My grandmother is almost 89 years old. She has been diagnosed with vascular dementia, and has been declining within the past 5 years. For about 3-4 years now, she has been in a memory care/nursing facility. A couple months ago, she had a stroke. It was considered moderate, but left her unable to swallow, walk, talk, etc. She doesn't show any reactions or emotions- doesn't seem to recognize anyone, show signs of pain, cry, etc. After her stroke (because she couldn't swallow), we had a feeding tube put in to see if she would make any improvements with swallowing, talking, moving, etc. She has not. Doctors estimate that she swallows 20% of her pureed food daily. She is being supplemented with the feeding tube. She is under palliative care, and they have asked if we would like to move her into hospice care. They said that if she is in hospice care, they would wean her off of the feeding tube, and focus on solely keeping her comfortable. They said that she IS medically stable- she is not actively dying, and not rapidly declining. I (and my family) do not want to prolong her suffering, or for her to merely "exist". We are unsure if we should or should not put her into hospice care and wean her off of the feeding tube. I'm so afraid that if we pull the tube, she will starve to death. I do not want her to feel hungry, starving, etc. I couldn't imagine a worse death for her- to slowly waste away. Palliative care made a comment about how sometimes when the remove the tube, the patient will try to eat more on their own, which further makes me think that they feel horribly hungry and malnourished. I DO NOT WANT THAT. Ugh. Does anyone know if there is a way that hospice care can make them NOT feel hungry, etc? My grandmother is the most important person in this world to me. I want to make sure that she is absolutely comfortable and not suffering in any way when she passes. I want a dignified end for her. Please help.
And it seems that sensory deprivation is a strong factor in her life at this point.
When my father had one, for several months, we had to change our entire life to accommodate tube feedings every 4 hours, and up until about 1 am b/c Medicare didn't provide larger capacity bags for 24/7 applications. It was a very difficult challenge for both of us. And it was depressing except for the fact that Dad was rapidly improving physically, so there were strong motivations.
My father was 85 at the time, my sister had just died, so I could focus all my caring on Dad. He eventually was able to eat normally again, although he developed dysphagia in his later years.
I can't answer your specific questions, but I know that if I ever face that situation, I WILL NOT have a feeding tube. If there isn't a strong possibility that someone can recover, I think it just accentuates the misery of aging adaptations.
If your GM hasn't progressed, and is swallowing (and possibly aspirating) about 20% ) I think you probably are aware that that can lead to aspiration pneumonia, or more obviously, choking. That kind of choking and coughing and attempt to clear even pureed food from the throat is hard to watch, and probably harder for the individual.
You seem very compassionate, and you're aware that your GM doesn't have much quality of life now. I think that would be a major consideration in considering whether or not to prolong her life with a feeding tube.
A very blunt but realistic question is what does she have to look forward to?
I hope you spend some time in solace, considering all the options, and asking yourself if you would want to spend your last years in a similar condition, and that you make a decision with which you feel comfortable. I offer my best wishes for comfort and peace to your family during this challenging time.
https://www.choosingwisely.org/patient-resources/feeding-tubes-for-people-with-alzheimers/
I fear from all you say that you will question yourself if you withdraw these feedings. I certainly would not, but you seem to be. I will tell you that these feedings often lead to diarrhea and bedsores, just more torment.
If you are ready for your grandmother to pass, if you accept that she is at the end of her life, then I suggest you do as the doctor has advised. If you do not accept that she is at the end of her life, and feel that you are starving her to death, then I suggest you withhold a decision until you discuss further with her MD. Hospice is for those who accept that the end of life is essentially now here. That while some interventions may prolong (the often tormented) few days, weeks or months, these interventions will not stop death coming. Being born is a pre existing condition; we will have to die. If you have hospice your loved one will not suffer agitation, hunger, air hunger, but will be medicated for peace and an almost dream like sleepiness. Will this cause an earlier death? Perhaps by some minutes or hours or days. But not by much more.
Your worry is now whether she will feel hungry if the tube comes out and she wastes away feeling hungry. You’ve been told that the opposite might happen, and she will start eating again. If she doesn’t, on hospice care in the end stages of life she is most unlikely to feel starving hungry. As the body closes down, it does not need food and can't digest it. Most people eat nothing at that point, and the most they want is something to keep their lips and mouth moist, painted on.
Perhaps you need to go back to your original ‘choice’ about the feeding tube. It’s hard to feel that you are making ‘life and death’ decisions for someone you love, but many of us are faced with it. A painless death with dignity is the best any of us can hope for. Love in a difficult time, Margaret.
Did your grandmother ever discuss HER preference about what she would and would not want at the end of her life? Much like Alva, my mom was very vocally against anything like a feeding tube.
I suggest strongly you reach out to hospice and put this all before them. Tell them you are only looking for information regarding feeding tubes at end of life. It doesn't obligate you to engage them just because you reached out to them for information! If you don't like what you're hearing from them, then don't engage their services. As Joanne said, my mom's hospice didn't encourage us to withhold food; rather they let mom decide how much she wanted to eat based on how hungry she was.
