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Author Topic: One year on dialysis - I still hate it....  (Read 6334 times)
Butterfly7
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Butteryfly7

« on: April 12, 2017, 08:45:32 AM »

One year anniversary on Hemo Dialysis.  sometimes can't believe it's been a year -and other times I still hate it. (I love this site because I still hate it....except Friday night at 8:30PM)
4 Infiltrations....but learning not to move at ALL.
3 years on UNOS list, April 2017.   - come on new Kidney!!!  I'm waiting for you!!
 :flower;
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Polycystic Kidney Disease diagnosed 38 years old
Brother, Mom, 2 Aunts and Cousin all have kidney transplants and doing well.
Started in-center Hemodialysis 5-16-2016.  On transplant list 3 years 4 months.
Hoping for a miracle in 2017!!
Rerun
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Going through life tied to a chair!

« Reply #1 on: April 12, 2017, 08:51:29 AM »

Come ON new kidney!   :bow;
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Butterfly7
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Butteryfly7

« Reply #2 on: April 12, 2017, 09:00:43 AM »

Thanks RERUN!   good to know there are a few listening out there!
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Polycystic Kidney Disease diagnosed 38 years old
Brother, Mom, 2 Aunts and Cousin all have kidney transplants and doing well.
Started in-center Hemodialysis 5-16-2016.  On transplant list 3 years 4 months.
Hoping for a miracle in 2017!!
Michael Murphy
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« Reply #3 on: April 12, 2017, 12:23:43 PM »

As your fistula enters the bumps (anyourism) stage the infiltrations become less frequent. I just had my four year anniversary and my bumps have gotten big enough that it has been several years since I infiltrated.  Hate the bumps love the effect.
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JVT90
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« Reply #4 on: April 12, 2017, 02:55:45 PM »

Happy anniversary. Hubby's been on almost 2 years.......1 infiltration. Not moving is a good skill to learn.  :thumbup;
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Husband started in clinic dialysis 2015
Simon Dog
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« Reply #5 on: April 12, 2017, 04:42:44 PM »

You can reduce the infiltration risk, and in many cases the amount of bumps that develop by using button holes and blunt needles.  The catch is this generally involves self puncturation.
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LorinnPKD
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« Reply #6 on: April 12, 2017, 10:17:31 PM »


You're doing great, Butterfly!
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Charlie B53
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« Reply #7 on: April 13, 2017, 06:25:50 AM »


Just the thought of an infiltration makes my skin crawl.  This is yet another reason I really REALLY love my perma cath.  But I know I can't keep it forever.  Qwap!
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Simon Dog
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« Reply #8 on: April 13, 2017, 08:27:49 AM »

perma cath.  But I know I can't keep it forever.
Oxymoron alert!!!

I did in-center cath, followed by in-center fisula until I could get my home hemo training.

The tech gave me a very nice going away present at my final regular in-center treatment - a huge infiltration.   She even managed to push a full 10cc into the tissue.     Was black&blue all the way to the shoulder for a few weeks.  No infiltrations since then (3.5 years or so at home)
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smartcookie
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LMSW

« Reply #9 on: April 13, 2017, 12:10:30 PM »

Congrats, Butterfly!  Each treatment you get is one step closer to transplant!  Here's hoping you get that call soon!
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I am a renal social worker.  I am happy to help answer questions, but please talk to your clinic social worker for specifics on your particular situation.
kitkatz
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« Reply #10 on: April 13, 2017, 07:14:35 PM »

Congratulations on one year!   I bring a cake to my center very anniversary to celebrate my life on dialysis.
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
LorinnPKD
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« Reply #11 on: April 14, 2017, 12:53:06 AM »

I love that idea, kitkatz!  I have an anniversary coming up and I might steal your idea & spread the love!
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Charlie B53
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« Reply #12 on: April 14, 2017, 03:35:31 AM »


I brought donuts once.  I was hungry and hadn't treated myself for a long time.


Simon, I hope you haven't jinxed yourself talking about not having an infiltration for so long. (Fingers crossed).
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Simon Dog
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« Reply #13 on: April 14, 2017, 12:11:40 PM »

I must have some sort of mental problem.  I don't mind dialysis - it's just something I do, and I find it hard to imagine any other life.   There are times where it really does get in the way with a deadline or something I want to get done.   Still arguing with my wife over the transplant (she does not want me to have one as she is convinced I will get rejection (acute and chronic), graft vs. host disease, blood clots, and at least 3 or 4 different cancers if I take the plunge).
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kickingandscreaming
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« Reply #14 on: April 14, 2017, 01:17:29 PM »

Quote
she is convinced I will get rejection (acute and chronic), graft vs. host disease, blood clots, and at least 3 or 4 different cancers

As a nurse, does she have some inside knowledge? Or is she just a glass half empty type?
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Diagnosed with Stage 2 ESRD 2009
Pneumonia 11/15
Began Hemo 11/15 @6%
Began PD 1/16 (manual)
Began PD (Cycler) 5/16
Simon Dog
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« Reply #15 on: April 14, 2017, 06:39:02 PM »

