Mood changes after transplant
I recieved my liver transplant end of Feb. 2023. I went from ecstatic, energized, grateful to depression, guilt, pain, loss of energy, no appetite, just not at all the optimistic person I have been pre transplant. Any one else feel these symptoms of loneliness, and depression?
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Thank you for this most important message. In my prayers everyday will be Gratitude 🌸🌷🌸🌷🌸
The most important message the Celebration Of Life is those who have made it possible, the precious gift of LIFE their families are honored..
God Bless each everyone of the families. 💚🌻
Hi , All the above comments r so true and very informative for new TP patients. I can remember feeling all the above and now almost 3yrs. I am feeling stronger and living my best life ever. My donor family contacted me after 6months and we stay in touch thru letters, I usually write the month of April every year. April is celebration of life for donor families and recipients. My donor was only 25.
Keep strong and know it will get better. So glad u found this site.😊💚
I'm so happy you had a successful transplant and a meaningful meeting with the donors family. I too search for knowing more about this wonderful woman and to share gratitude to her family.
Many thanks🩷
I'm grateful for your kind response and to know I'm not alone thru this. Best to your healing and thank you so much@
Congratulations on your transplant! I had my liver transplant in Jan 2020. While I was still in hospital I was encouraged to write my donor family. I must have started my letter over 30 times. I was fortunate to hear from my donor family first, which made it so much easier to put my words on paper. On my 1 year anniversary we were able to meet in person. Since our meet up we've kept in contact with an occasional card or text. This experience has been wonderful! Not only am I able to express my gratitude, but my donor family can see the hope their loved one has given to the recipient families. My donor saved 5 women's lives by being an organ donor...what a gift! I wish you the best! I hope your letter gets to your donor family!
To stephanierp
I have been on and off ballroom and social dancing for 50 years. I love Latin rhythm - so salsa, bachatta, rumba and more are my favorites and I still enjoy the smooth dances too.
Great advise. I will reach out to Mayo sooner rather than later. Thanks so much
Totally off topic, but what kind of dance do you do? I am also a dancer:)
I think you want a broad support system - those that have known & loved you for awhile, and some new people, who have been through a transplant. The old friends may not understand transplant specific things but they care about you. The new friends can help a bit with the transplant specific stuff.
Your medical team should also be a part of your support system. Let them know you are experiencing depression, anxiety, impatience, or whatever your emotions are. The meds are powerful, especially at first, and sometimes they need to be lowered or switched. They can definitely add to depression, because they are, in fact, designed to depress our system, so as not to attack our new organs.