Sitting across from my daughter at a tiny Starbucks table entirely taken up with two laptops, I’m wondering if I really want to write about anything, but in order to have her limited company this evening, I have to do something. My options are few: with a companion whose ears are plugged and whose attention is on her own blog post, I need to look like I’m busy and productive, not pining for conversation. It’s my second sojourn here today, two hours of the morning having been spent sketching out a story scene that I’ve been thinking about for a while.
~
One morning late last year I awoke from a dream about writing a book, and the storyline was detailed: an older woman, recently diagnosed with dementia, had enlisted the help of a younger man, perhaps her son, to guide her on a hike into the mountains, where she intended to let herself die by exposure to the elements. They had to hide the reason for their mission from her family, but were both convinced of the rightness of what they were doing.
It wasn’t a bad dream, on the contrary, I was quite intrigued about such a story because it linked two things that have long interested me – the right to die, and the looming pandemic of Alzheimer’s. In fact, it seemed like a clear message to get the lead out and write about it. And as if the message needed reinforcing, later that same day I had an experience that seemed coincidental at the time, and made the dream eerily prophetic in hindsight.
That afternoon, while driving to an appointment, my favourite Belgian spotted our neighbour Sophie walking along the road to the next village, a book tucked under her arm. Although we hadn’t seen much of her in recent months, we knew she had been diagnosed with Alzheimer’s, and he was surprised to see her out alone. When he stopped to ask if she was all right, she said she was on her way to meet her husband. Unconvinced of her explanation, FB called me to ask if I could come and pick her up.
Sophie didn’t blink an eye when I turned up. Just in case she had the story right, I drove her around for a little while looking for her husband. She chatted easily and issued a constant stream of almost expressionless directives, every short phrase with the same arc of inflection and always ending with my name. Be careful at this corner, Deborah. Watch your speed, Deborah. Turn left at this intersection, Deborah. You drive smoothly, Deborah. Finally it seemed like the best thing to do was leave a phone message for her husband and go back to my house to wait for his call.
It was a cool afternoon: while the kettle boiled, I built up the fire. Sophie commented on how well it caught: You make a good fire, Deborah. Oh that’s funny, I laughed, because my FB and I once had a ridiculous argument about the way I had laid the fire, not bothering with the small bits, and of course it didn’t take properly. He wanted to teach me how to do it in Boy Scout fashion and didn’t believe me when I said I knew all about the proper way to set a fire. I’ll tell him on Wednesday that you know how to make a good fire, Deborah. (Sophie played boules every other week with a group that included FB, and if her dementia had robbed her of her ability to calculate the score, her enthusiasm for the game was unaffected).
When I set the tea tray down, she eyed the oatmeal cookies sceptically: They don’t look like anything a French person would eat, Deborah. I wasn’t offended: Sophie had a fine reputation as a sophisticated cook, and did not suffer inferior food with diplomacy. The back of the kitchen cupboard yielded a box of iconic French biscuits, but when I returned with them, Sophie was already into the second cookie. These are superb, Deborah. I’d like the recipe, Deborah. All told, she ate fifteen of them.
We talked a bit: about her sons, playing boules, cooking. She tried to remember her husband’s cell phone number but was missing the last two digits. Now and then she picked up her book, tracing the words with her index finger but never turning the page. I wondered if she grasped what she was reading, and showed her a collection of political cartoons that poked satirical fun at the burqa, thinking that the visual humour might appeal to her. She got almost all of them, and asked if she could borrow the book. The afternoon lengthened. I think I’ll go home now, Deborah. It was awkward telling her that she really shouldn’t leave, and I wondered what I could do, other than accompany her, if she insisted. She didn’t.
