse I only saw our medical director make two home visits although certain FNPs took a great interest in their dying patients and would often visit the home, but of course they were nurses before becoming FNPs.

Pentobarbitol is not a drug I ever saw used and is generally discouraged for the elderly and not a first choice for the general population these days. Barbiturates were very commonly used 50 years ago and very effective for sedation. It was standard practice to use it as a pre op sedative for children.

My own husband spent most of his career as a Dr working in the pharmaceutical industry, developing some ground breaking drugs but as far as hospice care was concerned he deffered to me although he had had experience in acute medicine and general practice.

Was it your choice that Pentobarbital be used as a sedative for your mother? Not that I am suggesting it was the wrong choice if deep sedation was required.

I am in no way suggesting that drugs given at the end of life if they are needed to ease suffering may allow the patient to die more quickly and therefor suffer less.

Euthanasia is never the objective although there are frequently enough drugs in the home for caregivers to deliberately over dose.

Chemist I am so sorry that your mother had to suffer such excruciating pain but glad the end was finally peaceful.
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Excusé, Chemist. I'm confused about your post. How is someone giving your mom a dose of pentobarbital so she can sleep the same as performing euthanasia?

"they knocked her out with pentobarbital. I expressed my gratitude and they said, 'We would have done this last Tuesday, but I thought you still had some unfinished business.' Apparently they only do euthanasias on Tuesdays."

Thanks for helping me to understand this better. Seems to me they were helping her relax and sleep, which is what pentobarbital does, right?

Fwiw, my position is that I would hope someone would ease me into death if I'm suffering and ready to go... but that has nothing to do with giving an elder a dose to minimize anxiety and help sleep... does it?  
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Wow...
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Unlike most of the caregivers participating in this thread, I have experience in pharmacology (pharmaceutical industry scientist). I went through the caregiving/hospice experience three times within a year and a half and it was incredibly eye opening. Thank goodness for the skilled and compassionate hospice community. They are extremely good at their work. But have no doubt what their work is: to give you some quality final time with your loved one and then to create a peaceful death. It amazes me that even the hospice nurses appeared to be kept in the dark about the biological processes of death and the pharmacological effects of the drugs they were using. A major mechanism of the modern concept of a "good death" is dehydration. The trilogy of opioids, benzodiazepines, and Haldol is no different than what happens when you bring your beloved pet to the veterinarian to be "put down". It is just done more slowly.

I couldn't figure out why the hospice nurses kept asking me when my plane ticket home was. I finally found out when I begged them to finally stop her horrible pain and they knocked her out with pentobarbital. I expressed my gratitude and they said, "We would have done this last Tuesday, but I thought you still had some unfinished business." Apparently they only do euthanasias on Tuesdays.

When our pets no longer have a meaningful life, we hold them, tell them we love them, and let them go painlessly and peacefully in a matter of minutes. I'll never understand why we torture the elderly instead. It's inhumane.

Thank you to all those hospice nurses out there doing the compassionate work to minimize the torture.
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Soleo7, my heartfelt sympathy to you and your family.

As for the morphine given to your Mom, the dosage is similar to that one gets after they have had surgery. I remember having a morphine pump to help cut the pain. Once I was off the morphine pump there were zero withdrawals.

And it is not unusual for a patient to rally for a day or a month after being in a coma like state, both my parents did that.

When your Mom had to have her arms and legs held down, that is called delirium, which 90% of elders have when they are in the hospital. It is around 20% of much younger patients usually those who had major surgery. My Mom had delirium and she wasn't even on Hospice at that time.

