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Author Topic: My Transplant on Tuesday  (Read 6374 times)
BrandyChloe
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« on: January 01, 2010, 08:42:15 AM »

Hi all - Happy New Year! This is the first chance I've really felt up to posting so here is my transplant story -

As you know, my brother was able to donate one of his kidneys to me and the transplant was Tuesday. His surgery went well but took 6 hours instead of 4. My surgery took 2 hours so I was pretty quick but since I had still been creating urine while on dialysis, my surgeon decided to have a sonogram done while I was in recovery which turned out to be a good thing because the transplanted kidney wasn't working. They had to open me back up to try to determine what happened and it turned out my body had formed clots that clogged the artery so blood wasn't getting to the new kidney.

They unblocked the artery and closed me back up but the kidney was a little sleepy. My surgeon told me the kidney was already turning blue when she opened me back up but it had started to pinken back up by the time they re-closed me.

They havesince  been watching me like a hawk (which I am told is normal here at Mayo). My second sonogram on Wednesday morning was much better and my creatnine has been steadily dropping. Yesterday it was at 3.8 and this morning it's at 3.3. My urine output is excellent. They said they know my kidneys wouldn't be having that much output so they know it's the new kidney working. They said I am probably 1 - 2 days behind a normal live transplant recovery schedule.

Now they are trying to determine if I have a clotting issue that we didn't know about. The doctors have no idea why this happened and it has never happened to them before so they are in uncharted waters with me. For now, they are going to keep me on blood thinners for at least 3 months unless they determine I have an issue and then it will end up being a "for life" kind if treatment.

They are pulling me off all my IVs and drips but instead of going home on Saturday, they will probably keep me until Monday or Tuesday to complete the switch from the liquid to the oral blood thinner.

I"m not in a lot of pain, which surprises me. I feel more like I've done 100 sit-ups too many. Haven't used much of my pain meds and they have taken me off the "button" and are moving me to orals but they usually make me sick so I probably won't take many of those.

My arms look like I'm a drug addict and I'm retaining about 12 pounds of fluid from all the liquid they are pumping into me but all in all I feel ok, all things considered.

Right now my biggest concern is that something will happen to this kidney and my brother will have gone through all of this for nothing. I know it wasn't my fault what happened (truly, it wasn't anyone's fault) but it sure makes me nervous. I think I will end up being extra paranoid during my recovery.

Anyway, wanted to give you an update. I'll write more later.

Effie
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Darthvadar
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« Reply #1 on: January 01, 2010, 08:51:32 AM »

Great news, Effie...

Congratulations on your new kidney!...

Great praise to your brother... :bow;

Hope it all works out for you!....

Happy New Year..

Darth...

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Cared for my late mum, Elsie who had Kidney Failure... Darling mum died on July 15th 2014... May her gentle soul rest in peace....
okarol
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« Reply #2 on: January 02, 2010, 12:29:43 AM »

Hi Effie,
Thank you for the update. I appreciate your PM too.
Good thing they checked the kidney right away and were able to get it going again!
I hope each day is better and you can feel less worried. It sounds like they are taking good care of you. How is your brother doing?
Best wishes and Happy New Year to you both!
 :cuddle;
« Last Edit: January 02, 2010, 04:06:04 PM by okarol » Logged


Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
Hanify
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #3 on: January 02, 2010, 12:49:36 AM »

Wow how exciting - and scary at the same time.  Sending positive thoughts your way.
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Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
fc2821
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« Reply #4 on: January 02, 2010, 08:32:40 AM »

 :pray; that you and your brother do well and improve. 
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« Reply #5 on: January 02, 2010, 09:01:51 AM »

Effie,
Good to hear that things are improving! And I hope they continue on that course!

Your brother is an angel, but you already know that!

