Sunday, May 6, 2018

Things I learned about moving on from my mother's cat

I didn't want another cat, I really didn't, and certainly not my mother's finicky cat, Daisy. Nonetheless, when push came to shove, I couldn't bring myself to take Daisy to the cat rescue center after Mom died. Daisy made my dad smile eight years ago, just before he slipped into a coma. And Daisy was my mother's chief companion until Mom died in early April. So here she is, taking a nice nap on my bed.

Daisy and I are making the best of things as we learn how to navigate these first months since Mom died. She's even offered some good examples.

Daisy has her cat tree and her own room (temporarily) at my house, but she spent the first week refusing to eat or groom in what looked remarkably like sitting shiva. Then she decided it was time to take up the job of moving on, came out from under the bed, and started to embrace the new normal.

There is some real benefit in shutting down for awhile after someone dies, and I wish I'd followed the feline example. Instead, almost the day after Mom died of sudden cardiac arrest, I spent two weeks in a frenzied whirl preparing her house to accommodate out-of-state relatives, making arrangements, visiting the lawyer, and planning Mom's Unitarian memorial service and reception back at the house. I (stupidly) thought keeping busy would keep the grief of Mom's last day at bay.

Instead, by the day of the memorial, I was dazed, exhausted, and edgy. The reception was dominated by my dad's half sister and her adult children who, unbeknownst to me, started moving things from "their" side of the family out to their cars. My ditzy sister-in-law told them to take it. I made them put some things back, but a lot of stuff is gone for good.

I'm still fuming about their bad manners. Daisy,  on the other hand, didn't care about the Noritake china or the sewing rocker or the doo dads. She cared about Mom and their little daily rituals of  enjoying the garden, sunning on the porch, napping with a book, and watching CNN. Those daily intimacies are what make a life, not the "stuff."

Daisy has let me know that she's willing to work with me on new routines. She has become more cuddly. She has learned to eat dry food. She has quit hissing at the other cats when they put their paws under "her" door. Maybe, eventually, I will stop hissing over my sister-in-law and aunt for taking stuff I really didn't want in the first place.

What I want to remember about my parents was their kindness and their love for the natural world. Daisy, rescued from some neighbors who abandoned her, was the last burden  they asked me to pick up for them.

She is also their last gift.


33 comments:

  1. What a sweet kitty! I'm glad you are keeping her.
    Sorry to hear about the greedy relatives, don't know what gets into people, thinking about that kind of stuff when a loved one is barely in the grave.
    Unfortunately we usually don't have the option of shutting down after a death. What I remember most about the period after my mother's death is the fatigue. Now that the funeral is over be sure to get some rest.

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  2. Jean, thanks for this post. I am so happy that Daisy is getting to know you, Raber and the other cats. And I am so sorry about the difficulty with the relatives. I think I may have remarked before that when my grandmother died, it turned into a bit of a feeding frenzy at her house: she had antique furniture and other collectibles that various relatives had coveted for decades, and foolishly she hadn't made provision for any of it in her will. That meant that an orderly distribution depended on the backbone of her executor (one of my aunts) - it put her in a very difficult position. Folks, please make a will, and put your estate in the hands of someone who is willing to piss off all the siblings, nieces, nephews and other relatives in order to make sure that your loved one's wishes are carried out.

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  3. Mom's will was clear -- everything to me and My brother, 50/50. My brother's wife apparently felt fully staked in it all and, while I was talking to guests on the patio, she felt within her rights to give a bunch of it away. I told her that the appraised value of the stuff she made free with will come out of their share of the cash settlement. If she wanted the cash instead, she could round up the stuff she gave away and sell it to an antiques dealer. My brother agreed that was fair.

    I have never been one for bibelots and fine china. I do have a fairly extensive collection of vintage Fiestaware and salt and pepper shakers. Apparently I inherited Gramma's penchant for kitsch and loud colors.

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  4. Jean, I have never had the full load of funeral preparations dropped on my back, but in the funerals for which I had most, or a significant part of, responsibility, I had the impression the purpose of the funeral was to leave the most bereaved exhausted and ready to say, "We'll think about that tomorrow" to everything else. And maybe that isn't a bad way to handle it.