The Hospice group taking care of your Mom 24 hours a day, you were quite lucky, as the majority of Hospice groups do not do 24 hour care... one would need to hire Agency Caregivers. I needed to do that for my Dad.
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I had the same experience with my mother.She was told by her Dr at her last chemo visit that if she no longer wanted and was to tired to continue the treatment that they could have hospice come to house and make her feel more comfortable and at ease .She also was fine and alert the day they came. in fact she was due to have surgery 3days later on Monday morning to put something in or near her pancreas to make it function better for the time being. to give her just a little more time to be with us even if it would be just another day or another month.My mother was hesitant but she was also in some pain.But she had medication that would help her for pain already.But We were told shed be more comfortable with what they were giving her for a longer amount of time.Not once did they say Shed never speak walk talk orsay shed just plane sleep forever...But thats what happen.They gave her a morphine patch shot and something else also with ativan.For 2days i couldnt sit n watch her die like that.I called hospice and complained saying the nurse didnt know what he was doing.He was overmedicating her and i wanted him to leave n send a new person.They sdid but Monday came for her surgery and she was still out of it .we had to get her in car by my dad and son and i moving her out of bed struggling cuz she was hwavy and dead weight to a wheelchair and then up in car to hospital.Very difficult .When my dad admitred her andwe told them situation she was rushed to be seen right away.And we werw told her surgery could not be performed.She was to medicated they said.We had stopped hospice the 2nd night they came from giving her any more meds and 2 days later when we went for surgery they tell us shes to medicated,"STILL?"2DAYS LATER?She was overly medicated by hospice nurse is what they called it.What i called it was overdose by hospice.My mom took 3days to come out of it finally talking and having life in her again.But she wasnt herself.Not remembering everybody or who they were .Calling people names and being just so mean to everyone so bad they had to restrain her arms and legs .They said she was having withdraws but it pass.But vcuz the surgery was called off and her condition had worsened they said this time she can stay in hospital if thats what we prefer bcuz they gave her a week to survive.Or we can do hospice again but this time bed and all equipment needed for last days of life.She wanted to go home.I was angry that they took more time from us with her bcuz of too much Medsthe first time they went.i didnt want the same tging to happen again once home.My mother went home that night.Hospice wasmset up within hournor 2 at our home during time they were releasing her.Ambulance brought her home and she had hospital bed monitors needed walker a portable potty wheelchair etc....But no nurse.I had our priest come from our Church that night and read her her last rights and Baptize her which she had not yet been. But she didnt need one yet.i took care of her giving her same meds her Dr prescribed.And a week went by and not only was she still with us but she was back to her normal self again.And God Blessed us with more time after all. Hospice then came just to bath her and change linen and do vitals but id care for her.then when her pain started to increase and she needed a little more assistance it went to hospice coming few hours a day.Even when i knew i needed HOspice here more to help me i refused to say so But i was drained and when her body started the process of shutting down and i couldnt fight myself anymore to stay awake n stay up with her without sleep to care for her anymore i was devastated.I ended up going to emergency and found out id caught pneumonia So hospice was now caring for her 24 hours. I had no choice.She lived exactly 1month longer from day she was released and given 1week to live.It was feb25th ash wednesday she came home and until march 23rdshe spoke to us eyes open and still alert until 2days laterMarch 25th 2009 just a bit after 1am my mother took her last breath and with it my soul....But the woman nurses who were there to check on her those last weeks to takinturns daily in 24hr period were greatThey did great job and did allow her time with us that she was suppose to have.As for the hospice nurse that almost brought her to her deathto soon.Idk what happened to him.
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Karen you did not kill your mother it was simply coincidence that you gave it the day before she died. Starting dose is usually prescribed every four hours. The 5mg you gave would have been long eliminated from her system before she died.

It sounds as though the thing that is bothering you the most is the fact that the bottle was labeled "Opiod Tolerant" How the bottle was labeled is of no importace at this time it is the actual dose that matters. You only gave what was prescribed which you had done prior with no ill effects. Morphine is Morphine whatever the bottle says and the dose was reasonable. Drugs by mouth are not as effective as those by injection or IV By those routes the starting dose is usually 2 mg but is often repeated in less than an hour if the pain is not controlled
FF suggested that it would take 200 mg to kill someone. There probably is not an exact amount but that is certainly more than would be used. I saw one patient who was routinely taking 6mls every four hours because he had become so tolerant to it. But a dose of 200mg did not kill him.

Give yourself a break Karen you did not hasten Mom's death it was her time . Set this aside and concentrate on healing giving with assistance of a therapist or make use of the hospice bereavement councillor which is free for individual or in groups whatever you need. this is available for 12 months after a death.
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Be at peace, dear one!
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Dear SueC and BarbBrooklyn,
Thanks so much for your thoughtful insight into an issue that is causing me a lot of agony. Yes, I plan on seeing a therapist with the hope to work through it. When I agreed for my mother to enter home care, I requested that it be palliative - that she would continue to take her regular heart meds and eat. And that she did. But they sent a hospice nurse because Medicare does not pay for palliative. They told me to give my mother a small dose of morphine if she had pain/breathing problems. I gave her two doses (5mg) over a ten-day period. But it was the second one that was on her last day that bothers me. Even though the dose was 5mg, it came from a bottle that noted, "opioid tolerant." I was completely ignorant about all of this. Nevertheless, I will speak with a counselor. Thanks for the good advice.
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Karen,
I've been a nurse for 38 years and have given a lot of Morphine over those years. It is a narcotic. It deadens the pain centers in the brain, slows respirations, slows gastric movement in the gut, relaxes muscles, can make you sleepy and can give a feeling of well being.

