Showing posts with label alzheimer's disease. Show all posts
Showing posts with label alzheimer's disease. Show all posts

Sunday, September 11, 2016

Remembering 9/11 - 15 Years Later


[Editor's note: this post originally appeared here at Destination: Austin Family on September 11, 2008]

On the morning of September 11th, 2001, I was living in San Francisco out near Ocean Beach in a small one bedroom apartment where I had lived since 1993. It was a Tuesday and since I usually got up at 4:00 am to walk the dog and then catch a bus at 5:00 am to go to the gym, I'm not sure why I slept later than usual. All I remember is the phone ringing slightly before 6:00 am Pacific Daylight Time.

My first thought went to, "Why did I oversleep?" which was quickly replaced with, "Something is wrong." My phone just didn't ring at 6:00 am unless it was my mother in New York.

For years, Mom could never get the time zone thing right and I was used to receiving calls anywhere from 4:00 am onward. And after her early on-set dementia diagnosis in the summer of 2000, phone calls at odd hours of the day and night became commonplace.

As I said hello I could tell that my mother was flustered. First, she was at home and not working which concerned me. Second, despite suffering from memory loss, she had the wits enough to simply say "Turn on the television - something is wrong with the World Trade Center in The City." Having grown up only 90 miles northwest of Manhattan, we always called it The City.

Mom said "Call me back," and I quickly hung up and ran to the television. I was still half awake and was not understanding what was going on. I do remember Katie Couric's voice, or some other female voice, stating that there was something wrong with air traffic control perhaps since a large airliner had just hit one of the towers of the World Trade Center. It was only after having watched the second plane hit the other tower, live as it happened, did the announcer and I both know that this was no accident.

I sat mesmerized for the next 30 minutes before I put on some sweats and took the dog out for a short walk. My next task was to call George at his home in Oakland.

George and I had been dating for about 16 months and had not yet decided to move into an apartment together. He had been home sick the day before with a severe sinus infection, so I knew he'd be sleeping. And I also hesitated to call since he wasn't known to be entirely coherent in the mornings. But due to the nature of the events, I dialed the phone. As he answered I tried to explain what was going on, and realized I should have followed Mom's example and kept it simple. There are times when Mom really does know best. Finally, exasperated, I simply said what so many loved ones probably said that morning, "Turn on the television," and I hung up.

The rest of the morning is somewhat of a blur. I do remember calling my boss who lived in the East Bay and basically told him that I would not be coming into the office. He agreed that from a safety perspective, and what with working downtown in San Francisco's financial district amid large skyscrapers casting permanent shadows along Montgomery Street, being in an office was not the best place to be.

As I sat on the computer reading the news stories about the attack, the phone rang again. It was Mom and I could just feel the sense of confusion in her voice. I thought about what it must be like for someone who did not have all their mental faculties to witness such events and how they could possibly process them.

Did she think she was watching a movie? She probably wasn't the only one who thought that - many of us did as we first turned on the television. Then as I watched the first tower collapse, I said to Mom, "the building is falling." At which point she started crying and told me she loved me and that I should try to get out of the building if I could. I had to explain over the next 10 minutes that it was the building in New York collapsing, not my own apartment building.

Oh, if all the confusion and panic of those events had been so easy to explain in only 10 minutes that day. I do remember, as others have described, the "eeriness" of the streets, the buildings, the towns - big and small - and how things just didn't seem right. There was less traffic on the streets, there wasn't the usual small talk at the grocery store or the dry cleaner, if one could even think about seeking refuge in the mundane world of daily errands.

There was no air traffic. Planes were not crossing over from the Pacific Ocean only 10 blocks away to land at San Francisco International Airport. And for the next few weeks, once air flights resumed, their usual engine sounds which were usually ignored, seemed amplified at least three times by having witnessed those horrible events, that sad history.

And life did not resume quickly for me or for many others. Dinners out seemed like an extravagance, an indulgence despite the advice of television psychiatrists and counselors about the "need to take care of oneself." Music was not played loudly, jokes were not raucously repeated, kids did not run after each other during recess at St. Thomas' Catholic School across the street. In those few short hours which stretched out along my mental and emotional landscape for what seemed like months, the world had changed and would never be the same.

I had changed and would never be the same. Mom was going through her own personal terrorist attack, with daily pummelings to her mental capacity and her psyche. Before September 11, 2001, I already knew that she would never be the same. I was just hoping that the world around her would be and that I could still protect her from it, as much as an oldest son 3,000 miles away could do.

In those years since, time has passed quickly but not so quickly that I can't pause and take time to remember what was, what could have been and what may be because of those attacks. And as I remember I will do so as I hold my loved ones a bit tighter tonite, cherish the memory more fervently of those no longer with me, and pray not as silently as usual that we all appreciate what we have when we have it, thank those who protect us when we need it, and love those who love us despite the madness of the world around us.

 Photo: Rescue workers conduct search and rescue attempts, descending deep into the rubble of the World Trade Center. September 14, 2001. Source: U.S. Navy photo by Photographer's Mate 2nd Class Jim Watson. Public domain.

© 2016, copyright Thomas MacEntee. All rights reserved.

Wednesday, June 24, 2015

Passages: Jacqueline Barbara Austin, 1941-2015

Jacqueline Barbara Austin, 1941-2015
Jacqueline Barbara Austin, 1941-2015
It is with great sadness that I write these words: my mother passed away on Monday 22 June 2015 after a long illness. Many readers know that preserving my mother's stories during her struggle with early onset Alzheimer's Disease was one of the main reasons for starting Destination: Austin Family.

Below is Mom's obituary which I had written earlier in the year. I highly recommend that everyone compose an obituary now for not just their parents but themselves as well. A memorial service is being planned for August back home in Liberty, NY where I grew up and where most of my family and friends still reside.

Jacqueline Austin MacEntee
Jacqueline Austin MacEntee, former resident of Liberty, NY, died on June 22, 2015, at Mountainside Residential Care Center in Margaretville, NY after a long illness. She was 73 years old. 
The daughter of the late Alfred J. Austin and Anna Henneberg Austin, Jackie was born July 12, 1941, in Jersey City, NJ. A family statement reads: “Mom moved to Sullivan County as a young girl and raised two boys in Liberty while working at the New York Telephone Company, the Monticello Police Department and Mr. Willy’s in Forestburg. Many will remember her as an active, vibrant and gregarious woman who adored her children and grandchildren as well as all her family and friends. We are indebted to all those who helped out during the past 15 years while Alzheimer’s Disease slowly and painfully removed this bright light from our lives.” 
Survivors include two sons, Thomas MacEntee and his partner, George Arvanites of Chicago, IL, and Michael MacEntee and his wife Vicky Ferrell MacEntee of Charleston, SC; three sisters, Jo’el DeStefano of Toms River, NJ, Judith Froehlich of Honesdale, PA, and Jennifer Startup of Kerhonkson, NY; four brothers, Lawrence (Butch) Austin of White Sulphur Springs, NY, Lee (Jerry) Austin of Halcott Center, NY, Alfred Austin of Raleigh, NC, and Lemuel Austin of Loch Sheldrake, NY; five grandchildren, Amber Jane MacEntee, Corwin MacEntee, Conner MacEntee, Jacqueline Rose Pearson and Patrick Pearson, all of Virginia; and many nieces and nephews. Jacqueline was pre-deceased by sisters Patricia May, Joan Toher, June Finkle, and Julia Jackson. 
A memorial service is planned for August, 2015 in Liberty, NY. 
Donations in memory of Jackie can be made to: Catskill Area Hospice, 1 Birchwood Drive, Oneonta, NY 13820.

Source: "Obituaries," Times-Herald Record (Middletown, New York), electronic newspaper, archived, (http://recordonline.com: accessed 24 June 2015), obituary for Jacqueline Austin MacEntee.

© 2015, copyright Thomas MacEntee. All rights reserved.

Friday, March 20, 2015

An Alzheimer's Journey via StoryPress


Many readers of Destination: Austin Family know that this site started back in December 2006 as a way of coping with my mother's early onset Alzheimer's Diseases diagnosis in 2000. My main goal was to capture the many family history stories that I heard growing up.

Over the past eight years I've expanded the posts to cover genealogy and family history as well. An important element of many posts is the concept of "storytelling" and conveying the power of a family story with all its facets.

The written word can only go so far. So I've been working with a new platform called StoryPress (http://www.storypress.com) to create video stories using photos and text narrated in my own voice. Here is my latest video, My Mother and Alzheimer's Disease, based on an annual post entitled "Our Family's Journey to Remembering."  Here is the video and look for more video stories in the future:


© 2015, copyright Thomas MacEntee. All rights reserved.

