Living Donor: It's a huge responsibility
I am a match for my sister's kidney transplant and will be heading to Mayo next month for evaluation. My sister has told everyone she knows about me, even refers to me as her "kidney mama". I understand she is excited and I am as well, but now I wonder how I will feel if I don't "pass" and she has to continue her waiting and dialysis. Its a huge responsibility and a huge honor to be able to do this, but.....
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@dank, Congratulations on your transplant! There are several other liver recipients who are members. I am a liver/kidney recipient. And my husband an I enjoy our annual trip to Rochester, too!
Thank you for sharing and for joining us on Mayo Clinic Connect!
Rosemary
@dank, I want to add my experience: The results are already with my doctor when I have my afternoon appointment - same day.
How do they do that!
Rosemary
@rosemarya It occurred to me that back when I was talking to Mayo about possibly dual listing there I thought they said that after the first couple of months my care could be transferred to Mass General Hospital. Is that not the way it is done, or do you go to Mayo because you do not have a transplant hospital close to you?
JK
@rosemarya I had been going weekly for lab work and MGH had me using a lab that has facilities everywhere -- Quest. I would go in the morning before 9:00 and I would have the results in my email by about 2:00 in the afternoon. MGH had the Quest that drew my blood send it to the testing facility by courier STAT. Right now things are stable so I haven't gone in a few weeks but as of Saturday my drugs change again so I will resume next week. They are changing because I was on sirolimus but that that can interfere with healing so they switched me back to tacrolimus prior to my knee replacement and now I am going back to sirolimus.
JK
@contentandwell, I do have a transplant hospital nearby, It is only 45 minute drive. That is where I was originally listed for my liver transplant. But, due to complications, they sent me to Mayo, and that is where I received my transplant.
Mayo monitors me from a distance, and I return annually for my check-up. Every year they give me a standing order for my labs, and then my PCP writes it for the local lab with instruction to fax to Mayo. I usually get labs drawn 7:30 AM and I can go to the lab and get a copy later that morning. I like to be sure that they did get faxed. I also have a tacrolimus lab kit that Mayo supplies - the phlebotomist only has to fill the tube, then I put it the kit and I drop it in the outgoing mail. If I mail it on Monday, Mayo has it in my system on Friday. My transplant nurse will contact me about medicine changes. It is an efficient process for us.
If I am hospitalized, or need ER care, the attending physician will communicate with Mayo transplant Dept via a 24hr phone line. And this has occurred on several occasions. I also can call 24-7 when I need to.
We never considered transferring my care to local because of the level of care that Mayo was able provided for me. We return to Rochester annually for a 2 -3 day visit. I guess that someday, when the travel becomes too much, we will transfer to closer to home facility.
Rosemary
I am a living donor the transplant was March 15, 2016
I did not know the recipient at the time. She was a very sick woman and has since had a new lease on life. I feel incredibly grateful to be part of this miracle. My health is great my recovery was great, I was sore of course and it took time to heal but i would do it all over in a heartbeat.
GOD BLESS YOU !
thank you for posting this! If I have the timing correct, at this time next week, they should be finishing up with my surgery. I'm glad to hear that both you and the recipient are doing well.
I donated a kidney to my sister in August 2015. We are both doing great. Our family (my father's side) is affected by polycystic kidney disease (PKD) so many family members have undergone transplants mostly living donor. Besides a donor I have been on the caregiving side too as my husband had a living donor kidney transplant (2010) followed by a pancreas transplant (2015). He is now insulin free!
@dank, Thank you for your participation in this discussion. I believe that when recipients like you share experiences and send blessings, that we are able to give hope to others.
I invite you to stay in touch on this conversation, and/or to join in on any other discussion that looks interesting to you. At 6 years post transplant, I feel certain that you have a lot of practical experiences to share.
Rosemary