Advocacy, Antipsychotic drugs, Music, Videos

she couldn’t sing because she was sedated

My mother, who lived with dementia, was chemically and physically restrained every day for the forty-five months she lived in a dementia jail (aka a long-term care facility or nursing home).

These restraints could have been avoided if the medical personnel in charge of her care had addressed the root causes of the behaviours they found challenging in her. All they needed to do was to take a closer look at what was going on around Mom. If I could do it, surely they should have been able to.

When Mom was sedated, she was unable to do things she loved to do such as walking and singing. Here she is not singing (because she had been sedated an hour or so before), at some of the weekly sing-alongs conducted by volunteers at the place she resided:

Besides cruelly sedating her with antipsychotic drugs, no one who was involved with my mother’s care listened to my request to provide her with music therapy. So I hired a music therapist myself and the three of us enjoyed many happy afternoons together after the worst sedative effects of the chemical restraints had worn off. Here’s an example of one of those wonderful sessions:

a magical musical alzheimer gift

And this one was just four days before Mom died on August 17, 2016:

one last sing-along: august 13, 2016

I miss you Mom.

50 more pics that prove my mom was neglected and abused in long-term care

four years later is too late for my mom. but it’s not for others.

alzheimer disease didn’t do this. drugs and dementia jail did

10 reasons why neglect and abuse of elders with dementia may be the norm rather than the exception in long-term care facilities

25 practices long-term care workers know are elder neglect and abuse; it’s time to put a stop to it

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Advocacy, Care Partnering, Toward better care

50 more pics that prove my mom was neglected and abused in long-term care

If you don’t have proof, you won’t be believed. Sometimes, even if you DO have proof, you are not believed.

I learned that when I went to court to try to get control of my mother’s care in early 2014. I had lots of proof, but I still lost. I was devastated. But the loss didn’t stop me from documenting the neglect and abuse my mother continued to suffer until her death in August 2016.

The neglect included not having her incontinence pads changed as frequently as they should have been, having the pads put on backwards, not having wounds properly dressed and not having the level of one-on-one care she required.

The abuse consisted primarily of being chemically restrained with antipsychotic drugs (which caused her to stumble, bump into things, fall and sustain a continual stream of injuries), and being physically restrained with recliners, wheelchairs, and various types of alarms.

These fifty photographs (all taken in 2014), show what this neglect and abuse looked like.

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If you have a family member in long-term care:

  • learn what constitutes neglect and abuse
  • visit often at different times of the day
  • watch how staff treat other residents
  • document what you see and hear
  • advocate for proper care

25 pics that prove my mom was neglected and abused in long-term care

four years later is too late for my mom. but it’s not for others.

alzheimer disease didn’t do this. drugs and dementia jail did

10 reasons why neglect and abuse of elders with dementia may be the norm rather than the exception in long-term care facilities

25 practices long-term care workers know are elder neglect and abuse; it’s time to put a stop to it

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Advocacy, Care Partnering, Toward better care

who is responsible when people living with dementia are robbed of their dignity in long-term care?

Of the roughly seven hundred entries on seventy-five pages of nurses notes I was sent leading up to the court case I had initiated to try to get legal control of my mother’s care, the only one that made me cry was logged at 9 a.m. on June 26, 2013:

The second-floor “dining room” was small, more like a kitchenette really. It had a table in the middle at which six residents could be squeezed at mealtimes, a recliner (of course!) in one corner, and a rocking chair in the other. It had sliding glass doors that opened onto a little balcony where no one was allowed to go, and, at the opposite end, a sideboard with a sink and cupboards above.

I imagined Mom in there, needing to use the bathroom, but not knowing where one was. Maybe she had cramps in her tummy, as she often did in the morning. She suffered with diverticulitis. It flared up when she ate nuts or seeds or corn.

“Where’s the bathroom?” Mom would have asked other residents sitting at the table. “I need to go to the bathroom.”