Thursday, September 11, 2014

Remembering 9/11 - 13 Years Later


[Editor's note: this post originally appeared here at Destination: Austin Family on September 11, 2008]

On the morning of September 11th, 2001, I was living in San Francisco out near Ocean Beach in a small one bedroom apartment where I had lived since 1993. It was a Tuesday and since I usually got up at 4:00 am to walk the dog and then catch a bus at 5:00 am to go to the gym, I'm not sure why I slept later than usual. All I remember is the phone ringing slightly before 6:00 am Pacific Daylight Time.

My first thought went to, "Why did I oversleep?" which was quickly replaced with, "Something is wrong." My phone just didn't ring at 6:00 am unless it was my mother in New York.

For years, Mom could never get the time zone thing right and I was used to receiving calls anywhere from 4:00 am onward. And after her early on-set dementia diagnosis in the summer of 2000, phone calls at odd hours of the day and night became commonplace.

As I said hello I could tell that my mother was flustered. First, she was at home and not working which concerned me. Second, despite suffering from memory loss, she had the wits enough to simply say "Turn on the television - something is wrong with the World Trade Center in The City." Having grown up only 90 miles northwest of Manhattan, we always called it The City.

Mom said "Call me back," and I quickly hung up and ran to the television. I was still half awake and was not understanding what was going on. I do remember Katie Couric's voice, or some other female voice, stating that there was something wrong with air traffic control perhaps since a large airliner had just hit one of the towers of the World Trade Center. It was only after having watched the second plane hit the other tower, live as it happened, did the announcer and I both know that this was no accident.

I sat mesmerized for the next 30 minutes before I put on some sweats and took the dog out for a short walk. My next task was to call George at his home in Oakland.

George and I had been dating for about 16 months and had not yet decided to move into an apartment together. He had been home sick the day before with a severe sinus infection, so I knew he'd be sleeping. And I also hesitated to call since he wasn't known to be entirely coherent in the mornings. But due to the nature of the events, I dialed the phone. As he answered I tried to explain what was going on, and realized I should have followed Mom's example and kept it simple. There are times when Mom really does know best. Finally, exasperated, I simply said what so many loved ones probably said that morning, "Turn on the television," and I hung up.

The rest of the morning is somewhat of a blur. I do remember calling my boss who lived in the East Bay and basically told him that I would not be coming into the office. He agreed that from a safety perspective, and what with working downtown in San Francisco's financial district amid large skyscrapers casting permanent shadows along Montgomery Street, being in an office was not the best place to be.

As I sat on the computer reading the news stories about the attack, the phone rang again. It was Mom and I could just feel the sense of confusion in her voice. I thought about what it must be like for someone who did not have all their mental faculties to witness such events and how they could possibly process them.

Did she think she was watching a movie? She probably wasn't the only one who thought that - many of us did as we first turned on the television. Then as I watched the first tower collapse, I said to Mom, "the building is falling." At which point she started crying and told me she loved me and that I should try to get out of the building if I could. I had to explain over the next 10 minutes that it was the building in New York collapsing, not my own apartment building.

Oh, if all the confusion and panic of those events had been so easy to explain in only 10 minutes that day. I do remember, as others have described, the "eeriness" of the streets, the buildings, the towns - big and small - and how things just didn't seem right. There was less traffic on the streets, there wasn't the usual small talk at the grocery store or the dry cleaner, if one could even think about seeking refuge in the mundane world of daily errands.

There was no air traffic. Planes were not crossing over from the Pacific Ocean only 10 blocks away to land at San Francisco International Airport. And for the next few weeks, once air flights resumed, their usual engine sounds which were usually ignored, seemed amplified at least three times by having witnessed those horrible events, that sad history.

And life did not resume quickly for me or for many others. Dinners out seemed like an extravagance, an indulgence despite the advice of television psychiatrists and counselors about the "need to take care of oneself." Music was not played loudly, jokes were not raucously repeated, kids did not run after each other during recess at St. Thomas' Catholic School across the street. In those few short hours which stretched out along my mental and emotional landscape for what seemed like months, the world had changed and would never be the same.

I had changed and would never be the same. Mom was going through her own personal terrorist attack, with daily pummelings to her mental capacity and her psyche. Before September 11, 2001, I already knew that she would never be the same. I was just hoping that the world around her would be and that I could still protect her from it, as much as an oldest son 3,000 miles away could do.

In those years since, time has passed quickly but not so quickly that I can't pause and take time to remember what was, what could have been and what may be because of those attacks. And as I remember I will do so as I hold my loved ones a bit tighter tonite, cherish the memory more fervently of those no longer with me, and pray not as silently as usual that we all appreciate what we have when we have it, thank those who protect us when we need it, and love those who love us despite the madness of the world around us.

 Photo: Rescue workers conduct search and rescue attempts, descending deep into the rubble of the World Trade Center. September 14, 2001. Source: U.S. Navy photo by Photographer's Mate 2nd Class Jim Watson. Public domain.

© 2014, copyright Thomas MacEntee. All rights reserved.

Wednesday, November 20, 2013

Passages: Joan Kathleen Austin, 1936-2013

Joan Kathleen Austin - 1936-2013
I found out this evening that my mother's oldest sister, Joan Kathleen Austin, had passed away peacefully late this afternoon. Like my mother, she had been diagnosed with Alzheimer's Disease and her condition took a sudden turn over the past few weeks.

It would be easy to sit here and write about the toll that Alzheimer's has taken on my family. I've written about it several times and the post that best describes the impact of the disease can be found here. I would much rather focus on my aunt's life and how she impacted my own life.

Aunt Joan was someone who I saw on a regular, at least monthly, basis while growing up.  My first memories are visiting her and my Uncle Bill when they lived down in Hackensack, New Jersey. There were many weekends spent at their home - one visit I remember vividly is when Hank Aaron hit his record breaking 715th home run. It was at my aunt and uncle's house that we all watched that historic moment.

Soon she and Uncle Bill moved up to Wurstboro, New York which was much closer, yet they kept their jobs in New Jersey and commuted every day.  I don't know how they did it, but you knew better than to call or visit after 8pm because they were up and on the road each morning by 4:30 am for the long drive to New Jersey!

Aunt Joan was always indulgent - she was like a grandmother who didn't refuse you when you wanted another cookie or wanted to do something fun. She was also crazy - as in wacky - she had no "filter" and was very unpredictable. It was always fun to be around her and she always made you laugh or at least shake your head in amazement.

I will miss her. She was a big part of my family and rather than remember the ravages of a hideous disease, I choose to hold close the best memories I have of her and of her life

© 2013, copyright Thomas MacEntee

Sunday, December 16, 2012

Dear Mom: It's Best You Don't Know


Dear Mom:

This is one of these "letters in my head" that I've actually decided to put in writing this time, and do so publicly. You have no idea how many times a week I write one of these missives to you, knowing that while you can't read them, somehow across the miles you do get the message from me, your son.

Right now the world is a crazy place, and I hate to say it, but I'm actually blessed that you are in bed, adrift in your Alzheimer's Disease and what it does to your mind and body, not knowing what goes on in the outside world.

I remember back in 2001, as your diagnosed dementia progressed into early onset Alzheimer's (you had just turned 60), and the tragedy of 9-11 occurred.  To you it was unreal, like a movie, as it was to many of us. You imagined certain aspects of the events that didn't actually happen because that was the way your brain was wired. Again, I think you're the lucky one in that you never knew everything that went on that day or how it would affect all of us, as a nation and individually.

All this weekend I've tried to imagine your reaction to the school shooting in Connecticut and the murder of 20 young children, all first graders.  I know you'd be devastated, simply based on what I know about you and the way you were around children of all ages.

I was always amazed at how you would gravitate to almost any child and make a connection.  You held newborns almost as if you ached to do so. We'd be out in public, in a shopping mall or a store, and I'd turn around . . . and you'd have someone's baby in your arms. You were a mother to so many, in your own immediate family and to the extended family of Austins, MacEntees and more.

You counseled and cared for so many of my cousins, and even children of close family friends, knowing that a trip to New York City or that special birthday treat was a glimmering highlight in their life. You knew who had been abused, who had been neglected. It was almost a secret language you spoke with them. You connected instantly. And you let them know, based on your own experiences with abuse, that it does get better.  That there are kind souls out there. That good trumps evil each and every time, even if we don't see it in the short run.

As your disease progressed, this connection became a problem: you'd want to hold small babies and try to grab them from strangers. Or we'd be at a restaurant and you'd focus on smiling and waving to a small child across the room and ignore your food or the conversation.

