Am I losing it too?

Posted by wtr2026 @wtr2026, 4 days ago

Two weeks ago, I had my annual wellness visit and I scored 100% on the memory test, including counting back by 7's. Last week, my husband's brain PET Scan results came into MyChart. He has Alzheimer's. Since then, we have looked at senior living communities in person and rented an apartment near our children. I feel as if I can't remember anything and I think I misplaced my son's house key. I don't want to think I am losing it, yet that's how it feels. Very worried. Has anyone experienced this and did it resolve for you? Thank you!

Interested in more discussions like this? Go to the Caregivers: Dementia Support Group.

Profile picture for judimahoney @judimahoney

@georgescraftjr
Thanks ☺️
I am currently the only one awake, so I said, "Happy f@#&ing birthday" to myself.
Life is so weird right now, like we're all in a bad movie.
I will attempt to enjoy my birthday today, thanks so much for your kind words. 🤗

Jump to this post

@judimahoney Hope you have a sweet birthday!

REPLY

My husband was diagnosed with Alzheimers in 2018, but it is progressing relatively slowly. He's at home and with a little coaching can perform his ADLs. But I've noticed that I've started sundowning!
I can handle his repeated questions, etc., with equanimity during the day but after he gets up from his nap, around 5 pm, my temper is very short and the repetitions drive me crazy. He probably asks more questions then, too, and is more anxious (his own sundowning) but it was a real AHA moment to realize that I need to manage myself better in the evenings, and not be annoyed with him.

REPLY
Profile picture for annedallas @annedallas

My husband was diagnosed with Alzheimers in 2018, but it is progressing relatively slowly. He's at home and with a little coaching can perform his ADLs. But I've noticed that I've started sundowning!
I can handle his repeated questions, etc., with equanimity during the day but after he gets up from his nap, around 5 pm, my temper is very short and the repetitions drive me crazy. He probably asks more questions then, too, and is more anxious (his own sundowning) but it was a real AHA moment to realize that I need to manage myself better in the evenings, and not be annoyed with him.

Jump to this post

@annedallas you've lived with caregiving for such a long time. Do you know about the Guide Program? https://www.cms.gov/priorities/innovation/innovation-models/guide. It's a demonstration project to see if providing support for caregivers can keep people with dementia at home longer. Part of it is funding for some home care so the family caregiver can have a break. If you had someone during the early evening hours, that could be a godsend for you. It's human to get annoyed I think. Sending a virtual hug.

REPLY
Profile picture for dsand3 @dsand3

I felt that way yesterday! Forgot groceries in the car because I rushed in the house because we had a visitor! Seems there is so much to do, since you are thinking for two people. Seems like I’m living with a guest in my house sometimes, he rarely takes an active role or sees what needs to be done. It’s exhausting both mentally and physically. I’m looking forward to moving to a CCRC when it’s available. This situation is tough and we must give ourselves grace as maneuver through this new life!

Jump to this post

@dsand3 We only have Walmart as a grocery store and we are 25 min from the store. Yet they have in home delivery. It does cost $100 a year but there were half price sales last Thanksgiving. You are encouraged to tip. It's been a fabulous time saver for me.

REPLY
Profile picture for annedallas @annedallas

My husband was diagnosed with Alzheimers in 2018, but it is progressing relatively slowly. He's at home and with a little coaching can perform his ADLs. But I've noticed that I've started sundowning!
I can handle his repeated questions, etc., with equanimity during the day but after he gets up from his nap, around 5 pm, my temper is very short and the repetitions drive me crazy. He probably asks more questions then, too, and is more anxious (his own sundowning) but it was a real AHA moment to realize that I need to manage myself better in the evenings, and not be annoyed with him.

Jump to this post

@annedallas I've seen others suggest having a white board on the fridge with the day's activities to cut down on the questions. I've gone to a pocket planner by his recliner. I fill in his sports schedules for the whole month along with any other activities either of us have. He can just reach over and get it, which he does maybe twenty times a time. That has helped somewhat to save my sanity.

REPLY
Profile picture for grandmajoan @grandmajoan

@judimahoney Hope you have a sweet birthday!

Jump to this post

@grandmajoan
Thanks, it was OK.
Love the cake painting!

REPLY
Profile picture for wtr2026 @wtr2026

@annedallas you've lived with caregiving for such a long time. Do you know about the Guide Program? https://www.cms.gov/priorities/innovation/innovation-models/guide. It's a demonstration project to see if providing support for caregivers can keep people with dementia at home longer. Part of it is funding for some home care so the family caregiver can have a break. If you had someone during the early evening hours, that could be a godsend for you. It's human to get annoyed I think. Sending a virtual hug.

Jump to this post

@wtr2026
Wish we qualified for that program, it sounds great. We have Medicare Advantage so we're ineligible (I call it Medicare disadvantage).

REPLY
Profile picture for judimahoney @judimahoney

@wtr2026
Wish we qualified for that program, it sounds great. We have Medicare Advantage so we're ineligible (I call it Medicare disadvantage).

Jump to this post

@judimahoney I'm afraid you are right - although my sister and best friend have both done well with their Advantage plans. I'm going to sign up and will share how it goes.

REPLY
Profile picture for dederickve @dederickve

Well, wtr2026, this past week, I have had several bad moments of forgetting , confusion, thoughts of “is this actually happening , to me ? ! “ I talked to my doctor about it, yesterday. She said, stress, all the very hot weather, and I think also, too much to have to try to take care of, or try to get taken care of. The word to sum the causes would be OVERWHELMED ! Try not to worry too much ! You are more than likely, fine !

Jump to this post

@dederickve Thank you so much. Overwhelmed sums up our situation well. A long time ago, when I was facing a serious challenge said "You're going to get through this one way or another, you might as well get through it well." Of course I was a lot younger then :). My new mantra is "I can do hard things" - I don't quite believe it yet. How wonderful your doctor sounds. Thank you so much for taking time to help me!!!!

REPLY
Profile picture for Kathy @4goakley

I appreciate this post. I too have had periods of temporary memory loss caused by stress.
Thank you for the reassurance that we are not "losing it".
We are overwhelmed by our responsibilities and it is our body’s normal reaction.
Strength and courage !

Jump to this post

@4goakley Strength and courage - a winning combination. Thank you for saying this is our body's normal reaction.

REPLY
Please sign in or register to post a reply.