This and That and Talk - My Transplant
As our Mayo Connect community grows, I am constantly meeting organ transplant members on a wide variety of forums with a wide range of issues that are not directly transplant specific. However, because we are all transplant recipients, we have a special connection: a unique journey and best of all - a new life! We don't always need help or advice. Many times we just want to chat with someone like us! That is my purpose in starting This and That and Talk.
Drop in and say 'Hi'. You are welcome anytime.
What do you want t to talk about? What words can you offer to someone who is on the journey? Do you have any questions for another recipient?
Interested in more discussions like this? Go to the Transplants Support Group.
Awesome hope all is going well for you both !! We did look into the Riverview suites before we left and they look real nice ! Yes I will be getting help with the insurance for that also .. so basically should plan on 3-4 weeks then total with hospital stay then ... I remember my liver transplant was a little short of the full time they told me also but I was a lot younger back then ... I’m 52 and I work in a paper mill doing physical labor so yeah I will need a full recovery before returning... but hoping all goes right as planned !!
I had my kidney transplant 6 years ago at Mayo. My mom was my living donor. I stayed in the hospital 4 days postop. Then we stayed in a hotel that had a kitchenette for about 4 weeks from the time we went prior to transplant to when we left. As long as you schedule a stay for at least 4 weeks in a hotel, they will not charge you sales tax on your stay. This worked out great for us as there was a bedroom as well as a Murphy bed in the living room area. The only complication I encountered postop was with the Bactrim which they felt was the cause of interstitial nephritis and is now on my allergy list as being allergic to sulfa based antibiotics. I had a liver transplant in 1995 and a second one in 2007. The anti-rejection meds were the culprit for taking out my kidneys as well. As in all things we have to take the good with the bad, but always looking on the positive side we wouldn't be here without the miracles that can be done these days.
Wow sounds a lot like me only my liver is doing good 20 years and counting! Just hope I don’t have to have another liver transplant .. seems weird that after so much time it would fail !! But I know reading up on it that is what it’s says they only last 20-25 years ...well I’m planning on pushing that mark lol .. how many days before transplant did you have to be there just the day before ? So much to do and prepare but right now get thru the holidays and be thankful we are all still here to be with our families!! ❤️
My daughter and I both had last minute testing the day before. We we down to Mayo two nights before surgery.
Thank you and if there is anything else that comes to mind please let me know ...
threerrr3, I feel sure that this is going to be an exceptional Holiday Season for you and your family. You and your sister will be are starting the New Year with a blessed spirit of hope and love.
This is wonderful news to hear from you, and I want to tell you how much I appreciate that you have shared it here in the transplant group. I am following your story closely because I, too, am living with aransplanted organs and have been taking anti rejection meds for nearly 10 years.
When I was in Rochester in 2009, my husband and I stayed at the Gift of Life House for nearly 11 weeks. We were extremely pleased with our stay. In addition to a comfortable, clean environment, we enjoyed the support and friendship of the other guests. I want to share a recent blog post from Transplant Pages, for anyone who wants to learn more.
-Transplant Hospitality Houses - A Home Away From Home
https://connect.mayoclinic.org/page/transplant/newsfeed/transplant-hospitality-houses-a-home-away-from-home/
You and your sister might want to review these articles.
-Living Kidney Donation Surgery: Play-by-Play
https://connect.mayoclinic.org/page/transplant/tab/newsfeed/
-Countdown to Living Donor Surgery: Key Steps
https://connect.mayoclinic.org/page/transplant/tab/newsfeed/
cmael, I remember very clearly what I was doing/not doing during the holidays on the year before my transplant. Do you remember what your holiday was like last year?
Yes, last year was pretty typical of our usual Christmas activities...Christmas Eve at our son’s and Christmas morning at our house for Belgian waffles. We didn’t have a date for the transplant yet because my daughter had her testing planned for Jan. The idea of me having a transplant seemed so surreal. I had a hard time believing it was actually going to happen. I didn’t think I was that sick yet, despite the test results. Today I can sure see the difference.
However, this year my husband has pneumonia and I’ve been fighting a nasty cold for two weeks with an unrelenting cough. Hoping to feel better by Christmas.
🤞
I caught that and I’m post transplant and still coughing after 2 months ! A lot better but still a nagging cough !
So, this year you can celebrate that the transplant has already happened! It is amazing how much can change in a year.
I am sorry to hear that you and your husband are 'under the weather'. I do hope that you will feel better by Christmas, too.
I am getting over a cold. I have been so careful to avoid crowds and using my hand sanitizer, but a week after my husband came down with a cough and cold symptoms, I was suffering, too. I have observed, since my transplant, that I take a longer time to get over the symptoms. It took me a while to realize that it would be my new normal.
Will your transplant allow you to take anything for the cough?