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she is convinced I will get rejection (acute and chronic), graft vs. host disease, blood clots, and at least 3 or 4 different cancers

As a nurse, does she have some inside knowledge? Or is she just a glass half empty type?
She works on a unit where all the people who have xplant problems are treated.
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Charlie B53
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« Reply #16 on: April 14, 2017, 07:46:28 PM »


In my opinion, which is pretty much worthless most of the time, tissue make is still a very in-exact science, hense the demand for the anti-rejection meds which leave the body open to a whole host of other problems.
I am not a very good candidate for TX, which doesn't really bother me that much as fortunately for me, Dialysis is working very well.  The switch to Hemo was an experience, and truthfully those couple first months I seriously thought I couldn't live like this.  BUT.... figuring out how they had set my dry weight way too low, and adding a few kilos has made a substantial difference.  I am O.K. now.  I can do this without problems for a long time yet.  I do have to get my access and learn that I can get stuck, but that is coming.  I will survive.

I'm sure that none of us enjoy Dialysis.  But as a survival method it could be a lot worse than it is.
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Michael Murphy
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« Reply #17 on: April 14, 2017, 08:15:37 PM »

If you need a reason to go have a transplant Emory University created a app called iChoose that tells the mortality rate for a patient. I ran myself just now as a 65 year old white man with a heart condition by the app I have a 78% chance of being alive at the end of the year. With a  cadaver transplant that increases to
95.4%  chance and with a live donor 98.4% chance of being alive in a year.  That translates to me having a 1 in 5 chance of being dead on dialysis, a 1 in 20 chance of being dead with a cadaver kidney and with a live donor a little less then 1 in 50 chance of being dead.  Transplants are not perfect, the statistic show far more dead people on dialysis than after a transplant.  I am not transplant eligible since I have a melanoma removed at least once a year.  If that were not the case I would certainly list for a transplant.  The app is on iTunes for apple and I think somewhere there is a android version.  While depressing it's important to understand the risks involved with choices this important.
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Riki
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WWW
« Reply #18 on: April 15, 2017, 08:11:53 AM »

I'm coming up on 13 years on dialysis.  I don't think I'll ever get a kidney, but I'm hoping that something will happen eventually.  I'm actually keeping an eye on that implantable artificial kidney that UCSF is working on.  I'm hoping that it won't be too expensive to get.

I like the idea of the cake for the anniversary.  I'd do that too, except mine is the same week as my birthday, and I will most likely already have cake on the way. *G*
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Dialysis - Feb 1991-Oct 1992
transplant - Oct 1, 1992- Apr 2001
dialysis - April 2001-May 2001
transplant - May 22, 2001- May 2004
dialysis - May 2004-present
PD - May 2004-Dec 2008
HD - Dec 2008-present
Michael Murphy
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« Reply #19 on: April 15, 2017, 08:30:01 PM »

Riki my understanding is most if not all insurance companies pay for a transplant because in the long run it's cheaper then dialysis.  Even at Medicare rates my dialysis is about 50,000 dollars a year. If the new AIK (Artificial Implantable Kidney) cost 200,000 that would mean a 4 year pay back for the insurance company plus the additional savings on drugs.  If this thing proves out in testing I am sure you will not be stuck with the bill.
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Treasure
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Dialysis Schmalysis!

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« Reply #20 on: June 27, 2017, 07:12:30 AM »

It's been 12+ years since I started dialysis. I had 11 months in there with a failing transplant. I still hate dialysis, with a white hot hate! (I would use more exclamation points, but I'm an editor, hehehe). But I'm optimistic about the bioartificial kidney University of California San Francisco is working on. I trust that team because they did everything they could to save my transplant and include me in other research they have going on.

The hate keeps me hungry and in the game. I wouldn't last long if I just gave in and accepted being on dialysis. But that's just my personality. Other people deal with dialysis, differently. There's room for all viewpoints.

I wish you all the best, you hater, you.   :2thumbsup;

Treasure
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You may worship me anytime you like... go ahead...bow down.  Now! Ok, I'm hungry, go get the grapes.  What? They're not chilled. You're useless! Ok...I'll forgive you...this time hehehe
GA_DAWG
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« Reply #21 on: June 27, 2017, 12:08:46 PM »

While I still dislike dialysis, at the same time I am very thankful for its options. Without it, I would not have had the last five years and counting with my wife and kids. It is no fun whatsoever, but beats the alternative by miles and miles.
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Michael Murphy
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« Reply #22 on: June 27, 2017, 07:20:28 PM »

 I have a tee shirt that sums it up.
Dialisys Damned if you do
               dead if you don't
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Simon Dog
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« Reply #23 on: June 27, 2017, 11:44:39 PM »

I feel very fortunate to live in a country where dialysis access is not a choice between financial ruin and death, or death if one is broke.
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