The doses used after surgery (for pain control) range from 7.5 mg-15 mg every 4 hours, depending on the size and tolerance level of the patient. By giving your mom 5 mg (a low dose), there is NO WAY you could have caused her death. Maybe your dear mom was finally able to relax and her passing COINCIDED with the medication given. Be GLAD that she didn't have to go through an agonizing death (screaming in pain, screaming in fear, severely short of breath, thrashing around, etc.).

You can now relieve your mind that giving her the prescribed amount of medicine could NOT have taken her life. It's just not possible with that dose. Please stop beating yourself up. NOTHING would have prevented her passing away at exactly that time. That's the time God had planned for her. You just made her more comfortable for the journey.

As Barb said, you would benefit from some counseling. Hospice has follow up counseling for the family for up to a year. Maybe you'd feel comfortable talking to your pastor, priest, rabbi, etc.

Do NOT doubt your actions. You did nothing wrong. Everything you did was for her benefit. You loved your mom until she crossed over. I know she's grateful that you were in her life.
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Karen, go to Drugs.com and read about morphine dosages. They are divided into " opiod naive"-- patient who has not had morphine on a regular basis and " opioid tolerant"--someone who has been on morphine or other options before.

As I posted a few weeks ago, 200 mg of morphine, given at once is considered a fatal dose. 5 mg is not anywhere near that. You would need 40 doses of 5 mg of morphine, administered at once, to cause death.

You eased your loved one's pain, anxiety and breathing difficulties, if there were any. I wish you relief from your dreadful anxiety that you did something wrong.

I would like to suggest, gently, that it may be time for you, if you haven't already to get in touch with a counselor or therapist, to see if you can get some relief from the psychic pain that you are clearly in. Grieving is hard and hard work. It's more painful and complicated if we get bogged down in thinking that somehow we did something wrong, or that we, magically, could have made things " better".

Please be well and comforted in your good memories.
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Is 5mg (.25ml) of liquid morphine from a bottle that says "opioid tolerant" a high dose?
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ewinfrey64, my heartfelt sympathy to you and your family.

Please note, when someone is on Hospice or not, the patient will rally to a point where everyone will think the person is going to be fine. This is normal. Then a week or two later that patient will start to decline. They usually stop eating because any food in the stomach becomes very painful. One's body organs start to slowly shut down and there isn't anything one can do to reverse that.

Being that your Dad has lost so much weight, that in itself can cause a lot of back pain. My Mom had also lost a lot of weight and during her final month had been in so much back pain that the nursing home tried everything. Once on Hospice, the morphine quieted her pain, thankfully.

This is usually our first rodeo dealing with a death of a parent. With Hospice, they have been on this journey hundreds of times. They can tell just by looking at a patient if that patient is in pain.... if the organs are starting to fail... and are pretty good at determining how soon death will come.

Both my parents had passed in the wee hours of the morning. At the nursing home there was a head nurse who was able to confirm that my Mom had passed. For my Dad, he was in Assisted Living and we had to wait for the doctor to arrive to confirm my Dad, and that took an hour. We realized that my Dad wasn't their only patient to see, so the time frame was understandable.