The others, if there were any there, wouldn’t have answered because they wouldn’t have known. They would have forgotten, just as she had. If there were no other residents, Mom might have asked one of the care workers. If there had been any there, they might have noticed the telltale signs that Mom needed to got to the toilet. The signs were obvious, as I had explained to the Director of Nursing (DoN) four months earlier when she had asked me in a phone call whether Mom was in the habit of squatting and peeing on the floor. “No,” I said, surprised by her question. I wrote her an email the following day (February 5, 2013); it read in part:

“After I hung up the phone with you yesterday, I knew immediately why mom did this “squatting” behaviour in the living room at [the Dementia Jail]…she was desperate to “go to the peeps,” she didn’t know where to find a toilet, there was no caregiver…to help her, so she decided the best solution was to go on the spot rather than ‘in her pants.’

Even in her own room, she needs to be guided to where the bathroom is. For example, she may be sitting on her bed, facing the bathroom door, she will say: ‘ need to go to the peeps’, stand up, turn right, and head towards the closet. 

It’s easy to see the signs when [Mom] needs to go to “the peeps;” she starts to look distracted, she fiddles with the front of her pants, she may stand up, she may put her hand on her lower belly or between her legs, just like little kids do.”

The DoN replied saying she would share the information with the staff. It seemed strange to me that she hadn’t figured out for herself what lay behind the “squatting,” given that she was meant to be an expert in caring for people living with Alzheimer disease. Mom’s behaviour was basically Dementia Care 101, or at least it seemed so to me.

Had the DoN conveyed the information to the staff (who also should have known without having to be told), and had there been one of them in the dining room that morning, they might have wondered what my mother was doing when she went over to sideboard and took a piece of paper towel from the roll that was sitting there.

They may have kept watching when she laid the paper towel on the floor in whatever space she could find. But when she stepped in front of the paper on the floor, unbuttoned and unzipped her trousers and started to pull them down, surely they would have intervened and taken her to the toilet. Or one would hope they would have intervened…

But no one took my mom to the toilet, so it seems there weren’t any care staff there to help her preserve her dignity. Where were they? Around the corner at the nursing station, which was no more than twenty feet away, having a chin wag as I had observed them do on many occasions? Or maybe they were busy with other residents? Who knows?

What can be understood from the notes, which were written from the perspective of the charge nurse and not my mother of course, is that Mom had a bowel movement on the dining room floor and then tried to clean herself. How must she have felt throughout this episode? Confused? Scared? Embarrassed? Ashamed? Agitated? Upset? Surely she was robbed of her dignity, and that’s what made me cry when I read the entry. When I flipped the page to find the same thing happened the following week, I saw red.

I remembered the incident of the dirty pull-up. The week after, Mom was without a pull-up under her trousers, which were wet, two nights running. The next Saturday morning, I found her walking naked in the hallway; her bed was soaked and the room reeked of urine. Then there were the times her incontinence pad was so full it had leaked, and created crescent-shaped wet spots on her pants.

None of these had been mentioned in the eight months’ worth of nurses’ notes I was sent in advance of the court hearing. But fourteen other incontinence incidents had been recorded. They all implied the fault lay with my mother, when in reality it was the DoN’s responsibility to ensure her staff met my mother’s basic hygiene needs. Had the Director of Nursing done her job, my mother wouldn’t have suffered the indignities she did.

Likewise, my mother wouldn’t have been chemically restrained with antipsychotic drugs, physically restrained using recliners and other means, hospitalized with thrombosis in her leg, forced into incontinence, forced into a wheelchair, denied the right of seeing me, her daughter, during the last eighteen months of her life, and left in the bathroom alone to fall, break her arm and as a result of the trauma, die three weeks later.

Robbing someone of her or his dignity is tragic. Neglect and abuse are criminal. Those who are responsible should be held accountable.