When her husband knocked at the door a few hours later, he was upset and apologetic. Very unusually, he had left Sophie at home alone when he couldn’t persuade her to change out of her nightgown and go with him to take their grandson to his weekly sports practice. After he left, locking the front gate for security, she had obviously dressed herself – something she hadn’t done for some time – and climbed over the garden wall. No one with experience looking after a person with dementia would have blamed him for the sharpness with which he addressed his wife: he couldn’t contain his frustration and worry over the fact that she couldn’t safely be left alone for even a few hours. At the end of his ability to cope with a situation that had worsened significantly over the last six months, he told me that he felt like he was going mad himself, and that the only alternative was to put Sophie in a nursing home, an option the family supported but which she had vehemently rejected. They left for home, Sophie confused and defensive, her husband tired and despairing.
Nineteen hours later she vanished without a trace. After having lunch in a little hilltop village near Grasse, she headed out the door while her husband was paying the bill. She knew the place well and couldn’t go far, he reasoned, never imagining that the few minutes it took to complete the transaction and have a brief conversation with the chef would mean the difference between life and death for his companion of fifty years. Despite extensive searches by police, tracking dogs, friends and strangers, she wasn’t found until ten days later, by a boy hunting for mushrooms on his family’s holiday property. She had succumbed to exposure after falling from a large retaining wall, only 300 metres from the restaurant.
~
Did Sophie, in brief lucidity, set out to put an end to her misery? The morning of her disappearance she had told her husband that she felt she was good for nothing, unable to read, cook, or even use the telephone. She certainly knew, at breakfast, what kind of hell had her in its grip, and perhaps during lunch, she determined to find a way out of it.
Apart from the agony of the family, who alternately hoped and despaired during the ten long days of unknowing, and the terrible loneliness of Sophie’s death, I don’t think the end of this story is awful. Having watched her own mother die by increments from Alzheimer’s, Sophie had already said many times that she would never let herself go the same way. Whether she planned her end – it seems unlikely she was capable of it – or if by some beneficent inadvertence she found a way out will never be known, but I’m relieved for her that she did.
As a coincidence, the dream I had on the day before Sophie died is striking, but what both events have served to do is reinforce my view that the Damoclian threat of Alzheimer’s must be urgently addressed, and that the discussion of and concern about elder suicide should take into account that for some, death is preferable to a vastly-reduced quality of life. To act definitively against the inexorable grinding down of disease and infirmity should not always be viewed in a tragic context. Sophie’s family will probably never get over their anguish about the manner of her death, but they have found some comfort knowing that she was spared the emotional trauma and confusion of being put in a nursing home, and the further decline of her faculties.
And the book? It’s taking perceptible shape, and if I keep on paying for coffee, and finding some motivational, if antisocial company, there’s a chance it’ll continue to evolve.
As dementia has touched (and is still touching) my personal life twice Deborah - I am very interested in your story and book.
ReplyDeleteI am a psyche nurse too and my work involves caring for those with many kinds of dementia - in reality I live with dementia 24hrs per day.
The question of suicide is a difficult one and it is probably understandable and of course a right for those with insight to choose this path if they should so want... but then there is the real problem of the slippery slope... would some poor soul feel this was an expectation (and add to their angst?)...
It is a thing I think about often...
Anna :o]
Hello Anna,
DeleteYour persepctive is particularly relevant, although I wonder if, in a few decades, anyone will be able to say they have no experiene with dementia. The slippery slope issue always come up when euthenasia is discussed, and I think it's a very valid concern. Less so in the case of suicide, I think, but I might be naive. Fairly recently the whole issue of assisted suicide was examined again in Quebec, and one of the observations then was that slippery slope fears had not been borne out in juridictions where euthenasia and assisted suicide are allowed (Oregon, Holland etc). That's not to say that there is never pressure from caregivers or relatives who may not have the ill person's interests at heart, but it suggests that the safeguards put in pkace are sufficient to prevent abuses.
But your second-last sentence is sobering, indeed. Thanks so much for visiting and commenting.
I think that it is very touching that you have taken the time and made the effort to tell Sophie's story here. I cannot even imagine the grief her husband must be feeling except through a leap of empathy. Poor man. Oddly enough, the nature of Sophie's death resonates oddly with the death of English Rider's brother-in-law. I have a tendency to think that Sophie's own oversoul, if you will, was looking after her and taking her wants and needs into account at the end of her life. I am glad that she is at peace and not being forced to tolerate one more assault on her independence.