As I have said many times on this thread, a patient will die on the same timetable with or without Hospice.
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I was also concerned when my father was placed on Hospice back in april of 2016. He had been in a nursing facility for the past 3 months because my sister couldn't handle him living with her because he had dementia and would run sometimes if he was outside and she would have to call the police to help her. The second time this happened she called the police in Shawnee Oklahoma where she lived and they sent out a young police officer. He immediately called a mental health place and they came and took him to Henryetta an kept him drugged up to where he was on his stomach in the hallway scratching at the floor. He was there for 2 weeks before we could get him into an assisted living at Belfair in Shawnee Oklahoma. My father paid almost 4000 a month out of pocket to live in this assisted living. This place was a sad place for the poor individuals like my father. He would just walk up and down the halls on a daily basis. When I would go visit him, I would look for at least 30 minutes before I would find him in another persons room lying on their bed. They would allow him to feed himself even if he would only be able to get a bite of food in his mouth during the meal. Most of the food would go on the floor and all over him. I talked to them about helping him eat and giving him finger foods to help with his eating. They would give him sandwiches and he would get seriously constipated and would hurt so bad until I would have to beg them to get an order to get him an enema. My sister and I had decided to take him out in March of 2016, and place him back in her home. This time we were going to fence in her yard though. She lived in a trailor park, so they wouldn't allow her to build a fence around her trailor. So by the time we figured out what precautions to take so my father would be safe, it was to late. He had fallen at Belfair several times, and was rushed to the ER. The last time he fell was in the beginning of April 2016. They apparently weren't watching him and he fractured a small area in his hip. He was sent again to the hospital and this time admitted for surgery. The surgeon didn't completely sedate dad though. He numbed the area that needed a pin placed, which was a very small incision on his right hip. He had stitches placed and the surgeon said he should be up and moving in no time with some therapy. A rehabilitation therapist came in and worked with him after the surgery. He was very sore, and so they continued to give him a morphine drip until it was finished. The hospice facility called Faith hospice called my sister and she was concerned how we would take care of my father after all he had been through. I told Carolyn I wished he could go to here house and we could hire aides to come in and help take care of him. We sat down and talked to a doctor that saw dad, and the hospice coordinator. They were both ready to just give up on Dad of course. They said he would just continue to decline due to his dementia and the fall he experienced. So we wanted what was best for dad, and they said there would be nurses and aides coming in to help take care of him and they would provide the medicines, pads and the hospital bed. So we thought with only hours before he had to be released from the hospital that this would be the best option. We moved him into my sisters house, which not knowing at the time stopped me from having any say so in what happened next. Faith Hospice said they would take dad off of the morphine a little at a time until he was completely off of the medication. He was eating very well when we brought him home. They even told us he would be up and moving in a couple of days. I was so hopeful that he would get better and with his heart being so good and as strong as he was I just knew he would be better soon. My father was never a pill taker. He would tough out the pain if he even had a headache. He would have never wanted to be put on morphine for any type of pain. So I told them with in a week that I wanted my father off of the morphine. Of course they wouldn't listen to me though. I was a guardian of dad as much as my sister was but he was in her house. So she agreed to keep him on morphine and she would give it to him every 4 hours. I tried to be there as much as I could between working two jobs. I kept in touch with the nurses and even made them mad at me a couple of times because they would tell my sister one thing and tell me another. I couldn't get them to listen to me that I feared the worst if they continued to give him Morphine. So I would get into it with my sister and she would continue to side with them until I knew I was going to have to so something drastic. So I called an ambulance and was going to have dad transported out of there before it was to late. He wasn't eating very well by this time and he was losing a lot of weight. So the ambulance came and my sister was on the phone with Faith hospice who said they would have me arrested if I removed dad from her care. I even called them and said I want my father taken off hospice. They said that wasn't my decision to make. By the time the ambulance got there the police were surrounding the trailor. So I had to leave because I didn't live there. My sister banned me from her place for over a week. When I finally got to see my father again, he was almost gone. His mouth was rotting from the morphine and he was so tiny he looked like a skeleton. The hospice nurse came in and said well girls it could be very soon now because he was starting to turn blue in his hip area. I sat with him the rest of the night on May 30th, until he took his last breath on May 31, at 1:39 am. When I called Faith Hospice to find out if they were coming, they said No I am not coming right now, I will be there in a little bit, very hateful. I was so numb from my father dying, I couldn't say a word. I just hung up the phone. So I feel that some hospice places are in a hurry to get rid of the poor innocent elderly who should not be forced to die the way my father was. I don't think morphine should have been used on the elderly that wasn't use to taking medication and most of all because he had dementia. I believe if they would have taken him off of the morphine, a week after he was put on it and exercised his leg, that he would still be here today. My father was a very active and healthy man before he got dementia. So for him to be placed in a bed and put on morphine until he couldn't eat anymore was wrong. But no one would listen to me when I begged to speak with the hospice physician.
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Flymom, please note that amount of morphine given in Hospice is very similar to the amounts given to a patient after they had major surgery. I remember being on a morphine pump and all the morphine did was help cut the pain.

It takes 200mg of morphine to take down a person. Hospice uses only 5 to 15 mg for each dose. If Hospice was at home, no way would the Hospice nurse leave a huge amount. If Hospice was at Assisted Living or a nursing home or Hospice facility, as Veronica said above, it is strictly regulated and inspected [its a narcotic].

I was so glad that both my elderly parents were under Hospice care, as their passing was very peaceful, not one of sheer pain and/or gasping to breath. And also note, one's time table for passing is no different whether they are on Hospice care or not.
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Loveyourelders. I have news for you hospice is very strictly regulated and inspected regularly. The inspectors read all the records and go out on visits with the nurses.
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