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The Long and Winding Road…

~ An Alzheimer's Journey and Beyond

The Long and Winding Road…

Category Archives: Mom

Nine Months Later: We Walk to #ENDALZ

15 Sunday Sep 2013

Posted by Ann Napoletan in Advocacy and Awareness, ALZ Assn Central Ohio, Inspiration, Life After Caregiving, Mom, Ruminations, Walk to End ALZ

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Image-1Today marks nine months since Mom left this earth… The stack of cards and notes received upon her passing still sits in the same place it was in December. I keep thinking I’ll sit and read all of them one evening, but the time just hasn’t felt right.

Milestones

We’ve started to think and talk about what we’ll do to mark her birthday next month and then how we’ll spend December 15th. They should be days filled with love and laughter; that’s what Mom would have wanted after all…

I miss her so, so much… Fall was always her favorite time of year, and when we went to pick apples last weekend, I couldn’t help but remember the many times we’d visited that same orchard together over the years. Joyful memories to be sure.4M team.2013.c

Walking to #ENDALZ

Yesterday was our local Walk to End Alzheimer’s and what an event it was. A perfect crisp, cool autumn morning welcomed us to Huntington Park; the sun shone brightly as our ALZ angels smiled down on our new venue. The Central Ohio event has grown by leaps and bounds since 2009 when Marilyn’s Mighty Memory Makers were born. In five years, our little team has raised over $13,390 for Alzheimer’s research and programs, but there is much work yet to be done!

Here are a few photos from our special day in Columbus, Ohio…

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Arriving at the ballpark, bright and early… a beautiful day.

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Opening ceremonies…

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Jennifer Sega, the most AWESOME event organizer in the world! With hubby Bob, team photographer extraordinaire.

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Look at that glorious blue sky…

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Honor, remember, care, fight, – and love.

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The event brought out men, women, children…. and birds…. of all ages!

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Entering the field, nearing the finish.

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And we’ll keep doing it until there’s no more need.

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Caregiver PTSD: Fact or Fiction?

12 Thursday Sep 2013

Posted by Ann Napoletan in Caregivers, End of Life Signs, Grieving, Guilt and Regrets, HomeReach, Hospice, Kobacker House, Life After Caregiving, Mom, Ruminations, Saying Goodbye

≈ 75 Comments

Tags

alzheimers, caregiver ptsd, caregiver stress, death and dying, hospice

 

photo-41Post-traumatic stress disorder (PTSD):  An anxiety disorder that can occur after an individual has undergone extreme emotional trauma. It is most commonly associated with soldiers returning from war or victims of violent crime, but some experts now believe it can also befall caregivers. In fact, when I saw my doctor shortly after my mother died, it was something she mentioned.

Emotional Upheaval

In a way it sounds crazy; how could the impact of caregiving compare to war or violent crime? Obviously, they are very different, and I don’t think anyone is trying to imply they can be compared. But if you unravel what occurs in a caregiver’s life over many years, it’s reasonable to believe some form of PTSD is certainly within the realm of possibility – perhaps to varying degrees depending upon many factors.

Barry Jacobs is a clinical psychologist and author of The Emotional Survival Guide for Caregivers. Dr. Jacobs notes that many caregivers wrestle with uncontrollable disruptive, distressing thoughts months – and sometimes years – after a loved one has died.

It drives me nuts when well-meaning people say, “focus on the good memories.” (And for the record, I’m certain I’ve said the same thing to others a million times over my 47 years on this earth.) We’d all like to remember only the good times, and I imagine most of us constantly work toward that goal. But when you’ve watched someone suffer through years and years of an agonizing chronic illness, it’s tough to just flip it off like the light switch in the kitchen.

bearDr. Jacobs says, “Many people find themselves unable to stop thinking about the suffering they witnessed, which is so powerfully seared into their brains that they cannot push it away.”

Haunting Memories

My mom died almost 9 months ago, and try as I might there are certain moments that regularly haunt me. Some nights, when I lay down and close my eyes at bedtime, the images are more vivid than I can bear. I just can’t shake it, and the only way sleep will come is with television to distract my thoughts and melatonin to help me drift off.

Sometimes, the images pop into my head without warning – no apparent trigger – but there they are. It’s a vicious cycle; the mental pictures tend to bring forth more unpleasant memories, particularly of the last several weeks of her life. Those thoughts lead to unreasonable worry about things that I couldn’t control at the time and certainly can’t control now.

