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Q&A from Facebook

Caregiving For Dementia

Release Date: 04/12/2019

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

Once again this week I was on
Facebook. I was in some of the caregiving for dementia support group’s, and
I’ve got a few questions that I had answered and I thought I would just make an
episode out of the questions.

1:33 – 4:40         The 1st question that I come upon was, someone had
said something about getting their loved one in iPhone and iPad or an android.
I wasn’t really sure why they were talking about it, but my advice to the
writer was, don’t do that. Here in the house, Mama has times when she likes to
throw things and if we were to get her something like that. Mama is not a very
techie person, but if we were to get her something like that and she got into
this mood where she would want to throw it. She would just throw it not
realizing what it was or how expensive it was. You’re not only out the money of
the gadget, but you’re also out the money for the contract that you have to
have. Plus you would be out the money to get whatever it was fixed. So I
suggested due to the fact of the expense not to get an iPhone, iPad, or android
for this person.

4:40 – 8:00         Someone was talking about bringing their kids, or grandkids,
or great grandkids, to see their loved one in a nursing home. I suggested to
the writer to bring the children around as much as possible. You see, we now
have a lady from our church come in and sit with mom of 2 days a week. There
are times when this lady needs to bring her grandbaby with her, who is only
about a year old. Mama seems to perk up, Mama seems to be more alert, more
awake. Long story short, Mama seems to be more live with the child in the
house.

8:00 – 10:52       I also suggested to the writer, though if the children were
not able to come around, for the writer to get a baby doll about the size of a
new born baby for their loved one to play with. It’ll also stimulate them to
where they are more alive.

10:52 – 12:20     I’ve seen some film for Facebook, where people have give their
loved one, a newborn size doll baby and their reaction to that doll, and now
I’m not to put Mama on film for Facebook are you to be the one. I’ve been asked
not to put Mama on any kind of film for anything other than just pictures.

13:30- 16:45       Question number 3 was from another caregiving support group
page on Facebook and the question was whether or not someone with dementia
actually heard what you were saying or not? My answer to this question was, yes
they do hear you when you talk. I know every time we tell mom that we love her
we get yeah, love you too, and sometimes we get. I love me too, and then she’ll
laugh. So yeah they do hear you when you talk to them. They understand what you
say.

16:45 – 21:01 question for from of
support group page from Facebook was is it normal not to feel anything when a
loved one that you been taking care of passes. I don’t know what to say here. I
hope it’s not normal. I hope that I would feel something, but I know from the
family that has taken care of someone there seems to be a double feeling sort
of I guess yeah, there’s sadness their sorrow that there they’re gone, but
there seems to be as well. A feeling of relief, relief because it’s a lot of
pressure off with a off of you relief because it’s the blood loved one is not
suffering anymore. But yeah, there’s still the sadness there they’re still the
morning there. There’s still the sorrow there. My only advice that I was able
to give in the Facebook group was that put 1 foot in front of the other take it
day by day, moment by moment, because it gets easier as time goes on. So I’ve
been told you never forget them, but it seems to get easier as time goes on to
do things without them.
21:02
– 29:00     I want to throw out a question
to everybody, the question is would you like to see caregiving for dementia
turn into a live Q&A? Do you think it
would be a better show? Do you think it would be more of a help? Or would you
rather just have me sit here and talk like I have done for the past to have
years?