Falls and balance issues
My mom has Alzheimer's and still lives on her own but her short term memory is quite bad. She is falling out of bed in the middle of the night and has no memory of it. She has hit her head each time and has head, neck and back pain from these falls. Is this a common thing? My dad helps her up and puts her back in bed but he has major health issues also. I don't know where to step in or what to do. I have been managing all her meds (14 pills a day) and all her medical. The falls I don't know how to navigate, any suggestions?
Comments
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Agree that the falls are a significant issue. I would recommend immediately using a side rail (could a toddler rail work) to keep her in her bed or putting a padded mat next to her bed. I don't know how common bed falls are but in memory care, my mom's bed was lowered after a time, and a pad was placed next to it each night.
Do fall risks occur during the day as well? Is there a walker in the picture? Is this consistently utilized?
Please understand that a fracture would be incredibly painful for your mom. If it was a hip, she may lose her ability to walk.
They are so fortunate to having you manage all medication and doctors. I am assuming you are also ensuring there is appropriate nutrition and that there are controls in place such that there is no wandering or allowing strangers to enter their home.
I don't know what situation you are in. If you are retired, living alone, you may have the time to do all of this. If other family members rely on you or you have employment demands, you are going to need some support. Tell us more about your situation.
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Thank you so much for commenting.
This is all new or relatively new for me. My mom was diagnosed aprox 1.5 yrs ago. She lives with her husband (my dad) who has an inoperable brain tumor. I'm no longer working, I spent over 20 yrs in healthcare but it is so different on this side. The falls had initially been happening during the day but never witnessed. Sometime back they put her on seizure meds as she had a EEG with temporal lobe activity. That seemed to help but the last 2 were sometime in the night. Possibly getting up to use the restroom or wandering as she gets restless at night. She also has difficulty sleeping and is on generic Ambien and will get up in the night looking for more meds to take. My dad has tried hiding the meds but she always ends up finding something to take. My dad wakes when she falls but by then it is too late. She does not have a walker but that might be something to consider and maybe getting her a bed that only she sleeps in lower to the ground. I plan on moving the nightstand that is next to her bed as this is what she has struck her head on. I do not live with them but live close by. I feel like things have changed drastically since she had a UTI that we didn't know about and she ended up with sepsis and was hospitalized. The short term has gotten worse and I don't think she realizes her limitations. My family (husband & teenage son) have considered selling our home and building an ADU on their property but this is a huge consideration and still might not improve the overall situation. Phew, sorry to unload I have had no one to talk about all the issues going on and where to start. Sometimes it's overwhelming. I hope just being able to interact with others dealing with similar issues and get suggestions could be a big help.
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Hello I’m so sorry you’re going through this. This was my dad’s journey also, falls and UTIs which caused the dementia to progress and led to placement in LTC. My dad also has LBD where motor involvement is part of the disease and falls are common.
I’m sorry to say that once the falls start, they are hard to stop. She won’t ever remember she’s not supposed to walk unassisted and even remembering/learning to utilize the walker will probably prove difficult. I would look into in-home physical therapy which should be covered by Medicare.
The hard reality is that she should not be getting up at night unassisted (and most likely needs assistance during the day also). The bathroom at night was my dad’s undoing. I was so desperate until I could move him, I put his mattress on the floor.I purchased a floor bed for my dad. It’s a bed that can be lowered to only 2 inches off the floor and I have fall mats on either side. This way he would not hurt himself if he rolled out and while he was still mobile, because it was so low it was very difficult for him to get out of. He had a bed alarm so staff was alerted as he was trying to get up. You could try the alarm by itself to start so someone is alerted but if they don’t get there in time, then a fall can still occur as you’ve learned already.
