My mom 86 recently moved to assisted living lost her hearing aid 1st week. She is 86 very hard of hearing poor vision, and dementia. I'm working on replacing her hearing aid they say see needs two now as he hearing is so bad. Her dementia has worsen since loss of hearing aid of course some of it could be new assisted living environment.
I'm worried she will lose her new one how can I prevent or reduce the chances of it being lost. She does wear it all the time except sleeping and bathing.
When my sister was about 4-5 yrs old, got a new pair of shoes, playing in the backyard, kicked, & one shoe came off & went over the back fence down a steep overgrown hill. The shoe was lost forever, never to be found again.
When my mom was 82-3, had fractured hip surgery, which turned bad with anesthesia-caused stroke, so she was in the Restorative Care Unit of the hospital with an NG tube in her nose, her L side was paralyzed, she couldn't speak or eat solid foods - but there was an issue came up about the dental bridge on her front upper 4 teeth. The DDS made a "house call" to the hospital to look & assess -- upshot, in her condition HE opted not to do anything about it.
A couple years before, my dad had been in a convalescent home for PT, OT, & speech therapy following subdural hematoma & brain surgeries. There were issues with lost dentures with ALL the patients in the facility. The "green card" immigrant aides don't speak English - and many DON'T CARE about such things as the patients' dentures, etc. It doesn't pay to take our loved one's good clothes to such facilities because the aides will either steal them - and/or mix them up with other patients' clothing when they're in the facility's laundry. We really need integrity/ethics for facilities' workers - and/or caring agrarianism - but we can't legislate morality.... (sigh)
Now to CarolLynn's problem. I wish there was an easy answer to this problem. I live with my mom and have more than once had to hunt for glasses or dentures. We even had to replace one set of dentures and they are not cheap! Asking the staff to keep her hearing aids or glasses in a safe place is probably the best advice. This may not always happen because the information may not get passed on with shift change. Also, there are 3 shifts a day and if someone is sick or on vacation there may be part time or registry workers. Just keep in mind items may still might get lost. Painting the glasses sounds like a good idea but harder to do with hearing aids and impossible with dentures. As far as glasses, I would get a second cheap pair for back up. Take care of yourself and try to be patient.
1. Make sure the center has had training "in service" from the audiologist servicing their patients. This should include the understanding of the consequences of untreated or poorly managed hearing, proper handling and care, and proper protocols.
2. I do insist that the center lock the aids in the medcart at night after last meds and that they are returned in the morning to the patient with a working battery. If they are lost that day it is noted. The responsibility of the pm nurse is to back track and report ASAP so that there is a better chance of finding them An order can be written in the chart for this process. I take this seriously since every patient has the right to hear. It is as important as delivery of medications.
3. Otoclips or some kind of safety clip is important to keep the hearing aids secure. Staff can be overwhelmed, they cannot be your loved ones guardian angel every minute of every day. Things happen that are not controllable. I've even seen where a resident had taken an aid out of another resident's ear to wear. I recommend that if needed the safety is brightly colored and aids are labeled with the patients name if needed.
4. Please be proactive. Family support and involvement is imperative for this to work. I will usually recommend where possible that the family change the battery weekly and we teach them to clean the aids. I realize that staff changes and for consistency and because we are dealing with an investment of instruments and cognitive well being it's worth the extra effort on all parts. I sometime hear the comments of I PAY ALOT TO KEEP MY LOVEONE HERE. Understandable, but they are still your loved one and intervention and added support can go a long way to keeping that individual connected and engaged with the world around them. The family is the voice of that patient. With out that voice they are left sometimes very vulnerable. Be assertive not aggressive. Be kind to staff and they will be kind to you and your loved one. Caregiving is NOT easy. acknowledge the people who help only adds to the positive quality of life of the people who mean the most to us.
The other day Dad misplaced his large lighted magnifying glass. Dad's caregiver even put on rubber gloves and dug through the trash bins and recycling.... he looked high and low. Both searched for a couple of hours looking all over the house.
Then I walked into the house, found out about the missing magnifying glass, and went over to Dad's recliner and there it was, nicely tucked between the cushion and wood frame.... that is where I usually find missing things... even Dad's car keys last month were hung up on a wire underneath the recliner :)
Actually, I think it's because given (a) limited mobility (b) some age confusion....keeping things close by just makes common sense. The issue though is creating a nice place to keep those things that like to crawl away and hide in the sides of chairs so they don't keep escaping.
Then after the repaired one came back, soon after, he had removed one from his ear again, and he he'd had a habit of sticking them down his pants, and sometimes they would end up inside his Depends. So from there, this one fell on the floor and either he or I stepped on it and broke it. That did it! I wasn't about to spend another $350 to have it repaired.
My husband doesn't take to things very easily. He was constantly removing his hearing aids because he said "they hurt me." Okay, I'm done with this nonsense. I have put them away permanently. He is living without them. There comes a time when the caregiver has to make what she/he feels is the right executive decision, and I made it. I have no regrets!
Then I thought, how about an Over-the-Ear hearing aid, similar to ear muffs? Nearly impossible to lose, easy to adjust and longer lasting batteries, and no ear wax problems. I just started looking for a pair to trial and am still looking. Any comments/ thoughts?