Looking for what to expect as I consider Kidney Transplant
Hi, I was wondering if anyone can give me more info on what to ask the transplant team when I go for my evaluation. I'm struggling with whether dialysis is better or a transplant. I know any surgey has risks.
Interested in more discussions like this? Go to the Transplants Support Group.
When I got my 'call' I was living in Rochester at Gift of Life Transplant House. So My husband and I rode the patient shuttle for 7 blocks to the hospital. Originally I was listed for only a liver transplant in Kentucky. We live 45 miles from that facility and my husband could have done it a record speed, I'm sure. Complications resulted in a referral to Mayo for consult, but that never happened because I developed acute renal failure and was in critical condition. After a week was transported out of ICU to Rochester. So I got my liver and kidney at Mayo - one surgery with 2 organs from same donor.
That is really interesting that you drove past the donor hospital. And I cannot even imagine what you thought or felt to see that cooler with maybe your kidney. I've never heard that happening to anyone before!
As a liver patient, blood is always drawn in enormous volumes! I think they take at least 14 on my annual evaluations. I never did get used to it, and I still close my eyes during the stick and the draw! Fortunately, most phlebotomists understand and talk to distract me.
I will look for that building when I go to Rochester for my eval next spring. My husband asks if it is 'that tall colonial' structure?
Rosemary
Please check out the building, I do not remember what the building looked like it was new when my aunt and uncle moved in and had everything a retired person wanted. You would buy an apartment and when the time came you could move to assisted living, or full time nursing. They had all the activities anyone would ever want. When I was there for their 60th wedding anniversary the place was not able to maintain the dream the builders wanted, I do not know for sure but I think they were unable to attract as many residents as they needed.
My aunt and uncle were on the 14th floor across from the heli-pad at Methodist Hospital. They could walk all the way underground, from I do not remember from where, downtown maybe, to their building with access to the hospital and many other places along the way.
Because all my blood work lab results, goes to UCSF via computer, as well as staying here, I only have to have 7 vials drawn for my annual and 6 month draws, compared to the 4-5 I usually have drawn every 6 weeks. I close my eyes when I have my blood work done, where they do children and babies, so they are good. I usually let the "vampires" know when it is a good stick, because I have to have the draw done in my hand.
mlmcg
@mlmcg - Thanks for sharing your story. I agree with Rosemary, everyones stories are so different. Why do you need the blood draw one in your hand? I think those are very painful.
Lynn, I wanted to let you know that I just completed my evaluation this week in Rochester. Went very well and many of the things I feared would be issues were not. I will find out next Wed whether I am approved as a kidney donor for my husband, denied or deferred. But the entire team was very encouraging and I am going back to Arkansas tomorrow with tons of information and a much better feeling about the entire process. Love my donor nurse Lisa King who I will contact with any more questions that may arise. They are so thorough here you really are not left with many questions. I could easily check my test results and reports on my portal so that was handy. Was able to send my husband a picture of my left kidney which he will hopefully receive. They typically remove the left kidney for donation as the blood vessel is longer. Also found out that your test results are valid for 18 months.
Faune
Hi @mlmcg! I wonder if the building you have described here is the Charter house? https://www.charterhouse-mayo.org/
@jamienolson Thanks for the link Jamie. I think that @mlmcg is the member who you are referring to.
whoops. You are correct! Thanks, Rosemary. 🙂
The reason I have to have my blood drawn from my hand is that I "lost" my veins in both arms from the multiple surgeries I had to have to get a shunt or fistula in my arms. I have small veins that like to roll, blow and hide. Unless the person drawing blood or putting in an IV is very experienced the hand is the best place.
Yes, the hand can be painful because we have lots of nerves there and they cannot be seen it is easy to hit a nerve. If you have someone who does not hit a vein and moves the needle around trying to find blood they can and usually hit a nerve. My hands are cold so I am given "baby warmers" to warm my hand. It also helps when I can get someone who has drawn my blood before. I have asked for someone else to draw my blood if they believe they know my body better than I do.
mlmcg
@mlmcg - I did not know that is why needles in hands hurt. My veins are so visible in my hands but the few times I've had needles there I have found it quite painful and when it is an IV you can feel the coldness of the med going in. Good for you for advocating for yourself and asking for a different phlebotomist.
I completely agree, most people don't have a clue about transplant or dialysis...actually dialysis is worse but still it is hard to find someone that understands what we go through as patients and caregivers, I've had four kidney transplants, I did volunteer work at the hospital where I was transplanted after my third transplant and was on dialysis for thirteen years before my fourth. Looking forward to getting involved with something new, to better help bridge that gap.