Liver transplant - Let's support each other
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.
Good afternoon,
I was wondering how you met your living donor. What MELD score were you at the time of transplant? Any trouble with palpitations or fluid retention in the face or hands? Did you have any diastolic dysfunction on ECHO? I am new to the forum with a MELD-7 and concerned about the road ahead. I work full-time and am very active currently. We’re you able to work up until your transplant?
I am 15 months post TX at London UHSC. Good to hear you are trying to get something going there. The peer support is limited in our area but certainly needed. If I wasn't 5 hours away I'd come on by. Maybe next time I need to visit in person.
@lukef, Welcome to Connect, I had my transplant at Mayo in MN, and it is nearly 800 miles from my home. After I returned home, I was disappointed that there was no local peer support available for me, either. I'm glad that you have joined Connect where members give and get support from other patients who are living miles away from each other.
Congratulations on your transplant. Did you have a liver transplant? How has the first 15 months gone for you? What are you looking for in a peer support group?
@melissa0919, I want to invite you to this Support Group where you will be in the company of other liver transplant patients. I am sorry to learn that your early recovery is not going well and that signs of rejection are causing rising numbers and the need for increased medication levels. I, myself, do not have a similar experience that I can comment about, however other liver transplant recipients have had similar episodes and can guide you through this current situation. You are not alone.
Melissa, I will let you introduce yourself to this group.
I done introduced myself and told my story. Maybe I didn’t do it right.🤷♀️
@melissa0919 I think what @rosemarya was asking was if there is anything else you want to share, things others in this group may support you about. There is never any pressure to share more than you want to. I’ve found this to be very helpful to get reality checks when things are hard. For instance I recently had a scare about rejection or bile ducts as my numbers have been rising, and I reached out to this group to see if anyone had a similar experience and how they coped.
I’m sure you’re sick of all of this - sick of hospitals even though it sounds like this is the place for you to be. I’m praying for you and thinking of you, offering strength for this journey. 💗
Thank you. It is a lot to cope with. I figured once I got my liver and went through the initial recovery I would be ok. But that’s not the case at all. If there is anyone on here that has went through rejection please connect with me. I am extremely overwhelmed, because like I said I figured I would be better after recovering the initial part.
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?
Hi Melissa. I'm so sorry to hear you are going through this so soon after transplant. I have not experienced this but have seen many who have. It must be very scary but I've only seen positive outcomes. Wishing you well.
Melissa0919: Hi there! I received my liver tx at Mayo in Jacksonville 5 years ago and I appreciate what you are going through. For the first time at the beginning of this year, I experienced a bout of rejection and needed to go to Mayo (500 miles away) for anti-rejection treatment with SoluMedrol. That brought my LFT's down to acceptable range and I was able to go home on prednisone. I've been able to taper to 5 mg. of prednisone a day and, while I dislike the side effects, I'm glad to be able to take it and hang on to my tx liver. It has been my understanding from the very beginning that I will be fighting rejection to one degree or another for the rest of my life and this will not be smooth sailing, but I'm on the green side of the grass and able to do almost everything I enjoy doing most days. The way I figure it, I would have been dead from liver cancer 5 years ago this month and everyday is a gift to be delighted in and treasured. Keep your sunny side up.