Placement acceptance
Comments
-
Hi Saya-G-
It actually took my dad a whole lot less time than I expected as he tended to be a challenging individual-usually by choice- whenever possible.
He was stage 6ish with mixed dementia. His progression always seemed atypical in a lot of ways- the physical aspects of the disease always manifested earlier than expected while skills like speech and some memory remained better than one would expect. He was already in the stage when keeping his weight up was a challenge.
On admission to MC, dad was ambulatory- mostly a shuffle and unsteady on his feet. He would sometimes fall or even just crumble to the floor. He was mostly able to self-feed a range of foods- soup, ice cream, pasta, sandwiches, etc but not cut meat. He was not reliably continent, especially his bowel control but I think that was complicated by radiation for prostate cancer. He mostly remembered close family (me, mom, his grands) but was hazy on my husband of 35 years and couldn't recall if my sister was dead or alive. He was having a lot of hallucinations and delusions by this point- that his brother lived in another wing, that his golf buddies were in his room visiting, that he'd went clubbing in the basement of the MCF. His speech was remarkably intact- he was conversational until he died.
He was really angry for the first 2 weeks or so. His MCF wasn't one that suggested a period of no-contact, so mom and I visited daily initially. About 2 weeks in, we settled on one of us stopping in for a short visit daily. Sometimes, he and mom would have an afternoon nap together which he enjoyed; I usually came at lunch with something he might enjoy eating and a snack for later. The MCF had a monthly family event and the only picture I have of dad smiling in the last 6 years of his life was from a Valentine's party about 3 weeks after he moved there.
Hang in there. It gets better.
HB1 -
My mother was placed in memory care at very late stage 5 or early stage 6. She was physically still extremely healthy but incontinence and night waking hastened the decision to move her from home. The first two weeks were horrendous, the next two were slightly less horrendous, and about the 6 week mark she started to settle in and accept it. By 8 weeks she was happy and content, and has since had a great experience in long term care for the last 3 years. Hang in there, the early days are rough on both of you but it will get better. We had the best luck calling it temporary, the doctor ordered it.0
-
My mom, 91 at the time. Probably early stage 5. Still doing ADLs- needs cueing, shower resistant, no short term memory, unaware of time, year, weather. About 4-6 weeks to start to make sense of the routine of the place, about 3 months to really settle in.0
-
Here five years later—hoping to place DH soon—-so grateful for these words!!!!!!!
2 -
Kind'a glad this thread came back to the top… Just placed mom-in-law last week.
It is going rather, umm, ok, as far as I can tell. She wants to go home, but she wanted to go home when she was home. So no surprises there. We were able to get her in a bit faster than we thought, so it all worked out. She is probably mid-stage 6.
She is great eating with finger-foods, sandwiches, and the like, other things need to be cut and need a spoon. But the MC is doing great with that, because I'm sure they are used to it.
We made sure to label everything, and yes, the center agrees that they tell the folks 'doctor's orders'.
@AlzWife2023 ((hugs))
1 -
I hope things continue to go well @SusanB-dil
I hope all goes well for you @AlzWife2023
Peggy (my sister) was later stage 5 when I placed her .. fairly high functioning. She still had her phone, and knew how to use it!
She was pretty angry about memory care for about a week, and had one memorable meltdown, but after that she was good. She actually told me that she wished she had moved there sooner (!!)
1 -
Thanks so much @GothicGremlin .
She does seem to be fairly settled. I guess as well as to be expected. Stage 6, probably middle-to-late. We know having her at home, we did all we could for as long as we could.
0 -
I hear you. My DW was also stage 6 middle to late. It just got to be too much for me with the incontinence, helping her to eat, refusing showing, refusing to change her depends etc. I placed my DW into memory care going on three weeks now. She has adjusted better than I could have imagined. It has still been a tough journey for me. Even with all the work, I still miss her being at home. I visit her a few times a week and I know she's doing well. The adjustment for me is tougher than I thought.
0 -
I can soooo relate to that. ((hugs))
And now she isn't at the house, so she isn't there for dinner. Now I am finally missing what 'was'. Because although 'this' isn't her, but she was still there. sort of. You really can't explain it to someone who hasn't 'been there/done that'! And I know the wonderful folks here 'get it'.
Mom is also settled in. Brother placed her into the AL section when she was probably late stage 5 after dad passed. They were able to move her within the same facility to MC upon further decline, and she seems rather content, and sometimes even happy. She no longer refers to me as her sister, so now she has no idea who anyone is, but still greets everyone with a rather chipper hello.
2 -
I placed mom when she was stage 4. After 3 1/2 years she still doesn’t understand why she needs to be there. I guess she has accepted it, but only because she recognizes there is nothing she can do about it. She seems content and enjoys socializing and participating in activities. She usually isn’t openly angry, but I can’t help but feel a bit of tension in our visits. I think carefully before I at anything. I avoid any discussion of her house. Even bringing holiday decorations from her house can sometimes upset her. On a good day she said I know you are just doing what you think is best, but what you’re doing is wrong, I don’t belong here. I find there is an ebb and flow to her moods. She will be chipper and in a good mood for a few months then everything turns and she is furious I stuck her in a home. I think everyone is different. My mil never complained and was perfectly content.
0 -
My wife was probably in late stage 5 or early stage 6. The staff told me that the only problem she had was learning which room was hers. After that, she would still sometimes sleep in other residents' rooms
0
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
Read more
Categories
- All Categories
- 706 Living With Alzheimer's or Dementia
- 409 I Am Living With Alzheimer's or Other Dementia
- 297 I Am Living With Younger Onset Alzheimer's
- 19.2K Supporting Someone Living with Dementia
- 5.9K I Am a Caregiver (General Topics)
- 9.4K Caring For a Spouse or Partner
- 3.4K Caring for a Parent
- 249 Caring Long Distance
- 208 Supporting Those Who Have Lost Someone
- 13 Discusiones en Español
- 1 Vivir con Alzheimer u Otra Demencia
- 1 Vivo con Alzheimer u Otra Demencia
- Vivo con Alzheimer de Inicio Más Joven
- 12 Prestación de Cuidado
- 3 Soy Cuidador (Temas Generales)
- 8 Cuidar de un Padre
- 23 ALZConnected Resources
- View Discussions For People Living with Dementia
- View Discussions for Caregivers
- Discusiones en Español
- Browse All Discussions
- Dementia Resources
- 8 Account Assistance
- 15 Help