So what would you think of these 20 young lives eliminated by a madman? You'd cry, you'd talk to others about it, and you'd hold your own children a little closer and little tighter if you could.  Something I think every parent in America has been doing this same thing all weekend.

But you'd also wonder about the mother of the madman who was also killed.  You'd ask how this happened, and you'd have empathy for her and her family. That empathy is the greatest gift you've ever given me: the ability to picture myself in someone's else's shoes and ponder their plight before I jumped to conclusions.

My biggest fear over the next few days is that we as a nation jump to short-sighted, knee-jerk solutions to what is a serious problem: mental illness, access to guns, violence and the way media glorifies it at the expense of making a profit.

While it's better you not know these things, being the smart, capable and strong woman that you were, you'd find a way to make sense of it all. And you'd tell everyone not just how you felt, but what needed to be done. That's what I miss most right now.

© 2012, copyright Thomas MacEntee

Thursday, October 13, 2011

Update on Mom

Just a quick update on Mom's condition for friends and family. On my way back home from the Legacy Family Tree Cruise, we drove up to Margaretville, NY to visit Mom at the nursing home.

I actually was dreading this visit because back in May when I last saw her, she was bed-ridden, couldn't open her eyes and seemed very bloated. Imagine my surprise when she wasn't in bed but in her "geri-chair" (used for geriatric patients).

Not only did she look less bloated but occasionally she would open her beautiful blue eyes. My two aunts joined us and we spent about an hour just sitting there holding her hand, stroking her hair, massaging her shoulders and just plain "being there."

Just to be able to do this, to be in the moment, and so late in our Alzheimer's journey, was such a blessing.

© 2011, copyright Thomas MacEntee

Wednesday, September 21, 2011

Alzheimer's Action Day - Our Family's Journey to Remembering


[Editor’s note: Almost four years ago, on October 16, 2007, I posted about my family’s journey down a road all too familiar to many other families: the road called Alzheimer’s Disease. In honor of Alzheimer's Action Day - September 21st - is an excerpt from that post.]

Some of you know that my mother, Jacqueline Austin MacEntee, was diagnosed with dementia, one of the early indicators of Alzheimer's disease in 2000 at the age of 58. I can relate to you what I and my family had to endure just to get Mom diagnosed.

The diagnosis currently starts with a visit to a doctor for basic tests (blood, liver, cholesterol, heart, etc.) and then being sent to a specialist for neurological testing such as an MRI. Once everything is cleared as to possible causes, comes a visit to a gerontologist and a test consisting of about 30 questions. Questions are basic (the current day or year, the current president, etc.) and some are more complex (reading a small story and then relating what the story was about or who the main character was). This is usually when the diagnosis is positive as to Alzheimer's Disease.

And so it begins. You know it eventually has to end, and how it ends, but it just seems like it never ends.

You notice a marked change in behavior and instances where Mom just isn't herself. Many times you call and ask her what she did over the weekend or what movie she saw and she can't remember. Then it becomes the lack of remembering simple things like how to drive from point A to point B in a small town where Mom has lived for over 40 years.

The disease progresses to affect employment and the means of earning a living and surviving financially. You deal with the chief at the village police office where she works as a dispatcher and clerk when he tells her that she has "psychological problems." She loses the second job at a local restaurant because she can no longer handle the bookkeeping responsibilities. You step in to get Mom out on early retirement via Social Security and still you need to fight, hire an attorney, and attend hearings, meetings, etc. But you feel good that you are able to get Mom out on retirement early so that she can enjoy the few good years she has left going to movies, shopping, etc.

And the denial, the denial, the denial -- from both Mom and the rest of the family -- that this is really happening. Much of the denial is the realization that by watching Mom and the deterioration of her condition, you could be looking in a mirror held up to your face so that you know your own mortality. Even worse, you come to the realization that this could be you. "There but for the grace of God . ."

You drag your spouse or partner into the mess, the person you want to spend the rest of your life with, the person who may very well be doing all this for you one day. But you know that he or she would gladly make the sacrifices just as you would for him or her or for his or her parents.

Then there are the financial scammers that come out of the woodwork. Her "financial advisor" at New York Life who talked her into an annuity that only made money for the advisor. And then the same advisor selling Mom expensive health books and vitamins as a treatment for the disease. I know - I cleaned out the house, saw the books, and have the receipts.

And as the months progress into years, the gerontologist's test is given at least yearly and the number of correct answers dwindles from 22 to 20 to 17.

You decide to take the car away after several instances of U-turns through the grassy median of a 4-lane highway. You notice unexplained dents and dings to the car or even to the house or garage. You have to fight and get a letter from the doctor to give to DMV in order to take the car away.

If you are smart or lucky or both, you find a good elder law attorney and you do this early when Mom can adequately communicate her wishes. Wishes such as "do not resuscitate," funeral and burial, will, assets, care, etc. The power of attorney kicks in and you have so much more responsibility than just making sure Mom is comfortable. But you know you and your family are lucky, and smart, because you did this early. You didn't wait to find out that investments were sucked dry by scammers who sell home improvements or driveway repaving or annuities. Boy, were you lucky.

While you sort through the tangled financial web of the past five years, you try to arrange for in-home care for Mom, knowing that having the familiar around her is the best thing. You arrange for adult day care at the local hospital where on a given day she is probably the youngest one there but most definitely the most ambulatory. You bring in local women who specialize in elder care to stay with her the other 16 hours of the day and also to transport her to day care and doctors' appointments. You want to keep her in the home she bought 25 years ago, as a divorced parent with two boys and little credit. You know she deserves this and you and the rest of the family make sacrifices so this will happen.

You decide that while you've enjoyed living in California for the past 20 years, you can't handle all the tasks and responsibilities from so far away. The telephone, e-mail and the internet only work up to a point. You move to Chicago so you are at least a short two hour flight away, with three flights to New York each hour from O'Hare.

You get so caught up in the politics of family, and the squabbling and the pettiness that at one point you decide to walk away altogether. You decide it isn't that you aren't up to the responsibility but that you don't know why family has to make it all so complicated - especially those who are selfish and want this to be about them and not about Mom. A simple Thanksgiving day phone call turns into a yelling match with your aunt who doesn't know how to handle Mom or why she has been accused of stealing a book or moving furniture. You decide you need a break so you don't call for close to six months and you drop out. And you feel guilty, as you should. And every time you are willing to put it behind you and focus on what Mom needs now because you are back in the mix, someone is there to remind you of how you walked away.

And besides bleeding tears, you bleed money. Your mother's money. The money she worked so hard for at the phone company before she went out on retirement due to a bad back. The money she earned working for the state at the police station. The SSI money. You run credit reports and find out there are over 100 credit cards in her name, many from stores like Macy's (where she had 6 accounts!) with clerks who say, "would you like to save 15% today by opening a Macy's account?" knowing that Mom already had other Macy's accounts but the $5 commission was all that mattered. You close all the accounts, cash out IRAs and that damned annuity at a loss. You end up paying federal and state income tax as if Mom earned over $100,000 that year all because you had to cash in the investments for her care. But you also know that this is the best thing to do in this moment because it means months of in-home care, and safety and security. That's why we save for rainy days and right now it is pouring.

And the number of correct answers, at least on that test, becomes 15, then 12, then 10. For the rest of the process there are no correct answers, there are no touchstones because you've never been this way before. Oh how you don't want to be here right now but oh how you do because it's all about Mom.

Besides untangling finances, you have to untangle agreements and understandings that Mom entered into with other family members but had not the mental capacity nor the right to enter into. You deal with the house in Florida and you deal with Mom's home. You deal with the Grahamsville property that Mom inherited from her great-grandmother (Therese McGinnes Austin) for all her years of sacrifice and care. You realize that Mom entered into a purchase agreement with a family member who has since rented the property out but that person can't prove their payments to Mom or for taxes. You know that property meant so much to Mom as a kid but you also know the best thing is to let it go and realize that she was taken advantage of and to just deal with it. You deal, you deal, you deal. Until you think all the cards are dealt.

You fight with other family members who either think they know how to care for an Alzheimer's patient or want to keep denying that their sister has the disease. Because there's a small chance, given that the oldest sister already died from Alzheimer's, that they are next on the list to get it. But you also find other supportive family members who are glad to pitch in and actually make so many sacrifices for your mother when you know they already have their hands full.

Then comes the time to talk to Mom about finding a "facility" for her long-term care when either the finances or patience runs out, or both. You dread the discussion you have to have on Mother's Day, of all days, but you find she takes it well. Then you wonder if she really understands that a facility means a nursing home. You wonder if she is clear enough to figure it out over the next few weeks and retreat back into the denial stage. You have visions of that scene in the Exorcist when the priest puts his mother in an inner city nursing home yelling "Demi, why you do this to me? I'm afraid Demi." But you realize that when you see her a month later that she's lost over 20 lbs of excess weight, she's eating better, she has lots of activities. She is safe, she is happy, she is living in the moment.

