At last my father is going to a AL facility. I volunteered to help him move: my brother, the POA, is orchestrating it. I am an hour and a half away. Dad has early vascular dementia: He is happy about going to this AL. I wonder how to avoid him obsessing with his things as I organize and pack them for him. Got any suggestions?
If they allow them to have a mini refrig, think about getting one and putting it on a stand. This is a big trend for college dorms living. Pottery Barn has refrig, their stands etc in all sorts of colors for the college set that are ideal in size for AL. (We have a recent HS graduate about to start fall semester and dorms are nothing like my college experience)
No rugs!! & do what you can to secure cords & wires so no tripping. Good luck.
You might want to have a box of special items, things he likes to have around him, things that he can choose and pack. Label it with some special marking and have him open it as soon as he moves in. Hopefully it will help orient him and make his new facility have some semblance of what he's just left.
If he has things that remind him of home, the AL facility won't seem as drastically different.
Do you think he'll want to take everything? If so, and if there isn't room, perhaps you could ask/help him to identify what he wants first, indicating that you can pack it and bring it later. That way he's assured that he'll have what he wants but that his other possessions are still available.
Stop and talk periodically during the packing process, if he becomes agitated or obsessive, just reminisce, talk about what he enjoys, places you've gone as a family...soothing things.
Plan to put on CDs (or use an iPod if you have one) of his favorite songs. Again, if he becomes uncomfortable, take a time-out and just listen to music.
Try to make it a bonding session, one in which just a father and a son get together to perform a task, not one in which he's giving up his home.
Perhaps take snack or a lunch break, again just to relax and bond, and reinforce his decision if he begins to waver and become anxious.
Stay with him for quite a while after he moves, and visit the next day so he doesn't suddenly realize the drastic change he's made
Good luck; let us know what works for you!
We had already thinned belongings when he moved from his house to mine, so it was just a matter of packing up his room here and a few things he had in other rooms. For now his winter clothes and old tax papers are in my closet, I will worry about them later.
If you're downsizing from a house he's lived in a long time, it would be good for someone to do a walk-through ahead of the move to identify things that need to go and would be easy to miss. Medicines go at the top of the list. He'll want a favorite unbreakable cup or mug in his room. Tissues, towels, hand soap, toiletries. Batteries for any devices he's taking, including the alarm clock.
Suggestion from a social worker that was the biggest help for us was to have some activity for dad to keep him busy elsewhere during the actual moving process. We were only able to sort-of implement that--he was here while we loaded up his stuff, but I timed the move so we arrived at AL and he was whisked off to his initial visit with their physical therapist. By the time he was done, we had all the furniture in place and most of the rest more or less put away. We rearranged a few things to his preferences, showed him what went into each of the two closets. Pointed out the ice cream in his little freezer! Then the staff came in to introduce themselves, and the director talked to him about his meds and some other key items the doctor had noted on the 1823 form. We departed while that was happening, which I think was easier than if we'd had to just leave him alone.
Whoever is handling the 1823 form, if you have any doubts talk to the doctor who is completing it about what your dad can and can't handle. The AL is required to go by what the doctor marked, as to whether a person can do various things alone, with supervision, or only with assistance. If I were doing it again I would give the doctor a "pencil draft" with MY assessment of his abilities, since she is not the one who sees him day to day trying to dress, make phone calls, etc.
For my mom, she had lewy body dementia and although she was not blind, lewy for some does vision issues. She would see flooring with patterns (cobblestones) rather than flat carpeting or wood.. Odd shadows - to me the way she said things were was like things were lit with "cookies" aka cucoloris. Lewy has walking issues (tend to do a flat foot shuffle) so all this were an issue for her walking & gait. When she was in IL, I got rid of any dark and deep shelf furniture and got her shallow shelf furniture light in color and lower in height. Think IKEA birch rather than Ethan Allen mahogany. I Put torch lamps on timers in all rooms at her IL so there would be set time for daylight & night whether or not weather cooperated. For whatever reason, mom would not fuss with floor lamps but would with table lamps on timers. Why, well who knows, also put highest wattage bulbs you can.
If he has a private bathroom, figure out a light in there. Facility won't like a corded light but maybe you could get a motion sensor light battery operated to go on. Mount it with that 3 M sticky tape. college dorms don't let them nail stuff, so right now stores have mounting tape, sticky stuff, lightweight frames, cheaper lamps, etc for college in stock.
Also stuff just walks no matter how nice an IL, AL or NH. Sharpie or laundry marker clothes, shoes, anything fabric, etc. For my mom, I also put her initials & a little leaf design in screaming fushia nail polish on toiletries, brushes, eyeglasses, anything hers with a hard surface, etc. Nail stuff now comes in all colors, neons & metallics so you could find a "guy" polish to mark his stuff. Will make it easier to find stuff that walks.
I was so worried the first night he was alone in his new place, it was like giving up a kitten for adoption, you wonder about their first night away from home.