ReplyDeleteYour description of your dream reminds me of "The Ballad of Narayama." (http://www.nipponcinema.com/blog/the-ballad-of-narayama)
I thought the same thing, Ms. Pliers. I felt that English Rider's BIL had some guts, and that determing that life itself is not necessarily worth more than life under any conditions was an act of considerable character.
DeleteI like your term 'oversoul' - it perfectly fits the idea that the subconscious sometimes takes control, although admittedly that isn't always a positive thing.
And thanks for the reference to the film, which I hadn't heard of. It looks fascinating, and I'lm going to try and get my hands on it. Thank you.
This is a poignant and captivating description of something so real for many of us nowadays. My mother has been diagnosed with Alzheimer's and is in a care home. They let my Dad stay there as well, which is comforting as both of them are over 90. I feel that's the best for them, since my mom can be looked after 24 hrs. and they can still be together, after 60+ yrs. of marriage. I encourage you to finish your book for its relevance today. And hey, we all need to be a bit 'anti-social' to create... nurture the artist in us. BTW, have you seen the film by Sarah Polley "Away From Her", based on a short story by Alice Munro? It's a moving Alzheimer's story. I highly recommend it. Julie Christie got an Oscar nom. for her role as an Alzheimer-afflicted wife. If you're interested, here's the link to my brief review. The movie is a must-see.
ReplyDeleteHi ARti,
DeleteI did see 'Away From Her' and thought it was excellent. My mother also suffered from Alzheimer's, but well before that she used to say to me 'if I ever get like that, please shoot me'. It bothered me quite a lot that she lost all control over her life as dementia took her over, but there were some very unexpected moments of pleasure in her life.The first essay I wrote for my blog was about one of those, if you care to read it. theperfectionofbeing
Halfway through reading your post, my arms were covered with goosebumps; as my body's reaction shows, this issue and the way you write about it are moving and fraught and emotional. I ended reading, relieved that you are not a maudlin or sentimental person who needed to hit a "woe was Sophie's death" note. Rather, the pragmatism in your writing grants her a final dignity, just what she felt was ebbing away from her.
ReplyDeleteThe parallels between your dream and the reality prove, more than anything, that you've found your subject. Make your girl sit across from you and plug in more often, if it makes you feel you need to write.
Thank you, Jocelyn, for your constant support. No, I can't be anything other than pragmatic about Sophie's end, although admittedly it's much easier to be that way as an observer from outside her immediate circle. I like her as a person, but without emotional involvment with her, I can maintain a distance. I think there's a readership for this type of story - 'Still Alice' is the proof, and the film 'Away From Her' resonanted with a lot of people. We shall see - in any case, I'm going to have a plaster bust of you made to place on my desk, with wagging finger and maybe even a cord to puul that tells me - Chatty Cathy-like - to just FDI.
DeleteI think your dream arose more from your connectivity and less from coincidence.
ReplyDeleteAn uncle of mine died this week and the sadness is greater because he and his wife had not been together recently because of her Alzheimer's.
There certainly is great cause to push for assisted suicide. I also do think it is a slippery slope though and once on the downside it's very hard to maintain balance.
Arti's parent's are unusually lucky to be together in a nursing home despite her mother's condition, but Arti had to apply pressure for that to happen. It's very sad to see couple separated at the end of life, as if growing old wasn't bad enough already. Rather than repeat what I said to Anna (the first commentor) about the slippery slope, you might be interested to read there. Thanks Chris, for visiting. I look forward to reading you soon (that's a little nudge).
DeleteFascinating. I fear Alzheimers more than anything, both for my parents and for myself. The loss of the person you are and the total dependency seem like my personal hell, both for the sufferer and the carer. I too believe that the option of assisted suicide should exist although how difficult with Alzheimer patients to be sure that this would be their will and not that of their carer. Nevertheless I would come down on the side of allowing it. I am interested however that my son and daughter in law, both doctors and both pragmatic and caring people, are very uncomfortable with the idea and feel they have seen too many grasping and insensitive relatives to feel certain that it would not be abused.