Next you have to clean out the house you grew up in and you don't know where to start. You make six trips in one year, buying boxes when you step off the plane to Newark. Working long hours sorting through every scrap of paper, every wadded up tissue in a sweater or pants pocket because it might contain something of value, every book some of which would have a gold bracelet as a bookmark. You remember that Mom took care of your great-grandmother and your great-aunt (Ethel McCrickert Hannan) in that same house and realize that their possessions are still there. You get angry when you find all the crap and junk she's been sold, be it greeting cards (why are there 100 of the same Thanksgiving card from a Hallmark store? I know I won't ever live to see 100 Thanksgivings), or the wrapping paper that people sell for their kid's school, or the needless health books, vitamins, and other quackery and the expensive overpriced dolls from China which are probably decorated with lead paint. And you hope that however crappy or tacky or useless, these things brought her joy and made her happy, even if for a moment.

You sort, you throw away. You become cold, efficient, without feeling as you decide not to pause and look at a photo album - you just toss it in The Box. You donate clothing to thrift stores, you sell antique items that no one wants and that you can't send home to Chicago. Your aunt has a great idea to donate most of the 100+ dolls to a shelter for battered women and children. And when you are back home, you enjoy The Box and all its photos, diaries, etc. later in the year - it is the beginning of this project and other genealogy projects. You feel lucky to have photos from your ancestors and to begin to know who you are.

You have lots of help from family members that you can never thank enough. You didn't do it alone although you feel lonely and have a deep sense of loss most of the time. You thank your Uncle Jerry for all the help from the beginning - for attending hearings, meetings, taking care of finances, arranging in-home care and the nursing home. All of this was not possible without him and without Nan's support. You thank your Uncle Lem and Aunt Judy for helping clean out the house. You thank your Aunt Joan for providing a year of room and board to Mom despite the aggravation and the problems. You thank Beth for making the trip from Delhi and visiting. You thank all your other relatives who make visits at the nursing home, visits Mom won't remember five minutes later, but visits that you know make her happy despite the visitor being saddened by what they see or wanting to cry. And you thank all her friends, even the ones who no longer keep in touch because it is just too uncomfortable.

You keep in touch with family and friends who call and want an update on Mom. Or you get updates from them when they go for a visit at the nursing home. While you notice the deterioration in her condition on each visit, you hear from relatives that she has an ankle brace due to a fall, or this problem or that problem. And still you know you've done the best thing for Mom.

The time you get to spend with Mom becomes shorter and shorter - not because you don't want to visit, but because her attention span doesn't enable her to focus on any one thing for more than 30 seconds. You call the nurses’ station to talk to her and after a short conversation, you realize she put the phone on the counter and walked away. Not because there was something more interesting, but because she can't focus.

And the list of correct answers to that test are now in the single digits. You know what the future holds and you dread it. You don't want to go through the first time Mom doesn't know who you are, but you know it will happen. You already see the difficulty she has in eating, getting on and off an elevator, or getting in and out of a car. You know what the next steps are because just like this article, you've read them in some blog or book or news article or website. You know Mom will suddenly stop talking, stop walking, stop eating, stop breathing.

But you will always know that you are your mother's son. And that she knew that too.

I've decided that I can either be bitter or I can be better. And bitter won't change my mother's condition - just mine. I choose better and the way I can do that is to:

  • talk about my mother's experience with people like writing this article;
  • mention the bad times as well as the good times, the negative as well as the positive but focus more on the positive - the negative is there as a reminder but not something to regret for it can't be changed;
  • not regret the journey of Alzheimer's for me, for Mom and for the others involved - for a journey has lessons;
  • understand that I did and do the most that is possible for my mother's care given the circumstances, finances and that I was lucky to have other family members involved; and
  • honor my mother and the way she raised me by not forgetting her sacrifices and her love, her challenges and her gifts, her mistakes and her accomplishments.

And I intend to live life and every day as if it were important and my last. I wouldn't make someone else go through that dark twisting tunnel of care unguided and with those feelings of helplessness. Knowledge is power and power, be it the power of health, finances or love, can help you conquer all adversities.

© 2011, copyright Thomas MacEntee

Tuesday, September 21, 2010

My Recent Visit with Mom

This past weekend I made the trek to upstate New York to visit my mother who is in a nursing home. Many faithful readers know that I've been making this trip several times a year since Mom's dementia and early-onset Alzheimer's Disease diagnosis in 2000 at the age of 58.

I've written before about a typical trip of flying 800 miles then driving over 3 hours only to be able to spend 30 minutes with the woman who brought me into this world. This time was no different except that I keep telling myself, "This will probably be the last trip."

Family and friends ask about her condition, knowing, as I do, that there will never be improvement.  In summary, Mom can no longer walk, no longer opens her eyes, and really doesn't speak save for the occasional mumbling of words. It appears that the involuntary functions are shutting down - basically her body is "forgetting" how to perform functions that you and I take for granted on a daily basis. It will only be a matter of time before the forgetting takes over her ability to breathe.

* * *

One can only hope for comfort and that she go quietly into that dark and peaceful night.  This is my constant prayer, my constant thought whether I am there by her side holding her hand or home here in Chicago. And I appreciate everyone's support both here at my blog, on Facebook and through countless emails.

It has been a tough summer for mothers among my social group - I can no longer count on one hand the number of strong, vibrant and life-changing women who have been lost to various ailments and circumstances.

One might say this is only natural as we get older, but I somehow refuse to accept that. I just think that those of us who have been on the receiving end of their love, their wisdom, and their influence have just reached a point where we can finally go out on our own. And we can now be the influencers, the teachers, the ones dispensing love.

Letting go is never easy and the timing is never on our terms. Yet, let go we must. For how can we receive the next bounty in our lives with an open hand when we are still hanging on to a person, place or thing that is ready to leave?


© 2010, copyright Thomas MacEntee

Thursday, November 5, 2009

To Touch Mom's Face Again

This was a very difficult trip back to upstate New York to visit my mother over the past weekend. Some may look at the time, distance, and effort involved and ask whether it was worth it.

Was it worth it to get up at 4:00 am, scramble to O'Hare for a 6:45 am flight? Only for the woman who raised you to not even recognize you? To me it was. And I know in my heart and mind that she recognized me, even if only for a millisecond. And that the visit was important to her. This is the woman who woke up countless times in the middle of the night when I was sick to care for me. This is the woman who would rouse me early to go off on educational road trips all over the East Coast.

Was it worth it to fly 800+ miles for two hours then hop in a rental car and drive another three hours? Only to hear the woman who cared for you to speak gibberish, slur her words and yell loudly during a 30 minute visit? To me it was. This is the woman who would drive six hours at the drop of a hat just to see me in Washington, DC when I was going to college. Just as she had done for me oh so many years ago, I sat and held her hand, rubbed her shoulder and wished that her pain and suffering would disappear. "Comfort the ones that comforted you," I kept hearing my ancestors say.

Was it worth the lack of sleep, the restlessness and anxiety involved in a trip lasting only two and a half days? Only to see the woman you call Mother unable to walk, sitting in a wheelchair, unable to dress, feed or care for herself? To me it was. This is the woman who made sure I was comfortable that summer I broke my leg and couldn't walk.  This is the woman who dressed, fed and cared for me, her son.  Despite seeing Mom looking much older and not well-dressed, I noticed that she was safe, clean, warm, comfortable and just had a great hair cut. Mom was always so "put together" from what I remember growing up. I know that Mom's wardrobe is not the fault of the superb staff at the nursing home but the Alzheimer's Disease. They say that she won't wear a bra because she doesn't understand what is binding her and constantly tries to remove it. In a more comedic moment in my mind, I can just see Mom unhooking it, pulling it out of her blouse front, and letting it dangle from the side of the wheelchair. This from a woman whose favorite saying was "Would it kill her to wear a bra?" Sometimes you just have to laugh.

And each time I visit this woman, upon departing and knowing it may be my last visit, I bend down, stroke her cheek, and whisper in her ear, "I remember you and all you did for me. I love you and I will never forget you."

© 2009, copyright Thomas MacEntee

Sunday, August 9, 2009

Alzheimer's Redux

I'm not sure what got into me, but I've been thinking it's time for a repost of one of my writings about Alzheimer's Disease and how it has affected me and my family. Mom has been on my mind quite a bit lately and I also have some genealogy friends who are dealing with this same issue in their own families. I just pray that those with Alzheimer's find peace and comfort and that we, their caretakers, can find it as well.

