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Depression with Daughter, Mother's Senior Care

AnonymousPS profile image
6 Replies

I am not getting "my way" with my mother's care. I do not like my mother's care team: Caregivers, RN, and how her medical decisions are made. I don't see the best for my mother.

I am the youngest of the daughters, 33 yeards old. My mother is 74 years old. I feel side lined as a caregiver to her, and I do not have much input in my mother's health despite living with her. I have ordered her rehab equipment (i.e. Sara Steady a month ago) and earlier in the year bought with my mother's own money as well a Hoyer Lift in September to support my mother to get back to her life. Both of which she doesn't use because she hasn't met her physical therapy goals to get out of bed. This has personally upset me, and left me lost about how to go about encouraging her to get out of bed. I try to not show any emotion about it because I don't want her to get discouraged, disappointed and fall back into being "cozy" in her hospital bed longer. I want her out of her bed, walking. I want to enjoy my mother and her life.

How do I make life better and the best for my mother? I find that elder care does not have a lot of enhancing quality of life activities for those receiving care at a private home. I have looked online for most things for her to have at home so she is comfortable: table over bed, clothing rack, pillows (of all kinds), Hepa Filter (clean air), etc. But, right now she just watches TV. I have seen her quality of life drop to just watching tv all day. She asked 5 weeks ago to go outside and we have not done that yet. And, it bothers me. It hurts and it is a personal failure on my behalf to see her succeeed and be happy while she is bedbound. She is unable to use a wheelchair, and hoyer lift to get outside because she is not physically strong enough to get to sitting to the edge of the bed, which is a requirement by her physical therapist to do that before other moves such as getting into a wheelchair. The hoyer lift she is worried to use.

I need ideas of Quality of Life enhancing ideas: For example, entertainment, social support, daily fun, etc, for those bedridden, it takes away everything. I suffer caring for her and there isn't a lot offered by the public to alleviate these topics so that I can provide to my mother to enhance her life at home while she is bedridden.

My mother does not like skilled nursing facilities. However, with the doctor's not diagnosing her as hospice, I do not know what to expect for my mother's care and future. Every day is unknown.

Any advice, tips, recommendations, etc for me to add anything to enhance quality of life, and success for life.

I have suffered with depression from pitfalls, failures, trespasses seeing my mother suffer in pain. She has been suffering for 6 solid months. I have been suffering as well.

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AnonymousPS profile image
AnonymousPS
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6 Replies
Blueruth profile image
Blueruth

you mean the commenter not the OP right? :)

Dolphin14 profile image
Dolphin14 in reply to Blueruth

commenter sorry

Typing as fast as I can lol

I will try and backtrack and get the user name in. If you can help that would be fabulous :)

🐬

Blueruth profile image
Blueruth in reply to Dolphin14

It is pretty clear who you meant but I didn't want the op to feel bad if that wasn't obvious. People like the one you meant are usually stupider than stupid.

Dolphin14 profile image
Dolphin14 in reply to Blueruth

You are correct. When he gets taken down the only thing that will stay is my alert (I'm assuming )and I don't want these newer members to be confused.

Dolphin14 profile image
Dolphin14 in reply to Blueruth

Thank you for pointing this out. I back tracked I think I got them all and attached the bio

Blueruth profile image
Blueruth

Does someone in your family have power to make medical decisions? That’s who you should be talking to about the caretakers. My mother has an advocate too. Also most caretakers are grossly underpaid…like obscenely. That doesn’t excuse bad behavior but if they are overworked they may not be able to provide the best care. My mother was in a home where the staff was not well supported or trained. The advocate was able to be there to make sure they got her what she needed and she new the other facilities to recommend.

My mothers world got really small. You may have to honor that and accept where she is not where you want her to be. I used to bring an iPad with scanned photos of her childhood and mountains. I’d also record information that she told me. She liked that. You lose more recent memories first. She probably needs socializing. Just hanging out with peers. That is what a home would give her. I get the resistance though. They have a bad rap for good reason. I don’t want to end up there. It sounds like it might be best. That person with legal authority needs to help with that.

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