Caregivers Support Group
A voluntary caregiver is a spouse, relative, friend or neighbor of a disabled person or child who assists with activities of daily living and assists those unable to fully take care of themselves. The challenges of a caregiver are unique and sometimes it's hard to find people to talk to who know what you're going through. Join the conversation and find others who...
Maybe some of our other caregivers here can add their ideas.
Hugs, Phoebe :-)
My wife also had parkinson's and early onset dementia, and she too was very clingy. Any time I was out of sight she would start asking where I was, what I was doing, and when I would be back near her. Fortunately for me, this only lasted about 6-8 months, because it was very frustrating.
I don't know if there is anything that can be done to ease her fathers concern and need. Because of the dementia, reasoning with him is only temporary. Perhaps like my wife, this will only last for a few months and then pass.
Sorry I can't help more.
Hugs, Dan
My mother now resides in a nearby assisted-living facility and, even on days when I spend three or more hours with her, she still calls me no less than five times per day to complain and demand/request me to do or bring her one thing or another. On days when I don't visit, she's usually called between 5 - 10 times and, some days, it's as much as 15 times. I've always been a patient person, but it's really been wearing me out! Explaining to her that I need some "down-time" to process my grief over losing my father, handle estate matters, etc. has made no impact on her. It's all about her and what she wants/need when she wants/needs it, and the sooner I address her concerns the better....for us both. I've figured out that it's anxiety-based and also rooted in compulsion that coincides with the increased intake of Parkinson's medications such as Sinemet (carbidopa/levodopa), which is known to cause compulsive behavior (e.g., gambling, excessive shopping, etc.)
Recently, after a few months' break, my mother resumed taking 0.5 mg Klonopin (generic: Clonozepam) again as a sleep aid; her neurologist allows her to take 0..5 mg every six hours as needed ("PRN"). Her nurses and I have started encouraging her to take a Klonopin in the mid-afternoon since my mother wasn't requesting it but surely needed it to curb her anxiety. (She was not only constantly calling me but getting irritaged and demanding with nursing staff.) In short, on those days when she takes a Klonopin, life is gentler for her...and for me and others. I'm no longer being bombarded with all her many calls and even our conversations are more relaxed.
Although Klonopin is branded as an anti-seizure drug, it is also recommended to people with Parkinson's DIsease as a sleep aid as well as an anti-anxiety medication. It might be something to discuss with your friend so she can discuss it with her father's neurologist. At a low dosage such as 0.5 mg, it just helps to mellow the person with anxiety. When my mother takes it at night, at which time she's not anxious, that same dosage will enable her to sleep. While I'm not an advocate for lots of meds, especially medicating of the elderly, but this is a drug worth considering for anxiety related to Parkinson's Disease.
Hope this helps!