* * *

[This is a repost from October 16, 2007]

I heard the news yesterday that a new blood test was being developed at Stanford University in California that could help detect the probability of developing Alzheimer's Disease within two to six years.

While the results are still preliminary and the next step is to open up the testing to a larger test population, it has had a 91% accuracy so far.

Some of you know that my mother, Jacqueline Austin MacEntee, was diagnosed with dementia, one of the early indicators of Alzheimer's Disease in 2000 at the age of 58. I can relate to you what I and my family had to endure just to get Mom diagnosed.

The diagnosis currently starts with a visit to a doctor for basic tests (blood, liver, cholesterol, heart, etc.) and then being sent to a specialist for neurological testing such as an MRI. Once everything is cleared as to possible causes, comes a visit to a gerontologist and a test consisting of about 30 questions. Questions are basic (the current day or year, the current president, etc.) and some are more complex (reading a small story and then relating what the story was about or who the main character was). This is usually when the diagnosis is positive as to Alzheimer's Disease.

And so it begins. You know it eventually has to end, and how it ends, but it just seems like it never ends.

You notice a marked change in behavior and instances where Mom just isn't herself. Many times you call and ask her what she did over the weekend or what movie she saw and she can't remember. Then it becomes the lack of remembering simple things like how to drive from point A to point B in a small town where Mom has lived for over 40 years. But you also rejoice when your mother utters her disgust about Bush and the others in his administration who've hijacked our democracy. Part of you says "it's just the Alzheimer's" while part of you says it is clarity and another part of you hopes that all the years of discussing your own views have influenced her.

The disease progresses to affect employment and the means of earning a living and surviving financially. You deal with the chief at the village police office where she works as a dispatcher and clerk when he tells her that she has "psychological problems." She loses the second job at a local restaurant because she can no longer handle the bookkeeping responsibilities. You step in to get Mom out on early retirement via Social Security and still you need to fight, hire an attorney, and attend hearings, meetings, etc. But you feel good that you are able to get Mom out on retirement early so that she can enjoy the few good years she has left enjoying movies, shopping, etc.

And the denial, the denial, the denial -- from both Mom, me and the rest of the family -- that this is really happening. Much of the denial is the realization that by watching Mom and the deterioration of her condition, you could be looking in a mirror held up to your face so that you know your own mortality. Even worse, that you come to the realization that this could be you. "There but for the grace of God . ."

You drag your partner into the mess, the person you want to spend the rest of your life with, the person who may very well be doing all this for you one day. But you know that he'd gladly make the sacrifices just as you would for him or for his parents.

Then there are the financial scammers that come out of the woodwork. Her "financial advisor" at New York Life who talked her into an annuity that only made money for the advisor. And then the same advisor selling Mom expensive health books and vitamins as a treatment for the disease. I know - I cleaned out the house, saw the books, and have the receipts.

And as the months progress into years, the gerontologist's test is given at least yearly and the number of correct answers dwindles from 22 to 20 to 17.

You decide to take the car away after several instances of U-turns through the grassy median of a 4-lane highway. You notice unexplained dents and dings to the car or even to the house or garage. You have to fight and get a letter from the doctor to give to DMV in order to take the car away.

If you are smart or lucky or both, you find a good elder law attorney and you do this early when Mom can adequately communicate her wishes. Wishes such as "do not resuscitate," funeral and burial, will, assets, care, etc. The power of attorney kicks in and you have so much more responsibility than just making sure Mom is comfortable. But you know you and your family are lucky, and smart, because you did this early. You didn't wait to find out that investments were sucked dry by scammers who sell home improvements or driveway repaving or annuities. Boy were you lucky.

While you sort through the tangled financial web of the past five years, you try to arrange for in-home care for Mom, knowing that having the familiar around her is the best thing. You arrange for adult day care at the local hospital where on a given day she is probably the youngest one there and most definitely the most ambulatory. You bring in local women who specialize in elder care to stay with her the other 16 hours of the day and also to transport her to day care and doctors' appointments. You want to keep her in the home she bought 25 years ago, as a divorced parent with two boys and little credit. You know she deserves this and you and the rest of the family make sacrifices so this will happen.

You decide that while you've enjoyed living in California for the past 20 years, you can't handle all the tasks and responsibilities from so far away. The telephone, e-mail and the internet only work up to a point. You move to Chicago so you are at least a short two hour flight away, with three flights to New York each hour from O'Hare. You feel blessed because your employer in California believes in you and your work and the sacrifices you are making so much that they let you work from home in Chicago since they don't have an office there. You thank Heller Ehrman LLP and all your work family from California to London for being so supportive.

You get so caught up in the politics of family, and the squabbling and the pettiness that you decide to walk away altogether. You decide it isn't that you aren't up to the responsibility but that you don't know why family has to make it all so complicated - especially those who are selfish and want this to be about them and not about Mom. A simple Thanksgiving day phone call turns into a yelling match with your aunt who doesn't know how to handle Mom or why she has been accused of stealing a book or moving furniture. You decide you need a break so you don't call for close to six months and you drop out. And you feel guilty, as you should. And every time you are willing to put it behind you and focus on what Mom needs now because you are back in the mix, someone is there to remind you of how you walked away.

And besides bleeding tears, you bleed money. Your mother's money. The money she worked so hard for at the phone company before she went out on retirement due to a bad back. The money she earned working for the state at the police station. The SSI money. You run credit reports and find out there are over 100 credit cards in her name, many from stores like Macy's (where she had six accounts!) with clerks who say "would you like to save 15% today by opening a Macy's account?" knowing that Mom already had other Macy's accounts but the $5 commission was all that mattered. You close all the accounts, cash out IRAs and that damned annuity at a loss. You end up paying federal and state income tax as if Mom earned over $100,000 that year all because you had to cash in the investments for her care. But you also know that this is the best thing to do in this moment because it means months of in-home care, and safety and security. That's why we save for rainy days and right now it is pouring.

And the number of correct answers, at least on that test, becomes 15, then 12, then 10. For the rest of the process there are no correct answers, there are no touchstones because you've never been this way before. Oh how you don't want to be here right now but oh how you do because it's all about Mom.

Besides untangling finances, you have to untangle agreements and understandings that Mom entered into with other family members but had not the mental capacity nor the right to enter into. You deal with the house in Florida and you deal with Mom's home. You deal with the Grahamsville property that Mom inherited from her great-grandmother (Therese McGinnes Austin) for all her years of sacrifice and care. You realize that Mom entered into a purchase agreement with a family member who has since rented the property out but that person can't prove their payments to Mom or for taxes. You know that property meant so much to Mom as a kid but you also know the best thing is to let it go and realize that she was taken advantage of and to just deal with it. You deal, you deal, you deal. Until you think all the cards are dealt.

You fight with other family members who either think they know how to care for an Alzheimer's patient or want to keep denying that their sister has the disease. Because there's a small chance, given that the oldest sister already died from Alzheimer's, that you are next on the list to get it. But you also find other supportive family members who are glad to pitch in and actually make so many sacrifices for your mother when you know they already have their hands full.

Then comes the time to talk to Mom about finding a "facility" for her long-term care when either the finances or patience runs out, or both. You dread the discussion you have to have on Mother's Day, of all days, but you find she takes it well. Then you wonder if she really understands that a facility means a nursing home. You wonder if she is clear enough to figure it out over the next few weeks and retreat back into the denial stage. You have visions of that scene in the Exorcist when the priest puts his mother in an inner city nursing home yelling "Demi, why you do this to me? I'm afraid Demi." But you realize that when you see her a month later that she's lost over 20 lbs, she's eating better, she has lots of activities. She is safe, she is happy, she is living in the moment.

Next you have to clean out the house you grew up in and you don't know where to start. You make six trips in one year, buying boxes when you step off the plane to Newark. Working long hours sorting through every scrap of paper, every wadded up tissue in a sweater or pants pocket because it might contain something of value, every book some of which would have a gold bracelet as a bookmark. You remember that Mom took care of your great-grandmother and your great-aunt (Ethel McCrickert Hannan) in that same house and realize that their possessions are still there. You get angry when you find all the crap and junk she's been sold, be it greeting cards ("Why are there 100 of the same Thanksgiving card from a Hallmark store? I know I won't ever live to see 100 Thanksgivings!"), or the wrapping paper that people sell for their kid's school, or the needless health books, vitamins, and other quackery and the expensive overpriced dolls from China which are probably decorated with lead paint. And you hope that however crappy or tacky or useless, these things brought her joy and made her happy, even if for a moment.