ReplyDeleteI used to think I'd be spared any risk of dementia, probably for the same reason teenagers think they're invincible. It just wasn't anything that could happen to me. But after it became apparent that my brainy mother was developing dementia, I had to rethink the possibilities the future might hold. I too am frightened of it, and really wonder how I'd react to such a diagnosis, if it was in the early stages. Would I accept it? My mother didn't. Would I plan an exit immediately? Or would I wait just a bit longer, until it was almost too late, in which case it would almost certainly be too late.
DeleteVery interesting to know of your son and DIL's views (which should be personally reassuring to you!) I guess they would see the best and worst of human behaviour.
Sophie's family doesn't know how lucky they are, nor from what nightmare they have been spared. I just read another blogger's post on Oregon's laws enabling doctors to assist suicide in certain cases. So humane.
ReplyDeleteI was thinking of your BIL when I wrote this post, ER. And yes, I think the family does recognize that the outcome was not the worst possible.
DeleteMy mother had a "dementia of the Alzheimers type" and suffered from its affects for over 25 years. I so surprised myself at times by reacting logically to what sounded like a crazy event but, because it was my mother, the nurse, always with a pragmatic wisdom, who retold these events, I somehow believed them.
ReplyDeleteWhen she feared because of 'strangers' who peered into her windows, I made her curtains for her and had lights installed in the yard. She lived in a bi-level and anyone looking into her windows would need a ladder.
She also heard music many times a day: MacNamara's Band, Easter Bonnet, and I checked radios and tvs in her place over and over.
I also surprised myself with my lack of patience sometimes. I had three small boys at the time for whom I seemed to muster up all kinds of patience. And a teacher was used to reining in ill feelings all day! Why did this ninety year old lady bring out such anger from time to time?
One incident stands as frustrating at the time but comic now.
Costco had just introduced large containers of spices and herbs and I bought two of everything... oregano, marjoram, parsley. Finding them too large to store in the kitchen, I decided to transfer the contents into small bottles I acquired from my friend, who sold lab equipment. She supplied me with a huge bag of fecal collectors, the perfect size, and I set them all up on the kitchen table with the spices and labels. I began the transfer after church on Sunday with mom sipping tea and watching.
"Do your husbands know what you are doing?" she asked fingering a bottle of marjoram. She was convinced that my friend and I were getting ready to sell this stuff on the streets for a tidy profit. Or smoke it together I guess. No amount of explaining dissuaded her from this and I was soon fuming, more an expression for the loss of more of mom's logical capacity than from not being able to convince her I was not a drug dealer.
Mother never even heard of assisted suicide, but she had been a nurse, and I know from other nurses that they often participate, and have done for centuries, in helping someone "go" by slowly overdosing with morphine or other measures that seem normal humane practice. I do know she prayed for fifteen years that Jesus would come and take her, she was ready. I do believe that grasping relatives would abuse the power.
Dalhousie Neighbour
Anne, that story is both funny and sad. Mostly funny, although I can understand the frustration you felt. I remember you from that time as a caring daughter, who visited her mom regularly and was sometimes worn out by the responsibility of being the only one to care. Don't be hard on yourself. Besides, it's only when the irritant is gone that we really regain our patience and understanding - it's human nature.
DeleteI would love to read your book. If only because I know that you would be very careful in sketching out your characters. Letting them breathe, but at the same time reining them in if they got too capricious (and characters do). I was captivated by this Sophie woman. My late grandmother was the same when she fell prey to dementia. She would wander off on her own until a neighbour came to tell us. Luckily in those days in Cuba we still had a strong community.
ReplyDeleteThis is one of those posts that exudes elegance and humanity. Many thanks.
Greetings from London.
Cuban, I'd love to have the pill form of your kind of encouragement to take once a day. Thank you. Very much.
DeleteAs for wandering, sometimes I think that keeping Alzheimer's patients locked up so they can't wander off is just plain wrong-headed. I realize there's danger, but it's such a strong urge for many of them that one wonders if there isn't some 'oversoul' (as Ms. Pliers said) that drives them to such restlessness. In a perfect world, the community would always look out for them, bring them home, feed them, keep them safe. But I'm just dreaming.
