Liver transplant - Let's support each other

Posted by lmctif @lmctif, Oct 29, 2018

What topics do people who are waiting for a liver transplant want to talk about? Who has had a liver transplant and wants to talk about?

Interested in more discussions like this? Go to the Transplants Support Group.

@rosemarya

I hope that today brings some uplifting news to you about your current status. I am aware of how overwhelming this is for you. And I know how frightening it is when our precious organ is at risk. I imagine, too, that the medical terms and activities are confusing as well. I know it was for me. If you are feeling up-to-it, try to engage in conversation with your nurses, as doctors can be quick in /quick out due to their schedule. Are you at your transplant hospital?

@rickherman @silverwoman @gaylea1 @hdillon7 @ajdo129 @gerryp
I want to invite you to visit this conversation and meet @melissa0919 who is in hospital with signs of rejection of her recently transplanted liver. I know that she would appreciate your expressions of hope and encouragement during this difficult time, also Do you have an related experience to share? Have you dealt with rejection?

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To melissa0919
Before I even had a transplant and my friends were calling me to reassure me, I was surprised at how many liver transplants they knew. Friend Sharon has a brother whose third time transplant several years ago is doing well and a local vet is still taking care of the city's pups, cats and other critters after his second transplant. You are not alone.
Though I have yet to face confirmed rejection, at 18 months post transplant I have had several possible rejection scares. After six months post transplant, I would get urgent calls from Mayo after my weekly blood draw results. Over the course of a nine month stretch, Mayo would tell me to come immediately for a biopsy (3), am ultrasound (2) or an ERCP (2). Of course I researched what happens if your body rejects the liver and I learned rejection isn't like an "on/off" light switch. There are several interventions that can turn around the signs of rejection and, if needed, there are many successful repeat transplants.
I have been given a blessing since my original prognosis two years ago when I was told I have two months to live. I treat each day as a lifetime and embrace each moment, challenging or not, as the richness and depth of living. As I have realized that the depth of grief we suffer is the reflection of the love we have. So is the fear of death as the reflection of the preciousness of living. So I focus on the moments of living and fight for them if need be.
I do hope this helps. ajdo129

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recently my mom started getting soreness in her muscles. To where it’s effecting her walking. Has anyone else run into this? Her family dr stated it’s possible one of her medication could be causing it but her coordinator is stating that none of them do.
Hope everyone has a great and safe Christmas with their families.

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@tinamarie10 - when was her transplant? Calcineurin Inhibitors (Tacrolimus, Cyclosporine) can cause pain. I was an extreme case. Got to where I couldn’t get out of a chair without help. You can search for CIPS (calcineurin inhibitor pain syndrome) online. Usually starts within a year of transplant, but goes away within 2 years. Tell her to hang in there!

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@gphetteplace

@tinamarie10 - when was her transplant? Calcineurin Inhibitors (Tacrolimus, Cyclosporine) can cause pain. I was an extreme case. Got to where I couldn’t get out of a chair without help. You can search for CIPS (calcineurin inhibitor pain syndrome) online. Usually starts within a year of transplant, but goes away within 2 years. Tell her to hang in there!

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Thank you so much for answering. She’s on month 4 exactly since her surgery and on Tacrolimus. I will look that up for sure. I’m trying to understand, learn and help her get through this.

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@tinamarie10, I want to share the following support group discussion with you. You will be able to meet other transplant recipients who are also discussing muscle soreness and joint pain since transplant. You will also see that @gphetteplace has posted there, too!

Joint Pain - Liver Transplant
https://connect.mayoclinic.org/discussion/joint-pain-liver-transplant/
You are a good daughter and caregiver. Your mom is blessed to have you at her side. ❤️

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@rrichardparker

I am 6 years past my liver transplant

Support groups are very good with support. Just talking to people in the same boat as you leavens the horror of your situation.

Post transplant too.

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I'm also 6 years post transplant

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@kahlkream

I'm also 6 years post transplant

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Good Morning, @kahlkream. I want to welcome you and to inform you that as a member on Connect you are welcome to participate in any of the support groups that are of interest to you. I see that you are in your 6th year with your liver transplant and I know that your experience has had its share of ups and downs, As for myself, I'm going on 15 years with my own set of experiences as the months and years have gone by since my transplant surgery at Mayo Rochester. I am available to help you locate groups that might be of interest to you, and where you can share your own experiences and ask questions.

@kahlkream, Here are a few questions that I offer as a way for us to get to now you better and to learn about your transplant story. What brings you to Connect? How are you getting along since your transplant? What would you like to share about your liver transplant?

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@myfablife

Hi All, I am also 3years Liverversary. I had my LTP 2020 developed hernias by 2021 I was scheduled for AWR with hernia repair. I also had acute rejection in 2022. With all that I am doing well I don’t have pain but my incision/scar feels hard when I touch not sure what that is could be the mesh they used.
It is definitely a journey that TP patients r on we just have to stay positive 💪.. day at a time. I wish u all the best😊💚

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If you don’t mind me asking, I have a brother in law that is in need of a liver transplant due to HCC (cancer) and hepatitis B. Were you really sick prior to transplant? He’s tired all the time and can not walk very far and doesn’t eat much. How long was your wait?

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Hi,
I was in end stage liver disease so my wait on the TP list was very short 9 months. I had great Drs. and was very blessed to have been given this second chance. I 🙏🏻🙏🏻 that you will be blessed to. Is he on the TP list.

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@oooanooo

If you don’t mind me asking, I have a brother in law that is in need of a liver transplant due to HCC (cancer) and hepatitis B. Were you really sick prior to transplant? He’s tired all the time and can not walk very far and doesn’t eat much. How long was your wait?

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@oooanooo, Welcome to Connect. Before my own liver and kidney transplant, I had the tiredness/fatigue, couldn't walk far, no appetite, etc. These are some of the symptoms that can occur with liver disease and advanced cirrhosis.
Here is some information about liver disease if this is new to you.
- Liver Disease
https://www.mayoclinic.org/diseases-conditions/liver-problems/symptoms-causes/syc-20374502
.
Here is a Connect discussion with members who have experience with liver cancer HCC
- Anyone waiting for liver transplant and diagnosed with liver cancer?
https://connect.mayoclinic.org/discussion/liver-transplant-6/
@oooanooo - Where is your brother-in-law in his current need/journey to a possible liver transplant? Has he been treated for the HCC and Hep B?

@katebw Do you have any information about Hep B before liver transplant?

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