My mother was 68 years old. Her health was bad she was on dialysis.23 hour oxygen and her heart was weak.We all knew she was dying and had known for two years.Mom fought death with all she had.Her doctor on the other hand didn't seem to fight all that hard.He was 9nly concerned with mom stopping dialysis he seemed to be trying to talk my mom into dying but she wasn't giving up.Her doctor knew how sick she was and he gave her med to make her sleep she would fall asleep so easy and she did one night while sitting on the toilet my sister in law talked her into going to the hospital two days after she fell.She was in the hospital one week before she died.she had a black eye and a nasty cut on her head but she was awake alert responsive eating and drinking just hrs before being told her doctor had order she be taken off dialysis a hospice nurse talked her and my dad into in hospital hospice until the time came that her body shut down from not being on dialysis. Hospice was going to make her comfortable until the end we were told she would probably last about two weeks.She was moved from her room to a hospice care room giving a shot of morphine as soon as she got on the hospice floor. She went to sleep five mins later and was dead six hours later she never even got to yell us bye.I feel so guilty for not taken her home to care for her.If oo nly we would've knew about hospice killing off their patients with morphine we would have done things differently. She may have only lived a day without that shot we don't know but I do know I would give anything for one more day with my mom
She died on her own schedule. Hospice is set up to decrease the pain and distress of the final passing. They do not take lives. I've experienced Hospice with my mother (who got better and "graduated" from the program) and my husband who was on it five weeks before dying. Initially hospice expected Mom to die within days. But that was not her agenda. She got well. She certainly still has dementia but two years later she is pleasant and enjoying her days. Hospice was expecting my husband to live a few more weeks and was very surprised when I called to say he was gone and I needed them to arrange for the body to be removed. An autopsy showed that he did die of the dementia he had lived with for ten years, but that he was very close to dying from a heart condition -- it was surprising he hadn't died of that.
Many of us would give anything to have our loved one with us even one more day. Anything but watching them suffer, be in unspeakable pain, or be heavily in distress.
Your mother died when her body was ready for her to die. I am very, very sorry that it was in her sixties. Certainly you wanted her longer!
Taking your mother home to care for her may not have changed anything -- probably not. You made the decision that you honestly thought was right at the time (and it probably was right.) Don't let feelings of guilt get in the way of the genuine and legitimate feelings of loss and mourning.
Please try not to torture yourself. Your mother in heaven may be irritated that she didn't get to say goodbye, but that happens to lots of people. Your mother showed her love by the way she treated you when she was alive. For me, my late mother isn't really gone, because she lives in my heart every day.
Would your mother want you to be at peace? I bet she would. Remember her and enjoy her memory, and remind yourself that her pain is over. I hope that time brings you acceptance, as it did for me.
But truth be told your Mom died from heart failure and kidney disease.. To help her cross over peacefully is what hospice did..
Again I'm sorry you feel guilty.. Hopefully time will heal.. But there was nothing you or hospice could do to make your Mom healthy again.. Hugs..
Try and find peace in that she died comfortably. The Drs knew from her blood work that the dialysis was no longer working so no point in continuing to put her through. Kidney failure is not a nice way to die so try and be thankful for the care she received.
My Mom was not in hospice care when she died. She was in palliative care in hospital. Which amounts to the same thing. They were giving her morphine at regular intervals to keep her comfortable. One time when I was sitting with her she started to moan and cry cause the morphine had worn off. Would I have liked her to be awake and with me? Yes.......but I did not want her to be in discomfort so I agreed to the morphine. Period. They did not kill her.
So sorry for your loss, and that you did not get to say goodbye.
I never want them to come near me when I'm ready. I see lots of you have had similar experiences with hospice. I hate them so much!!
Please, please note that the amount of morphine given is no different than the amount of morphine given to a patient after a major surgery to help cut the pain.
And if the doctors/nurses had up the amount it would be from 5mg to 15mg and no more. It would take 200mg to kill someone. Morphine is highly regulated, every mg has to be accounted for.
I was glad both my parents had Hospice. Especially my Dad who had aspiration pneumonia, otherwise he would have died choking to death. Believe me, that would NOT have been gentler. The morphine helped relax his throat.
My deepest condolences and sympathies. I'm very sorry for your loss. I know it hurts. We always want things to be different. Its been almost 10 months since my father passed and I still wished his last moments could have been different. We all have these questions during our grief journey. Try to be kind and gentle with yourself. I know its easier said than done. Thinking of you.
Dialysis does not work forever. It is a treatment meant to assist the function of the kidneys, when they stop working, to filter toxins out of the bloodstream. But it is not a replacement for the kidneys. Eventually, kidney function will cease altogether and dialysis will be of no real benefit to the patient. When a doctor recommends ending dialysis, it is to end a person's suffering because the treatment is no longer helping them.
I am sorry for your loss. I know it's extra hard because stopping dialysis feels like making a choice about death. In truth, it is only a choice to discontinue treatment that is causing suffering, and at the same time, is no longer benefiting the recipient.
there well run hospice groups and maybe not so well run hospice groups.
I'm certainly not discounting the concerns of those who feel their loved ones death
came sooner than necessary. There are also many who feel that their loved ones
lingered in pain longer than they wanted. So complaints about hospice care can cut
both ways.
It's so frustrating and leaves one feeling helpless when we don't always know the
best course of action. And sometimes we don't feel we're given all the info we need to
make best decision for our LO's . My sincerest condolences to all who have lost a parent
possibly before their time and with any lingering questions regarding care.
now please read this ....
the symptoms of morphine overdose is clear, this so called MD has tried to cover the symptoms of MORPHINE OVERDOSING BY STATING THESE ARE NATURAL SYMPTOMS OF EXPRESSING PAIN. anyone with concerns should call the police , this is murder and nothing else!! listen to your gut feeling, i am in the same place with this and i am about to go give a statement, my loved one was not given 6 months or less to live they gave her Morphine and she was on no pain at all NONE , yes that is right NONE they upped the dose until she couldnt breath and told me they where gong to up it again , i confronted the doctor who looked and acted worried after the death of my loved one i had to keep it together for my family , only now am i strong enough to tackle this head on
Nursing homes will not accept a patient unless the patient qualifies for the care.
I would rather die relatively pain free rather than in agony - I don't see the point of making dying people suffer more. Some of this concern about hospice seems to be related to the idea that incurable disease can be cured.