3 weeks post liver transplant: when will I feel better?
I had a liver transplant 3 weeks ago because of an autoimmune disease. I don't feel like myself right now. My face is all puffy and swollen which I assume is from the high doses of steroids. I've always been a thinner person but now I feel so fat and that is weighing on me mentally. My legs are still swollen. If I keep them down for even a short time, they become heavy and make it hard to walk. Everyone keeps telling me to be patient but right now nothing feels like it'll get better. I guess I just stupidly assumed things would bounce right back and that frustrates me. Im so miserable and even becoming more depressed. I tell people that and they make you feel guilty for feeling depressed. I guess I'm just looking to talk to people who actually been thru a similar experience. I would like to know how things went for you. Did you have bad side effects to the medicines? Did you ever get depressed after? Do things actually ever go back to normal again? As far as swelling and water retention. When they lowered your steroids did you lose weight and puffy ness in ur face?
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Footballmum, yes this happened to me last November . I was in acute liver rejection, I was admitted to the hospital put on high doses of steroids and increased my immunosuppressant's. Today my liver test is stable and hope to start decreasing immunosuppressants. The TP team takes baby steps after rejection.
If they were concerned about rejection they would probably have told u this. Did they increase your immunosuppressant meds? R u getting blood drawn every 2weeks to monitor them.
Best of luck hoping all will stable .💚😊
Rejection is gnarly and needs close supervision. Think of your anti-rejection meds as your partners, they allow you to keep this foreign body(the organ) mellowed out and that allows you to live. It can be a roller coaster but you and your team will find what the magic dosage is. It will happen and it will be well worthwhile. Happy summer back at you, honey!
Gracias por responder! You are right, no matter how complicated this all is, it definitely beats the alternative as one only gets a liver transplant when it is the last resort. Each day truly is a Gift! Saludos.
Hi Vivian, I will definitely look at it that way, thanks again for your input, it really makes a lot of sense when you put it the way you did.💚🌺🌻🌼
Hi footballmum. My liver transplant was in April 2022. Starting December I have had 4 incidents where all 3 liver enzyme markers have spiked high. The first 3 times I had simple biopsies. The 4th time I had an ultrasound. My liver was doing fine. Mayo is still keeping a close eye on me. I usually have the alksline phosphate enzyme high. I think I am just an anomaly so they keep exploring causes for the spiking.
Just stay in touch with your transplant team, follow your healthy living guidelines. Best of luck, Barbara
Thank you and I will.