For instance, in her last few days before going into the hospice facility, I had to administer morphine. Of course I was doing so under the direction of hospice nurses, but it was horrible. She was in so much agony; the morphine was the only thing that brought her peace. I know that. Yet, I still struggle and wonder if there was something I should have done differently.

Defying Logic

An image that is burned into my psyche is that frail, almost unrecognizable woman who, for nine days, occupied the bed in room 16 at Kobacker House. Face sunken in and unresponsive; so thin that at one point, I touched the sheet, wondering what the pointy thing was under there – only to realize it was a hip bone jutting out of her tiny body. I can still see her like it was yesterday, and if that’s not painful enough it’s a visual that never fails evoke memories of the moment she took her last breath.

Something that has bothered me for the past nine months; was I holding her hand at the very moment she crossed over or had I let go? Now what a ridiculous thing to obsess over! Even if I knew the answer, I couldn’t change it, yet I have to consciously remind myself how illogical it is to allow that thought to take up residence in my head!

I don’t doubt some people will read this and wonder why in the world I would put myself through reliving such painful memories, but it’s not a choice. I’ll be honest; I wish I understood it. What I do know is that I watched my mother’s gradual decline for almost a decade; it’s nearly impossible to even remember her BA (before Alzheimer’s).

PTSD or Not, Caregiving Takes Its Toll

Symptoms of post-traumatic stress disorder include flashbacks, feelings of anxiety, dread, guilt, apathy, numbness, and depression, but as Dr. Jacobs points out, each of those issues are common in caregivers. It’s really up to a physician to determine whether what you’re experiencing might be a form of PTSD.

Do I think I have it? Probably not. The thoughts and images I’ve described aren’t constantly present; they come and go. But at the end of the day we have to realize that years of witnessing the unthinkable, being forced to make life’s most troubling decisions, never being able to completely settle our racing minds, constantly facing wildly fluctuating ups and downs – all while confronting life’s “normal” daily challenges… it takes a toll.

I remind caregivers all the time they must be gentle with themselves, but the truth is, it’s still something I have to work at everyday. It’s only since my mom’s passing that I’ve realized the need extends well into life after caregiving…

I would love to hear your thoughts on caregiver PTSD, as well as how you’ve dealt with the unwelcome images and memories that come calling at the most unexpected moments.

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World Alzheimer’s Month: Free Streaming of Critically Acclaimed Documentary

11 Wednesday Sep 2013

Posted by Ann Napoletan in Advocacy and Awareness, Behaviors, Films, Helpful Resources, Mom, Ruminations, World ALZ Month

≈ 4 Comments

xposter-smallIn recognition of World Alzheimer’s Month, Independent Lens|PBS will offer free streaming of the documentary You’re Looking at Me Like I Live Here and I Don’t from 9/15 through 9/25!

Told exclusively from the perspective of Lee Gorewitz, a woman living with Alzheimer’s, all of the filming took place in an Alzheimer’s care unit. The film originally aired on PBS’ Independent Lens series and has received rave reviews from the Alzheimer’s community as well as film critics far and wide.

This riveting film grabbed my attention immediately and held it through the final scene. When it ended I felt sad — not because of the subject matter but because I wanted to spend more time with this unique and endearing woman with whom I’d fallen in love. I missed her, so I turned around and watched the entire movie again. – Marie Marley, Huffington Post

I must say that after reading just a bit about Mrs. Gorewitz, I am very anxious to see the documentary. Described as a charismatic, “exceptional and resilient soul… who often shakes a tail feather long after the music has stopped… and who will not let us forget her, even as she struggles to remember herself,” I can’t help but think how much that sounds like my mom!

The following synopsis was taken from the film’s website:

In Danville, California, Lee Gorewitz wanders on a soul-searching odyssey through her Alzheimer’s & Dementia care unit. Confined by the limits of her physical boundaries, she scavenges for reminders of her life in the outside world. Yet her search is for more than a word, or a memory, or a familiar face. It is a quest for understanding.

A total immersion into the fragmented day-to-day experience of mental illness, You’re Looking at Me Like I Live Here and I Don’t is the first documentary filmed exclusively in an Alzheimer’s & Dementia care unit, and the first told from the perspective of someone suffering from Alzheimer’s disease. The film reveals Lee’s penetrating ruminations and charismatic vitality, challenging our preconceptions of illness and aging. Here is the journey of a woman who will not let us forget her – even as she struggles to remember herself.

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Marilyn, BA (before Alzheimer's)

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