Kidney transplant - The Journey from the Donor's Side
I'm headed to Rochester on the 10th for surgery on the 12th. I'm excited and nervous! I didn't know the recipient but have gotten to "meet" her and some of her daughters through phone calls and emails.
I've had labs done at my doctor's office and went to Mayo a few weeks ago for a million more tests. My case was presented to the donor board a few days before Christmas and I was approved and notified the same day. It seems like everything took so long and now is going so fast.
I'm interested in hearing from donors but haven't had a lot of luck. It seems like the recipients are the ones who post the most, which gives me some info and reassurance but it would be nice to hear from the other side too.
Interested in more discussions like this? Go to the Transplants Support Group.
@hopefulgirl the testing process is pretty amazing, isn't it?
It took me until almost the end of the evaluation to realize that all of those tests were to make sure I was safe to proceed. I had thought most of it was for the recipients information.
There were a few family members worried about my donating so I sent them my schedule of tests to show how thorough it was.
The stress test was rough for me but now that you've gotten the 18 & 24 hour tests done, everything else is easy!
I'll be thinking great thoughts for you.
Rosemary,
Thank you for suggesting the transplant pages. I found several helpful articles there! You are such a great facilitator btw!
@rosemarya I wore a 24 hour blood pressure monitor from Friday after until Saturday afternoon. It pumped up every half hour, hourly during night/sleeping hours, but never made any noise! I did find it annoying though. I am hoping that my BP won't be enough of a problem to prescribe medication, I think I take enough already, just no BP medication.
JK
BP control plays an important role in protecting our kidneys. So as a transplant recipient it is important to monitor and/or treat. I do take BP meds and have a home monitor that I record my readings regularly.
@rosemarya I never really thought about BP affecting kidneys. I only thought it about affecting my heart. If I do need to start taking it I will tell him I want to wait until after our trip to Denver. I would hate to be there and discover that it did not agree with me in some way as lisinopril did.
JK
I have new, since my transplant, home bp monitor that has Bluetooth so all of my readings are transferred to my phone. That makes it easy to share with the doctors.
You are way ahead of me! I have BP recording booklet that I use.
@cmael @rosemarya I actually do not record mine, I just take it to see how it is doing. My doctor has never mentioned wanting me to record it. When I am home it's always pretty good, but I guess high for today's standards -- systolic in the 130s, and diastolic in the high 60s. I am dreading my appointment tomorrow.
JK
I have “white coat syndrome”. Whenever I’m at the dr my bp is elevated and when I’m relaxed at home it’s good so it helps to have proof.
My PCP used to ask me to jot down a few numbers between my 6 month check ups with him. But it is my Kidney transplant team who is keeping a close watch. I only see them tyearly, so they gave me the small booklet. I will return it at my annual visit.
My PCP has been working with me when my BP meds were giving me trouble after the Kidney folks made a change. He is my GoTo person, but he knows that the Kidney (and Liver) get priority treatment.