I Hate Dialysis Message Board
Dialysis Discussion => Dialysis: Home Dialysis => Topic started by: NCspinner on December 27, 2018, 07:15:25 AM
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I hadn't realized when I agreed to train as a home hemo care partner that it would be so difficult to get even a couple of days off to visit my family, who all live very far away. (We're in NC and they are in MA, ME, ID & WA). Our home hemo nurse is willing to help but she's very busy and the last time I visited my 93-year-old mother, the cannulation did not go well. It appears that if I need to be gone my husband probably ends up going in center for dialysis using sharps. Not a good alternative except in dire emergency. We've tried to find qualified people to come and do the dialysis here at home if needed but it's proved amazingly difficult ... and DaVita absolutely refuses to talk about it. Why isn't there a resource for locating respite caregivers? Has anyone out there found a way to deal with this?
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I hadn't realized when I agreed to train as a home hemo care partner that it would be so difficult to get even a couple of days off to visit my family, who all live very far away. (We're in NC and they are in MA, ME, ID & WA). Our home hemo nurse is willing to help but she's very busy and the last time I visited my 93-year-old mother, the cannulation did not go well. It appears that if I need to be gone my husband probably ends up going in center for dialysis using sharps. Not a good alternative except in dire emergency. We've tried to find qualified people to come and do the dialysis here at home if needed but it's proved amazingly difficult ... and DaVita absolutely refuses to talk about it. Why isn't there a resource for locating respite caregivers? Has anyone out there found a way to deal with this?
One BIG WORD: LIABILITY!!! Says it all.....
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I know, I know. Our local center is making a big push for patients to do dialysis at home--lots of posters with smiling faces all around--but IMHOP this is the dirty little secret they don't mention when they're telling you how wonderful it is.
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If I remember correctly, Fresenius allowed respite maybe every 2-3 months. I think I posted about it. Hubby had to go in-center during that week. I probably should have regularly taken some time off.
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IMHO the only thing worse then a being a patient is being a home health giver. The never ending grind is bad enough if you are the patient. Worst case see if you brought hubby and nexcare box do home hemo on the road, I figure if Bill Pulham can do it in the middle of the Grand Canyon on a river raft it should be possible to set him up at a relatives house.
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I know, I know. Our local center is making a big push for patients to do dialysis at home--lots of posters with smiling faces all around--but IMHOP this is the dirty little secret they don't mention when they're telling you how wonderful it is.
What is the dirty secret?? There is no secret that the push is for home dialysis over in center dialysis. Trying to cut costs by shifting the responsibility onto the patient..
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I was treated in center for 3.5 years and found it good. I would think a week of in center treatments would not be that bad for many patients. So unless you have had bad experiences in center I recommend trying it so you can have your break.
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I hadn't realized when I agreed to train as a home hemo care partner that it would be so difficult to get even a couple of days
NxStage is FDA certified for solo (no caregiver) home hemo as long as the patient is not doing nocturnal.
Fresenius supports this, and it is possible to be certified to do your own D without a caregiver present.
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I know, I know. Our local center is making a big push for patients to do dialysis at home--lots of posters with smiling faces all around--but IMHOP this is the dirty little secret they don't mention when they're telling you how wonderful it is.
What is the dirty secret?? There is no secret that the push is for home dialysis over in center dialysis. Trying to cut costs by shifting the responsibility onto the patient..
I wonder how much the cost of those cute plastic measuring cups and teaspoons with the Fresenius logo on them handed out as Xmas gifts was shifted to the patients. >:(
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I know, I know. Our local center is making a big push for patients to do dialysis at home--lots of posters with smiling faces all around--but IMHOP this is the dirty little secret they don't mention when they're telling you how wonderful it is.
What is the dirty secret?? There is no secret that the push is for home dialysis over in center dialysis. Trying to cut costs by shifting the responsibility onto the patient..
It's the only reason this (slow) shift is happening though. A bit like the abolition of slavery. Nothing happens unless there's an economic adnantage to the powers that be. But in this case I can see the patient as a huge winner too.
I have independence back which I had lost.