Note: To add insult to injury, there were no “public toilets” on the second floor where Mom did not have a room of her own (her room was on the third floor). So when she was “toiletted,” she was taken into one of the second floor residents’ rooms too use their bathroom. But if she “wandered” into one of the second floor residents’ rooms on her own, she was admonished for doing so, dragged out into the hallway and made to sit in a chair in the corner by the elevator. Naturally she protested by striking out, and was then written up in the nurses’ notes as being aggressive and uncooperative.

which way to the bathroom?

hail mary i need to pee

5 ways we rob people with dementia of their dignity

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Care Partnering, Death & Dying, Life & Living, Love

7-part palliative care plan works (for people AND cats)

About a month after Mom died in August 2016, her little kitty cat Pia Roma, who had lived with me since late February 2013, began to behave strangely. Coquetishly cute Pia, with her big yellow eyes, had always been a little odd, but this was different. She wasn’t herself at all. There were continence issues, a lot of meowing and more vomiting than usual.

“She has chronic kidney disease,” the vet told me after some blood tests and an overnight stay at the clinic. “And probably a bit of feline dementia too.”

The vet gave me medication for the CKD, and put Pia on a special diet. Pia continued to enjoy an active life for an older cat, despite her dementia. When I took her back for a check-up in 2017, Pia’s kidneys had actually improved. In the four years we’d been together, we’d grown really close, and I was delighted she continued to be so well. I was equally devastated, however, with the results of this year’s check-up, which took place last week. I wrote about it on my personal FB page:

“I took Pia to the vet yesterday afternoon. Unfortunately, the news isn’t good. The vet was impressed with the great shape she’s in for a cat her age, which I think is 16. The vet said her heart is in fabulous condition; she was surprised and impressed when I told her that Pia still runs around, plays, and jumps up and down from my desk to the floor and onto my very high bed.

The blood tests, however, told a different story. The results showed that, while her thyroid is fine, her kidney disease has progressed from stage I, which is was two years ago, to stage III, which it is now. The vet reckons she only has about six months more in this world.

The only thing that can be done for her now is palliative care to keep her comfortable. Of course I feel desperately sad, and I can’t stop crying, but what to do? This is life. And death.”

As with any terminal illness (e.g. Alzheimer’s disease, kidney disease, etc.), the patient does not suddenly die the minute she or he is diagnosed. People (and animals!) can continued to live relatively well until they die. I believe our job as care partners is to support those we love in living as they go through the process of dying. If I’m not mistaken, that’s what palliative care should be about. Hard as hell in the midst of our own grief, no doubt about that. But I know it’s possible.

So I have a palliative care plan for Pia. It’s essentially the same as what I tried to do for Mom, even though my hands were tied in many ways. Here’s the plan:

1) watch and listen carefully to try to determine what her needs are and do what I can to meet them

2) focus on what she can do each day

3) make her life as joyful as possible

4) maximize comfort

5) minimize pain

6) let her be the driver

7) respect the process and hold space for both of us

I know all these things worked a treat when I was with Mom, and I believe they’ll help Pia as well. Maybe they’ll be a blessing for those you love too.

https://myalzheimersstory.com/2018/02/25/3-wise-thoughts-on-being-with-someone-you-love-as-they-die-which-also-apply-to-being-with-someone-with-dementia-as-they-live/

https://myalzheimersstory.com/2018/04/27/understanding-the-suffering-associated-with-dying/

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Challenges & Solutions, Tips, tools & skills, Videos

20 questions to ask yourself about dementia-related incontinence

One of the first things we learn to do as toddlers is to eliminate our waste in socially acceptable ways, usually in private. The cultural norms and taboos associated with this normal bodily function are deeply ingrained; they remain with us for our entire lives.

The elderly, and people who live with dementia in the later stages may experience incontinence, and, as a result, have to wear adult incontinence products. Sadly, they may also be forced into incontinence, as my mother was, in understaffed long-term care facilities either because the staff don’t understand incontinence or they don’t have time to properly care for people.

I developed this list of 20 questions to help all of us, particularly care partners and care workers, to reflect on some of the issues surrounding incontinence in dementia care, whether that care is administered at home or in a facility.