You sort, you throw away. You become cold, efficient, without feeling as you decide not to pause and look at a photo album - you just toss it in The Box. You donate clothing to thrift stores, you sell antique items that no one wants and that you can't send home to Chicago. Your aunt has a great idea to donate most of the 100+ dolls to a shelter for battered women and children. And when you are back home, you enjoy The Box and all its photos, diaries, etc. later in the year - it is the beginning of this project and other genealogy projects. You feel lucky to have photos from your ancestors and to begin to know who you are.

You have lots of help from family members that you can never thank enough. You didn't do it alone although you feel lonely and have a deep sense of loss most of the time. You thank your Uncle Jerry for all the help from the beginning - for attending hearings, meetings, taking care of finances, arranging in-home care and the nursing home. All of this was not possible without him and without Nan's support. You thank your Uncle Lem and Aunt Judy for helping clean out the house. You thank your Aunt Joan for providing a year of room and board to Mom despite the aggravation and the problems. You thank Beth for making the trip from Delhi and visiting. You thank all your other relatives who make visits at the nursing home, visits Mom won't remember five minutes later, but visits that you know make her happy despite the visitor being saddened by what they see or wanting to cry. And you thank all her friends, even the ones who no longer keep in touch because it is just too uncomfortable.

You keep in touch with family and friends who call and want an update on Mom. Or you get updates from them when they go for a visit at the nursing home. While you notice the deterioration in her condition on each visit, you hear from relatives that she has an ankle brace due to a fall, or this problem or that problem. And still you know you've done the best thing for Mom.

The time you get to spend with Mom becomes shorter and shorter - not because you don't want to visit, but because her attention span doesn't enable her to focus on any one thing for more than 30 seconds. You call the nurses’ station to talk to her and after a short conversation, you realize she put the phone on the counter and walked away. Not because there was something more interesting, but because she can't focus.

And the list of correct answers to that test are now in the single digits. You know what the future holds and you dread it. You don't want to go through the first time Mom doesn't know who you are, but you know it will happen. You already see the difficulty she has in eating, getting on and off an elevator (she won't get on because she thinks you are getting off to visit her), or getting in and out of a car. You know what the next steps are because just like this article, you've read them in some blog or book or news article or website. You know Mom will suddenly stop talking, stop walking, stop eating, stop breathing.

But you will always know that you are your mother's son. And that she knew that too.

I've decided that I can either be bitter or I can be better. And bitter won't change my mother's condition - just mine. I choose better and the way I can do that is to:

a) talk about my mother's experience with people like writing this article;

b) mention the bad times as well as the good times, the negative as well as the positive but focus more on the positive - the negative is there as a reminder but not something to regret for it can't be changed;

c) not regret the journey of Alzheimer's for me, for Mom and for the others involved - for a journey has lessons;

d) understand that I did and do the most that is possible for my mother's care given the circumstances, finances and that I was lucky to have other family members involved; and

e) honor my mother and the way she raised me by not forgetting her sacrifices and her love, her challenges and her gifts, her mistakes and her accomplishments.

After all this, would I want to take a blood test, or any test, that would help predict whether or not I was to have Alzheimer's Disease? You're damned right I would. Not only would it help progress the research that has already been done, but it would help me prepare for the future. And I could live life and every day as if it were important and my last. I wouldn't make someone else go through that dark twisting tunnel of care unguided and with those feelings of helplessness. Knowledge is power and power, be it the power of health, finances or love, can help you conquer all adversities.

Would you take the test?

[This is the first off-topic topic that I've posted but in way it does relate to genealogy in that some forms of Alzheimer's Disease is hereditary or genetic (I believe the percentage is 15%)]

Monday, November 10, 2008

Alzheimer’s Disease – A Duty and A Toll

This post was written for the 60th Edition of the Carnival of Genealogy hosted by Jasia at Creative Gene.

[Editor’s note: A little more than a year ago, on October 16, 2007, I posted about my family’s journey down a road all too familiar to many other families: the road called Alzheimer’s Disease. In that post, I discussed recent developments in a blood test that could predict the probability of developing Alzheimer’s Disease. I challenged readers with this question: would you take such a test, even if you had already traveled through what I call “the long goodbye” with a loved one? Would you want to know your chances of having to walk that same path? Below is that post in its entirety.]

I heard the news yesterday that a new blood test was being developed at Stanford University in California that could help detect the probability of developing Alzheimer's Disease within two to six years. While the results are still preliminary and the next step is to open up the testing to a larger test population, it has had a 91% accuracy so far.

Some of you know that my mother, Jacqueline Austin MacEntee, was diagnosed with dementia, one of the early indicators of Alzheimer's disease in 2000 at the age of 58. I can relate to you what I and my family had to endure just to get Mom diagnosed.

The diagnosis currently starts with a visit to a doctor for basic tests (blood, liver, cholesterol, heart, etc.) and then being sent to a specialist for neurological testing such as an MRI. Once everything is cleared as to possible causes, comes a visit to a gerontologist and a test consisting of about 30 questions. Questions are basic (the current day or year, the current president, etc.) and some are more complex (reading a small story and then relating what the story was about or who the main character was). This is usually when the diagnosis is positive as to Alzheimer's Disease.

And so it begins. You know it eventually has to end, and how it ends, but it just seems like it never ends.

You notice a marked change in behavior and instances where Mom just isn't herself. Many times you call and ask her what she did over the weekend or what movie she saw and she can't remember. Then it becomes the lack of remembering simple things like how to drive from point A to point B in a small town where Mom has lived for over 40 years. But you also rejoice when your mother utters her disgust about Bush and the other's in his administration who've hijacked our democracy. Part of you says "it's just the Alzheimer's" while part of you says it is clarity and another part of you hopes that all the years of discussing your own views have influenced her.

The disease progresses to affect employment and the means of earning a living and surviving financially. You deal with the chief at the village police office where she works as a dispatcher and clerk when he tells her that she has "psychological problems." She loses the second job at a local restaurant because she can no longer handle the bookkeeping responsibilities. You step in to get Mom out on early retirement via Social Security and still you need to fight, hire an attorney, and attend hearings, meetings, etc. But you feel good that you are able to get Mom out on retirement early so that she can enjoy the few good years she has left going to movies, shopping, etc.

And the denial, the denial, the denial -- from both Mom, me and the rest of the family -- that this is really happening. Much of the denial is the realization that by watching Mom and the deterioration of her condition, you could be looking in a mirror held up to your face so that you know your own mortality. Even worse, that you come to the realization that this could be you. "There but for the grace of God . ."

You drag your partner into the mess, the person you want to spend the rest of your life with, the person who may very well be doing all this for you one day. But you know that he'd gladly make the sacrifices just as you would for him or for his parents.

Then there are the financial scammers that come out of the woodwork. Her "financial advisor" at New York Life who talked her into an annuity that only made money for the advisor. And then the same advisor selling Mom expensive health books and vitamins as a treatment for the disease. I know - I cleaned out the house, saw the books, and have the receipts.

And as the months progress into years, the gerontologist's test is given at least yearly and the number of correct answers dwindles from 22 to 20 to 17.

You decide to take the car away after several instances of U-turns through the grassy median of a 4 lane highway. You notice unexplained dents and dings to the car or even to the house or garage. You have to fight and get a letter from the doctor to give to DMV in order to take the car away.

If you are smart or lucky or both, you find a good elder law attorney and you do this early when Mom can adequately communicate her wishes. Wishes such as "do not resuscitate", funeral and burial, will, assets, care, etc. The power of attorney kicks in and you have so much more responsibility than just making sure Mom is comfortable. But you know you and your family are lucky, and smart, because you did this early. You didn't wait to find out that investments were sucked dry by scammers who sell home improvements or driveway repaving or annuities. Boy were you lucky.

While you sort through the tangled financial web of the past five years, you try to arrange for in-home care for Mom, knowing that having the familiar around her is the best thing. You arrange for adult day care at the local hospital where on a given day she is probably the youngest one there but most definitely the most ambulatory. You bring in local women who specialize in elder care to stay with her the other 16 hours of the day and also to transport her to day care and doctors' appointments. You want to keep her in the home she bought 25 years ago, as a divorced parent with two boys and little credit. You know she deserves this and you and the rest of the family make sacrifices so this will happen.

You decide that while you've enjoyed living in California for the past 20 years, you can't handle all the tasks and responsibilities from so far away. The telephone, e-mail and the internet only work up to a point. You move to Chicago so you are at least a short two hour flight away, with three flights to New York each hour from O'Hare. You feel blessed because your employer in California believes in you and your work and the sacrifices you are making so much that they let you work from home in Chicago since they don't have an office there. You thank Heller Ehrman LLP and all your work family from California to London for being so supportive.