Congratulations.  :cheer: :cheer:

Keep the good news coming!  :bandance;

Aleta
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Wife to Carl, who has PKD.
Mother to Meagan, who has PKD.
Partner for NxStage HD August 2008 - February 2011.
Carl transplanted with cadaveric kidney, February 3, 2011. :)
kellyt
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« Reply #6 on: January 02, 2010, 01:25:49 PM »

Congratulations on your transplant!  Prayers that everything works out and you don't need the blood thinners forever.

I know it's hard, but don't think about your brother right now.  Concentrate on your recovery.  Now that I'm 1 year post transplant I think about my donor (sister-in-law) all the time in regards to what if something happens to the kidney and all this would have been for nothing.  But in the beginning you must concentrate on you and your new kidney.  He won't be thinking it's a waste if something happens.  He'll be thinking how much he loved you enough to try.  Everything will turn out fine!   Rest and recuperate.   :cuddle;   And  :beer1; to your brother, the Hero.
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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
cariad
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« Reply #7 on: January 02, 2010, 03:34:19 PM »

That sounds like quite an ordeal, Effie, but you made it through.  :cheer:

Best of luck with your ongoing recovery.    :flower;
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« Reply #8 on: January 02, 2010, 03:55:09 PM »

WOW, I'm thankful they decided to do the sonogram to find the new kidney was plugged up.  I'm sure you will do well from no on.  I hope your brother has a speedy recovery.  Nice guy!

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Chris
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« Reply #9 on: January 02, 2010, 05:33:45 PM »

Congraats on transplant, but sorry to hear what you have gone through. Hope creat and bun get even lower when you read this.
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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?
BrandyChloe
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« Reply #10 on: January 02, 2010, 06:15:43 PM »

Hi all. Creatnine was 3.2 this morning which is down from 3.8 yesterday and I'm putting out a lot of urine so the docs are happy, all things considered. The cath is gone so I am peeing on my own and they have removed all IVs except the blood thinner. They are targeting me going home by Monday.

They said the kidney is a little sleepy from the ordeal it went through but since they know it's working and I'm not on dialysis, they are very positive all will be well. They said it will just take a little longer than anticipated but what do I have if I don't have time?

Today is my last day of prednisone and I'm so glad. I'm nervous enough as it is but the prednisone makes it worse. Mayo's policy is to only have you on the steriod for 5 days and then they take you off. I wasn't even aware of this but was so happy when I found out. The bruises on my arms are yucky and they said the prednisone makes it worse.

Thank you so much for your advice and encouragement. I know you are all right when you say my brother wouldn't see this as a waste. He's a good person and I'm so grateful for his gift. He is recovering well at home which makes me very happy. Can't wait to see him again!

TTYL
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kellyt
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« Reply #11 on: January 02, 2010, 09:16:50 PM »

You lucky dog, getting to come off the Prednisone so soon!  I'm jealous!   I'm currently at 4 mg and we're starting (again) the decline to get off the Prednisone 100%.  I would have been off a long time ago, but I had this stupid lymphocele problem.  I can't wait to get off of it completely.

Take care!!  Keep us posted of your progress.
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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
Hanify
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #12 on: January 02, 2010, 09:18:14 PM »

Sound good. Yahoo.
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Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
flipperfun
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« Reply #13 on: January 03, 2010, 01:00:01 AM »

Hi Effie, congratulations on receiving a new kidney from your brother.  I wish you and your brother a very speedy recovery.

Denise
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Des
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« Reply #14 on: January 03, 2010, 02:21:06 AM »

 :cheer:

I was on holiday so let me just say  :bandance; :cheer:
I am so glad both you and your brother are doing well. May you have a fantastic 2010!
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Please note: I am no expert. Advise given is not medical advise but from my own experience or research. Or just a feeling...