  1. How often do you go to the bathroom every day? If somebody told you you couldn’t go when you needed to go, what would you say?
  2. When you need to use the toilet, do you know where to go? What would happen if you didn’t know where to go? How would you feel? What might you do?
  3. What is it like to be in a public place, to be desperate to go to the bathroom and to not be able to find one? How might you feel? What might you do?
  4. What would it be like to be in a strange country, to need to use the toilet, and not know how to ask where to go?
  5. What would it be like to be told you can only go to the bathroom at certain times, according to an arbitrary schedule and not when you need to?
  6. How does it feel when your bladder or bowels are full to bursting?
  7. If somebody told you to urinate or have a bowel movement when you didn’t feel the need to, would you be able to? How would you feel about it?
  8. When was the last time you peed your pants? How did it feel physically and emotionally?
  9. When was the last time you wore a diaper? What would it be like to have to wear a diaper today? If you had to wear a diaper from now on and forever, how would you feel about it?
  10. What would it be like to not be able to take care of your own personal hygiene?
  11. Have you ever been on a long drive, needed to use the toilet and been too far away from the next rest stop to hold it until you got there? What did you do?
  12. Have you ever been so desperate to pee, that you have urinated somewhere that you otherwise might not?
  13. What kinds of signs and signals do people (think children) exhibit when they need to go to the bathroom? What about you?
  14. How would you feel about having to wear a full diaper that weighed more than a kilo (i.e. more than 2 pounds) for several hours? Do you think having to do so would affect your mood and outlook? If yes, how?
  15. How often do you use the toilet with someone else in the room, or in the case of a public washroom in the cubicle with you?
  16. Would you feel comfortable having somebody clean your genitals and behind after you had urinated or had a bowel movement? If not, why not?
  17. How would you feel if, when you needed to urinate or have a bowel movement, you were told to do it in your pants?
  18. What is the relationship between bodily functions and human dignity? What is the relationship between bodily functions and shame?
  19. How would you react if you were told to do things or you started to do things that you had been told all of your life were taboo?
  20. What do you think of people who are incontinent? Do you treat them any differently than you do people who have control over their bladder and bowels? How would you feel about yourself if you were incontinent?

In closing, find good information about adult incontinence products, and watch this powerful scene from the movie Still Alice:

More lists of 20 questions related to other dementia care issues here.

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Advocacy, Care Partnering, Poetry

hail mary i need to pee

In March 2017, I wrote an open letter to Québec’s Minister of Health regarding the rationing of incontinence products in the province’s long-term care facilities. The letter includes a two-minute video, which demonstrates the amount of fluid required to fill an incontinence brief to overflowing, as I found my mother’s to be on numerous occasions. So far, a year later, I’ve not received a reply.

I’ve also written a short vignette on incontinence (based on my mom’s real life experience), in the voice of my fictionalized character Alzheimer’s Annie. Meanwhile, care workers in Ontario held a news conference and talked about how they had no choice but to force residents into incontinence. This poem is about that.

hail mary i need to pee

This poem is dedicated to older adults forced into incontinence. The shame belongs to someone else.

©2018 punkie

hail mary i need to pee

which way to the bathroom?
how and where should I go?
there’s no one to tell me
and no stopping the flow

I really am desperate
can’t afford to delay
“help me, please help me,”
to a young woman I say

“there’s not a minute to take you,”
she replies with a sigh
“i’ve got twenty more like you,
some near ready to die

“you’ll just have to wait
or go in your pants,
stop your complaining,
give up with your rants

“can’t you see we’re all busy
we’re run off our feet
that’s why we can’t let you
get out of your seat.”

“oh my goodness,” i say
“i’m in such a state,
to pee in my pants
is a shame that’s too great.”

“don’t worry my dear,
you’ll get used to it soon.
here the rule to obey
is you sing to our tune”

my bladder releases
it’s wet on my thighs
my cheeks turn red hot
my eyes start to cry

i want to go home
get me out this place
hail mary please save me
with your heart full of grace.”

