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Author Topic: My turn soon.  (Read 15780 times)
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #50 on: July 20, 2011, 03:13:26 PM »

 :2thumbsup;
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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
sico
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wheres my bike gone?

« Reply #51 on: August 10, 2011, 01:28:58 AM »

So on my 34th birthday I visited my Renal Clinic, my creatinine is at 107.
Not back there for 3 months now, got a big bag of drugs so all sweet for a while...lol
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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.
Rodneyss1
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« Reply #52 on: August 10, 2011, 02:43:08 AM »

Glad to hear that you are doing well.  My turn will be on September 9.  A really close friend of mine is donating.  Are there any serious side effects of the medication that you are taking?  Can you give me any pointers on the proceedure?
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Diagnosed with FSGS- 2003
End Stage- December 2010
Dialysis Journey Started- December 2010
Transplant List- December 2010
Living Donor Transplant Non-Related Surgery at St. Vincents (Indianapolis)- September 9, 2011
***Living life like its Golden***
edersham
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« Reply #53 on: August 10, 2011, 01:14:26 PM »

Most of the drugs tx patients take have an assortment of possible side effects. Serious is in the eye of the beholder. Also, every body is different so you just never know. With the assortment of things you will be taking after transplant tracking down which drug or supplement is responsible for a given side effect can be a process .  There are a lot of threads on this site discussing different side effects. The bottom line is that for the great majority of transplant patients the side effects are a minor blip compared to the miracle of a healthy kidney.

Godspeed
Ed
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Ang
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« Reply #54 on: August 10, 2011, 04:23:13 PM »

Glad to hear that you are doing well.  My turn will be on September 9.  A really close friend of mine is donating.  Are there any serious side effects of the medication that you are taking?  Can you give me any pointers on the proceedure?

you should be given plenty of reading material after your transplant
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live  life  to  the  full  and you won't  die  wondering
RichardMEL
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« Reply #55 on: August 11, 2011, 02:09:30 AM »

107 mate? that's awesome!! 3 months?!?! even more awesome!! LOL. I'm still at 3 weeks haha
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
sico
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wheres my bike gone?

« Reply #56 on: April 07, 2014, 06:08:14 PM »

Well thought I'd jump on here as it's been quite a while.

Today is the 4th anniversary of my transplant and it has performed faultlessly.
My last creatinine reading was around 114(aus reading).
Dad is doing well and I am too. So hoping to get lots more D free years.

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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.
SooMK
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« Reply #57 on: April 08, 2014, 07:56:57 AM »

Congrats!
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SooMK
Diagnosed with Uromodulin Kidney Disease (ADTKD/UMOD) 2009
Transplant from my wonderful friend, April 2014
Volunteering with Rare Kidney Disease Foundation 2022. rarekidney.org
Focused on treatment and cure for ADTKD/UMOD and MUC1 mutations.
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