• Home
  • Helpful Resources
  • Reading List
  • Recommended Blogs
  • Marilyn’s Legacy: A World Without Alzheimer’s
  • About Me
  • Contact Me

The Long and Winding Road…

~ An Alzheimer's Journey and Beyond

The Long and Winding Road…

Tag Archives: caregiver stress

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

≈ 73 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.

Share this:

  • Click to share on Twitter (Opens in new window)
  • Click to share on Facebook (Opens in new window)
  • Click to share on Pinterest (Opens in new window)
  • Click to share on Reddit (Opens in new window)
  • Click to share on LinkedIn (Opens in new window)
  • Click to share on Tumblr (Opens in new window)
  • Click to email a link to a friend (Opens in new window)

Like this:

Like Loading...

Coming Soon….and a Fabulous Read for Caregivers

29 Thursday Aug 2013

Posted by Ann Napoletan in A Place for Mom, Advocacy and Awareness, Blogging, Caregivers, Films, Inspiration, Life After Caregiving

≈ Leave a comment

Tags

alzheimers, caregiver, caregiver burnout, caregiver stress

Ah, it’s been a busy week and I’m already asking myself how in the world I was managing three weekly posts for APFM. For some reason, this week I feel like I’ve been running at hyper-speed yet have gotten very little accomplished!! wheel

I promise a review of Angel’s Perch by the weekend, so be sure and check back. It’s been two weeks since the Columbus screening, and I’m still hearing from people who thought the movie was just incredible!

In the meantime, I want to leave you with this wonderful article from Mark B. Perry for dnj.com. It’s been awhile since I’ve read something that hit home so deeply and on so many levels.

The original article can be found in its entirety here –> PERRY: Alzheimer’s takes its toll on those in daily battle

____________

Alzheimer’s takes its toll on those in daily battle

by Mark B. Perry

For those of you who have had an experience with someone with Alzheimer’s, you are fully aware of the toll it can take on you.

I recently saw pictures of soldiers that had been in Afghanistan; they were before and after pictures. It was obvious that the constant worry and stress of their situations as well as the loneliness of missing their loved ones back home, had taken its toll on them. It reminded me a bit of what I see in the mirror every day.

I know I haven’t had to go through the horrors of what our soldiers have gone through, and I haven’t had the stress of literally fearing for my own life on a daily basis, but in the mirror, I can see what a long drawn-out battle has done to me and the toll it has taken.

I can see it in the faces of people who are taking care of their parents and their spouses. The hours of furrowed brows and thousands of tears have etched and grooved and new landscape across our faces that no amount of smiles can smooth away. Just as gravity pulls at the body and ages it, so stress and worry weigh us down

We are at war; we are in a battle. We are fighting something bigger than ourselves that we cannot defeat. Our days are long and drawn out and we are forced to do things we never thought we could do mentally or physically.

We are fighting a disease that knows no enemies and has never been defeated. We fight to keep our loved ones safe from harming themselves, wandering off, or simply from falling down. We fight to keep them involved while fighting to protect their dignity. We fight our frustrations in them not knowing who we are.

We fight the urge to argue when they want to go home even though they are already in their own home. We fight to convince them to do the basics of daily life. We fight to keep it together when they tell us the same thing every five minutes.

We struggle daily with the guilt of our bad decisions and letting someone else help to take care of our loved ones. We worry when we leave them alone with caretakers that they will be watched after and cared for and that no one will show them their own anger and frustration. At night we lie awake and worry about the day we just had and how we will handle the next one.

But each day, we gear up and face the battle. We do it to protect our loved ones. We do it because we have to and we want to and we are scared to death not to. The toll it takes on us is great. As hard as we try, our minds never really wander away from our task at hand.

Just like a soldier that comes back from war, when our loved ones have passed away, we need time. We need time to re-adjust when it is all over.

We are battered, shell-shocked and tired, but in time, we will pick up the pieces and find the good to remember and take pride in knowing that we made a difference; we did our best, and even though probably never expressed, it was appreciated. No one can really understand unless they have been through it. We can’t expect them too. What we must do is continue to pursue a happy life that we know our loved ones would so desperately want us to have.

Once a year we all come out of the trenches for a moment, and we join together, we march, we walk. In over 600 towns across this country, we gather in groups and walk to show our support for all the work that is being done to fight this horrible disease.

If you would like to help and join forces in time, support or even with finances, you can go to www.alz.org and look for the Walk To End Alzheimer’s in your area. There are many teams from healthcare organizations, caregivers and families. For my mom, Ann Perry, we are www.thememoryjoggers.com.

Don’t be discouraged if you don’t have the funds to help out financially. There are other organizations that require nothing more than a click.

