Overcoming Resentment

Overcoming Resentment

overwhelmed woman

When caregivers recognize they need help, they sometimes find it takes time to research, and asking seems an uncomfortable admission of need. When it seems no one understands or hears their urgency, frustration that breeds resentment sets in. When a caregiver begins to feel disappointment as they see the dream of a life that never happened fading, or their future seems grim and unclear because of this unanticipated circumstance, resentment can show up unexpectedly. 

Resentment is defined as indignation at having been mistreated or treated unfairly, offended or insulted.

Many caregivers for those with memory loss begin their journey with a heart full of optimism, love, and a good dose of desire, to take care of a family member or good friend – all hopeful intentions. But over time, reality reveals that initial aspirations are not so easily attained nor sustainable.

Discoveries about the nature of the particular dementia disease become a daily education and often classes from various professional groups substitute for personal activities. Frequently, new behaviours require understanding and research to develop new management strategies as the disease progresses. 

Eventually, the wish to make life better for a loved one dissolves into a mixture of dread and desperation as caregivers wade through the fog of unfamiliar confusion. The psychological state of the loved one begins to need attention while caregiver self-awareness calls for new caregiving know-how. 

In time, caregivers recognize new financial responsibilities they never dealt with before, and realize they are making unexpected sacrifices in their personal lives and activities, all of which demand time to learn new life-and-management skills. Relationships that once felt comfortable begin to shift and change and the resulting uncertainties can tend to eat away at original foundations.

The caregiver’s life tends to change far more than initially envisioned. Any impact from the new role and tasks required generally are not evident right away. However, when that initial confidence shrinks, fear can slowly begin to fill the void.

THE THING ABOUT CAREGIVING

The caregiver is usually so wrapped up in the tasks of their new role that they rarely see the personal transformations happening. When caregivers are climbing the steep learning curve, swamped by all that is required of them to observe and learn, they quickly become desperate and feel the need for support, for someone to talk tofor reassurance that they are doing OK, and especially not to feel alone while caring for their loved one. This period, when fear is creeping into daily thoughts, is when caregivers sense the anxiety of panic. It is a time when they might begin to seriously feel the need for help, as they realize that they cannot carry the entire caregiving responsibility alone. They then recognize the importance of connection to others, the inspirational support that caregivers can share, as well as the value of professional counseling, therapists, and support resources. It is then, when they begin to come face-to-face with their own exhaustion, their overwhelming desperation from the losses endured, and the sacrifices made, that they might feel a sense of resentment bubbling just below the surface

While it might not be the norm for every caregiver, you would be normal if you were to go through a period of resentment. And while it might not be the norm for every caregiver, you would definitely be normal to try to find help to eliminate resentment.

You are may find yourself asking what is normal, what is typical. There is no such thing. But for the sake of understanding others in a similar situation, you might want to know if others feel as you do.

It would be normal to feel anger if it has been difficult finding support.  It would be OK to admit you have exceeded your abilities, It would certainly be reasonable to feel frustrated by the losses experienced because the person you care for has changed from the person you originally knew. You could rightfully feel you found it tough to be grateful, or to find positive aspects in a situation where you felt abandoned by a system of health care that is also overwhelmed. You would be normal to feel disappointed, bitter or even angry at the a situation you find yourself living in. You would be normal to feel alone. 

Although resentment does not happen often, nor to every caregiver, it does happen…and it is truly unbelievable how fast it happens.

CONSEQUENCES OF RESENTMENT

No matter what stage of memory loss, no matter which of the dementia diseases your loved one may be battling, caregiver emotions still build up and resentment can be a consequence. 

Caregivers are so busy and most times exhausted, that they might not realize they feel resentment. The cost of not recognizing it can impact your health, can bring on depression and other stress issues. At a time when you need all your energy and attention to stay well to care for your loved one, you want to avoid the chance of stroke, anxiety, ulcers, migraines, or other health issues.

If you address the resentment that comes from mistreatment or grudges, you can avoid additional anger and stress in your life.

We suggest that 
to overcome and eliminate resentment,
first seek professional help,
a trained counselor or therapist.

IDEAS FOR REDUCING RESENTMENT

While it is unlikely that a caregiver will resent each task,
it would be helpful to list the
(1) tasks. (2) reasons where resentment comes up.

