Followers

Showing posts with label visions. Show all posts
Showing posts with label visions. Show all posts

Monday, July 27, 2026

Fresh Air...


Since moving back home, I find myself sitting out on the front porch every morning, when weather allows. In my younger days, we spend so much time outside and sitting on each other's porch. Just talking, laughing and playing. And I just love this. I love it so much. And when I bought my house well, when I was looking for a home, I was looking for one with a front porch. Unfortunately, you had to live in a certain area to really get a porch. Because further out the houses, are more modern, and the porch was no longer there, they had stoops to sit on.


For those with dementia, fresh air is very good for them. Exercise is good for them, just regular everyday routines is good. However, with my mother, I have some issues getting her to do certain things. Especially sitting out on the front porch. She surprised me one day, asking me did I want to go out on the porch with her? Trust me, I jumped up and went with her. Can you believe we sat out on that porch for 5 hours!  Of course, we had some hiccups here and there, because with Dementia, you're just gonna have it, it's not gonna be a day without some type of little up-and-down. But it was still a good day.

There is one thing I notice with her after sitting on the porch and getting the fresh air was that she was sleeping better. We were having a little better evening, once we go inside too, things were a little calmer. Like I mention, you still have some ups and down. But at least they weren't major (that's what sundownin is).  I am working hard to get her back on the porch. Especially when the weather is very good, we had a couple of cooler days. Because it had been cold or cool  she hasn't want to go out because she thinks every day is cool outside but we're going to get out there as much as possible rbefore the summer ends.

Need more of that...



Friday, July 17, 2026

Caregiver life...

Until you have to pause a good portion of your life, to care for a parent(s), grandparent(s) or a love one, you won't know the decision and sacrifices a person has to make to become a caregiver to someone!

To be honest, I didn't believe the doctor when she told me, mom won't be able to live alone. Not knowing what Dementia was and how it affects the person that has it, and telling me someone needs to stay with her. My mother at that time was still able to take care of herself and still can for the most part. So why did I need to stay with her?

One night, I decided to go home and go back after I went to church. Well I got back to the house, I quickly learned that being gone all night was a big mistake. I found her in a state of confusion and fear. Trust me, I did not do that again. It hurt me seeing her that way, to the point that I was scared that I may have hurt her in some way. That Sunday in early 2025, my life was no longer mine.

Here is the crazy part, I had to change the way I lived my life, for my mother prior to being diagnosed with Dementia. My mother would worry about me, especially at night. If I had somewhere to go at night, I learned she wouldn't go to bed until I got back home, and call her to let her know I was in the house. It was so bad that she would not go to bed until she heard from me. 

Since moving back home with her, I have learned just how deep this worrying and fear she has, been going on for many years, and as far back as childhood. My mother has so much fear and worry in her still with this Dementia to a point it is scary for me. You would think she would relax now that I am living with her, but that is not the case.

I wish it would stop, but I know it won't until the final call from the Lord. So I got to find a way to adjust to this change and the others that may or may not come.

Grace and mercy goes with us...

Friday, July 10, 2026

Back home...


After 43 years, I am back at my family home. Never thought it would be to care for my momma, but now that I have relinquish the keys to the home I raised my son in, I'm not sad at all, just glad I can be here for the woman that raised me, no matter how hard it may be.

The constant worrying she was doing about me over the years, kept me from doing so many things I wanted to do. I know most would not let that stop them, but my conscious wouldn't let me be selfish that way. So now all the worrying and stress has taken its toll on her. This past year and half has shown me just how much she stress and worry, even when I am in the house with her.

So, I trust God more now, I pray more, I'm becoming Ms Domestic too! 🤦🏾‍♀️😅 And most of all, I need to be here, no matter how hard it can be. 🙏🏿 Yet, I do pray that more family will step up to the plate, and offer more assistance to me, but to be honest, I don't see that happening any time soon. Not sure what it is with family when it comes to sickness that actually needs assistance. It seems everything else is more important than helping love ones. I maybe wrong, and I pray it's not true.

I will say this, I am so thankful for those who has helped me along the way. If it wasn't for them, my move back home would not have been as smooth. God has truly watched over me during this time. The most stressful time is when she doesn't recognize me when she looks at me. That is really painful for me to endure. So as I sit outside to give her mind a break, I pray that when I go back in, she will see me again.

Now you see me, now you don't...

History does repeat itself...

A week or so ago, mother and I had a 11:30am hair appointment.  My only issue was if she would recognize me that morning, so that we will be...