My first visit here (from Nance's Mature Landscaping). But on the strength of this post, if I were your burgeoning novel I think I'd be very happy about my future.
ReplyDeleteThanks!
Now that's a POV I hadn't considered - how would my novel feel if it couldn't look forward to being done? This might add guilt to my procrastination!
DeleteThanks for your visit, JES. Much appreciated.
You're welcome, JES.
DeleteI remember you telling me this story and if it makes you pick up your pen and knuckle down, I'm glad.
ReplyDeleteOn the whole, I agree with you and other commenters that finding a way out of Dementia and into an early death (early in the course of the illness), is much preferable to a long drawn-out process of dying inch by inch. Having said that, I have a friend who has had Alzheimer's for over12 years, she is still alive, at home, being cared for by her husband and other carers who come in several times a day. I haven't seen her out for years; she is now unable to walk or sit upright and should, be, by rights, in the very final stages of the disease. yet she still 'lives'. Her husband has never wanted her to be institutionalised; he is an artist and has made sure that there are always hours when he can immerse himself in his work. He is still sane, 12 years later.
Janet's (my friend's) death will not be as lonely as Sophie's, but Janet hasn't been aware of her own existence to any meaningful extent for a long time. When she was like your Sophie, we did indeed all look out for her, stop her from wandering into danger, take her in or take her home. She was still invited to social gatherings, which she enjoyed, although she made now sense when she spoke.
So you see, it can be done. But it takes a very special kind of person to do it and a very special kind of humanity. I doubt that I'd be able to measure up myself.
I think it must be a characteristic of dementia that those who have it wander. I finally realized that I would have to put my mother in an institution when neighbors were picking her up a mile or two from home. But I don't think she ever wanted to die. When she finally did, at the age of 100, I think she left this world with regret. I think it's possible that at least some people with dementia still have times when they enjoy life. The will to live is very strong in some of us. It sounds to me as if your friend Sophie enjoyed the afternoon she spent with you.
ReplyDeleteI realized that something was "wrong" with my mother the day I took her to the grocery store and found her aimlessly pushing her cart up and down the aisles with no idea where she was, or what she was supposed to be doing. The look in her eyes was terrible - flat and empty, as though the life had been snuffed out. It wasn't long until she was herself again - perhaps only 20 minutes - but we both knew that something had happened, and it wasn't good.
ReplyDeleteSometimes, the decline was funny, as it was the afternoon I went down to visit and found her prepared to go out for dinner dressed only in a leopard-print shirt and high heels. Other times, it was terribly sad, as it was during her last hospitalization when she insisted, over and over, that she was going to go home. She nearly made it once. She removed all of her IVs, telemetry and such and headed for the door. If it hadn't been for the catheter, she might have made it to the nurses' station before anyone noticed her black monitor and came running.
The reality of things is that I will have no one to care for me when I'm "really" old. I can't imagine taking my own life, but I have no desire to rot in a corner and absolutely no desire to land in government care. Obviously, the only solution is to remain completely healthy until I'm hit by a bus on my way to a dance at age 93!
Linda,
DeleteWhile I don't ever want my children to bear the burden of my care, I do assume (correctly, I hope) that I won't be completely alone to face whatever old age brings me. My childless friends worry about that sort of thing, even more so when they're single. A friend's MIL, 85, looks in on several older women in her neighbourhood, all of whom are alone and still living in their own houses. She keeps an eye on their situations and helps out, if not physically, and it's this kind of community that both keeps her active and feeling useful, and allows them all to live relatively safely in their alone-ness.
Sometimes I wonder if the wandering is an ancient response, like what the INuit elders used to do when they left their communities to go off and die, and that perhaps we thwart that when we lock the doors on an Alzheimer's ward. But I'm romanticising a real problem, perhaps.
I like the ending to your life story. I wish it for you!