Example:

  • Are you angry because you are being told to do things for which you previously have asked for help but never received it, so you feel inadequate to do the task? 
  • Are you feeling cheated because you have given up all your time to care for your loved one instead of giving any care to yourself? 
  • Do you feel the tasks seem to end up with negative results instead of positive? 
  • Are you associating emotions of this experience with those from earlier, unpleasant times?

The Australian. website, Start With Self, offers more: “How to let go of resentment”
Read their page. This is my recap:
1. Become aware of your resentment
2. Analyze the cause of your resentment
3. Begin to heal when acknowledging responsibility for your emotions
4. Find compassion for yourself inside
5. Learn the power of forgiveness

TAKE TIME to self-evaluate, and take action
if you sense any resentment.

MOVE BEYOND RESENTMENT

For the good of your mental health and your ability to continue caregiving, you may want to address the mistreatments that trigger your feelings of resentment.   It may take a day, a week, or one month, or maybe a year to find your way through the process, depending on the depth of hurt and amount of work you are able to exert to move through it – it takes the time it takes. A professional can help with that.

You may need professional help. Find it. There is no shame in needing and asking for help for something we cannot correct on our own. The knowledge professionals bring to their work will help in our growth as a caregiver as well as a person in our own life. We can also learn from this experience for future issues.

You may need to forgive in some way. Forgive. Forgive yourself for not knowing everything. Forgive yourself for not being able to foresee the behaviors that prompted the initial mistreatment. Forgive yourself for not always finding the positive side of an issue. Forgive yourself for having guilt or bad thoughts about the issues. We are all imperfect humans trying the best we can.

You may need to find aspects of your tasks for which you are grateful. Be grateful. Just feeling good about some part of what you do can change your attitude and emotional connection about the entire task. Be grateful that caring for a loved one means spending time together you otherwise would not have spent. Be grateful you could give back love to someone who gave love to you. Be grateful for the help you did get rather than resenting the help you did not get. 

Sometimes seeing a task from a different perspective helps remove resentment about it.  Look for a new perspective. I resented showering my loved one every day, having to prepare his clothes, undress/dress him became tedious to me.  I found that by getting service workers to come in for twenty minutes each morning to shower him, I could help by having his clothes clean and ready. I had reduced demands on me for that task and my perspective changed by having someone else doing the dressing.

Sometimes, raising the vibration of the emotion that you associate with the resentment of the task can be enough to lessen the emotion causing resentment and thus eliminating the resentment. Redefine and reframe the task and thus the emotional connection – for instance going from anger to frustration to annoyance. Feeling the emotional change might take time but be well worth it.

~

My loved one makes me angry because I have do everything to shower him in the morning.

My loved one frustrates me because I have to do everything to shower him in the morning.

My loved one annoys me because I have to do everything to shower him in the morning.

Annoyance does not make me feel resentment and so I can accept that I am annoyed with my loved one because I do everything to shower him in the morning. I even can detach enough to seek out help.

~

Those emotionally charged thoughts that caused your frustration, anger, disappointment, or despair, can be revisited. You can realign your situation from a positive perspective.  Consider yourself normal if you find you not only need help from other caregivers and support systems, but also from the world of professionals.

In time, those redefined and realigned thoughts and perspectives will give you space to find the wisdom and courage, love, hope and desire that you felt when you began your caregiving journey.

With the help of caregivers, of a counsellor, or professional therapist, you will find that overcoming the impact of resentment will be a gift to yourself that will last the rest of your caregiving journey and, hopefully, for the rest of your life.

Love and be well, 🌷 Judy

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Learn from our stories… BOOKS FOR CAREGIVERS and those who support them. Finding you are a caregiver, without warning, without training, without intention, all make the tasks ahead overwhelming and many caregivers become desperate at the thought of it, as they begin to learn all their new responsibilities entail.

Read our story, about out ten year journey while I cared for my loved one, who was diagnosed just after our retirement, putting a new spin on our plans for our later years.


Overcoming Resentment (c) 2023 Judith Allen Shone

Capturing Memories

Capturing Memories

Do you hear it, too? Some families are already making plans for Thanksgiving. Can you believe it will be here in just a few weeks!

Many times when families get together, the photo albums come out and everyone looks at pictures from the past years. There is laughter, reconnection, memories of good times together when recognizing family from years before. Time goes so fast. While peeling carrots or setting the table, or sharing the meal, take pictures to add to that album.

