Fascinating article on wearable artificial ... - Kidney Disease

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Fascinating article on wearable artificial kidney

Bassetmommer profile image
BassetmommerNKF Ambassador
21 Replies

This is a fascinating report on the progress of artificial kidneys. Very promising:

mddionline.com/behind-inven...

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Bassetmommer profile image
Bassetmommer
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21 Replies
Bunkin profile image
Bunkin

Very exciting to me! 😀

RhenDutchess123 profile image
RhenDutchess123 in reply toBunkin

they are also working on a Biotic Kidney too.....except it is about the size of a normal kidney and implanted into the body

Bunkin profile image
Bunkin in reply toRhenDutchess123

Yes I follow both of those things. I’m confident it’s just around the bend😀

RhenDutchess123 profile image
RhenDutchess123 in reply toBunkin

me too...they say as early as 2020...2025...

Bunkin profile image
Bunkin in reply toRhenDutchess123

I’m hoping for 2020!!😂😂

steve680 profile image
steve680 in reply toRhenDutchess123

Right, the USF project. That sounds more appealing to me as it avoids dialysis completely and in some ways better than a transplant since you won't have to take anti-rejection medication.

steve680 profile image
steve680

They sure make hemodialysis sound like a total nightmare. I guess it is.

Bunkin profile image
Bunkin in reply tosteve680

I hate reading negative stuff. It’s like every time you read about it, it’s horrible but I’ve seen posts from people on this site who’ve said dialysis makes them feel better. That’s what I’m aiming for and that’s how I’ll be going into it. Attitude is important 😀

RhenDutchess123 profile image
RhenDutchess123 in reply toBunkin

i am going to try the peritoneal dialysis at home....until a transplant and/or new technology....Dialysis doesnt sound fun...but at the same time i feel grateful that there IS a treatment...many diseases dont have any and are far worse

Bunkin profile image
Bunkin in reply toRhenDutchess123

Me too! I feel the same as you. I can do it til new technology comes along and remind myself that at least there is something that can be done😀

RhenDutchess123 profile image
RhenDutchess123 in reply toBunkin

are you on transplant list ?

Bunkin profile image
Bunkin in reply toRhenDutchess123

Yes. Went on list 2 years ago. But don’t have a living donor and have pretty much decided against transplant and just go with dialysis til something better comes along. I don’t feel the risks from all the medicine would be worth it

Bassetmommer profile image
BassetmommerNKF Ambassador in reply toBunkin

I really like your positivity. I too am hoping for something to come along other than dialysis. I am not a candidate for transplant.

Bunkin profile image
Bunkin in reply toBassetmommer

I am on transplant list but have no donor. Since I went on list 2 years ago, I’ve pretty much decided against it and just go with dialysis til the new wearable kidney or bionic kidney comes along. Due to my age and I don’t want to take all the drugs involved with transplant. To go thru all that for maybe 5 years, just doesn’t seem worth it. If I were younger, I may feel differently. Most people wouldn’t understand my way of thinking but everyone feels differently I guess.

Bassetmommer profile image
BassetmommerNKF Ambassador in reply toBunkin

HI Bunkin, I get what you are saying about the medications for transplant. That is one of the reasons I would not be a candidate. The other reason is that I would feel bad at my age taking a kidney when someone who is much younger could have used it. I just can't seem to get past that.

Bunkin profile image
Bunkin in reply toBassetmommer

I hear what you’re saying. I did try to get a donor in the beginning but no one wanted to. Then after reading about cadaver kidneys and how they don’t last that long, I just couldn’t see going thru that. Plus I get colds and stuff very easily now, getting one with no immune system would probably do me in. Plus I find it ridiculous that you have to go and get all that testing done every year for no reason. There’s no way I would get a kidney before 6 years anyway

RhenDutchess123 profile image
RhenDutchess123 in reply toBunkin

i know that bothers me too....the heartbreak of going through the testing and not accepted....but you still have to pay for it....and even if you are accepted..just a change in health or insurance coverage can make you have to be re-accepted......if you have a live donor than you can somewhat pick your day of surgery...if you have to go with a cadavar it could be anywhere from a couple months to a couple years...living on edge ..waiting for phone to ring...would be hard to make plans for anything else

Bunkin profile image
Bunkin in reply toRhenDutchess123

Exactly. And there was one test they wanted me to go have every 3 months. I did it a couple of times then thought that’s silly. New rules are even if you’re on the list, if you’re not on dialysis, all dialysis patients will be put ahead of you. I got on the list in 2017 and that test is very expensive and basically useless.

RhenDutchess123 profile image
RhenDutchess123 in reply toBunkin

are you on dialysis yet...and if not..what type are you considering ?

Bunkin profile image
Bunkin in reply toRhenDutchess123

Not yet but will be soon. I’m going for PD

daxielovinglady profile image
daxielovinglady

In the United Kingdom we have a different way of dealing with the situation, thank goodness for our much beloved NHS (National Health Service) it's there for everyone.

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