You get so caught up in the politics of family, and the squabbling and the pettiness that you decide to walk away altogether. You decide it isn't that you aren't up to the responsibility but that you don't know why family has to make it all so complicated - especially those who are selfish and want this to be about them and not about Mom. A simple Thanksgiving day phone call turns into a yelling match with your aunt who doesn't know how to handle Mom or why she has been accused of stealing a book or moving furniture. You decide you need a break so you don't call for close to six months and you drop out. And you feel guilty, as you should. And every time you are willing to put it behind you and focus on what Mom needs now because you are back in the mix, someone is there to remind you of how you walked away.

And besides bleeding tears, you bleed money. Your mother's money. The money she worked so hard for at the phone company before she went out on retirement due to a bad back. The money she earned working for the state at the police station. The SSI money. You run credit reports and find out there are over 100 credit cards in her name, many from stores like Macy's (where she had 6 accounts!) with clerks who say "would you like to save 15% today by opening a Macy's account?" knowing that Mom already had other Macy's accounts but the $5 commission was all that mattered. You close all the accounts, cash out IRAs and that damned annuity at a loss. You end up paying federal and state income tax as if Mom earned over $100,000 that year all because you had to cash in the investments for her care. But you also know that this is the best thing to do in this moment because it means months of in-home care, and safety and security. That's why we save for rainy days and right now it is pouring.

And the number of correct answers, at least on that test, becomes 15, then 12, then 10. For the rest of the process there are no correct answers, there are no touchstones because you've never been this way before. Oh how you don't want to be here right now but oh how you do because it's all about Mom.

Besides untangling finances, you have to untangle agreements and understandings that Mom entered into with other family members but had not the mental capacity nor the right to enter into. You deal with the house in Florida and you deal with Mom's home. You deal with the Grahamsville property that Mom inherited from her great-grandmother (Therese McGinnes Austin) for all her years of sacrifice and care. You realize that Mom entered into a purchase agreement with a family member who has since rented the property out but that person can't prove their payments to Mom or for taxes. You know that property meant so much to Mom as a kid but you also know the best thing is to let it go and realize that she was taken advantage of and to just deal with it. You deal, you deal, you deal. Until you think all the cards are dealt.

You fight with other family members who either think they know how to care for an Alzheimer's patient or want to keep denying that their sister has the disease. Because there's a small chance, given that the oldest sister already died from Alzheimer's, that they are next on the list to get it. But you also find other supportive family members who are glad to pitch in and actually make so many sacrifices for your mother when you know they already have their hands full.

Then comes the time to talk to Mom about finding a "facility" for her long-term care when either the finances or patience runs out, or both. You dread the discussion you have to have on Mother's Day, of all days, but you find she takes it well. Then you wonder if she really understands that a facility means a nursing home. You wonder if she is clear enough to figure it out over the next few weeks and retreat back into the denial stage. You have visions of that scene in the Exorcist when the priest puts his mother in an inner city nursing home yelling "Demi, why you do this to me? I'm afraid Demi." But you realize that when you see her a month later that she's lost over 20 lbs, she's eating better, she has lots of activities. She is safe, she is happy, she is living in the moment.

Next you have to clean out the house you grew up in and you don't know where to start. You make six trips in one year, buying boxes when you step off the plane to Newark. Working long hours sorting through every scrap of paper, every wadded up tissue in a sweater or pants pocket because it might contain something of value, every book some of which would have a gold bracelet as a bookmark. You remember that Mom took care of your great-grandmother and your great-aunt (Ethel McCrickert Hannan) in that same house and realize that their possessions are still there. You get angry when you find all the crap and junk she's been sold, be it greeting cards (why are there 100 of the same Thanksgiving card from a Hallmark store? I know I won't ever live to see 100 Thanksgivings), or the wrapping paper that people sell for their kid's school, or the needless health books, vitamins, and other quackery and the expensive overpriced dolls from China which are probably decorated with lead paint. And you hope that however crappy or tacky or useless, these things brought her joy and made her happy, even if for a moment.

You sort, you throw away. You become cold, efficient, without feeling as you decide not to pause and look at a photo album - you just toss it in The Box. You donate clothing to thrift stores, you sell antique items that no one wants and that you can't send home to Chicago. Your aunt has a great idea to donate most of the 100+ dolls to a shelter for battered women and children. And when you are back home, you enjoy The Box and all its photos, diaries, etc. later in the year - it is the beginning of this project and other genealogy projects. You feel lucky to have photos from your ancestors and to begin to know who you are.

You have lots of help from family members that you can never thank enough. You didn't do it alone although you feel lonely and have a deep sense of loss most of the time. You thank your Uncle Jerry for all the help from the beginning - for attending hearings, meetings, taking care of finances, arranging in-home care and the nursing home. All of this was not possible without him and without Nan's support. You thank your Uncle Lem and Aunt Judy for helping clean out the house. You thank your Aunt Joan for providing a year of room and board to Mom despite the aggravation and the problems. You thank Beth for making the trip from Delhi and visiting. You thank all your other relatives who make visits at the nursing home, visits Mom won't remember five minutes later, but visits that you know make her happy despite the visitor being saddened by what they see or wanting to cry. And you thank all her friends, even the ones who no longer keep in touch because it is just too uncomfortable.

You keep in touch with family and friends who call and want an update on Mom. Or you get updates from them when they go for a visit at the nursing home. While you notice the deterioration in her condition on each visit, you hear from relatives that she has an ankle brace due to a fall, or this problem or that problem. And still you know you've done the best thing for Mom.

The time you get to spend with Mom becomes shorter and shorter - not because you don't want to visit, but because her attention span doesn't enable her to focus on any one thing for more than 30 seconds. You call the nurses’ station to talk to her and after a short conversation, you realize she put the phone on the counter and walked away. Not because there was something more interesting, but because she can't focus.

And the list of correct answers to that test are now in the single digits. You know what the future holds and you dread it. You don't want to go through the first time Mom doesn't know who you are, but you know it will happen. You already see the difficulty she has in eating, getting on and off an elevator (she won't get on because she thinks you are getting off to visit her), or getting in and out of a car. You know what the next steps are because just like this article, you've read them in some blog or book or news article or website. You know Mom will suddenly stop talking, stop walking, stop eating, stop breathing.

But you will always know that you are your mother's son. And that she knew that too.

I've decided that I can either be bitter or I can be better. And bitter won't change my mother's condition - just mine. I choose better and the way I can do that is to:

a) talk about my mother's experience with people like writing this article;

b) mention the bad times as well as the good times, the negative as well as the positive but focus more on the positive - the negative is there as a reminder but not something to regret for it can't be changed;

c) not regret the journey of Alzheimer's for me, for Mom and for the others involved - for a journey has lessons;

d) understand that I did and do the most that is possible for my mother's care given the circumstances, finances and that I was lucky to have other family members involved; and

e) honor my mother and the way she raised me by not forgetting her sacrifices and her love, her challenges and her gifts, her mistakes and her accomplishments.

After all this, would I want to take a blood test, or any test, that would help predict whether or not I was to have Alzheimer's Disease? You're damned right I would. Not only would it help progress the research that has already been done, but it would help me prepare for the future. And I could live life and every day as if it were important and my last. I wouldn't make someone else go through that dark twisting tunnel of care unguided and with those feelings of helplessness. Knowledge is power and power, be it the power of health, finances or love, can help you conquer all adversities.

Would you take the test?

Thursday, May 8, 2008

That Month of Three



This post was composed for the 1st Edition of Smile For The Camera ~ A Carnival of Images

That Month of Three

In your arms, that month of three,
you held and loved and carried me.
Our blue eyes, our skin both fair,
your gaze told me you'd be right there,
by my side, through good and bad.
And oh what times, what times we had!

Trips away were so much fun,
more so with me, your oldest son.
We saw things that touched our heart
and laughed and laughed at stuff called "art."
We flew, we drove, saw it all
and took it in, both big and small.

When Dad left (men always go . . .),
I promised you, "Not me! No! No!"
You had hoped I'd be right there,
but knew deep down that wasn't fair.
"Go," you said, and with a smile
I went away for quite awhile.

School was far, so far away -
my hopes, my dreams to find one day.
Way out West, each week I'd phone,
"Please be careful," you'd intone.
"When will you come home again?"
"It will be soon, you'll see me then."

The empty nest, you did fill
with work and church and visits 'til
something came, took over you.
You struggled so with what to do.
"What is it?" you asked, "Will it stay?"
"It will," I knew but dared not say.

You knew too, but built a game
of cover, of lies, and of shame.
We cried, we fought, and we tried
to stop the loss, as mem'ry died.
"This road's dark, it's hard to see!"
"I'm right here Mom. Remember me?"