For many families, holidays are a time of excitement, kitchen action and chatter, of family members huddled together, cherishing special moments. Sadly, sometimes, smiles and hugs among family members are not able to happen even once a year. This is a reminder to take family photos. Remember to have a camera, and to use your camera. Maybe set your phone alarm to remind you!

**If you care for someone in your family who is older, sick or especially with memory loss, or even someone you don’t see frequently, it might be a good time to take a family photo, or prepare questions and record a video talking about family history. **

CAREGIVERS:
It seems when family members get together folks want to reminisce about their childhood, or meaningful holidays. New voices chime in and new happy memories are made while reliving ‘old times.’ Please understand, those with dementia don’t always remember what you remember.

BEAR IN MIND:
if someone with dementia is among your guests, understand they may feel tired, may become annoyed if surroundings become too loud or busy, may need to have someone beside them so they don’t feel alone.

In some cases, our loved ones may relate some history that you feel is inaccurate. We know those without dementia often see events differently, so it is no wonder those with dementia might also. Go with the flow.

You may have heard the story of five people going to an event. And after the event, they were asked to write up their report on what had happened. As each one read their account to the group, the descriptions were so different that it was not evident that anyone had witnessed the same event.

And so it might be with those with memory loss. It is the perfect time to let others know that your loved one is telling their story. You are witnessing their reality as they interpret their reflections of time past. Arguing never works. Instead, join in and accept your loved one’s reality.

Gatherings can also be a time to pay attention, to ask questions. These members of our families hold memories that we may never hear about otherwise. Take photos. Record their answers for the years ahead, for future holiday gatherings or for someone looking into family ancestry. You can be one taking pictures. You can be the one who reminds everyone to stand by the fireplace or the in the garden for the family picture.

Invite guests to help! Ask them to put a reminder for Alexa or Google to announce out loud. Even ask them to set an alarm on their phone to remind everyone.

Maybe, before guests come to dinner, suggest each one to be responsible for one photo of a certain person during the day. Let them know you are making an album of this gathering so they will want to contribute ‘the best’ picture.

“Jill, please take a picture of your sister when she arrives with her new baby. Be sure to capture the smile when she introduces her to everyone. . Harry, see if you can get pictures of Mom cooking the meal…in her normal director stance. Jim, you are responsible for getting a great photo of Grandpa relaxing during the day. He might sit outside with Grandma. Patrick, please take a picture of the family seated at the table. It will be one of the few times we are all together. And, Patrick, if you can, video it when they are laughing and telling stories. Pauline, please take Grandma aside and let her talk to you about her time in grade school, or college, or when she and Grandpa got married. Try to catch the twinkle that surfaces in her eyes as she remembers.”

Many times, I’ve wished I had disconnected from my intense tasks of caregiving enough to be prepared for the time ahead when I would no longer see the twinkle in My Love’s eye, or would no longer be able to hear his voice. I loved his expressive eyes and speaking voice. Now I can’t ‘see or hear’ either in my mind – and I have no recording of his voice. I truly wish I had. But….you know.

Maybe put a note on a side table to remind you, or someone else at that gathering, to take a family photo or a family video when everyone is happy and talking. Or make a tradition that no turkey service until the family photo is taken. And then you know it will happen. Even use that one last chance….suggest taping over the car handle so no one gets in their car to leave before taking a family photo.

Of course, you do not need a holiday to take photos or record videos, however, you can make a point of having people help you in remembering to take pictures.

There are likely many other ways to capture the moments with loved ones for remembering later. I think most important is remembering to do it. Talk about it before hand. Make plans so it happens. There are no do-overs. Action makes it happen, not talking. Find motivation that works.

I have been to visit family when so much chatter and memory-sharing and doing together was happening in a short time…and nobody took one picture. Not even catching folks as they were leaving, as sometimes we have done. I felt horrible. There we were, all together, all with phones or cameras, and no one stopped to take a photograph, or record a video of the occasion. I imagine this has happened in other families, too. Who will be in charge of taking photos?

These are the memories that will be shared in the future, year after year, even when most of us are gone and the next generation brings out the photos. (By then, who knows how the current photography method will be.) Plan to leave the best stories, the best photos, and best videos possible from this event.

