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Mental Stress

Caregiving For Dementia

Release Date: 03/08/2019

27 Months Without Mommy show art 27 Months Without Mommy

Caregiving For Dementia

This is just an update of the family. 27 Months after losing Mommy!

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Life After Caregiving Part 2 show art Life After Caregiving Part 2

Caregiving For Dementia

This Episode is a continuation of what went on after Mommy was picked up.

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Life After Care Giving show art Life After Care Giving

Caregiving For Dementia

This is the first of a few episodes that goes through what you may feel right immediately after your loved one passes away. There's not a whole lot of show notes of these episodes it's just me talking about what happened immediately after mommy's death. What I thought would happen that didn't and that kind of thing. I hope these few episodes help you get along for a few months immediately following your loved one's death.

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A Happy Thanksgiving Message show art A Happy Thanksgiving Message

Caregiving For Dementia

This episode is a brief message to all those who are still downloading the podcast happy Thanksgiving to all

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Caregiving journey ended show art Caregiving journey ended

Caregiving For Dementia

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The hardest talk a family can never have. show art The hardest talk a family can never have.

Caregiving For Dementia

Episode # 93 There comes a time in caregivers journey that they know time is very close to running out. We hear caregiving for dementia have realized that fact. The past five days Mama has not eat anything at all, the past four days Mama has not drank anything, and for the past three days Mama’s been very hard to wake up at all. When she is awake it’s about two minutes and she’s right back out. Mamas, breathing has also changed its no longer normal breathing. Doesn’t look the same, doesn’t sound the same as the normal breathing does Mama breeze through her mouth...

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Things we take for granted as Caregivers show art Things we take for granted as Caregivers

Caregiving For Dementia

Episode #92 Show Notes There are so many things in life that normal people take for granted. This becomes more apparent the longer you take care of your loved one. There are things that I take for granted because there things that come natural to me that Mama can no longer do for herself. Mama can no longer wash her face, brush her hair, brush her teeth, or even talk. Mama tries so hard to talk to us and you can see the frustration in her face as she tries to say something and can’t. Mama tries to hold a cup of something to drink and because of her Parkinson’s she...

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Caregiving Mistakes,Regrets show art Caregiving Mistakes,Regrets

Caregiving For Dementia

In your caregiving a lot of times you do things in the heat of the moment. After time goes by you wonder whether or not what you did was the right thing to do.

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Caregiving Mistakes/Regrets show art Caregiving Mistakes/Regrets

Caregiving For Dementia

Episode #91 Show Notes In your caregiving a lot of times you do things in the heat of the moment. After time goes by you wonder whether or not what you did was the right thing to do. A lot of caregivers won’t tell you everything that they go through in their caregiving. I am one of those people who won’t tell you every little thing that goes on in in the house with the caregiving I am one that won’t tell you what Mama has done to us I won’t tell you what we’ve done to Mama. What I tried to do in this podcast is tell you what we do and what we don’t do because...

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Know It All Doctors show art Know It All Doctors

Caregiving For Dementia

While in your caregiving journey there will be a lot of things that happened that you don’t understand. I know when not when we first started there was a whole lot that went on that we didn’t understand there’s a whole lot that I haven’t gone into with this podcast that went on when Mama first got dementia. That’s one reason why I started this podcast

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More Episodes

Mental Stress

Episode # 75

In this episode, I talk a little bit about mental stress while
caregiving for our loved one. There are a whole lot of things that goes on that
I don’t share in the podcast. There may come a time when I’m able to do so, but
as of right now I don’t feel comfortable sharing everything that goes on.

There’s a lot of times when there is of good bit of back and
forth between Stephanie and I, Michael and I, Stephanie and I and Michael that
we don’t go into in the podcast.

There’s a lot of things that Mama does and says that she
would not do or say, if it were not for this devastating disease of dementia
and there are times when you have to step back and catch your breath to where
you can handle some of the things that are said and done that are quite hurtful
at times

I do not have any real good answers for anyone who’s dealing
with stress while they are caregiving. My solution a whole lot of the time is
getting on the computer. This is where I spend most of my time that I’m not
caregiving for mom.

I also honestly do not think that the doctors have very good
answers, either, except to push pills. They don’t even seem to know where this
dementia comes from, or even how you get it.

You also have some mental stress when you 1st
start taking care of a loved one with their medications, especially if you are
on medication yourself for an issue. You worry about whether or not you’re
giving them too much or not enough of their medications, but you work through
it and you relax as time goes on.