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Author Topic: Update almost 3 weeks out.  (Read 2172 times)
bette1
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My dear daughter

« on: June 11, 2010, 10:27:31 PM »

I had my transplant May 24th.  My labs have been very good with my creatinine at 1.2.  Although I feel much better than I did on dialysis, I am still weak and find myself needing to rest a lot.  I've mostly been at home, though I did go to a program at my daughters school.  I find myself wanting to do things around the house and then realizing that I don't have the stamina to do everything I want to do. 

I am not having too many problems with the prograf or the prednisone, but the cellcept is giving me a lot of stomach cramps.   I'm hoping that they lower the dose when I go for my follow up appointments.  I am also having a bit of a problem with insomnia. 

I also miss my coffee.  The transplant center doesn't want us to drink it so I switched to herbal tea.  It's just not doing it for me.  I think a lot about my deceased donor and I feel bad that their family is going through this time of loss while I am so happy. 

I have a 10 year old, and she worries about me.  She asked me what would happen if the kidney failed and I told her I'd go back on dialysis and that seemed to calm her down.   I'm looking forward to being able to drive again so I can take her out to the park and stuff. 
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Diagnosed with FSGS April of 1987
First Dialysis 11/87 - CAPD
Transplant #1 10/13/94
Second round of Dialysis stated 9/06 - In Center Hemo
Transplant  #2 5/24/10
Chris
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« Reply #1 on: June 11, 2010, 10:58:53 PM »

Bette, do they have you on an anti acid like Zantac (Ranatidine), Pepcid (forgot prescrition name)? That is usually taken to help with the CellCept and other transplant meds  problems on the stomach. Also there is Myfortic that is similar to CellCept that is suppose to be easier on the stomach that they may want to try.
 
As for the coffee, that's odd that they want you to stop drinking that. I'm curious to what their reasoning behind that. I thought my center was odd when they told me to stop drinking caffeine, but years later didn't tell cariad that same waning with her transplant (we went to the same center). Most aren't told to stop drinking coffee or avoid caffiene from what I have read on various sites.
 
Good Luck at next check up.
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Diabetes -  age 7

Neuropathy in legs age 10

Eye impairments and blindness in one eye began in 95, major one during visit to the Indy 500 race of that year
   -glaucoma and surgery for that
     -cataract surgery twice on same eye (2000 - 2002). another one growing in good eye
     - vitrectomy in good eye post tx November 2003, totally blind for 4 months due to complications with meds and infection

Diagnosed with ESRD June 29, 1999
1st Dialysis - July 4, 1999
Last Dialysis - December 2, 2000

Kidney and Pancreas Transplant - December 3, 2000

Cataract Surgery on good eye - June 24, 2009
Knee Surgery 2010
2011/2012 in process of getting a guide dog
Guide Dog Training begins July 2, 2012 in NY
Guide Dog by end of July 2012
Next eye surgery late 2012 or 2013 if I feel like it
Home with Guide dog - July 27, 2012
Knee Surgery #2 - Oct 15, 2012
Eye Surgery - Nov 2012
Lifes Adventures -  Priceless

No two day's are the same, are they?
Dianejt
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« Reply #2 on: June 12, 2010, 05:54:48 AM »

So glad to you are doing well. I hope they get your meds straightened out. How wonderful you where able to go to your daughters program, I'm sure it meant the world to her to have you there. Keep resting when you need to you have been through alot & need to take the time to heal, it has only been 3 weeks.  :flower;
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caregiver to husband Frank

bladder cancer 1994
renal failure April 2009 due to blocked right ureter. Left kidney 20% function
November 18 2009 surgery to remove right ureter.
April 3, 2010 removal bladder, prostrate, left kidney.
June 11, 2010 started Hemo @ hospital
July 2, 2010 Embolized right Kidney due to hemoraging of tumor
September 11, 2010 RIP my love
kellyt
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« Reply #3 on: June 12, 2010, 12:15:22 PM »

I felt/feel the same way, Bette.  You seem to be right on track.  My creatinine is also hanging around 1.1 and 1.2.   :cheer:
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1993 diagnosed with glomerulonephritis.
Oct 41, 2007 - Got fistula placed.
Feb 13, 2008 - Activated on "the list".
Nov 5, 2008 - Received living donor transplant from my sister-in-law, Etta.
Nov 5, 2011 - THREE YEARS POST TRANSPLANT!  :D
natnnnat
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« Reply #4 on: June 12, 2010, 07:01:03 PM »

Takes a little while for the body to get used to the new situation too.  For example, Gregory had restless leg syndrome for about a month, then it went away.  Good to hear things are progressing well.  Nice answer to your daughter.   :thumbup;
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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.
bette1
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My dear daughter

« Reply #5 on: June 19, 2010, 06:06:08 AM »

Things are still going pretty smoothly,  I am feeling better every day - more like my normal self.  I think I may be a little euphoric.  The myfordic still gives me gas pains but the transplant docs don't want to lower it because I'm high risk due to this being my second transplant and I'm african-american.  I'm tolerating the drug better now though.  I am also starting to get the fat cheeks from the prednison, but I can live with that.  The huge appetite is hard though.  I don't want to get too fat, but I am starving all the time.  I'm trying to fill up on fruit and veggies.

My only problem is that I wake up in the morning feeling great, start planning my day and then putter out.  I know that this is just temporary, so I allow myself to rest as needed.  I am also still having abdominal pain, and they don't seem to want to give me anything stronger than Tylenol.  What's up with that?
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Diagnosed with FSGS April of 1987
First Dialysis 11/87 - CAPD
Transplant #1 10/13/94
Second round of Dialysis stated 9/06 - In Center Hemo
Transplant  #2 5/24/10
monrein
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Might as well smile

« Reply #6 on: June 19, 2010, 06:19:02 AM »

You're still recovering from a pretty major surgery so the abdominal pain and puttering out both sound fairly routine to me.  Things ought to slowly improve until you're feeling stronger and stronger.  So glad to hear that you have no major issues to report.   :cuddle;
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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
Dianejt
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« Reply #7 on: June 19, 2010, 09:39:10 AM »

 :clap; Glad you are doing so well. Please take it slow, rest when needed & don't push yourself. As far as  fat cheeks I love far cheeks they are the best to paint on (LOL I am a face & body painter). So happy to hear you have "The hungry horrors" & you know what foods to stay away from so enjoy one of lifes pleasures. Keep up the healing & enjoy your new freedom.
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caregiver to husband Frank

bladder cancer 1994
renal failure April 2009 due to blocked right ureter. Left kidney 20% function
November 18 2009 surgery to remove right ureter.
April 3, 2010 removal bladder, prostrate, left kidney.
June 11, 2010 started Hemo @ hospital
July 2, 2010 Embolized right Kidney due to hemoraging of tumor
September 11, 2010 RIP my love
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