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Author Topic: My Arm Is Swollen  (Read 27337 times)
Rerun
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Going through life tied to a chair!

« Reply #125 on: April 25, 2009, 06:09:52 PM »

His reply is in bold:

Dr. Davis,

Will this axillary vein prosthetic be visible; like a tube under my skin across my collarbone?  I'm not vain at all,  but I don't want to look like more of a freak then I do.

I think we can bury it pretty far down so it won't extrude-I will try not to make it too visible
 

Have you done this procedure on others, and if so, can I talk to someone who has one?

Sorry, no.   While putting a graft in is something I do every day, this graft (axillary vein to axillary vein) is pretty uncommon.    Usually, in your situation we end up developing the other arm for access.

Even with my left arm... it has always had problems and Dr. Park (in Sacramento) told me I would have problems because I had bad veins from 22 years of Prednisone.  How would my right arm be any different?  To me it would be even worse because they chose the "good" arm.

Like I said, you have fairly good vein on the right arm
 

I went ahead and had the left arm fistual against my better judgement because my transplanted kidney had not failed yet and it would be a slow death with it still trying to work for me.  I'm just telling you how it is.  Now it would be quick.

In my experience, very few people, when push comes to shove, are willing to stop dialysis and die.   What I think will likely happen is that your left arm will fail, and then you will decide you want to live.   And then I will be several months behind, be forced to develop your right arm (we likely would not be able to save your left arm fistula), and you will have a right neck catheter or femoral catheter for several months

I am willing to try anything once.  I have done home hemodialysis, PD, transplant, incenter hemodialysis, and nocturnal dialysis.  I have had probably 4 catheters and countless fistulagrams.  I am not a quitter, but my gosh it comes to a point where I feel guilty for costing the tax payers so much money, and I get tired of contributing to the health care crisis.

Neither option will cure me, and what future do I have in dialysis with no hope for a transplant.  All I can see are more problems. You have to realize there is no break from dialysis.  There is no two weeks off to go to Hawaii and then come back and hit it again.  It is every other night with Saturday night off.  I guess that is not enough for me.

Maybe you could get back to me with a name and phone number of someone who has this axillary vein prosthetic?

I have yet to see Obermiller, so I emailed him today reminding him that if he doesn't visit the center in April he won't get paid by Medicare.  That may set a fire under his ass!

I stopped the nurse last night before he put heparin in the wrong line.  That is just another example of why I'm tired of dialysis. 

I really hope you understand my decision, but maybe we can agree to disagree.  Isn't that politically correct these days?

Mrs Irwin, you're the patient.   You are always the one in charge.  It's your body, and I will respect whatever decision you make.   
 
Thanks,

 Darla Irwin~

 

 
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Rerun
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Going through life tied to a chair!

« Reply #126 on: April 27, 2009, 11:19:08 PM »

Monday April 27, 2009

I'm in the hospital because there is a spot on my fistula that does not look good.

I saw the surgeon and he is getting his way.  Tube across the chest and start on the right arm.

I was concerned that he had never done the tube across the chest and his analogy was like riding a bike up a hill.  You know how so it doesn't matter what hill you go up.

Let's hope!     :flower;
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Wattle
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« Reply #127 on: April 28, 2009, 01:28:47 AM »


 :flower;  Hugs Rerun. I am glad you are giving it a go. Hopefully it will go smoothly and all the drama will be behind you. We need you around for a while yet!!   :cuddle;
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PKD
June 2005 Commenced PD Dialysis
July 13th 2009 Cadaveric 5/6 Antigen Match Transplant from my Special Angel
paddbear0000
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« Reply #128 on: April 28, 2009, 09:56:11 AM »

I hope this works so you can hang around for a long time to come!!  :cuddle; :cuddle; :cuddle;
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I HAVE DESIGNED CKD RELATED PRODUCTS FOR SALE TO BENEFIT THE NKF'S 2009 DAYTON KIDNEY WALK (I'M A TEAM CAPTAIN)! CHECK IT OUT @ www.cafepress.com/RetroDogDesigns!!

