My mom has been in a nursing home for over 4 yrs. she has dementia and recently has not been able to figure out how to eat her breakfast. Once out of bed and into her wheelchair the breakfast is delivered to her room. ( My mom WILL NOT EVER go to the dining room). Once the meal is delivered the staff leaves the room. My mom sits there for hours crying and trying to figure out how to eat. My sister and I both have witnessed this happening and have started going to the NH before breakfast to help her. Her dementia is terrible in the morning so breakfast and rising is very difficult. While this everyday appearance by my sister and I is working (we stay 2 hrs min) we are finding we cannot keep it up everyday of our lives. The nursing staff will not help her eat breakfast. If she wants their help she must go to the dining room. What shall we do? We are getting worn out.
Anyway, I'm beginning to dislike these 'skilled nursing facilities'. My mother is in a so called Medicare Five Star Rated facility. While I like the various entertainment, the CNA's, the aides, etc., I'm not too fond of the RNs (of which there is one at each station doing paperwork, it seems). Don't even try to ask THEM a question. I always go over their head to the social worker who then goes to the RN's. Also, you need to call the doctor to get the RN's to do anything, there are so many rules and regulations as to why they can't do things on their own. Quite frankly, I don't blame them, everyone is suing today.
Something needs to change because the largest group of people are starting to get old and that's me, and probably a majority of you guys out there, who are baby boomers. It somehow always falls to us to exact change.
My MIL is in assisted living in AZ. No one can eat meals in their room, there.
I would hire a private person to feed her in the mornings, I think.
My mother is now in a memory care facility. She can still feed herself. There are other who cannot. Some family members will come to spend the time and feed them, others cannot because of working. There is one man who cannot feed himself and I have seen the staff (with gloves on) hand feed him because this man will not sit down. He is on the move all the time, pacing, walking.
BTW - Just because she does not fit the cookie cutter mold of sundowning instead of not being a morning person....- well, is there some med they are giving at night, maybe in too high of a dose for her, that is leaving her confused in the AMs?? This ought to be reviewed.
Second, I assume your goal is to have her transition gently into her day and eat breakfast without being upset. Might she do better eating breakfast later? Would the staff have more time to help if she isn't doing it during normal breakfast times?
It sounds like your presence is a comfort to her and you are willing to do this, but not on an every-day schedule. Is that right? How many days would be reasonable? I like cwillie's suggestion of hiring someone else to come in and help on the other days.
Thirdly, have you had a conference with the staff? Perhaps at the next Care Plan meeting, or a special conference just for this topic. Approach it as "one of your residents has a problem related to her dementia. How can we work together to solve it?" They may have some suggestions. Don't be accusatory or demanding. This problem is a result of the dementia and is nobody's fault. Do they have a dementia wing and are they more flexible with their scheduling and one-on-one help there? (Even if they have such a unit it may or may not address this kind of issue.)
Alos, at my mother's NH there really is a desire to provide each resident with quality care. They do listen to family. They have constraints with staffing but they are good at brainstorming and trying to work around obstacles. If you haven't already had discussion about this, with at least DON and Social Worker, I'd start there.
Lastly, it sounds like Mom is especially anxious in the mornings. Perhaps an anti-anxiety med would help. If she is already taking something, perhaps a change in the timing or dose would help. Drugs don't solve everything, but they are worth at least considering.
Your dear mother is very fortunate to have two advocates working on her behalf. I hope you come to some comfortable resolution. Do let us know how this works out. We learn from each other, and we care!
And as Babalou had asked above, why doesn't your Mom want to go to the dining room?
Would they provide someone to feed her for a fee? Or could you afford to hire someone to come in to help her in the mornings on the days you can't be there? I know it seems that you are paying more than enough already, but you really can't expect to get preferential treatment without paying for it, imagine if they had everyone wanting room service?