Taking Loved Ones from Memory Facility for a Holiday
I have moved from physical caregiver to an overseer, an advocate, a visitor now that my husband is in a Memory Care Facility. Each day feels like a learning curve. The book 36 Hour Day has a chapter about taking residents out, but it is clear, that every resident is different. My daughter and I took my husband to a nearby doctor's appointment. It was the first time out of the building in 3 weeks. Returning to the facility spun him around, and he had great difficulty reorienting himself again after acclimating very well initially. I would welcome comments on how to make this transition easier on the family and the loved one. Holidays are coming up and bringing my husband out of the facility to home with many family members whom he no longer recognizes may be too much. I'm looking for advice from people who have done this. My daughter asked," Are we bringing him over for a holiday celebration for him or for ourselves?" I'm very concerned that it would cause more harm than good.
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When my father was in memory care we did not bring him home because we feared it would cause him more confusion and anxiety. For special occasions the facility always had celebrations on a day around the holiday. One or more of us always attended and he had no idea what the date was. I think we, at first, overestimated his ability to reason and keep track of time. Once we settled in to this new routine all was well.
I hope this helps.
I had multiple reasons to not bring my LO home from Memory Care for holiday celebrations. One was her mobility and inability to walk. The house was not equipped for her wheelchair. And, she was fully incontinent. Also, she became disoriented and upset whenever she left the facility and returned….even for doctor appointments. We took the party to her instead. We took her gifts, treats, decorations to the facility and celebrated there. She tolerated that pretty well.
Home trips may work for some, but not in our case.
Thank you. Yes, your comments do help. I find solace in hearing from those of you who have walked the walk.
The facility did a fabulous Halloween buffet with great decorations. They make an effort to bring the fun to the residents. I don't know how this will turn out in the future, but for now, we are going to let my husband find his footing there.
Sometimes taking loved one out of familiar environment can be very stressful for them and very disorientating.
Just from my experience it did complicate my wifes situation in Memory Care. I was told by the CNA's that I should not do it for some time but I didn't care, I wanted to bring her home often and it turned out that they were right because it did confuse her and it was really difficult getting her to go back. After a few tries at it I stopped taking her out for a few weeks and it did help lessen her confusion over, where does she belong in her eyes. It was very hard on me to not be able to take her home because that was always what she wanted to do, was to be at home. I felt guilty doing so which hurt me a lot but it did help her acclimate better to the memory care estab.
thank you for sharing about the article on taking your loved one out for an excursion. I haven’t come to that point yet so it was good to read these comments right now. We are at the stage where hubby is still at home but showing more and more signs so, I took him to a beach excursion to watch our church baptisms. He grumbled about going and was in a depressed place; nevertheless, As soon as we went for a drive, got to sea and sunshine with church friends and Acquaintances, his demeanor lifted. No sooner did we return home, the dark side Resumed. I just happened to read these comments and kind of connected the two situations.
Every day is a new day and is totally unpredictable. As much as you would like to live your life logically and on a straight path, that isn't how it works. It may be that taking him to the baptisms again would be upsetting, and he may not be able to convey why he feels that way. My husband has always remembered his sister and lit up when she called. Last time, we Facetimed and he turned away refusing to speak to her. "For what purpose?" was his comment. I figured out that his sister must be 19 in his mind, not the 86 year old woman who was on Facetime. The next time she called, we made it just a phone call and that was fine. You just have to keep batting the ball, no matter where it lands.
You make good points about expectations. I learned to curtail my expectations of what my loved one might enjoy, as opposed to what someone who didn’t have dementia. I would imagine she would enjoy adult coloring books, music CDs, and a tv. Problem was that she no longer had the ability to focus on coloring. And, she never thought of turning the tv on or putting music on to play. Someone had to do it for her. She could only give her attention to certain things for short times. So, all these activities I thought of for her weren’t feasible. Short activities with direct supervision by staff were really the only things that worked.
I also learned that things that I thought would make her happy, might not anymore, such as a drive to the country, opening gifts, dining out…….