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Author Topic: What are some things u wish u were told BEFORE transplant?  (Read 3148 times)
gothiclovemonkey
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« on: March 31, 2011, 07:18:39 PM »

What are some things u wish u were told BEFORE transplant?

If you had to do it again would u?
« Last Edit: April 01, 2011, 04:59:10 AM by gothiclovemonkey » Logged

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rsudock
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will of the healthy makes up the fate of the sick.

« Reply #1 on: March 31, 2011, 11:39:43 PM »

you may get high blood sugar resulting in the use of insulin b/c of the Prograf....that was a bit of a slap in the face....

xo,
R
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Born with autosomal recessive polycystic kidney disease
1995 - AV Fistula placed
Dec 7, 1999 cadaver transplant saved me from childhood dialysis!
10 transplant years = spleenectomy, gall bladder removed, liver biopsy, bone marrow aspiration.
July 27, 2010 Started dialysis for the first time ever.
June 21, 2011 2nd kidney nonrelated living donor
September 2013 Liver Cancer tumor.
October 2013 Ablation of liver tumor.
Now scans every 3 months to watch for new tumors.
Now Status 7 on the wait list for a liver.
How about another decade of solid health?
sutphendriver
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« Reply #2 on: April 01, 2011, 04:31:29 AM »

the weight gain associated with the steroids.  I gained 70lbs over a few years.  When my transplant failed and they took me off the steroids, I lost 81lbs.  It didnt matter how hard I excersised,  I had to eat constantly or get sick.
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gothiclovemonkey
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« Reply #3 on: April 01, 2011, 04:58:50 AM »

yikes with diabetes running in my family, this is no good.
also weight gain, after it took this long to get the weight off FOR transplant, that would make me a bit angry! lol

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natnnnat
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WWW
« Reply #4 on: April 01, 2011, 07:09:02 AM »

"...that the medication would give you cancer.  That I would have trouble with my bowels. That getting the transplant is just the start.  I had to find that out for myself.  Cos I thought that once you got it that would be it.  But it was just the start of a very long road," says Gregory, from another room.  I know from asking him other times, that he is glad of his transplant and yes he would do it over again.  Just to check, I ask him again:  "Yes, definitely.  It's worth it, every minute of it.  Even though you go through a lot of pain and bad experiences, its worth every second of it."
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Natalya – Sydney, Australia
wife of Gregory, who is the kidney patient: 
1986: kidney failure at 19 years old, cause unknown
PD for a year, in-centre haemo for 4 years
Transplant 1 lasted 21 years (Lucy: 1991 - 2012), failed due to Transplant glomerulopathy
5 weeks Haemo 2012
Transplant 2 (Maggie) installed Feb 13, 2013, returned to work June 17, 2013 average crea was 130, now is 140.
Infections in June / July, hospital 1-4 Aug for infections.

Over the years:  skin cancer; thyroidectomy, pneumonia; CMV; BK; 14 surgeries
Generally glossy and happy.

2009 - 2013 PhD research student : How people make sense of renal failure in online discussion boards
Submitted February 2013 :: Graduated Sep 2013.   http://godbold.name/experiencingdialysis/
Heartfelt thanks to IHD, KK and ADB for your generosity and support.
Brightsky69
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« Reply #5 on: April 01, 2011, 08:16:28 AM »

This is my 2nd transplant so not much was a surprise. Somethings were new...like the drain line they put in after the transplant. Never had that before. Yucky.
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Transplant June 11, 1991 (1st time) my mom's kidney
Received my 2nd kidney transplant Oct. 19th 2010.
RightSide
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« Reply #6 on: April 04, 2011, 04:42:18 PM »

Two things:

1.  That I would have to travel back to the transplant clinic every week for blood tests and consultations, at least for the first three months.  (For me, that's a very long drive and a very long time to wait before eating anything, since I must take my anti-rejection meds before eating like I do on the other days.)

2.  That it's practically expected that I'll catch at least one or two low-grade infections in the first 6 months after transplant.

My transplant was January 26, 2011.  And already I've picked up jock itch (haven't had that in 20 years) and now I just got a mild sinus infection (stuffy nose and discolored yellow post nasal drainage).  I haven't had time to tell my transplant team about the sinus infection yet, but I did tell them about the jock itch. And they said "Sure, topical fungus infections are quite common."  They didn't tell me that before I got the transplant though.

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Sugarlump
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10 years on and off dialysis

« Reply #7 on: April 04, 2011, 07:09:25 PM »

Rightside I am 4 months post tx and still on weekly visits (150 miles roundtrip) due to medication problrms.  :waiting; Takes big chunk of day.
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10 years of half a life
3 years HD 1st transplant Feb 08 failed after 3 months
Back to HD 2nd transplant Dec 10 failed after 11 months
Difficult times with a femoral line and catching MSSA (Thank you Plymouth Hospital)
Back on HD (not easy to do that third time around)
Fighting hard (two years on) to do home HD ... watch this space!
Oh and I am am getting married 1/08/15 to my wonderful partner Drew!!!
The power of optimism over common sense :)
Ang
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« Reply #8 on: April 05, 2011, 11:48:37 PM »

pretty much knew what to look for,was given plenty of reading material re: anti rejection meds and what they can do.
do it again- won't have to i hope
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live  life  to  the  full  and you won't  die  wondering
rsudock
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will of the healthy makes up the fate of the sick.

« Reply #9 on: April 06, 2011, 07:07:15 AM »

Another thing be careful about going to public gyms. (Rightside's comment about jock itch reminded me about something) Post transplant like 7 or 8 years when I was in college I kept going to this gym and and working out on this machine you had to put your thigh on and push. Well I got RINGWORM!!! At first I couldn't figure it out and I went to the gyn doc and as soon as he saw it he was like, "Gosh you never seen ring worm before?" SO I STOPPED using the college's gym asap. It took forever to go away and I even had to use some type of liquid metal stuff to rub on it to make it go away...the over the counter stuff wouldn't work....nasty!

Oh I make sure to paint my toenails before transplant b/c it might me awhile before you can bend over and do it yourself!!

Again yes I would get a tranplant again.

xo,
r
Logged

Born with autosomal recessive polycystic kidney disease
1995 - AV Fistula placed
Dec 7, 1999 cadaver transplant saved me from childhood dialysis!
10 transplant years = spleenectomy, gall bladder removed, liver biopsy, bone marrow aspiration.
July 27, 2010 Started dialysis for the first time ever.
June 21, 2011 2nd kidney nonrelated living donor
September 2013 Liver Cancer tumor.
October 2013 Ablation of liver tumor.
Now scans every 3 months to watch for new tumors.
Now Status 7 on the wait list for a liver.
How about another decade of solid health?
wj13us
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Paul's ride 2011

« Reply #10 on: April 06, 2011, 07:29:49 AM »

I wish they would have told me it would last 38+ years.  Would have saved me a a LOT of worry.

Bill
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Brightsky69
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« Reply #11 on: April 06, 2011, 08:04:42 AM »

wj13us - 38 years is awesome!!
Mine is plugging along. I worry too about some stuff like when my socks leave a slight impression. I start to think OMG the kidney isn't getting rid of all the fluid!!!!
My doc always checks for puffy ankles and said to me if you notice swollen ankles then let us know and we'll prescribe a diuretic....like it's no biggie.
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Transplant June 11, 1991 (1st time) my mom's kidney
Received my 2nd kidney transplant Oct. 19th 2010.
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