He was recently placed in a care home during this whole Covid pandemic after a fall and a stint in the hospital. He had a cell phone with him that we could call him on so although it was difficult not being able to see him, we could still talk to him. The care home have misplaced 2 of his phone chargers now that we've brought in and so I've started to call the care home instead to speak to him. They do have a phone booth specifically for calls with the residents or sometimes a portable phone.
I've just been told by a nurse today I can't call him every day and that most families don't do this. He has dementia and also doesn't speak much English (hardly at all) and so doesn't really communicate with the staff or the residents. They already confirmed they don't have staff there that speak his language.
I understand it's not the staff's job to bring him the phone or wheel him to the booth every time but I got a bit upset as I feel if we don't call him, he won't have anyone to speak to all day and with his dementia, I don't think it will help. He already doesn't understand this pandemic and the fact we can't see him at all. I also can relay information to the nurses like the one time he said he was in pain and felt a bit unwell. He can't tell the nurses this.
Am I overreacting? I just don't know if I should limit my calls now as I've annoyed them but then I don't want to leave my grandpa alone. I'm sure it will be better once visits are allowed again but I feel it's difficult in the meantime as we are all a very close family. Any advice would be great. Thanks.
(Sorry for the lengthy post).
It is difficult for residents when they first go in to a seniors home, especially when they have little comprehension of English. Indeed, your calling can help the nurses if there is a problem with the staff because of language problems.
Yes it is challenging for the staff but that is their own fault for misplacing the recharger
You are to be commended for your loving concern. It is sadly lacking in todays society.
I have numerous years experience as a volunteer in seniors homes.
Have you explained all the reasons why you wish to speak with him daily. I think these reasons should be added to his file and posted prominently for the staff to see so that no-one gives you a difficult time in the future. Perhaps you should address you complaint to a supervisor.
You sound very kind and loving. I hope my grandchildren care as much when it is my turn to be in a care home.
I would talk to someone above the nurse/aide level and focus just on the language issue. People with dementia need that contact - it does help a little keeping them more in tune with reality. Since no one there can speak his language, he NEEDS the contact and it should be daily!
I think I would start with finding out what the best times to call would be. IF you start with being amenable and trying to work with them, it might be better than being accusatory. Obviously getting them all up in the morning or to bed at night, meal times and medication times would be the worst time to call. Most of those should be a set time, but medications can happen throughout the day. Still, there should be times that are better - maybe not every day, but most days.
As for the missing charger - I wouldn't hold my breath getting them to replace it. Items go "missing" all the time and they don't replace them. Dentures. Hearing aids. Clothing. Other personal items. A charger would just fall into the same abyss. Mom's hearing aid ended up going through the laundry (we were letting her "maintain" it, with me having to locate it sometimes and change the batteries - I requested they do that every 2 weeks, because she wouldn't remember, but it didn't happen.) The replacement was rechargeable, so I gave the charger to the nurse as mom would likely lose it (mom is in MC, not NH.) Plan was to charge it overnight and give it to her in the morning (she only wore one, so the other was a "spare".) Within a few weeks, maybe a month or so, it was lost - probably wrapped in tissue or napkin and tossed. From that point, they kept taking it away from her, as she kept taking it out. NO was the answer on helping pay the $400 replacement charge (the purchase included loss insurance, so much less to replace than buy new!)
Even with the hearing aid, I chose not to put a phone in her room. She would only use it to call for a ride home or to her mother's. I didn't want her sitting in her room all the time, so no phone, plus even with the hearing aid she had trouble hearing us. No window access. Lock down since 3/16. Hoping she still remembers me when I can finally visit! They are allowing short outdoor visits, with mask and distancing, which in her case will be difficult because of the hearing issue. Not sure what state you are in, but you could ask if they allow any outdoor visits.
If they can't work out a good time to call, perhaps you can work with them to bring the charger once every day or couple of days, and charge it while you wait or return to take the charger back. Usually phone charges are good for 1-3 days, so it probably wouldn't have to be every day. Another option is to have a nurse take charge of the charger and have his phone charged overnight in a safe place.
Will this be his home going forward or is this a rehab type of set up? If it is his permanent home, admin should be willing to work something out that works for everyone. They *SHOULD* be understanding of this issue, since he can't communicate with anyone there! Also, just because other families don't call every day should NOT be a reason why you can't. Some don't have families. Some families don't care. YOU do and that should be something they appreciate!
If they don't want you to continue to call daily ~ ask them to help you come up with a plan and make it STAT... Doesn't take long to forget how to use the phone.
I'm actually happy to hear this coming from a grand-child. He'd be very proud of you.