Advocacy, Death & Dying, Life & Living

a young hospice nurse makes a promise to her dying patients

Emily Gagnon is a hospice nurse. She lives in Waterdown, Ontario. Her Facebook post to mark the end of National Nurses’ Week 2020 brought me to tears:

“As we wrap up National Nurses Week 2020, I’d like to share a little bit about what I do as a hospice nurse. For those of you who are not familiar, hospice is a facility where people come to live out the remainder of their days. Many of the residents that I care for have a terminal and/or life limiting illness with limited time left to live.

What I love most about hospice is watching the residents and their families surrender all of the burden they carry and make the best of the time that they have left. In my three years of practice, I’ve witnessed miracles, tragedies, beauty, pain and everything in between. Residents and their families put all of their trust in us to ensure their wishes are fulfilled and their dignity is maintained.

I am honoured to care for, help and serve the residents that come to our hospice. End of life care is my biggest passion, one that I hold so close to my heart.

I will sit with you and hold your hand.

I will brush the hair from your brow.

I will do my best to explain why this is happening.

I will tell you that it’s going to be alright.

I will comfort your family as you transition.

I will tell you when there are weeks and not months, days and not weeks, hours and not days.

I will be there for you till the very end and beyond, this is my promise.

Thank you Emily and your fellow hospice nurses. Thank you nurses everywhere.

3 wise thoughts on being with someone you love as they die, which also apply to being with someone with dementia as they live

3 things to know when you can’t be with someone you love as they are dying

understanding the suffering associated with dying

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Advocacy, Death & Dying, Life & Living

3 things to know when you can’t be with someone you love as they are dying

Palliative care physician Dr. Mike Harlos gives advice to other palliative care doctors and nurses on how to best support people who are dying, as well as their family members and friends who may be going through the process with them. I love Dr. Harlos’s wisdom and gentle manner, which I have also featured here, and here I wish I had known of these videos before I sat by my mother’s side as she took her final breaths.

According to Dr. Harlos, there are three important things people should remember if they can’t be with a loved when he or she is dying:

  1. Not being in the room at the time of death does not mean you are absent at the time of death
  2. You are connected in spirit and in soul to the people you love
  3. Connection does not require physical proximity

When a family can’t be be present at the death from Canadian Virtual Hospice on Vimeo.

 

3 wise thoughts on being with someone you love as they die, which also apply to being with someone with dementia as they live

understanding the suffering associated with dying

dying with my mom

 

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Care Partnering, Challenges & Solutions, Toward better care

7 ways to transform dementia care grief and suffering into joy and healing

Are you a dementia care partner who lives in a world full of grief, loss and suffering? What if you didn’t have to be in that dark, depressing place? What if you could transform your suffering into healing? What if you could release your feelings of grief and loss?

Moreover, what if changing your world was simply a matter of changing your perspective? Would you choose to do it?

When I chose to reframe the way I saw dementia and the people who live with it, I completely changed my experience as a care partner. Others have done the same. Here’s an excerpt from an email I received from FK, a long-time follower of MyAlzheimersStory.com:

Susan,

I really need to thank you so so much for changing my perspective on what was happening to my parents as they both lived with dementia. I have responded to your blog from time to time, mentioned that I was caring for my parents, both of whom had Alzheimer disease, and shared my experience about being with my sister when she died when your mom was approaching that point.

I had moved to [Some Little Town] from [A Big City] in 2011 when my parents began to lose their abilities to live independently, and I eventually became a full-time care partner.  For the first few years after I noticed the first signs of memory loss, I was stuck in that  intense grieving phase and could only see the losses and mourn what felt like my parents disappearing before my eyes.

But after discovering your site/blog and following it, I gradually learned to see that they were still there, still my parents, still loving and able to share many things with me.  My focus changed from mourning each new loss and grieving what lay ahead in the future, to living with them in the moment and trying to share as many moments of joy as possible.  That made a world of difference.  I was able to love them and keep sharing laughter and love until they died (my dad on April 02nd, 2017 after a long, slow decline and many false alarms; my mother very unexpectedly the very next day, April 03rd, 2017.  Thanks to you, I look back on those years as, in many ways, a happy time despite all the difficulties, frustrations, fears and tears.

