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Letting Go - A Good Death

Letting Go - A Good Death

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With permission, I am sharing this post she sent me, because it is a wonderful testimony to the loving care her mother received, and the persistence required of the family to be sure she got it! The Moyers series on death "On Our Own Terms" could have used this as an example of how Hospice care for the end of life when a person is so terribly ravaged by disease, is the best option. However, please note that Ruth and the others were following *her mother's wishes*--- and that is the important thing-- no one should be forced into someone else's idea of "a good death". Thanks you very much for sharing this moving account with us all.

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Mom was under hospice care and on a pain patch and morphine push through her IV. The doctor at first had a hard time that we wouldn't put in a feeding tube and some other things, but finally was wonderful and understanding. I guess it was hard for him to just let her go naturally.

How to describe it: my sister and I were with her, talking to her, kissing her and holding her hands. It was both terrible and beautiful. She just stopped breathing, had a few last breaths quite far apart, and her heart stopped. She was in no pain and as best we could tell there was no anxiety. The doctor told us the morphine would prevent any anxiety.

She had been basically non-responsive except to pain for a few days. This after she had broken her hip while lying in bed here at home. We took her in for x-rays and they wanted to keep her to set up a pain protocol and that is where she died. One of her daughters was with her 24 hours a day. They did a simple hip repair (took 15 minutes) to stabilize the bone which was only done to lessen the pain. Test results in the hospital showed she had at some point in the past suffered a severe heart attack, x-ray of the hip area showed she had bone cancer (doctor thought that was why the hip broke so easily), was in renal failure, had pulmonary hypertension, and a severe urinary tract infection. She of course developed pneumonia on top of all this.

She had gone on Hospice on August 10, I knew that it was time. She seemed to go down hill very fast from that point, but breaking the hip kind of accelerated everything. When I finally convinced the doctor that we and Mom were against things like the feeding tube, since any prolonging of her life would only be short and probably painful for her, he discharged her to hospice respite care so she could stay where she was and not be moved home. Hospice continues with a grief support program for 13 months after the loss, which I will be taking as much advantage of as possible.

Dad had not gone in to the hospital to see her, and we convinced him that he should go for her to see him and for him to talk to her and tell her it was okay to go. It was beautiful what he did and she died about 3 hours after he left. He had sat and held her hand and talked to her, told her he loved her and that it was okay to go, that he would miss her and would always love her.

As much as I know we did the right things, there is sometimes some guilt feelings about denying her life sustaining support. I know that will ease and I know that we did what she wanted, no matter how hard it was. Even the doctor felt we had made the right decisions, so I have that to hold on to, and all her daughters agreed on every course of events.

She was cremated, as was her desire, and on the 23rd we are having a memorial service for her in Allegheny State Park in New York, one of her most favorite places in the world. We are taking pictures of her throughout her life to display and many of the things she made and having food catered, and will have a family gathering to celebrate her life after the minister has finished the religious part of the day.

Sorry for rambling, I hope I was able to answer your question. This has helped, to write this out and sort out my jumbled thoughts a little. If you feel that this information is okay for the list, I don't mind you posting it for the others.

My love and thanks to everyone on the list, I will continue to lurk for a while. It has been so comforting through the stress, and I know it will be for a time to come.

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Thank you so much for forwarding the letter. My mom is 83 with advanced PD and in a nursing home. She is on her third round of antibiotics in a month for a really bad UTI. So far, no relief. She is not drinking enough liquids (swallowing is all the harder since the medications exhaust her), is hardly eating, and has intermittent pain on urination and low stomach ache. She is pretty much bedridden at this point, even being up in a chair is exhausting and causes neck and shoulder spasms. She is lucid but it is difficult to understand her, since her voice has faded to a whisper. We have always been able to discuss end-of-life issues and she has been adamant about preferring comfort to cure.

I have just contacted Jansen Hospice nearby to find out what our options are as far as palliative, non-invasive care if she is not responding to the meds. Apparently, Jansen has a hospice program in the nursing home Mom is in. And I also want to find out about possibly moving her back home if it looks like there is no option for her, except extensive invasive tests and perhaps surgery. Thank God for the Moyers program. It couldn't have come at a better time to help my West-coast sister and I feel less isolated and better informed as to our (and Mom's) choices.

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You are facing a difficult time, but you seem to be moving in the only appropriate direction, given your mother's condition and her wishes. I'm glad if our discussion has been timely, and the Moyers series also---you are NOT alone, for sure, and your mother will be grateful for the comfort care you are arranging for her. Stay with us, and tell us how it goes, because your experience will help others, and because we care--
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