    Our wills say that any "little personal things" any of the kids want will have to be appraised and deducted from their share of the settlement. We have tried two ways to discourage such sentiment, however. First, we haven't got much left that is of any value -- the baseball autographs (which include Ty Cobb and Cy Young) and a painting of unknown but possibly significant value that was a gift. The rest we shed. We may get shed of the autographs, too, if we ever get a break between doctors' appointments. Second, from the time they were young we have tried to impress on them that all stuff is just stuff,
    Unfortunately, we won't be around to see if that worked.

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  5. My mother has had conversations with me and my wife, and each of my siblings and their others', about who gets what. She has figurines, china and the like (some of which came to her from my grandmother, I think). Honestly, I don't have any interest in that stuff; if any of my brothers or sisters wants all that junk, more power to 'em.

    Once the sharks had swum away from my grandmother's house, I ended up with the leftovers, which turned out to be a player piano and a cabinet full of piano rolls. They're in the room where I'm typing this. I play the piano as a piano. The rolls are all of songs like "Lady of Spain" that none of us can muster any interest in listening to, once the novelty has worn thin.

    Isn't there a word for the thing that nobody wants? That's what I ended up with. I'd love to get rid of the stuff but have lacked the motivation so far to venture onto Craig's List. Actually, the piano roll cabinet would make for a decent bookshelf.

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  6. Thanks to Jean's post below on old people in novels, I thought of David Lodge's novel, "Deaf Sentence." That brought me to the shelf that turned out to have most of his novels, most of his lit crit, a play, and two volumes of memoirs. I am now immersed in the questions, "Why Lodge? Why so much Lodge? What is Lodge up to?" Work-in-Progress.

    But so many books! This is to speak of the topic at hand.. Accumulation. We have lived here for 45 years! As the children left, more space opened up and it has been more than filled mostly with paper, books, magazines, laundry lists, etc! I doubt there will be a trove of relatives eager to haul this off. Any advice?

    In the meantime, speaking of books, David Leonhardt (NYT columnists and former economics reporter) has a pleas to save Barnes & Noble and some critical remarks about Amazon. Perhaps of interest to book lovers here.

    https://www.nytimes.com/2018/05/06/opinion/save-barnes-noble.html?rref=collection%2Fsectioncollection%2Fopinion&action=click&contentCollection=opinion&region=rank&module=package&version=highlights&contentPlacement=4&pgtype=sectionfront

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  7. Raber suggested the Amish way of liquidating the estate. You have a silent auction, and anything you "win," you pay the estate for. Then it's all liquidated, and the funds divided amongst the children.

    Tom, yes, Raber and I have made a vow not to leave The Boy with the burden of all this stuff. I already have what Raber calls my Death Folder. A list of all assets, funds, passwords, service preferences, POA, will, and obit.

    I do want to talk to the doc about a DNR order. Mom should have had one, and I fault the doctors for not discussing it with her. I don't want my family to have to make that decision for me.

    Jim, I love player pianos. Our neighbor had one in her basement. Her granddaughter used to visit in the summers and we would sit down there drinking A&W root beer and singing "Shine on Harvest Moon" and "Just a Closer Walk with Thee." Good times!

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  8. Margaret, am reading "Deaf Sentence" right now! I also have high frequency hearing loss like protaginist Desmond. I am constantly hearing things wrong. Raber was talking about "endangered Australian koala bears" this morning and so heard "enamored of Australian foreign affairs."

    Being in a crowded restaurant is a nightmare. The food needs to be extra good because I can't have a conversation.

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    1. Yes, Ears! Yes, High Frequency Lost! Both of us. We keep discussing hearing aids. And then go back to reading and writing, which do not require ears.

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  9. On hearing aids: Remember, if not hearing well is a pain in the neck for you, so is it a pain in the neck for anyone trying to communicate with you and not knowing whether you heard him or her. I know several people with hearing aids who used to not hear and now do. I am married to one.

    There was a time when hearing aids were more trouble than they were worth, but those days are over. (Some day someone will tell me electric shavers finally work, and on that day he will be right, for a change.) Anyone who can endure eye glasses can endure modern hearing aids, and anyone who does will be more fun to be with.

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    1. Good advice... Have you any recommendations..Brands? Costco? Audiologist? etc.?

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    2. Cost of hearing aids puts me off. Does Medicare cover them?