If I could, that month of three,
know all the pain you couldn't see,
I'd hold it close so deep within,
but you'd find out, and smile and grin.
"Let go, please. Give that to me.
Now, what's your name? My name's Jackie."


Copyright 2008 by Thomas MacEntee

Photo: Jacqueline Austin MacEntee holding her three-month old son, Thomas James MacEntee, March 1963, Liberty, New York

Monday, April 14, 2008

My Stuff And What My Ancestors Would Think About It

Larry at Passing It On, has a great post which is sure to start the cogs and wheels in your brain spinning this morning: What would your ancestors think about your stuff?

He poses this question in light of how Americans buy, use and dispose of items and comparing such consumption to the practices of our ancestors. Well, it certainly got me to thinking!

I've noticed various consumption patterns among my family:

- my mother was a product of the Great Depression and lived with 11 other siblings. This meant there often was not enough to go around in terms of food. It also meant there were never any new clothes but hand-me-downs from older siblings. The most profound effect was my mother's purchasing habits later in life. As I cleaned out my mother's house over the past three years, I noticed that she had bought almost 10 of every food item, whether she needed them or not. Cake mixes, canned goods, spices, baking goods, etc. At first I attributed such consumerism to her early-onset Alzheimer's Disease. But then I remembered that Mom always shopped like this. And we never threw anything away! Much of the food had to be disposed of during the cleaning process: most food pantries would not accept expired dry goods, open items but would gladly take canned goods.

- my great-grandparents were definitely thrifty. I think my great-grandmother (Therese McGinnis Austin) still had the first nickel she ever received. They too lived through the Great Depression and my great-grandmother grew up very poor in New York City at the turn of the 20th century. The farmhouse that she and my great-grandfather (John Ralph Austin) purchased in 1947 as a retirement home was stocked with lots of items I would now consider antiques. And my great-grandmother was the first "green" person in our family as far as I was concerned: she had canvas and mesh shopping bags to take to the store; she would sort all the garbage and place organic items in the compost bin; she would make use of all the produce, nuts and fruits she could find near the house; an item was used until it was beyond death.

As I get older and more in middle-age, I find that not only do I not need as much, but I don't want much. And my trick to minimizing consumerism: downsize. At home here in Chicago, we live in a small 2 bed/2 bath condo with almost no storage space. This has forced us to justify each and every purchase and decide if we really need it and where we will put it.

Recycling has always been big with me after living in California for close to 20 years. San Francisco had a great program that worked very well. Chicago's program has been dismal up until recently. They had a "blue bag" program where you actually had to pay for the bags into which you placed your recyclables! Now, our neighborhood is one of the first to have tall, bright blue recycle bins. My only complaint is that they aren't emptied but twice a month and are constantly overflowing.

Finally, one way in which I've changed my consumerism is shopping at and donating to my local non-profit run thrift store. I use the Brown Elephant which benefits the Howard Brown Health Center here in Chicago. I keep a large bin in the hallway closet and over a three month period I will add items that I don't want or can't use anymore. Then I'll haul it up Clark Street and drop it off. I also shop at Brown Elephant especially when I need a book to read on a long trip or on vacation. They sell hard cover books for $1 and if I leave it on the plane I don't feel so bad about it. Also, if I finish the book, I'll either leave it at the hotel if they have a library/reading room or I'll drop it off at a local thrift store.

I think many of my ancestors who came before my great-grandparents would be amazed and even a bit outraged at the level of consumerism we see these days.

Tuesday, March 11, 2008

I'm Back - But Not For Long

I was able to get through my visit back home to New York to check on my mother and I really appreciate everyone's support during this tough time. Since much of my information about Mom's condition and progression of Alzheimer's Disease is second and third hand, I figured I needed to make a quick trip and see for myself.

Things were as bad as I had heard and then again, not as bad and could be worse. I think what has really struck people is the sudden decline since October and another turn in December 2007. She is definitely entering the late stages where the effects are beginning to show physically: she won't eat (because she can't focus on the act of eating); and she walks but only if she can look down at her feet and even then she rocks side to side when doing so.

So, we gathered up her remaining sisters and made a great visit on Sunday. While her state was sad to see, and we all knew she wouldn't remember the visit an hour later, it was well worth it. Every so often, these "rays of recognition," as I called them peaked through: she would remember someone sitting at the table and then something that took place 30 years ago. But just as soon as that happened, she wouldn't know that same person or scenario five minutes later. While she knew me the minute I walked in, at the end of the visit when one of the nurses asked Mom, "Is that your son?" while pointing to me, she said, "No. That's not him."

As much as you prepare for that point of progression in the disease, nothing can take away the pain you feel. You are just glad that you have friends, family, and fellow colleagues like my genea-bloggers to get you through it. I appreciate all your thoughts and prayers - they really do work.

So, I will be here the next two days catching up on my blog reader, making comments on some great posts, fulfilling some carnival and meme deadlines, updating my McEntee information, and then taking off for a scheduled mini-vacation on Thursday.

Thursday, December 20, 2007

Death Doesn't Take A Holiday

[Author's note: This post was originally done on November 29, 2007 but has been repackaged for the Advent Calendar of Christmas Memories - Day 20 - Christmas and Deceased Relatives.]

Funny how you sit down to write about one topic and then it is taken over by another that is more important. This one started out about wills and estate planning, then and now. I'll save that topic for a later date. Today I had to "stop for Death" as Emily Dickinson once wrote. He was too important to ignore.

I am sitting here ready to post after a rough day but one that has really emphasized to me the "cycle of life." While I'm all hopped up and ready for the holidays, Christmas trees, baking, seeing friends and family, at the same time I am dealing with loss and death on many different levels. Death doesn't take a holiday. But if it does, some years it seems like my family is its prime vacation spot.

Yesterday, while I was in the middle of writing out my estate planning details, I received news that one of my partner's aunts was declining quickly. She had been quite ill for months and at a stage where hospice care was brought in to care for her last days at home. And then the call came about 5:30 pm that she had passed on. Her sister had just passed away during this year's Easter holiday.

This post is not about death but more about remembrance and ways we can embrace and cherish those memories. This post is really more about pausing and recognizing the cycles of life and how they seem most evident when a death occurs around a holiday such as Easter or Christmas.

Death amid a time of joy tells me that death is just a part of nature, it is part of what should be expected but is not always anticipated, it gives meaning to holidays and to life. If we had no sorrow, no loss, no death, we'd have no touchstones with which to measure our joy. Joy would be a constant, a flat line with no spikes and simply rendered a non-emotion.

But why do our losses seem more obvious when we should be filled with the holiday spirit? I know that last week's holiday was rough for those of us with recent losses and not so recent losses. Holidays emphasize togetherness and family for many of us, and the absence of a loved one during this time seems more intense, and the separation more vivid and painful.

I caught myself on Thanksgiving Day wanting to call Mom and ask if she watched the Macy's parade while she was stuffing the turkey. This was our ritual, our nod to continuity from year to year, something she and I shared. With phone in hand, I started to dial and then I remembered: she wasn't home stuffing a turkey or over at one of her sister's houses. She was in the nursing home this year. Maybe she was watching the parade, but the Alzheimer's would make sure she couldn't remember it even 15 seconds later.

So, I paused and put down the phone. I put my hands back in the bowl of stuffing. And I remembered for her. I remembered holidays, turkeys, and parades. I remembered learning how to make this exact dish that I am literally up to my elbows in. And I cried. And then I laughed because how can you wipe a tear when your hands are practically breaded and battered?

Sure, a cycle ended when I couldn't experience that holiday tradition this year. But cycles that seem to halt their movement - frozen in time - allow new cycles to begin. I now make stuffing with my own family in Chicago. I now call Mom on holidays and try to help her remember.

There will be many tears shed by me this holiday season. And that's not a bad thing, really. The tears tell me that a memory had meaning, that loss is real, that a loved one was important, that death hurts, that a ritual was worth repeating even to the point of aggravation, that there will be new tradtions in the years to come, and that more loved ones will all too soon be missing at the table.

That piece of a life is gone, and it isn't ever coming back. Choose to chase after it, blindly follow its path, and forget the life and rituals going on right now around you. Or choose to embrace its memory, wrap it around you like a colorful and warm Mom-made afghan, and make it live by telling it to others in your family.

This is what we do. We are family historians. We engage in The Telling. In a way, we bring life to the dead and memories to the living.

Photo: grave of my great-grandparents, John Ralph Austin and Therese McGinnes Austin. Grahamsville Rural Cemetery, Grahamsville, New York. My great-grandfather died two days after Easter, 1988.