Somehow - this brought tears to my eyes. I have to think there was something important in your dream..and that you have a story within you that's going to be written with heartfelt beauty and grace.
ReplyDeleteThank you for reading and leaving such kind words, Marcie. Time will tell if I can get my act together for this story, but I'm working at it!
DeleteI share Marcie's tear, Deborah, because this really is close to home, as you know. The thing is, I just assume I have the Alzheimer's gene from Mom and would like to be pleasantly surprised NOT to get the disease rather than the other way around.
ReplyDeleteAstrid and I have already talked about living together in assisted living, if the day comes. I've paid my premium for it and hopefully her own added expense would be significantly less. She has promised me that we will dance together whenever possible. When I worked with Alzheimer's residents years ago, that seemed to be a bright spot in the day. The body knows. The "oversoul" also.
My sense about euthenasia here in Holland (you know how I feel about this) is very highly regulated...such that it is the doctors who have their second opinions, come to agreement, and give their seal of approval. Not the relatives. I'm not sure Alzheimer's fits this category in most situations. It's not a disease that can be taken care of by any one person or family, in most situations, but in the proper setting, there are wonderful facilities that give "quality of life" I would not fear even for myself. However, if Astrid could be with me because she'd not have it any other way, I'd be so lucky.
Mom had it for probably 3 years (one year when Dad didn't let us know!) and then died peacefully in her sleep after an unusually lucid evening. In fact, she died 30 minutews before Easter Sunday, two years after Dad was buried the day before Easter. THAT would be its own book!
Carry on. It's all there in you. It just has to all come out...in its time and rhythm.
What an astonishingly pragmatic person you are! You’ve always come across that way to me, and this confirms it. Instead of hiding your head in the sand, you’ve faced the very real possibility head-on and made contingency plans. I admire that kind of clear-headedness.
DeleteThe fear of Alzheimer’s is the perspective of healthy people but from what I’ve seen (admittedly not a lot close-up except for my mother) the damage to the mind from dementia protects the mind from awareness of that. You could argue that people so afflicted really don’t know what they’re suffering from and in some cases, seem like happier individuals. My mom did suffer, though, although not constantly by any means. For at least 18 months, she was very bothered by the fact that something was going wrong with her but couldn’t figure out what it was. What a terrible conundrum – to try and get your addled brain to figure out why it feels addled!!
The thing that bother me about the possibility of Alzheimer’s is the effect on my children. Although there too, I look at my own case and cannot say I suffered because of my own mother’s illness. It was just hard to watch sometimes. She had the funds to be taken care of, and my older brother made sure she had the best. But the responsibility was heavy for him.
There are days when I think I know how I feel about this subject, and then I hear a voice like yours, and suddenly I’m not sure anymore. But it is in the process of talking and writing about it that things become clearer, and I thank you so much for adding your very important bit to this discussion. Your own mother was so lucky to go the way she did. A friend is currently waiting out the long, long decline of her 98-year-old mother who has had A. For 15 years and is now inching towards death, suffering physically despite the care she’s getting. Her body just won’t let go. I have trouble accepting that ‘it’s her journey’, because it’s awful for the her, and for her daughter. I would want a pillow over my face at that point, I’m pretty convinced.
My husband's aunt passed away a few months ago after spending her final years in a nursing home. Each time we visited we saw so many patients who stared without seeing, sitting in bed or in wheelchairs, unable to shower or use the bathroom or even stand without a nurse's assistance. Just a steady decline with few if any lucid moments.
ReplyDeleteIt seemed cruel to me. I cannot speak for others but I can say that for myself, I would rather die. With dignity. Like the character in your book, I would enlist the kind and humane services of my son or some other loved one. We would find some beautiful and isolated place. Sometime after sunset, there would likely be a combination of vodka and pills to put me to sleep and never wake up.
Your post on this subject is both riveting and respectful of Sophie's dignity. Can't wait to read your book, Deborah.
This is a great posting I have read. I like your article.
ReplyDeleteThe obvious snag is how to judge how capable someone is to decide for herself on euthanasia , by the time it becomes clear that it's dementia she's suffering from , rather than vagueness or depression .