©2018 Susan Macaulay. I invite you to share my poetry widely, but please do not reblog or copy and paste my poems into other social media without my permission. Thank you.

understaffed nursing homes force residents into incontinence

20 questions to ask yourself about dementia-related incontinence

crazy daughter weighs mom’s wet “nappy” and writes open letter to minister of health about it

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Advocacy, Toward better care, Videos

understaffed nursing homes force residents into incontinence

In summer 2009, author Lise Cloutier-Steele complained to the administrator of the long-term care facility in which her father resided that she had found his catheter bag full to capacity four times in the previous five weeks.

“If it happened when I was there, it probably happened just as much when I wasn’t,” Cloutier-Steele wrote in her 2010 book “There’s No Place Like Home: A Guide for All Caregivers,” which documents her quest for basic services for her aged father while he was in an Ottawa, Ontario, nursing home.

Cloutier-Steele, a frequent visitor to the home, regularly found other incontinent residents in soiled briefs, but was powerless to do anything about it. Nurses and staff were as scarce as hen’s teeth, and often of little help when they were finally located.

“On one occasion, I was fortunate enough to find a nurse on the floor,” Cloutier-Steele writes, “but when I told her about the resident in need, she said that she would have to wait because all the healthcare aids were on a break!”

Even more frustrating, Cloutier-Steele says she was “viewed as a troublemaker” if she complained about the negligence and abuse.

“I talked to other ‘troublemakers’ who visited the home as much as I did,” she says in her book. “Like me, these folks simply could not turn a blind eye to what happened to their institutionalized loved ones. Family members and designated guardians are only trying to make the best of a bad situation.”

Family members who complain risk retribution such as being denied access to their loved one. Three Ottawa women, for example, were slapped with no trespassing orders in separate cases in autumn 2017 after advocating for better care for their parents. My own visiting hours were restricted to between 1 p.m. and 3 p.m. during the last 18 months of my mother’s life as punishment for advocating on her behalf. I too complained about poor hygiene, and, after Mom died, wrote an open letter to Quebec’s Minster of Health about the issue.

Clearly, not much has changed in the seven years since Cloutier-Steele published her book. In fact, they may have gotten worse. In 2017, the Canadian Union of Public Employees (CUPE) in Ontario lobbied hard for legislative changes to LTC regulations.

Here’s what one 19-year care veteran, said of the dire situation at a November 1, 2017, news conference:

Candace Roddick, CUPE Ontario’s Secretary Treasurer followed, calling the situation “a crisis:”

Bill 33, called the “Time to Care Act,” would require Every licensee of a long-term care home [to] ensure that the average number of combined hours of nursing services and personal support services offered at the home each day is at least four hours per resident.”

A step in the right direction to be sure, but so very much more remains to be done in Ontario, as well as throughout the rest of Canada, the US, the UK, and Australia. I am convinced that elder neglect and abuse are pervasive, persistent and systemic worldwide. It’s time to put a stop to it.

https://myalzheimersstory.com/2017/03/31/crazy-daughter-weighs-moms-wet-nappies-and-writes-open-letter-to-minister-of-health-about-it/

https://myalzheimersstory.com/2017/12/03/four-years-later-is-too-late-for-my-mom-but-its-not-for-others/

More links on why elder abuse remains prevalent in care institutions here.

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Advocacy, Toward better care, Videos

crazy daughter weighs mom’s wet “nappy” and writes open letter to minister of health about it

“Rationing” incontinence products in long-term care facilities (LTCFs) is not unique to the province of Quebec, Canada, where I live. An Ontario-based claimant in a class action suit against LTC giant Rivera told investigative news magazine W5: “Diapers in these homes are like cigarettes in prisons – they’re currency.”

When a student care worker blew the whistle on the issue in Quebec in autumn 2016, her Facebook post went viral and an investigation by the province’s ombudsmen ensued. The investigation outcome prompted me to write this open letter to the Quebec Minister of Health and Social Services. The letter and video are available in French here.  Une version française de cette lettre est ici.

