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Stephanie Wetzel
  • Female
  • Champaign, IL
  • United States
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Latest Activity

Jason Boyd and Stephanie Wetzel are now friends
on Saturday
August 18
August 17
hey girly! this is an awesome idea! i am hoping to get to south africa! i will email you about a shirt! they are adorable!! xoxo
August 17
August 17
I have been on the waiting list 3 1/2 years for a new kidney! Actually my second kidney! My first transplant was from my brother, my hero! Sadly, I had been living with undiagnosed pulmonary hypertension for years (shortness of breath was bad enough…
August 17
For those on the waiting list. Come find support and encouragement from others who are waiting.
August 17
Hey all!!! check out my new site http://transplantswim.webs.com/
June 8

Profile Information

What is your city / state and country of residence?
Champaign, Illinois
USA
How are you touched by transplantation?
I am a Recipient
If you are a recipient, what type of transplant did you receive?
Kidney
Recipients: In this space, feel free to list those you are grateful to for receiving the Gift of LIfe:
My older brother Doug! He donated me his kidney in November 2002.
If you are a recipient, what type of donor did you receive your Gift of Life from?
Living Donor
What is your principal transplant med(s)?
Prednisone and Plaquinel
What is your hospital and, or doctor's name, city / state and country?
University of Chicago 2002-2003
Barnes Jewish/Washington Medical 2003 to present
If you are on the transplant waiting list, what type of transplant are you waiting for?
Kidney
If you are on the transplant waiting list, please use this space to write about your experience:
I had my first transplant from my brother in 2002. In 2005 I got sick from too much stress and my fistula started growing again causing cardiac overload. After it was removed in 2006 after some complications, I was left with only 20% kidney function in my "new" kidney. So the process began again to get back on the waiting list and I made it March 2008.
What do you do for a living?
Part Time Admin. Asst. at Windsor Road Christian Church
About Me: Please use this space to tell the community about yourself and your unique experience with transplantation:
I think everyone's story is unique in some way. We all go through different struggles but are able to relate to others through our varied experiences. I have been blessed to be apart of Team Illinois with the Transplant Games and am looking forward to representing Team USA!
My story began in 1986 when I developed a "mysterious rash" from swimming all the time and being baked in the sun. I was diagnosed with discoid lupus in the fall and my future swimming plans were scrapped because I could no longer go out in the sun. My disease progressed into systemic affecting my blood, joints, liver, stomach and kidneys. By 1995 I had kidney disease and began treatments like imuran, cellcept and large doses of prednisone. The lupus was scarring my kidneys down. In 2001 I started the process to get on the waiting list and my family was tested. My dad and I weren't a match and my mom was, but because of high blood pressure she wasn't a candidate. My brother tested and we were a perfect match! I then had some complications getting ready for surgery and had to have a hysterectomy and 2 fistula surgeries. My brother had some borderline blood pressure issues and had to lay off exercising for a few months too. In June of 2002 we were all set and I had a kidney biopsy to see if there was any treatment to be done to prolong the kidney function I had left. The biopsy pierced a blood vessel inside the kidney and the outside healed over it causing the blood to fill up in my bladder and back up into my kidney. The doctors wouldn't do a CAT scan even though I was in horrible pain because there was no bruising apparent under my skin. They sent me home and the next day I couldn't go to the bathroom because my ureter was clogged with blood. I went to the ER and the $%^^% hit the fan. My kidneys failed and they had to plunge my bladder with what looked like a turkey baster! I spent 3 weeks in the hospital before they tried an angiogram to cauterize the bleeding vessel. After that I went on dialysis. My brother and I had to re-do all our cross matching because of all my transfusions and we got the clear for late September. On Labor Day he went for a bike ride and was run over by a drunk driver (at noon). He had a broken clavical and scapula but no internal injuries. It was so stressful and I found out on dialysis so I was "tied" up and couldn't go be with him. Our surgery was then moved to November and on November 18, 2002 I had my last dialysis and November 19th I was given a second chance at life because of my big brother!!!

The saga continues as I am now back on the waiting list for another kidney and we just pray the ones I have hang in there! The Games have been such a huge therapy for me and my family dealing with this kind of lifestyle. I love swimming and to be able to be apart of this is so wonderful!
Please help us reach other members by telling us how you found Transplant Cafe:
NKFI website
What is your relationship status?
Single
My Personal (non-commercial) Website, Page, or Blog URL:
http://www.stefswimz.webs.com

Comment Wall (33 comments)

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At 7:40am on August 18, 2010, Jason Boyd said…
Hello Stpehanie,
thanks for dropping by to welcome me. I am glad your brother was able to help you in your time of need. I am sure he does not feel like a super hero, but definitely happy he will continue to have his sister healthy and happy.
All my best
At 8:04am on May 24, 2010, Kim Jacques said…
Hey!! Thanks for your words of encouragement!! I saw via Facebook that we have some mutual friends (including a specific Jen Klouse). WOO HOO! I hope we can meet up in Wisconsin!! Hugs!! :-)
At 2:01pm on July 21, 2009, Little_Jen said…
How are you feeling?
At 7:40pm on May 29, 2009, Jen said…
I'm thinkin' of you lady...you're gonna pull through this!!! xo
At 5:49pm on March 3, 2009, Jen said…
Hey chickie....How the heck are ya?? xoxo
At 7:51pm on February 24, 2009, Jen said…
I'M SO EXCITED!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
At 6:58am on January 30, 2009, Little_Jen said…
Hey Stephanie! I'm actually going to room with my mom. I didn't want to because she snores, but I don't want to make her pay extra for a single. Plus, she turns 65 while we are there! Maybe we can all stay in the same "area." I think you share a kitchen and living area, right?
At 2:58pm on January 29, 2009, Steve Diamond said…
Hi Stephanie,

Thanks for the advice. I did have the chance to have a long phone conversation with Bill a couple of weeks ago. What a nice guy. He was very helpful. I would try swimming but I would need scuba gear since I am as likely to sink in water as stay afloat. I will try to start up slowly. My problem is when I start working out I forget what slow and easy means. Must be short-term memory loss.

Thanks for the feedback on Cellcept; I get nervous thinking about a change to my meds.

By the way if you have a chance to forward information on fundraising it will be greatly appreciated.

Steve
At 3:35pm on January 28, 2009, Steve Diamond said…
Stephanie,

That is exactly why I was told to stop all exercise until they got my Creatinine gets under control. I do tend to train hard and my Neph did a blood test for toxins released from muscles when they are under stress. The med change isn't due to the exercise tho, the levels were rising anyway.
At 2:03pm on January 28, 2009, Steve Diamond said…
Thanks Stephanie,

I am excited about Australia and the US games next year. I am planning to do the Cycling events and am thinking of exploring some other events also. I have had to put my training on hold for what I hope is only a short time due to rising Creatinine levels. My Neph is going to take me off of Rapamune and switch to Cellcept. Hopefully this will do the trick and I can resume training.
 
 
 

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