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    3. Hi Jean--No, unfortunately Medicare does not cover hearing aids. However, some Medigap plans do cover them, as long as you use their dispensaries.

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    4. Then Raber will have to learn to repeat himself a lot. Fortunately, to Tom Blackburn's point, there are ways to be fun to be around that do not involve talking ...

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    5. Raber and I also do like the Millennials and text each other in the same room together!

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    6. Can you and Raber text? It beats me.
      My wife's is a basic (I think) StarKey. It took three trips to the audiologist for her to get the settings and earbuds right. Now it's just a once-a-year checkup, and the audiologist thinks Marilyn and I are fun. A friend got a pair just like hers, hated them and kept turning them off. Then, all of a sudden he said, "Eureka" or something and he can hear again with them. So I guess they take some getting used to. M's were about $2,000 and a big chunk of that was covered by our secondary insurance.

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    7. We text on our phones.

      A big problem for me is that Raber blabs through TV shows and movies. That means I can hear neither of them. He tries to shut up, but watching the news is especially awful.

      Some of it is noise, but some of it is that blabbing pulls you out of the narrative or story, and then it's hard to reimmerse yourself.

      He thinks that whispering makes it OK.

      Talking is overrated.

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    8. Talking during the news. I have been asked to keep my comments and observations to a minimum. It is very hard. I am a multi source news junkie and honestly I know more, or think I do, than Judy W. and the amateurs who seem to be replacing her. (What is going on at the Newshour?)

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    9. I dislike their "Politics Monday" feature, which is really predictable, and Any and Tamara are lightweights. I am also wearing of Shields and Brooks, much as I like their winning personalities.

      Judy needs a partner.

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    10. Promoting Women! which seems to be one thing going on at The Newshour is a good idea, on the face of it. Why is it looking so pathetic?

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    11. I dunno, I compare it to commercial broadcast news, and it's still better. Low bar, I realize ...

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  10. Tom, all hearing losses are not alike. And even if it's no fun for you to live with a hearing impaired wife, it is worse for your wife.

    I have suffered hearing loss for about a decade, steadily worsening. Right now, I have a "profound" high frequency loss. "Profound" means I don't hear certain frequencies at all and hearing aids cannot make up for that loss. The severity of this loss was brought home to me when my husband tested some alarms on our house. We travel a lot, and we decided to put window/door alarms on the house after several houses in our neighborhood were broken into. They don't call the cops, just make very loud noise. The local police said they run off about 80% of housebreakers, and since breaking/entering/burglary have been rare events where we live, we decided those odds were OK. Just draw attention to the house. But, when my husband was testing them, I could hear nothing at all - even though he said the alarms were indeed very, VERY loud.

    Hearing aids are very different from glasses. I am also severely myopic - if I don't have on glasses/contacts, I cannot make out the features on the face of someone sitting only a few feet away from me. With glasses/contacts, I have "perfect" vision. Hearing aids do not EVER restore hearing to "normal" or "perfect" even though they cost in the thousands of $ instead of hundreds. Hearing loss that is severe to profound, as opposed to mild - moderate (fortunately that is what most experience) leads to emotional challenges, primarily due to the fact that it is very isolating. I can no longer attend lectures or classes. Hearing with ANY background noise doesn't work well, which leaves out most social gatherings. I can understand homilies at church because it has assistive devices available. Otherwise I just hear sound, without clear words. If my husband and I watch TV together (closed captions of course), and he comments, I have to mute the TV sound and have him repeat it. I have told my husband for YEARS now that it doesn't matter how loudly he shouts at me from upstairs when I am downstairs, or from any room other than the one I am in, that I can't understand what he says. It's not volume, but clarity - as Jean pointed out in her example. Hearing aids do NOT solve all of these problems for those whose hearing loss is greater than mild-moderate.

    Those with hearing loss, and those who live with people with hearing loss should read this book:

    https://www.amazon.com/Shouting-Wont-Help-I-Americans-Cant-ebook/product-reviews/B008MWG7R8/ref=cm_cr_arp_d_paging_btm_2?ie=UTF8&reviewerType=all_reviews&pageNumber=2

    The top reader review for this book is in the next comment, and it is one that I appreciated deeply - few hearing people (including myself before my loss) understand the emotional consequences to people with severe-profound hearing loss.