I would also suggest you talk more in depth with GM's medical team. I would specifically ask if she is swallowing 20% of her food, is that enough to keep her from painfully starving to death, which seems to be your main concern. It could be that the 20% she is able to swallow is enough to keep her comfortable. The last few weeks of my mom's life she ate less and less; she was also having trouble swallowing, and everything was "dry", even stuff covered with gravy. But she never complained about being hungry, and I let her eat however much she wanted. Frankly, as the end came, I was more worried about complications from her eating too much rather than not enough.
I hope you can find an answer that will give you and your family peace. I am sorry that this is so difficult for you. (((hugs)))
If she had been on Hospice PRIOR to the stroke they would not have recommended the feeding tube and probably not approved it. (but not 100% sure on that since the stroke was not what made her eligible for hospice)
Weaning her off the tube is probably the best. When the body no longer "needs" food if you were to continue to supply the food it is not digested properly and that can lead to problems. The signs that she is not needing the food are missed when a feeding tube is in place. Turning away form food, eating far less, closing the mouth when a spoon is brought to the mouth. With a feeding tube all of these signs are ignored or are unable to be given. Also the feeling of hunger is not the same as what we experience.
If she is eating 20% of her food orally that should be what she needs now and more frequent offerings of food and food that is higher calorie dense might help.
You also have to remember that her need for food has declined, she is not expending calories at a high rate.
I would remove the feeding tube.
Hospice will make sure that she is comfortable.
We moved him to hospice and I broke down in tears when I asked how painful it was to die from dehydration. The thought was horrible! We just didn't want him to suffer. They assured us that they would keep him comfortable and pain free. The truth was, he would've been suffering had we tried keeping him alive. It was a difficult decision, but it was the best decision. The right decision. Hospice did a great job. Just be warned, it is only a myth that you die without water in 3 days.
I wish you peace with whatever decision you come to.
I would not want to be kept alive by a feeding tube.
I would have it removed and have her on a liquid diet using a straw and let her live or die in peace.
Prayers
The thing is. If your grandmother is stable and shows no signs of distress, what is the rationale behind changing her management? It might be a relief to remember that you don't have to make this decision. Waiting for developments is a valid option.
There are many things that happen at the stage of life your grandmother is in and I found Hospice was helpful in understand all of it. Ask as many questions as you need to. Get that understanding. Remember, to quote you: "She doesn't show any reactions or emotions- doesn't seem to recognize anyone, show signs of pain, cry, etc" then, as I remember the decision, it was time for "me" to let go also. I had to remind myself that most of my questions were to keep her with me and not what was best for her.
Making that final decision to let our loved one go is the hardest thing I ever have had to do. But at the same time it was also the greatest release. Does your Mom have a DNR, do you know what her final wishes really are, I pray you do, that is what you need to work with now. Taking our own wishes out of this situation is so very hard.
I would say, ask your self only what would she say. What would be her answers to all these questions. Loving Prayers for you and your family.
A dignified end is one that allows her to pass when it is her time, My feeling is that her memory care unit is suggesting speeding up the process. Given her age, there doesn't seem to be a reason to "speed things up" except for the suffering of the family members who remember her as a more vibrant person. If you do not change anything, she will eventually pass sooner or later.
That said, I will share my experience with two patients I cared for in Hospice. One woman had deteriorating Alzheimer's. She developed a blood cancer. Her 4 adult children discussed with the oncologist about putting a feeding tube in. Doctor said no surgeon would agree to that surgery and the cancer would most likely hasten her death. My colleague and I did a family meeting one night with the 4 children (2 women, 2 men). The sons were afraid she was starving to death and uncomfortable. I gave the example of when we are busy working, hungry, no time for a meal and shortly after, we no longer feel hunger pangs. Also, the dying body no longer requires what it did while we were active. My colleague then asked them, "if Mommy could come out and tell you what she wants, what would she say to you"? That made the decision in peace for them all as they immediately replied, "don't you dare keep me going".
The second patient was a man terminally ill with Alzheimer's. He lived alone with his wife who took exceptionally great care of him. She opted for a feeding tube due to her fears of his starving. For FIVE years he hung on. My colleague visited her one day and she said, "if I had known, I never would have allowed them to put in a feeding tube"
These just give you some food for thought. Lean on Hospice. It is the work that they do and will support you. This is a decision that ONLY you can make. Wrap yourself in teflon as people will have opinions about whatever you decide. Do not take on any of others' comments. Prepare a response. Maybe something like this: "I'm sure you are trying to help me, but until you have walked in my shoes, I'd appreciate your support, not suggestions or judgments".
Know that this is the most difficult decision you will ever make but others who have been faced with this, support you. Godspeed to you and the journey Gran is making.
And i agree 100% with your words to those in pain and dealing with these decisions. And yes they are the hardest you will ever have to make. God bless your decisions in love and what is best!!
Liz
As I said, nobody really knows what it is like at the very end, but we make decisions based on the best knowledge and experience we have.
Praying for a peaceful release for your grandmother and comfort for you and the rest of her family.