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 I understand your frustrations and sadness. As you said there are other ways for you to help. I tried to be my husband's donor but was unable to do so. It is so disappointing when you want to do whatever you can to help someone.
Prayers for peace and guidance for you.
JoDee
hopefulgirl, I have heard others speak of their own disappointment after being unable to be a living donor. They also struggled with their emotions about it. As a recipient, (deceased donor) I think I can confidently say that your courage, your love, and commitment to be evaluated is a sign of HOPE to patients who are waiting for organs.
I look forward to continuing conversation with you whenever you feel ready.
Hugs.
@hopefulgirl I applaud your efforts. We all do. Remember, the transplant team wants you healthy, also! Can you consider bone marrow or stem cell transplants to help someone, after all your testing? You are a hero.
Ginger
@hopefulgirl how disappointing and frustrating, especially knowing that donors are needed and you were willing to be one. Thank you for sharing your story here. As @jodeej knows, not being able to donate is a reality and it helps for people to know that side of the story too and to be supported by people who have “been there”. By your sharing on Connect, you will help many.
I agree full-heartedly with @mauraacro that the positive outcome is that the medical team detecting FMD at an early stage that may have gone unnoticed. Should you wish to share with others about FMD, here is a discussion on Connect:
FFibromuscular dysplasia (FMD) https://connect.mayoclinic.org/discussion/discussion-fmd/
Thank you Colleen! I didn't realize there was a group for FMD. It will be interesting to learn more.
@gingerw Thanks for the encouragement! I will consider other ways to help. I appreciate this group and being able to connect has been so helpful.
hopeful, April is the National Celebration of Donate Life Month. There should be lots of activities for involvement on many levels for you to consider.
@rosemarya how did I not know that April is the “National Celebration of Donate Life Month”? I probably did and forgot.
JK
Bigger question is how did I know😉.
It is my anniversary month and my annual checkup month, too. So that is how I remember it.
@rosemarya I picked up a “Donate Life” green rubber bracelet when I was in the MGH transplant center in December. I don’t remember to wear it often but I will make an effort in April.
JK