ReplyDeleteWe'll all experience dementia , whether as a sufferer or a family member , and no matter how many books one reads on the subject , nothing prepares one for the reality .
Your post is so vivid and at the same time so delicate – this is a hard subject. I hope some cure can be found. Last week, the doctor told us that some type of vaccination against the disease (which is in research right now) was looking very promising. I hope it is.
ReplyDeleteYou must write this book, absolutely! The topic alone is important; but the characters, the love and humanity that you have already woven through this post, and illuminated for us, all these characters are just versions of people we all know something about, yet need to know more.
ReplyDelete(I signed up to follow your blog through email, yet, I don't remember receiving this one. So, I tried to sign up again, and Google kindly informed me that I was already signed up. I'm not sure what to do next.)
rosaria ~ I've had the same problem trying to follow Blogger blogs. I get some emails and not others. Sometimes these things resolve themselves - but you're not the only one. ;)
DeleteThanks for your latest comment. She's great, isn't she? When I saw her in concert recently, opening for the Cuban pianist Roberto Fonseca, I was afraid she might upstage him. So good was she. But no, Fonseca came up with the goods, too.
ReplyDeleteHave a nice week.
Greetings from London.
Wonderfully written. This is part of the book, yes? The prologue, perhaps?
ReplyDeleteWho needs to make up stories when there's Life to be observed and recorded? The only trick is to do it well, and you've succeeded so well here.
How kind you are, and how lucky Sophie was to have spent such a wonderful afternoon. As Nance says, this is beautifully written, Deborah.
ReplyDeletea/b
Hi Deborah, I have started to read this a number of times since it posted. I finally finished tonight. Sophie's end reads like a work of fiction, not because it's not believable but because it seems poetic. I had to re-read the first part about your dream, then you & FB seeing Sophie out, to to see if her story was a continuation of the dream as a compelling work of fiction. Her death is romantic in a sad way. I understand why it's also a brave ending. I have not personally dealt with Alzheimer's within my family but have several friends whose parents suffered.
ReplyDeleteThank you very much for your comment on my latest post, Deborah. And believe me, I never intended to show you up! :-) Keep snapping away, especially if you have musician friends! :-D
ReplyDeletePunter is slang for customer in London. I should have made a note of that. Sorry.
Greetings from London.
Your book needs to be written, and the subject of choosing to die rather than suffering until the poor old diseased body gives up, however long that might take needs to be explored and explored.
ReplyDeleteMany of us have watched in anguish as loved ones go through so much pain and indignity, with no hope of improvement and no way out. Write the book!
Well, here's hoping that the book is coming along nicely now. I definitely miss your columns. The wit and humour of them.
ReplyDeleteGreetings from London.
Get thee back to blogging! You are even worse than I am!
ReplyDeleteI hope all is well. xx
btw your word robot thing is awful. for heavenssake turn it off and get another platform if you get too much spam. I had to try about ten times before I could find somethng I could read, and I am not a robot.
ReplyDeleteVous pouvez quitter diablo 3 gold la zone à moins que vous n'ayez ultérieur vous aux Missions totales. Et être dans une région pour finir les Quêtes pourrait être extrêmement plaisant. Vous pouvez posséder l'opportunité de continuer aussi beaucoup comme le métal précieux En argent le mars de bois ou même Gratuit dès que vous avez réalisé avec les quêtes. Je pourrais extrêmement suggérer que vous restez simplement là jusqu'à ce acheter diablo 3 gold que vous soyez dans une région au degré riche quelque chose comme 20. Quand vous êtes questing vous obtenez la pièce, l'expérience, la fraction minoritaire avec quelques augmentation d'information. Dans le cas où vous découvrez des Fentes et commencez à vous occuper d'eux vous obtiendrez un peu d'incroyablement grande expérience, pourtant, pas offres ou fractions minoritaires dont vous avez besoin. Vous pouvez profiter de l'occupation faisante à la main dans la diablo gold Fente aux quantités augmentées.
ReplyDelete