Open letter to Dr. Gaetan Barrette, Minister of Health and Social Services, Government of Quebec

March 31, 2017

Dear Dr. Barrette,

I was hopeful when the Protecteur du citoyen initiated an investigation into a young whistleblower’s charges regarding the rationing of incontinence products in Quebec’s long-term care facilities (LTCFs).

I know the torture of seeing an elder family member neglected, and I hoped the Protecteur du citoyen‘s investigation might lead to change. Thousands of other Quebeckers like me witness the ill treatment of people they love in Quebec’s LTCFs, both public and private, on an ongoing basis.

My mother, who lived with Alzheimer’s disease, entered a private LTCF on November 16, 2012. She declined more during her first two months in “care” than she had in the previous two years. Things deteriorated further over time. One day in September 2013, I noticed her incontinence “pad” was overflowing. It wasn’t the first occasion, nor would it be the last. Discouraged and dismayed by the indignities Mom was suffering, I took a picture, and later weighed the incontinence brief. Watch the video:

As I’m sure you know, Dr. Barrette, the average daily output of urine for a healthy adult who drinks about two liters of water per day is between 800 mls and two liters. That means, depending on her output, there was between 11 and 27 hours’ worth of pee in my mom’s incontinence brief when I visited her that day.

In response to my repeated requests for Mom’s briefs to be changed more often, I was told that she was toileted every two hours. That was not true. I regularly found Mom’s briefs either wet or soiled or both when I visited, regardless of when I arrived. Worse than the discomfort and humiliation she endured, poor hygiene practices caused my mother to contract urinary tract infections (UTIs), She was treated for the last in a series of UTIs just six weeks before she died on August 17, 2016. During the time I cared for her myself, she never had a UTI.

I was keen to participate in the Protecteur du citoyen’s investigation, and I spoke to a Protecteur representative at length on the phone. I recounted my story, including the incident above. The interviewer appeared to be listening, and then she asked: “But did the facility have quotas for the incontinence briefs? This investigations is about quotas.” I explained that we paid for my mother’s pads; there was no reason for the facility to ration them. I told her that Mom’s experience had nothing to do with quotas, and, in my opinion, had everything to do with lack of staff, lack of training, lack of care, lack of awareness, lack of resources, lack of compassion, and most important, lack of understanding of the needs of an elderly person living with Alzheimer.

The first paragraph of the Protecteur du Citoyen’s “Intervention report concerning quotas on incontinence products” states: “The purpose of the investigation was to ensure that the rights of the seniors lodged in these centres are upheld and that these residents are treated with dignity and respect.”

Where are “dignity and respect,” Dr. Barrette, when an 86-year-old woman’s brief is full to overflowing and weighs more than a kilo? Can you imagine how uncomfortable that would feel? How humiliating it would be?

The Protecteur du citoyen’s investigation and report miss the point, as does all the brouhaha around once-a-week baths, potato flakes versus “the real McCoy” or whatever other eldercare scandal of the day pops up. These are symptoms of much deeper problems: how we devalue our vulnerable elderly and those who live with dementia, and how compassionless and broken our so-called “care” system is. Pervasive and systemic overmedication, short staffing, a dearth of training, low pay, insufficient funding and a whole host of other deficiencies result in a toxic environment for residents, family members and workers alike.

Nurses and other front-line workers employed by long-term care facilities (LTCFs) don’t set out to deliberately neglect and abuse residents, or at least the vast majority don’t. Unfortunately, neglect and abuse are results of the system of which they are a part, and unintentional neglect and abuse are still neglect and abuse. The underlying issue is the absence of a culture of care, compassion and competence in LTCFs.