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  11. From the Amazon reader reviews of Shouting Won't Help

    For the adult with late onset hearing loss, there is no recovering the person you used to be."

    By Amelia Gremelspacheron February 19, 2013

    "Katherine Bouton has been a writer for the New Yorker, and her literate and informative writing skill come to serve us very well in this book which is part memoir. Clearly this book is going to attract those people with hearing loss or who have family with hearing loss. ...More to the point, hearing loss is associated with extensive emotional and social loss that the hearing understand only marginally.

    ...my mother is struggling with hearing loss. She had shared her , anger and depression with her isolation. This book is able to greatly enlarge my understanding of her struggle. Bouton has met with professionals in every facet of this loss. She provides vignettes with people in specific fields who have lost their hearing. These people include nurses and opera singers. ...Most striking for me is the sheer exhaustion of effort that is required for a person to cope with conversation even with good hearing aids.


    I wish to draw attention to the bold - hearing aids are NOT a panacea. They help hearing impaired people to cope, but do not bring "normalcy" , A person who needs crutches to walk can move around, but with difficulty - not normally - and some places are unreachable without more assistance than the crutches provide. For many, hearing aids allow us to hear, but not normally - they are like crutches in that way. We still need assistance from those who are speaking to us even though we have hearing aids. We need closed captions on the TV - even with hearing aids. We need people to look at us when they speak to us. Do not SHOUT, it doesn't help - as the title of the book emphasizes.

    Back to the reader review

    ... Finally she is able to offer some solutions, notably ways to move away from the effort to return to one's former self and towards one's new identity, even though this is certainly difficult.

    Some of the other reviews note that the author did not cope well with her hearing loss - she resisted, and was in denial for years (her loss started when she was in her 30s). This is, however, not an uncommon reaction. It was mine, and still is after 9 years of trying to deal with an ever worsening hearing loss. I dread every hearing test, as it confirms what I already know - my hearing continues to deteriorate. Even though I know what to expect from each new hearing test, it depresses me quite severely for a couple of weeks - to see it in black and white on the audiogram. So, I think that even the author's "whining" as some reviewers put it, is a good lesson for readers - both those of us who suffer hearing loss and those who live with us.

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    1. Anne, sounds like you have similar hearing problems to my dad. He has hearing aids, some of the high tech kind, and it's better than nothing. But by no means like natural hearing. His problems are a cumulative effect of allergies and working on noisy farm equipment for a lot of years. He is introverted, so maybe the social aspect doesn't bother him as much, but he does like to visit with family members. My sister in law doesn't understand why he doesn't want a big 90th birthday party. Hello...bunches of people and background noise, not to mention a degree of social anxiety.

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    2. Katherine, at the rate things are going, by the time I reach your dad's age (if I'm still around!), I will probably be totally deaf. But I am still a bit more than 20 years away from your dad's age. Perhaps they will have improved the cochlear implants by the time I go totally deaf, and I will get one if that becomes necessary. Medicare doesn't pay for hearing aids, but it does pay for cochlears - IF you are totally deaf. Fortunately, I am not - yet. Medicare will also pay for a partial cochlear for just high frequency loss. I would be eligible for that. But when I read about it, and the clinical trials, I learned that 40% of those who got the partial cochlear lost their residual low frequency hearing and then needed a full cochlear. I can still hear lower frequencies, and I am not willing to risk losing that part of my hearing. I will just limp along with my hearing aid/crutches.

      I am also an introvert and have always hated large parties and other large gatherings. However, I do like being with close friends and family, and it's difficult to try to follow conversations these days. I also like to learn, and DC is a great place to live for access to interesting speakers, sponsored by many organizations here, mostly free, and interesting courses available at the universities in the area, some of which let seniors audit for free. Unfortunately, I can't understand the speakers/professors unless I am right in front of them in a smallish room with decent acoustics.

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    3. Anne, I hope they perfect cochlear implants in time to benefit you, and others who are losing their hearing. Which can happen suddenly. My late mother in law didn't have hearing problems until she fell and hit her head. I know a couple of teenagers who have had the implants. It's not perfect yet but hopefully the process is getting there.

