Anyone Got Off Of Dialysis?
I was wondering if there are those who were on dialysis and were able to get off of dialysis without having any kind of …
Dialysis is a type of renal replacement therapy which is used to provide an artificial replacement for lost kidney function due to renal failure. It is a life support treatment and...

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My experience on CAPD.
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Continuous Ambulatory Peritoneal Dialysis (CAPD) or just (PD).
I don't want to scare you but you need as much information, good and bad, to make decisions in your new life as a kidney dialysis patient. I had an awful experience on PD which is not to say you will. Everyone is different. I've heard of others who did just fine. You know the advantage: freedom, continuous dialysis, etc. I exchanged bags in the desert, on top of parking structures, in my car while working, in my office at noon time and of course at home. The problem came up as I slowly got sicker over the 15 month period of CAPD. My dialysis nurse and doctor just kept increasing my exchanges and larger amount of fluid going in. Instead of recognizing that it just wasn't doing a complete job and switching over to hemodialysis they kept me on it. I primarily blame my CAPD nurse whose job depending on getting and keeping patients in his program. I ended up so sick I could not work, period. I was on my death bed when they told the transplant surgeon to put me on the top of the list. Back then I had waited 15 months which was a little longer than usual so it was not a big effort in my opinion. Anyway if you are unable to work full time after being on it awhile, and continue to feel worse and worse consider switching. Here is what you should feel. You will be very sick when you start as they will not start you on any dialysis until your body is really bad. Probably not working. You'll feel much better in comparison but you'll not be normal. But OK. Then you should stay OK. If, over a period of months, things get worse then reconsider. But for a start its a great way to go. One secret I learned was the use of sterile saline (salty) water to clean all wounds and around where the tube enters the abdomen. Clean all of them with each exchange. For some reason the saline works much better than alcohol. Use a device to switch the tube from the old bag to the new. It's much faster and cleaner than doing the switch by hand. DO NOT HESITATE to go to the emergency room if your used solution is the slightest bit cloudy. YOU WILL GET abdomonical infections. Peritoneiumitis if I spelled it right. Everyone gets them. It DOES NOT go away by itself. You can die. By getting IMMEDITE diagonis you can cure it quickly and avoid a LOT of pain. Always carry the instructions on what the EMERGENCT ROOM doctors should do when you walk it. It's call the Protocol. Few medical people know anything about dialysis so they will very happy that you can show them what to do. YOU ARE RESPONSIBLE FOR YOUR HEALTH. You cannot assume that any medical personnel know how to treat your unique problems. Be a boy/girl scout. Be prepared. If it seems right for you go for it. There is only one way to find out and that's to do it. I hope that things will go great for and and it's like that the will. Please don't be scared of what I've said. It's just my experience. If in time you see yourself going my direction don't hesitate to consider some form of hemodialysis. And don't be afraid of the needles if you go to hemodialysis. It's OK. Posted on 09/30/07, 11:09 am |
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Thank you for this post.
I am planning IF/OR when I go on dialysis to do CAPD. I can't stand the thoughts of having the fistula in my arm o( My creatinine is 4.3, but all of my other blodwork is still remarkably good, so my drs. say I can wait for a while. I feel good most of the time, just get aggrevated because of constipation...sorry! Does everybody else have this same problem? Does anyone have a solution? I would love to know it! If I can lend an ear or shoulder to anyone, please let me know! Take care, Carol
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Carol there have been some Threads on this issue. Try the search option above to find them. If you can't make it work send me a message and I'll try to help.
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I'm glad you got your transplant. I hated hemo when I was on it. I had opted for PD but my kidneys failed before I could get my catheter put in and I ended up on hemo anyway. I spent a little more than a month on it before I was able to do my PD on my own. I've had Peritonitis twice since then. Besides that however, my life is pretty much the same as it was before my kidneys failed. I work full time and I go to school. For me, hemo was worse because it took away too much of my freedom. Despite the fact that dialysis was sustaining my life I felt like I was dying.
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I just started CAPD beginning of Dec. I still have some function left so I am basically doing 2 exchanges a day to help them out. I am also working with constipation. I take a stool softner with my daily medications and have increase my "fiber" and fresh fruit. It has helped a bit, I am going a bit more frequently. If you can and like prunes, my grandmother used to drink a cup of prune juice and a splash of hot water every morning as soon as she got up. Needless to say, she was regular! :) Hope you get some relief, if you haven't already started CAPD, you will find the two don't go well. I am sure it is a space issue. Email me if you would like to compare notes or just to say hello. Best of luck
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