...or sponsor me at http://walk.kidney.org/goto/janetschnittger
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Diagnosed type 1 diabetic at age 6, CKD (stage 3) diagnosed at 28 after hospital error a year before, started dialysis February '09. Listed for kidney/pancreas transplant at Ohio State & Univ. of Cincinnati.
kitkatz
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« Reply #129 on: April 28, 2009, 02:44:09 PM »

Oh my Rerun! I wish you luck!
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Remember your present situation is not your final destination.

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

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David13
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« Reply #130 on: April 28, 2009, 03:09:05 PM »

I genuinely hope that everything turns out okay.   :cuddle;
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monrein
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Might as well smile

« Reply #131 on: April 28, 2009, 03:30:49 PM »

Rerun, I'm thinking of you and hoping for a positive outcome with every fibre of my being.  We need and want you back here with us.
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
paris
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« Reply #132 on: April 28, 2009, 03:41:25 PM »

Rerun,  Lots of prayers for a good outcome.  Your surgeon seems to respect your opinions, and at least is listening to you.  I hope the surgury is fast and you have good drugs!       :grouphug;
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
Zach
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"Still crazy after all these years."

« Reply #133 on: April 28, 2009, 08:59:31 PM »

 :cuddle;
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Uninterrupted in-center (self-care) hemodialysis since 1982 -- 34 YEARS on March 3, 2016 !!
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
No transplant.  Not yet, anyway.  Only decided to be listed on 11/9/06. Inactive at the moment.  ;)
I make films.

Just the facts: 70.0 kgs. (about 154 lbs.)
Treatment: Tue-Thur-Sat   5.5 hours, 2x/wk, 6 hours, 1x/wk
Dialysate flow (Qd)=600;  Blood pump speed(Qb)=315
Fresenius Optiflux-180 filter--without reuse
Fresenius 2008T dialysis machine
My KDOQI Nutrition (+/ -):  2,450 Calories, 84 grams Protein/day.

"Living a life, not an apology."
Deanne
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« Reply #134 on: April 30, 2009, 03:28:18 PM »

Rerun hasn't posted in a couple of days. Has anyone heard how she's doing?

Rerun, Get well soon!!!!! I mostly lurk these days, but I miss you.

Deanne
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Deanne

1972: Diagnosed with "chronic kidney disease" (no specific diagnosis)
1994: Diagnosed with FSGS
September 2011: On transplant list with 15 - 20% function
September 2013: ~7% function. Started PD dialysis
February 11, 2014: Transplant from deceased donor. Creatinine 0.57 on 2/13/2014
Wenchie58
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Always carrying the big silly grin!

« Reply #135 on: April 30, 2009, 03:43:00 PM »

I was also questioning today whether anyone had heard from/about her.  We are all mother hens to each other.  I love it!

Here's hoping all is going well for Rerun!  :grouphug;
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Live your life in such a way that when your feet hit the floor in the morning Satan shudders and says "Oh s**t, she's awake!"

Right nephrectomy 1963
Diagnosed ESRD 2007
"Listed" summer 2007
Transplant 3/6 match  10/24/08
jbeany
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Cattitude

« Reply #136 on: April 30, 2009, 07:53:51 PM »

Thinking of you, rerun.   :cuddle;
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circleNthedrain
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« Reply #137 on: April 30, 2009, 10:35:12 PM »

Thinking of you Rerun and hoping for a good outcome here!
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1979 Diagnosed with kidney failure
1979 Right arm fistula
1979 Start hemodialysis
1980 CAPD catheter
1980 Start CAPD
1989 Cadaveric kidney transplant
1995 2nd cadaveric  kidney transplant
2007 Start hemodialysis
2010 Still drawin' wind
paris
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« Reply #138 on: May 01, 2009, 01:38:06 PM »

We keep praying for you Rerun.    :grouphug;
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
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