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  12. Margaret, since hearing loss is highly individual, there is no one brand that will suit everyone. The first thing to do is get a hearing test. Costco gives those. If your hearing loss is relatively simple (mild-moderate), the Costco hearing aid technicians can fit you. They sell the same brands as the private independent audiologists at less than 1/2 the price. Costco gives 90 days for the trial period - the hearing aids can be returned during that time, no questions asked. I have done it. Independent audiologists with advanced degrees usually give a 45- 60 day trial period. Unfortunately, my next stop will be a private audiologist, as my hearing loss now requires a more complex set of devices - hearing aids PLUS microphones, transmitter, receivers, bluetooth perhaps.

    There are also hearing aids that are made for smartphones - primarily iPhones. If you have an iphone, you might want to ask about those - they stream phone calls to the hearing aids directly. They are made by Starkey and ReSound and , now perhaps a couple of others have new aids that will do the same. Costco carries ReSound but not Starkey.

    Although I have spent $11,000 on hearing aids out of pocket during the last 9 years, I will probably be spending another $6000-7000 this year. Medicare does not cover the cost of hearing aids.

    I had good luck with Costco in the early years, but the complexity of my hearing loss now means that my next stop will most likely be with an audiologist with an advanced degree. This was not necessary during the early years of my hearing loss, but it is now.

    Good luck.

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    1. Hi Anne--My hearing loss is not nearly as severe as yours, but I can confirm the difficulties you endure. I can’t watch TV without closed captioning; I don’t go to movies. However, I would like to say that the Bluetooth option with hearing aids is really worth pursuing. It allows you to hear cellphone conversations very clearly through your hearing aids, and--best of all--the hearing aids (at least mine) automatically block out surrounding noises. In any kind of noisy environment, it is far better to listen to your cellphone through your hearing aids, even--or especially--on the street. I will admit though that it can be tricky to coordinate the phone, the hearing aids, and the Bluetooth device--it’s not automatic.

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    2. Thanks, Bob. With my next hearing aids, I plan to ask about bluetooth - and your experience with them making the phone calls possible again might motivate me to grit my teeth and make an appointment sooner, rather than later. Phone calls are a nightmare these days.

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  13. My friend Charlie Seitz, GRHS, had a penetrating voice that could be heard over any ambient noise, even ski lift machinery. I don't remember ever asking Charlie "what?". I don't remember ANYBODY asking Charlie "what?" If you could make a device that digitized a voice and morphed it into Charlie's, it would make for an interesting hearing device experiment. I am only half-kidding. For a sample of the impish but audible Mr. Seitz, here's an abbreviated rendition of his skiing-isn't-fun-it's-just-something-that-has-to-be-done routine.

    https://www.facebook.com/HuntingdonValleySkiClub/posts/10151370798966851/

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  14. I can hear volume fine. It's just that people who are not looking directly at me or are speaking where there is a lot of background noise sound garbled.

    I need CC for movies, so I don't go. The rising/falling volume and the intrusive musical scores often interferes with my ability to make out words. I hear TV better. If we go to a stage play, I'm fine if I sit close.

    At Mom's memorial service, there was an hour of visitation, and I found it hard to hear some of her elderly, frail friends against the piped in music and background chat. But, then, they were all saying the same thing, and, "It's nice to see you, thank you so much for making the effort to come," pretty much covers the contingencies.

    I've also learned you can fake a lot by assuming the right facial expression for the event.

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    1. Just last night we were invited for pizza and a movie (the new, not as good as the old, Murder on the Orient Express) in Century Village, one of the famous or infamous huge developments built for the unloaded over-55 crowd. The movie was in the CV theater, and what I am getting to is that it was closed captioned. That's appropriate for the clientele. (It was a little odd when the translations from the French or German in the regular audience version appeared in different type.) My point is, there are probably general public theaters that could serve an audience and benefit themselves from regularly scheduling showings with cc.

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    2. I live in the suburbs of DC. We aren't movie buffs, and mostly see movies on long airplane flights. If a movie is of real interest, we wait for Netflix, which almost always has CC. But, even though I am not a movie patron, I do know that most of the movie theatres in the suburban malls and downtown DC have some kind of device for the hearing impaired. But since I have not been to a movie theatre in more than 20 years, I don't know what the hearing assist device is, or how it works. But, I imagine that this type of help is available in many places.

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