One great organization that is working hard to get the government to increase the funding for Alzheimer’s research is http://www.usagainstalzheimers.org.This is a powerful group that is really starting to make things happen by making our government understand the epidemic situation we are facing and the economic impact it will have on our future.

Another that I love is the grassroots campaign to get a postage stamp (much like the one for breast cancer) for Alzheimer’s. These type stamps have raised millions in the past. That site is https://www.facebook.com/HelpStampOutAlzheimers.

Whatever you can do, do it. Do it for those you love and do it for future generations so that years from now, the Walk to End Alzheimer’s will be nothing more than a distant memory.

Source: http://www.dnj.com/article/20130820/OPINION/308200013/PERRY–Alzheimer-s-takes-its-toll-on-those-in-daily-battle?source=nletter-news

Share this:

  • Click to share on Twitter (Opens in new window)
  • Click to share on Facebook (Opens in new window)
  • Click to share on Pinterest (Opens in new window)
  • Click to share on Reddit (Opens in new window)
  • Click to share on LinkedIn (Opens in new window)
  • Click to share on Tumblr (Opens in new window)
  • Click to email a link to a friend (Opens in new window)

Like this:

Like Loading...

The Skinny on Caregiver Burnout

08 Saturday Jun 2013

Posted by Ann Napoletan in Blogging, Caregiver Burnout, Caregivers, Caregivers.com, Helpful Resources, Tips

≈ Leave a comment

Tags

caregiver burnout, caregiver stress, caregiver tips, caregivers blog

Caregiver burnout is a serious issue that can lead to a number of physical, mental, and emotional ailments. Do you know the red flags? You can learn the most common warning signs and get some tips on keeping your stress in check – it’s all in my latest Caregivers post:

Identifying Signs of Caregiver Burnout – And Then What?

no-caregiver-burnout

Share this:

  • Click to share on Twitter (Opens in new window)
  • Click to share on Facebook (Opens in new window)
  • Click to share on Pinterest (Opens in new window)
  • Click to share on Reddit (Opens in new window)
  • Click to share on LinkedIn (Opens in new window)
  • Click to share on Tumblr (Opens in new window)
  • Click to email a link to a friend (Opens in new window)

Like this:

Like Loading...
Newer posts →
© Copyright 2020
All Rights Reserved
The Long and Winding Road

Between 2009 and 2015, Marilyn’s Mighty Memory Makers have raised over $22,000 in the fight to #ENDALZ! To all who have supported us, THANK YOU!!

Marilyn, BA (before Alzheimer's)

Contributor

Contributor

Recent Posts

  • June 7, 2021: A Historic Day
  • UsAgainstAlzheimer’s National Alzheimer’s Summit: Don’t Miss It!
  • Happy 84th Birthday, Mom.
  • Mother’s Day in Heaven
  • World Alzheimer’s Month

Enter your email address to follow this blog and receive notifications of new posts by email.

Join 1,325 other followers

Archives

Blog Directory & Business Pages at OnToplist.com

Blog Stats

  • 129,796 hits

Meta

  • Register
  • Log in
  • Entries feed
  • Comments feed
  • WordPress.com
stats for wordpress

Categories

Popular Posts

  • About Me
  • Thank you!
  • A Special Bond
  • Telling the Story
  • Monday ... on Caregivers
  • Caregiving: Imperfections, Weaknesses, Acceptance, and Forgiveness
  • Walking a mile in his shoes...
  • Look for me on VoiceQuilt!
  • CGSN: Focus on YOU!
  • Hiding In the Canned Goods Aisle...and Other Stuff

Recent Comments

  • Ann Napoletan on Caregiver PTSD: Fact or Fiction?
  • Ann Napoletan on Caregiver PTSD: Fact or Fiction?
  • Ann Napoletan on Caregiver PTSD: Fact or Fiction?
  • Ann Napoletan on Caregiver PTSD: Fact or Fiction?
  • Tasha on Caregiver PTSD: Fact or Fiction?

Pages

  • 2013-2014 News Archive
  • Helpful Resources
  • Latest News & Events
  • Postmaster General Letter – Alzheimer’s Semipostal
  • Reading List
  • Recommended Blogs
  • About Me
  • Contact Me
Coming Soon!
Marilyn's Legacy: A World Without Alzheimer's, Inc.
Stay tuned!!

Blog at WordPress.com.

  • Follow Following
    • The Long and Winding Road...
    • Join 1,325 other followers
    • Already have a WordPress.com account? Log in now.
    • The Long and Winding Road...
    • Customize
    • Follow Following
    • Sign up
    • Log in
    • Report this content
    • View site in Reader
    • Manage subscriptions
    • Collapse this bar
 

Loading Comments...
 

    %d bloggers like this: