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Instead of feeling like I’m going to end up like my elders, I’m doing my best to stay independent, continue challenging myself, keep learning tech, embrace change, declutter, all the stuff I saw my MIL doing, but she still got Alzeheimers. My own mom did very little of those things, and she is dealing more with loss of mobility, but def has dementia. Both our parents have official diagnoses of memory loss disease, but their memories are better than they are bad, now. They still know us kids, remember lots, but forget lots.
So if it gets me, I’d appreciate opting out, but will plan, with my husband for what we do, if not possible. We used to joke that since we want to go together, we’d simply jump on an iceberg, and float off to our fate, happily heading for whatever is next, together. As we age, we realize it is better to make actual realistic plans, because burdening our children, with our lack of preparation, or because we wanted things done our way, with no regard to the burden it will bear on our two kids, is not for us.
I feel like a traitor, even writing these words, but living under this, the past 4-8 years, watching our parent’s deteriorating health, and their increasing dependence, on their youngest daughter, our youngest sister, has also made life tough. I won’t go into it here, but things are the way they are because it is the way our mom, dad and sister want it. They live together, always have, their choice, never discussed with the three older sisters. It is what it is.
This is my first post, and the subject brought me out from under the covers, as I’ve been lurking this forum, for over four years. You’ve helped keep me sane. We’re all just doing our best to support our sister and parents, always have, too much to say to tell the story, but know that lack of communication is deadly, and memory loss disease, combined with immobility, incontinence and poor health, is a lot to deal with, so I want the easy way out, in case doing everything possible to avoid it, does not work.
Thanks for having a place for people to go for excellent, honest, caring advice. I’ve experienced how much people can help each other, just by sharing their troubles and solutions. It works!
Do know that even when we have "intent" not to "go there" very few of us, even when we have a means at hand, willingly exit this life. Even those in pain at the end of life. When I was in nursing I was taught that by a Priest. So dire was his condition that nurses went in two by two and wept outside his room questioning why "his God" didn't take him to peace. Yet one night he said to me "If the pain meds put me out could you wake me at 9?" I said "Sure, but WHY?" and he said "Quincy's on then". So while we prayed for him to die this gentle man wanted one more episode of that Coroner's program, Quincy, on TV.
Believers would say it isn't to us to make the time. Others say is is/can be. I think most of us would be comforted to know we COULD have a painless exit if we wanted it, even tho few of us would likely use it.
As for my interest in assisted suicide, I've lived with a serious and complicated mood disorder since I was about 7. I'm now 66. I have pursued treatment for years and years and really there is not much medicine has to offer. I spent a few hours today looking for research studies but so many of them cut off at 65 if not sooner. I am looking for an interdisciplinary mood disorder program that will help me give me as accurate a diagnosis as possible,. I'm also interested in the brain-gut axis, which addresses microbiome health, newer talk therapies, and psychedelic treatments like ketamine. So I'm not giving up just yet. Even so, what keeps me sane through all this is the knowledge that I can quit when I want, albeit after my husband is gone if I outlive him. I think I've had enough and the significant possibility I will get dementia ties it up like a bow. My best to you.
My frustration with my mother has to do with a number of issues. She has had so many periods dating back to my childhood when she couldn't cope and stayed in bed. She practiced Christian Science. That did not solve two hip and one knee replacement along with countless other issues. I tried to have her be healthier.
During Covid she developed a septic infection. She spent time in a hospital and was released to rehab and then SN. She hasn't walked since. 9 months ago she was dropped by an aid who went against protocol and both her femurs were broken. She then developed a horrific bedsore which she still has. She has to be catheterized. I feel very bad about all of this but there is nothing else for me to do but visit and see countless residents whose quality of life is nonexistent at least from my viewpoint. Crying, screaming for help or totally out of it. I don't know how anyone could want this.
If a medication comes along that actually does restore cognitive integrity, I’ll want it to be tried on earth.
My own LO is presently declining significantly, as did her mother and my mother, but SOME of the other members of this side of my family, even with significant disease process (PD), retained their cognitive integrity to the very end. No extraordinary measure will be provided, but she receives exemplary care in her SNF, and I keep an eye on things almost everyday.
I’m too nosy to want to cut myself off from my natural future, whatever it may hold.
Nothing at all contentious here. We all need to think this out and do the best we can for ourselves.
Years back, an article came out about how ppl were going to Mexico for bottles of liquid barbiturate intended for animal euthanasia. The people would just drink them and hope to go out like Marilyn Monroe.
So, now at 68, I see my friends watching and caring for their 95 year old parents, watching them swim upside down like a dying goldfish for what seems like forever, fighting with siblings for time or inheritance, and I am so thankful my parents (my step father, too) went so early and quickly. It is the most loving thing to do. At some point, it will be too late to have any say in our treatment. That is the what scares me the most. Thanks, mom, and don't worry about me, kids, I have a plan.
Do it where nobody but wild animals will have to see your carcass.
It was horrific for the family, for the boy and for our entire neighbourhood. We all heard the shot.
I am also concerned about my own possible end of life, as my mother died from dementia and both my sisters have Alzheimer’s. I’ve care for them all and I don’t envision that for myself. I volunteer with End of Life Washington and have assisted 30 or more people using Death with Dignity, otherwise known as medical aid in dying. It is fast and peaceful and the body does not blow up, as one person below indicated. However, it is not available for Alzheimer’s and dementia patients. There are two other options. VSED or Voluntarily Stopping Eating and Drinking is one way. It takes about two weeks and requires caregivers and a death doula is recommended. One drawback is that the required care for two weeks is expensive and usually out of pocket. See VSEDResources.com for more info.
Another option is Final Exit Network. Both are legal and can get the job done.
I’m only providing information and not making recommendations. But, I am passionate about both my roles of caregiving and helping people die. Feel free to reach out if you want to talk more or just visit Endoflifewashington.org to see what kind of advanced planning options there are.
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