These beds are expensive but for my dad it was worth every penny and I could finally sleep at night knowing he was safe. My experience (and what I was told) is that the falls don’t stop once they start and are very difficult to manage. For my dad, they led to several injuries/hospitalizations. I would remove all trip hazards, use a bed alarm, look into a lower bed with rails, etc. but at some point, additional care may be needed. Medicare will cover a regular hospital bed but it was still too high for my dad—I think they are more like 8-12 in off the floor at lowest height. My dad has not fallen in the over two years he was moved to an RCF, got the bed and bed/chair alarms utilized.0 -
My DW took a major fall necessitating a trip to the ER. CT scans and x rays showed no problems. 2 weeks later another fall, this time showing a major brain bleed requiring neurosurgery. It took 2 weeks for the bleed to develop from the initial fall. Falls are not to be taken lightly. Docs told me that I got her in (hospital, the second time) just in the knick of time. Any longer could have resulted in a stroke or death. two more smaller falls while she was in hospital recuperating.
Meds, Physical Therapy, constant vigilance…so far no more falls. It is exhausting, on top of all the other issues relating to her dementia - Capgras syndrome, delusions / hallucinations, Anger with me for not letting her drive, wanting to leave our home to go "home" to where she grew up, wanting to go teach the children who have set up appointments (retired teacher), wanting to phone deceased relatives, anosognosia. I sleep with one eye open…when she gets up to go to bathroom, so do I. I would love a full night's sleep.
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My Mom fell last week. I had to call EMS to have them help get her up and help us get her to bed that night. Last month I had to call EMS because my Dad fell and he needed help getting up. I had to take my Mom to the ER twice in the past 3 months and my Dad had to go to ER once. The ER doctors were not much help. The rest of the staff was better. The ER doctors wanted to get them in and out ASAP. I think I have PTSD from dealing with my parents for the last 3 years. Dealing with my Dad when he had sepsis 3 years ago was rough and Mom had gout and some other stuff 3 years ago. Many hospital visits. It never gets better. Good luck with everything and I hope things get better for you soon.
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With an ADU, a fall could still happen while you are looking at the little home out your kitchen window.
It may be time for a live-in caregiver which is costly. You would almost need three—one for days, one for nights, and one for the weekend. Perhaps you could visit a memory care and ask how they would handle. I recall restraints not being allowed while sleeping to prevent a fall out of bed. Perhaps your mom could adjust to a wheel chair. PT or OT could be scheduled such that she could continue to exercise by standing and walking under guidance of others. All this sounds extreme but my point here is to gather information and brainstorm further.
UTI's can drive extreme behaviors. They are tough to prevent though, as my mom, for example, taught herself not to drink because she didn't want to have a bathroom accident. The dementia would not allow me to reason with her or educate her on importance of hydration. At one point, she was prescribed a basal level of preventative antibiotic that perhaps could help your mom if the infections are frequent.
Hang in there. Perhaps folks with parents in memory care who are extreme fall risks could post.
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The UTI and subsequent infection can definitely cause balance issues. Also, your mother is on a lot of medication that causes balance/falling issues (seizure medication, Ambien, plus 12 unknown others). I'd recommend reviewing all of her medication. If you haven't already, look up side effects and potential interactions. At one point, a reaction to two medications was causing my mother to have syncope episodes. The doctor who prescribed it had no idea. I had to do that research and have it changed. Problem resolved. Also, my mother was on a low dose of seizure medication that immediately caused issues with balance and falling. Please review her medications and then discuss with her doctor to see if all are needed or if changes need to be made. It may be she needs the medication even though it is causing this issue. Then strategies need to be developed to prevent the falls.
She is most likely not falling out of bed but falling when she is trying to stand up when getting out of the bed. Try looking into the guard rail as mentioned above but be aware they can also create a bigger issue if she tries to climb over it. A bed alarm may help. There are some that can go under her when sleeping, and when she moves it will go off. That may help to alert your father before she has a chance to get out of the bed and fall. They can go off often though so it may be disruptive. You want to get to her before she has a chance to stand up at night so the fall can be prevented (or rolling out of bed can). Perhaps the bed alarm plus the guard rail would work until you find the cause of the falling issues. Is your father capable of assisting her to the bathroom when she wakes to prevent the falls? I'm thinking the bed alarm will go off and the guard rail will slow her down to give your father enough time to assist. This may be too much for your father to handle though, so an overnight aide may be needed.
I do think there's a good chance this is medication related. At least it should be ruled out. Once you figure out why it is happening, you can determine how best to prevent. I wish you the best of luck with this.
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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
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