It’s time to stop defending the system, and start defending the people: the residents, their families, and workers who want to do the right thing and truly care for people instead of being forced to neglect them in what are essentially warehouses for the old, infirm and/or neurologically challenged. It’s time to ask better questions, listen to whistleblowers and others who speak the truth, and take immediate and effective action to fix what’s broken in Quebec’s LTCFs.

Advocates such as myself want to work with you to create positive outcomes, but we need you to listen and address our concerns; we need you to include rather than exclude us from the process; and we need you to work with us in a spirit of cooperation instead of against us as if we were the enemy rather than your constituents.

We need to do this now. For the sake of our elders, as well as our own.

I look forward to your collaborative response.

Susan Macaulay
Dementia care advocate

https://myalzheimersstory.com/2017/05/26/12-uti-symptoms-experienced-by-the-elderly-and-what-theyre-like-in-real-life/

https://myalzheimersstory.com/2017/12/03/four-years-later-is-too-late-for-my-mom-but-its-not-for-others/

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Advocacy, Annie & Cricket, Antipsychotic drugs, NHBPS

which way to the bathroom?

Which way to the bathroom cropped

This is one in a series of vignettes based on the Nursing Home Behaviour Problem Scale (NHBPS), which is used to measure agitation in people who live with dementiaThe vignettes are told from the point of view and in the voice of a fictional character called Annie, a woman in her mid-eighties who lives with dementia of the Alzheimer’s type in the mid- to later-stages of the disease. Annie resides in a long-term care facility somewhere in Canada. This vignette is called “what a shame.” There’s a link to all the vignettes at the end of the post.

what a shame

I have to go to the bathroom. I’m desperate. I really need to go.

I walk down the hall looking for the ladies’ room, but I can’t find it. What a strange hotel. It doesn’t have any toilets. The doors to the rooms are open, but most of them have stop signs in front of them. I guess I’m not allowed to go in, but I’m not sure. I’m not sure. What an odd place. Here’s a room with no stop sign, there’s an old lady inside; I’ll ask her. The old lady is in a chair. The chair is tilted back. She has a blanket across her legs. When I walk in, she leans forward, and stretches her arms out to me like she wants something.

“I have to go to the bathroom,” I say. “Do you know where the toilet is?”

Ahhhhhhh ahhhhhhh ahhhhhhh,” she says. I don’t understand what she’s saying. It looks like she’s trying to get out of the chair. But she can’t. Maybe she needs help too. Maybe she can’t hear me. I walk closer.

“I have to go to the powder room. Do you know where it is?” I repeat a little louder in case she’s deaf.

Ahhhhhhh ahhhhhhh ahhhhhhh,” she says again as she takes hold of my wrist. Her fingers are bony; her grip is light. Old ladies aren’t strong. The poor thing. I wish I could help her, but I can’t. I have to find a bathroom. I feel wetness between my legs. I put my hand there, and press it into my body. I walk knock-kneed out of the room, my inner thighs rubbing together. The hall is empty.

I can’t wait. I can’t. I’m going to pee my pants. I’m going to pee my pants. Oh no. Oh dear. Quickly now. Undo the button. Pull the zipper down. Pull the pants down. Quick. The pee is already coming. Squat. Put your hands down so you don’t fall over.

Dark yellow liquid gushes from me onto the floor. Relief. A sunny puddle spreads on the white linoleum. It surrounds my shoes. Move your hands! Move your hands!

“Annie! What are you doing?” A young woman is walking down the hall toward me. “What are you doing Annie?”

My hands are wet. My cheeks are hot. I can’t stand up. “I had to go to the bathroom.”

“I see that,” the young woman says. “But why are you doing it on the floor? You have to go to the toilet when you need to pee.”

I know. I know. I couldn’t wait. I couldn’t wait. She helps me stand up; she pulls up my underwear and pants. The puddle is still spreading. I feel sick.

“My hands are wet,” I say.

“C’mon, let’s get you cleaned up. And next time, when you need to pee, go to the bathroom, okay dear?”

“Okay,” I say. “Okay.”

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©2016 Susan Macaulay / MyAlzheimersStory.com

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