What has changed in a year and a half
Greetings all.
In September 2023, I moved both my parents into my home. My dear mom has Alzheimer's. My dear dad has mild cognitive impairment. They are 85 and 87 respectively. For more background, see the discussion at https://alzconnected.org/discussion/64542/moving-my-folks-into-my-house#latest
btw - I copied and pasted the link to the prior discussion on this forum….maybe it works. maybe it doesn't. moving my folks into my house
In the year and a half since they've lived with me:
My DM's disease has progressed.
- She can no longer attend her day program 3 days a week.
- She uses a walker to navigate the home.
- She is currently on Home Health Care provided by the local medical center.
- She will be reassessed by the physical therapist today.
- Her short term memory is short.
- She often asks the same questions repeatedly.
My DD is displaying more frequent signs of mental decline.
- His executive function is not as keen as it was 2 years ago.
- His most recent SLUMS score was 24 out of 30.
- DD is a retired engineer. His focus remains solving the disease, instead of dealing with the condition we are in.
Our current care team has included additional private caregivers:
- Me
- My Dad
- Private caregivers
- MWF 8-3:30 pm
- Tues and Thus 8-7:30 pm
- Saturday 8-1 pm
My goals:
- Survive caregiving
- keep my folks and myself clean, safe and calm….happy would be nice, but I have accepted that happy is a bonus, not a requirement
- maintain boundaries to keep me calm which include daily exercise and a hobby and a volunteer activity and time with my best buddy Hap (my dog)
Overall, our set-up is very good. But it is still stressful. This is a difficult, chaotic and unpredictable journey. I still HATE THIS DISEASE.
Blessings to you all.
Lady Texan
Comments
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LT- so good to hear from you. I’m so sorry though that you are having to deal with this double duty after going through it with your spouse. I’m glad you are using caregivers this time. I don’t think I could do it again so soon after my parents - and they were in an AL.
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@LadyTexan
I think of you and your situation often. Thanks for checking in although I wish the news was better. Give good old Hap some scritches from me.
HB0 -
@LadyTexan Folks on the "Just need to talk to my Friends" 208 are asking about you and if you are ok after the storms in Texas. Just wanted you to know we are thinking of you. ❤️
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Thank you JeriLynn66. I am grateful to share that My family and I are safe. My community is hurting. I am definitely shaken. I will write soon.
Peace and grace to you all ❤️
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Miss your clear voice and organized way of viewing caregiving
When you get a chance I, and I'm sure others would love to hear from you.
Wishing you the best
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Greetings all.
It has been quite a while since I have visited ALZconnected. I have missed you all. This resource was a life saver as I muddled through the Alzheimer's journey with my dear husband Jesse. After Jesse's death, I put on my caregiver cape (blue gloves) again, to care for my dear mother.
I seriously could not have survived without the knowledge, skills and support of the caregiver warriors here. I will check in again soon. Much has changed in my life. One constant that remains: I HATE THIS DISEASE!
Blessings to you all.
LT
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@LadyTexan
It's lovely to hear from you.0 -
Hi LadyT - agree - Great to hear from you.
also agree - HATE 'this' dreadful thing. Still dealing with it, and yes, grateful for the wisdom and support on this forum.
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Catch us up when you can!
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Hi Lady Texan, it's wonderful to "see" you again. I have been thinking of you recently, hoping you and your family were makin' it through ok.
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The Texas Hill Country, including Kerrville, had another flooding event. My family and I are safe. Thank you for your thoughts and prayers. ♥️
2
Commonly Used Abbreviations
DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
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