Have a happy family gathering. 🥰 ~judy


Capturing Memories © 2023 Judith Allen Shone

Beyond Caregiving

Beyond Caregiving

Since My Love passed, my life has not been the same. He took part of me with him. Thankfully, he left me his love.

Beginning again

“When the world feels like a roller coaster, steady yourself with simple rituals. Do the dishes. Fold the laundry. Water the plants.  Simplicity attracts wisdom” ~ Gregg Braden

I know my caregiver commitments are over. But, even though I was privileged to be My Love’s caregiver, if I can be honest with myself, I really was ready for the exhausting daily tasks of feeding, washing, organizing, nursing, and chauffeuring to end. I have nearly recovered from the unbelievable desperation and caregiving frazzle of those ten years. Yet the love I felt while fulfilling those responsibilities still remains. It is from the memories of our relationship, buoyed up by the love we had, the love that did not die with him, that I will begin to build a new life .

The grief I continue to feel may stay with me forever. It just confirms for me that our love never dies.

Alan D. Wolfelt, PhD., one of North America’ s leading death educators and grief counselors, shares these words from Henri Nouwen

Every time we make the decision to love someone, we open ourselves to great suffering, because those we most love cause us not only great joy but also great pain. The greatest pain comes from leaving…the pain of the leaving can tear us apart.

Still, if we want to avoid the suffering of leaving, we will never experience the joy of loving. And love is stronger than fear, life stronger than death, hope stronger than despair. We have to trust that the risk of loving is always worth taking.

But it was the grief that allowed me to process so many thoughts of our time together, that allowed me to reflect on areas of our life, even of my life before ‘us,’ that inspired me to fill that vacuum with a new life. I envisioned that my new life would give value to what we’d just been through, celebrate that I had learned so much, and honour the relationship of love we had throughout out nearly thirty years together…the good times and, yes, some not-so-good times.

In one grief group each week we were to leave by saying the one word representing how we felt at that moment. As we talked among ourselves over the months, I felt a ‘mental graph’ of emotions go from desperate, angry, unconnected, sad, lonely, floating, to annoyed, ‘pissed off’, improving, to encouraged, optimistic, to content. Of course, there are lists on the internet you can check with. But we all experienced a wide range of emotions on our journey…I would add I did not feel them in any order, and not for any particular length of time. Overall, I discovered grief takes it’s own path, and takes the time it takes.

Passion, Purpose and Service ahead

Mike Dooley’s words from his daily emailed
Notes from the Universe resonated with me,
“Passion. Purpose. Service. In that order.”

I appreciate the insights I received from other caregivers while I was walking that path; I know they were priceless. I will continue to be an encourager because it meant so much to me to be inspired by others.

Perhaps my years of caregiving have turned to Passion, now an enthusiasm to further share my experiences with those who are fearful, who feel alone in their new and unfamiliar role. There are still experiences to share and stories to tell.

Going through grief I’ve been trying to heal from a deep wound of loss I did not think I could bear. And then these words from Gloria Steinem showed up, perhaps just to confirm I was on the right track.

The final stage of healing is using what happens to you
to help other people. That is healing in itself.” 

And so, even though My Love has passed, I sense that my Purpose has identified itself as Service to others through the stories I can share about caregiving. It is what I ‘studied’ in the last ten years. Caregiving is what I have my most recent ‘life-degree’ in, and therefore, it makes sense, that while I won’t be writing from a perspective of sitting across from My Love reporting current actions, I can share the rest of the story. And I will in months ahead.

I hope you will check in here once in a while when I, and perhaps new guest authors, share more information for caregivers. There will be static posts on this site as well as periodic blog postings. I put most on static so it is sort of organized. I know no other way!

Thanks to you and those we met along the way, for support and kindness toward My Love and me, and toward other caregivers. Thank you for being examples of how kindness is the way for us all to live. I am glad our paths crossed.

Have you had a chance to read “Imagine You Have Dementia

Love and be well. It’s a beautiful life!
~ Judy

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© 2023 Judith Allen Shone


Caregiver Heroes– These books are for you! Insights revealed from the moment of diagnosis, through the years while I was always learning. Then through the harder years when he was progressing along the Alzheimer spectrum. I wrote to share so others won’t feel so lonely or alone, and hopefully will look for help and comfort during those desperate years.

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