I lost a legal bid to get control of my mother’s care in February 2014. Shortly thereafter, I launched MyAlzheimersStory.com. I wanted to share my journey and learnings as a care partner, and help others avert some of the challenges and pitfalls I had faced.

As I learned more about Alzheimer disease and other illnesses that cause dementia, I also came to realize we can radically change our experience of dementia and the people who live with it by reframing the way we see it and them. Helping people transform their experience from suffering to healing has become an integral part of my advocacy–one that’s working as FK’s email demonstrates!

Here are seven ways you can reframe and change your dementia care experience:

  1. Focus on what remains rather than what has been lost
  2. Look for potential rather than staying stuck in deficit
  3. See the person, not the disease
  4. Understand that people who live with dementia are still people, not “empty shells”
  5. Understand that people who live with dementia have the same needs we all have
  6. Create opportunities to experience joy and happiness
  7. Find things to laugh at instead of things to cry over

I did it. FK did it. You can do it too.

17 links to the “other side” of dementia

do you see what i see?

3 excerpts from the best article on dementia i have ever read (and a link to the full meal deal)

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Advocacy, Death & Dying, Life & Living

understanding the suffering associated with dying

Palliative care physician Dr. Mike Harlos gives advice to other palliative care doctors and nurses on how to best support people who are dying, as well as their family members and friends who may be going through the process with them. I love Dr. Harlos’s wisdom and gentle manner, which I have also featured here, and I wish I had known of these videos before I sat by my mother’s side as she took her final breaths.

The thoughts Dr. Harlos shares in the three-minute video below won’t stop the pain of being by the side of someone you love as she or he nears death, but the reflections and advice might alleviate the pain a little; they might ease the suffering overall, and thus allow for a deeper, richer and more meaningful final life experience.

Final hours at the bedside: Is my loved one suffering? from Canadian Virtual Hospice on Vimeo.

Here’s a transcript of the video:

“In palliative care, we don’t treat pain or we don’t treat shortness of breath, we don’t treat nausea; we’re treating suffering. We’re helping people with suffering. Suffering is the total experience related to a certain issue. So the person with pain is experiencing a physical symptom, but there’s also a meaning to that symptom, there’s an emotional context to that symptom, there’s a spiritual context, there’s a cultural context and that whole package is the suffering.

Sometimes the suffering is mostly physical, and sometimes it’s mostly spiritual or emotional or cultural and sometimes it ripples out to others in the room, and you can actually sometimes be aware of the total suffering in a room. So when someone changes, when someone is declining, it’s often seen that this person is suffering, even if they look comfortable. In fact families might say in the same breath “he had a good night, he looks good now, I think you’re on top of the pain,” and there might be a pause and then they might say “how can you let him suffer this way? You would not let an animal suffer this way.”

That sounds contradictory, and how I would try to discuss that is to say “I understand that this is really difficult to be part of and to watch. You’ve just mentioned that he looks comfortable, so I’m wondering, I’m wanting to hear more about what you’re seeing as suffering. Sometimes when people describe that they’re describing the total suffering related to this circumstance and that includes what he’s going through and what you’re going through. And I think he’s comfortable, and I’m wondering how we can help you with what you’re experiencing, which I think is contributing to what you’re feeling as his suffering.”

Also I think what people are describing in that situation isn’t so much his physical comfort, it’s the huge gap between who he was and who he is now. And often in the last few hours of life particularly, there are physical changes that happen that you can’t change. Like people lose weight, their skin colour changes because there is not enough oxygen being circulated, they become cool. And I think it’s important to make a distinction between who this person is in their spirit or in their soul, versus the physical changes that are happening to the shell of that person because people might see those changes and think of it as suffering.

Sometimes even the breathing pattern is changed and it almost looks like they’re struggling for air because they’re taking deep breaths, or periodic breathing, and there’s a gasp, and really what’s happening is that their regulatory centre for breathing is changing and becoming weaker so the breathing is erratic and there’s a long pause, and then there’s a big catch-up breath which then may be seen as he’s “gasping.” So it’s important to be aware that some of those physical changes don’t relate to the experience that the person is having. It’s simply the way the body is changing in a very physiological or biological way.”

Thanks again for this palliative care advice and wisdom, Dr. Harlos.

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

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