South Africa
PKD
Jan 2010 Nephrectomy (left kidney)
Jan 2010 Fistula
Started April 2010 Hemo Dialysis(hate every second of it)
Nov 2012 Placed on disalibity (loving it)
fc2821
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« Reply #15 on: January 03, 2010, 12:20:40 PM »

 :yahoo; and  :2thumbsup; Glad you are both doing well and I hope you both will continue to do so. Let us know.  :waving;
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« Reply #16 on: January 03, 2010, 06:52:52 PM »

Gee Effie what a start for your kidney. Lucky they picked up the clot. I hope it's smooth sailing from here on for you.
Thats great to hear you're getting off the prednisone so soon.
 :bestwishes; to you and your brother.
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Brad      "Got myself a one way ticket, going the wrong way" - Bon Scott

6/11/08 diagnosed with ESRF, dialysis that day

HD and PD

8th of April 2010 Live kidney transplant from my father.
Jean
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« Reply #17 on: January 04, 2010, 06:54:42 PM »

What wonderful news!!!! Congrats, and keep on P ing!!!
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BrandyChloe
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« Reply #18 on: January 06, 2010, 06:20:49 PM »

Hi all. Thanks for all the encouragement! Sorry I don't write more but it's amazing how tiring it is trying to heal.

Creatnine dropped to 2.7 four days ago but hasn't budged since. They made me come in today for a sonogram to make sure the kidney was ok. They said they didn't see anything out of the ordinary. I have a day off from traveling to Mayo tomorrow and don't have to go back until Friday morning for more blood work. Hopefully my creatnine will go down some more.

One of the anti-rejection meds is giving me gastro issues. Hopefully my body will adjust soon because this sucks. They are pushing me to eat but it's not fun when your stomach is nauseated most of the time.

I had forgotten I can now eat dairy again so I had a yogurt today and that seemed to help.

Anyway, I'll let you know how the labs look on Friday.
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Chris
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« Reply #19 on: January 06, 2010, 09:20:11 PM »

Are you on CellCept? If so, did they prescribe pepcid,ranitidine (Zantac) (higher dose and quantity than on the shel) to help with te effects?

Hope your creat goes down Friday. :bandance;
Logged

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?
Sunny
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Sunny

« Reply #20 on: January 07, 2010, 04:00:09 PM »

I'm happy things are going well for you and your new transplant now. Mayo sounds like they are taking good care of you. I hope your donor is doing well.
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Sunny, 49 year old female
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BrandyChloe
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« Reply #21 on: January 08, 2010, 06:24:45 PM »

Are you on CellCept? If so, did they prescribe pepcid,ranitidine (Zantac) (higher dose and quantity than on the shel) to help with te effects?

Hope your creat goes down Friday. :bandance;

Yep, on Cellcept, Prograf and Prilosec. Had to break down and get a pill for the nausea today. Creatnine is up to 3 but they think it's because my Cellcept dose is too high so they dropped it from 5 mg twice a day to 4 mg twice a day. My level was 10.5 and they want it to be around 7. Hopefully this will help the creatnine go down. More blood work on Monday.
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Chris
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« Reply #22 on: January 08, 2010, 08:21:44 PM »

Sounds like you are talking Prograf dosage there and level. I forgot to mention the nausea med, but hope the doctors warned you about prolong use of that med.

The dosage change should work, that is a normal thing they do and it works.

Good Luck on next labs. :2thumbsup;
Logged

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?
okarol
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« Reply #23 on: January 08, 2010, 08:37:02 PM »


I am sure they have you drinking tons of water, and that will help you avoid dehydration, which can cause toxicity of the meds. Prograf is usually the one that gives you a spike in creatinine, as I recall.
Hope it gets better!
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
BrandyChloe
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« Reply #24 on: January 10, 2010, 08:27:26 AM »

I drink as much water as I can but also drink hot tea (I'm so cold all the time) and cranberry juice watered down with seltzer water. My doctor did tell me it's the Prograf causing the stomach issues so hopefully lowering the dosage will make some of that crappy feeling go away. He told me it could take up to a month for the creatnine to be where they want it so I just need to learn to be patient.
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