Question for RNs and LPNs. I was told today by representatives of a private duty home care company that pureeing food for a client is considered skilled nursing and can only done by someone qualified as such. Any input on this? I asked a relative about this but was confused at the time and can't recall her answer!
So all in all and completely unscientifically, I regard plastic in microwaves as suspect and am now using only glass or ceramic ware. Which is a pain, I realise, if you have to decant everything; but you can get toughened glass or Pyrex containers reasonably cheaply.
I still use plastic for freezing, and I do defrost food in those containers - but then the food isn't getting hot, just up to room temperature, and there's no sign of wear. So I suppose that's all right?
It's at times like this that I wish I'd paid more attention to molecular chemistry (hangs head)...
What the company CSR asked me was how long was the container being microwaved. That's when she said 30 seconds, and maybe another 30 seconds, but definitely not more.
The containers are not designed for more than a quick warmup.
She also said not to use the containers any more, as it MIGHT BE that the plastic was deteriorating. She suggested throwing them away. Yikes.
Microscopic bits of plastic in food was my concern as well, which is why I now have over a dozen or so containers that can't be used for anything, well, maybe except storing screws, nails, sewing needles, thread, and things that aren't edible but always seem to escape open containers and wander around the house, hiding out in chair cushions or on the floor.
I too have switched to glass and some ceramics. But they do get hotter and need to be handled a bit differently. Easy for me, but not for Dad.
The only plastics I've used for freezing are ones that I bought years ago, the Ball containers for storing canned foods. When I was dreaming of living more off the produce from my garden and fantasizing that I would soon be digging out a root cellar, I bought a few dozen and have enough to last for years.
At that time I also bought other plastic ware but stopped using it when I saw a little "tail" of plastic separating from the bottom of a container. Those too are relegated for nonfood storage. I guess I'll have to stock up on nails, screws, tape, string, and whatever to make use of them.
I could recycle them, but would they be used for food storage? Who knows?
If you're not seeing any deterioration of plastic, I think they could still be used, but then that raises the issue of whether they were manufactured when BPA was still being used in plastic. I wouldn't be as concerned about the ones that are BPA free. And that raises the issue of the safety of the old Ball containers.
Sometimes I think animals have it all over us. Squirrels just have to bury their food or find a nice hole in a tree. Carnivores either consume food right on the ground, or hide it with brushes or something and come back later.
We humans have to deal with all sorts of safety issues, although at least we don't have to have bearproof containers. Well, maybe that's not so - I've seen some amusing photos of bears in a swimming pool and others not so amusing when they're getting into cars. If they're in the swimming pool, what do they do when someone barbeques?
Molecular chemistry? I literally faint at the thought of trying to understand chemistry. It's waaaaayyyy beyond me!
BPA.
The thing is, you need to weigh the pros and cons of it all - the bento containers are easier to handle, can go in the freezer, and the compartments keep things separate. They are also relatively cheap, so they can be replaced fairly often.
At his age I doubt that the cumulative effects of microwaved plastic containers are ever going to cause any adverse effects, if it was for a child I would think differently.
My father was diagnosed when he was in the hospital for something else at 88 yrs old. At 87 he had started having repeat pneumonias. He had been pretty healthy up til then. I thought it was viral and washed all bedding, etc. I had never heard of dysphasia - (swallowing problem, usually lots of coughing when eating) - or of aspiration pneumonia - (bacterial infection due to food or liquid getting into your lungs) - or of "silent" aspiration - (where you have a dead spot in your throat and you can't even feel the liquid going down the wrong pipe) .
A rather brusque nurse showed me what to do - like it's just simple, you just do this. "He can't even drink water??" (I pictured him not being able to just go and get a glass of water - he certainly would not be able to do this thickening thing. I was kind of shocked that no he couldn't get water and yes this is what I would have to do.)
The nurse never said a thing about skilled care for this. Later we saw a Speech Therapist, had a flouroscope done and watched. Thin liquid went right down into his lungs.
He had a slow swallow. It should happen in 1 second, his took 2. The "flap" didn't close fast enough. No one could figure out why. Mini stroke that doesn't show on scans? Side affect of cough drops or pain meds? (I asked). No one knew for sure.
The Speech Therapist said his food has to be something that will form a "bolus" - a ball that will slide down his throat without breaking up. And that all liquids had to be "honey thick". That's pretty thick. Later, he actually improved to "nectar thick" for a while.
We also tried electrical stimulation to his throat. Sometimes that does help. And exercises which he hated. He was too old and not well enough to really pursue these. In the end this throat problem was his worst problem and it got worse. That was the reason he passed away.
But anyway - the original question - no I don't think there is a requirement for skilled nursing. All of my father's care in this area was up to me. I had a sheet of things to avoid and a few tips that the hospital gave me.
The nursing home (he was there a few times for rehab) does note this condition and tries to create food that will work. It's very tricky. Even pureed stuff sometimes doesn't work - it gets hung up.
One thing that worked well for my father was lasagne. The cut bite sized pieces seemed to slip right down. He hated pureed stuff and really, it didn't work as well. Bananas and avocados were good - a little catalina dressing in the avocado half. Moist and slippery is good. Dense meat loaf with a lot of ketchup. Strawberry shortcake with ice cream, whipped cream, chopped strawberries with sugar to make a sauce, and those soft commercial cake things. It is a learning curve for sure.
Also we tried a lot of different thickeners. Some are cornstarch, some are a seaweed thing I think. We didn't like the cornstarch ones. The best one, to us, was Nestle's Thicken Up. They have good customer service. They have prepackaged juice, water and milk which I bought and found useful for car trips, emergency rooms, immediate needs...
You have to watch the hospitals closely as the workers make mistakes and give thin liquids when they shouldn't. I tried to be there all the time, especially at meals. Difficult. Even the nursing homes occasionally make mistakes. They actually required me to be with him if we wanted him to eat in the rehab dining room. Otherwise he would have to eat in the main room with the permanent residents. The dining room was nicer.
You just do your best and hope it works. There's only so much you can do.
I sympathize so much with you and wish you and your loved one the very best. It's not hopeless. It can sometimes improve.