TransplantCafe.com - The Gift of eLife!

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

doing better all the time! dialysis is going well most days. is it true i can't compete in 2010 because i am on dialysis??
October 13, 2009
Unfortunatly prednisone is a beast all on its own. I have been blessed/cursed to be on it since 1986 with the same types of side affects--uumpa luumpa mean anything to you? i take lasix for water weight and watch my salt carefully, unfortunatley pr…
October 13, 2009
Cloyce--thank you for sharing about your daughter! I have had lupus (a relative of CF) since I was 14 and my first kidney transplant was in 2002 from my brother. I am unfortunately back on the list after losing my new kidney to cardiac arrest from p…
October 13, 2009
hey all! i haven't been on much since returning home from the hospital but am keeping up with your excitement. i am still totally bummed i can't make the trip and ironically, the day i would have been swimming my favorite race, i will now be having…
August 7, 2009
July 21, 2009
hello everyone! i am finally home from the hospital! I have started therapy and hope to be able to walk on my own again soon! thank you so much for supporting me and lifting me up in prayer...they have been heard and answered in so many ways! i am j…
June 23, 2009
Members who are planning on swimming at the 2009 World Games in Australia
June 22, 2009
May 29, 2009

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 (31 comments)

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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.
At 3:10pm on January 27, 2009, Stephanie Wetzel said…
haha oh sister i will be out of my mind on xanax!! tee hee we will sleep like babies! tee hee this could be really entertaining if they have wine on the flight too! i hope we don't get kicked off!! ha ha ha
At 3:37pm on January 26, 2009, Little_Jen said…
Hey.. I'm on the team flight on the 19th.. you too? I will be majorly drugged on Ambien tho, so don't know if we will *chat* then. Or we could, but I won't remember it!
 
 

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my good friend christy rec'd her 3rd liver transplant last week and is doing nicely....she has two girls 12 and 9, and a great hubby and host of friends...im glad to report she is doing well at Duke Univ Med Cntr....she is young, 30 ish....
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Hello, Anyone out there that had a liver transplant at the Royal Free London? Just curious Regards
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Please post jokes, funny stories, and anything humorous. It is healthy for our minds, bodies, and spirits. Very healing. So let's get those endorphins swimming around, and keep it clean.
55 minutes ago
Hi there, Im from London although had my kidney and pancreas transplant in Oxford in March 2007 (was 3 years ago Monday). I am keeping really well and enjoying life! Hope everyone is okx
1 hour ago
Hi there. I am from Aylesbury. You are even more more recent than me. Hope all is going well? Cheers.
1 hour ago
I'm on Cellcept (brand name from Roche) for SLE. Works great for joint pain, but I really can't afford the medicine. Aetna makes me pay a 1/3rd copay, and that is near $564/mo. for the therapeutic dosage (3000mg/day). No one can help, not even Roche…
1 hour ago
Thomas awad and Scott Schafer joined TransplantCafe.com - The Gift of eLife!
1 hour ago

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