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.

@tayloryvette

Thanks and yes. I struggle with even wanting to eat sometimes. I only weigh 125. I lost another 3 lbs. this week. Thank you for the encouragement. so needed and appreciated. Congrats on your recovery! Gives me hope!

Jump to this post

Tayloryvette, I am post transplant and lived with liver disease for 10 years from the first signs that was a almost fatal esophageal varasies to acites 10 years later. I lived with a MELD score in the teens for Years. Acities kicked in 6 months before my transplant . I went about my daily life until I had sever flue like symptoms at which time I was addmited to the hospital and then transferred to the transplant hospital. It sounds like you already have selected a transplant hospital so you should be in good shape. It's a good thing that you are reasonably heathy with a lower Meld score. Good luck.

REPLY

Thanks and yes. I struggle with even wanting to eat sometimes. I only weigh 125. I lost another 3 lbs. this week. Thank you for the encouragement. so needed and appreciated. Congrats on your recovery! Gives me hope!

REPLY
@tayloryvette

I too am a pre-liver transplant candidate and have just as many questions, however, I wanted to introduce myself. Taylor is my nick name, I live in very rural part of Michigan with my husband, a dog and a cat. Now a Real Estate Agent, I was a Restaurant/Bar owner and in the business for 30 years. . Just never thought Liver Disease would slowly creep in and take over my body without feeling or knowing a thing. Scary! I am in my 4th year with end-stage and getting more and more scared. My meld score went from a 16 down to a 10, 2 years ago, however I am scheduled for a current assessment and labs to determine if it has gone back up. My symptoms slowly returning are telling me to get the transplant process moving. Waiting on a number is insane.

Jump to this post

Hi and keep strong. I'm a post transplant patient. Are you having any problem with fluid build up? I sure did. Talk to your Dr's. They can petition you to get higher up the transplant list based on your situation.

REPLY

I too am a pre-liver transplant candidate and have just as many questions, however, I wanted to introduce myself. Taylor is my nick name, I live in very rural part of Michigan with my husband, a dog and a cat. Now a Real Estate Agent, I was a Restaurant/Bar owner and in the business for 30 years. . Just never thought Liver Disease would slowly creep in and take over my body without feeling or knowing a thing. Scary! I am in my 4th year with end-stage and getting more and more scared. My meld score went from a 16 down to a 10, 2 years ago, however I am scheduled for a current assessment and labs to determine if it has gone back up. My symptoms slowly returning are telling me to get the transplant process moving. Waiting on a number is insane.

REPLY

@luckonetj My creatinine levels were up around 140 and even some times up to 150. That was why I was switched to sirolimus. I actually like the sirolimus more because I only have to take it once a day and I choose to do that in the morning about an hour or more before breakfast. As with tacrolimus, you can take it with or without food but you must be consistent. If I had to take a second dose later in the day it would be more difficult for me to be consistent, especially when we are in a different time zone. I like taking it without food because I was able to lower my dosage from 4mg to 2.5mg. Anytime I can take less medication I consider it a win.
JK

REPLY

@christinelouise I to have higher creatinine levels with Tacrolimus just past the normal range. I'll mention sirolimus to my nurse next time. They attributed the hi levels of creatinine to the Antiviral I was on. I do have to drink more water during the day. Doctors orders.

REPLY
@christinelouise

I am a transplant patient too and I too am interested in how you came to be in the hospital. I was in the hospital at Mayo for 6 months after my transplant with complications. Let me know about your transplant experience( all of you in this conversation.)
Christine
Christine

Jump to this post

@christinelouise I am not sure of exactly what you mean. I was in a hospital a number of times pre-transplant, for short stays. A few hospitalizations were due to HE episodes, and then a couple were for other problems, like very low blood counts -- hemoglobin and hematocrit. Those numbers were so low that the doctor at my local ER said I could have gone into cardiac arrest. I was sent by ambulance to Mass General and had a few transfusions which solved the problem.
I was only Mass General for six days following my transplant. I'm sorry that you were in for so long, what was the cause of that? I can't imagine being in a hospital for six months. When was your transplant and how are you now?
My experience was very positive. I recovered amazingly quickly and have felt great ever since. I feel very blessed to have been given this second chance at life.

@luckonetj Having a potential rejection must have been scary. I am glad you are doing well now. I am thankful that my new liver and I have gotten along well right from the start. The only problem I have had was that tacrolimus was causing my creatinine to go high so first, they had me drinking 80 - 100 ounces of fluid a day. That didn't have the desired results so they then changed my immunosuppressant to sirolimus. That has worked out well. I do still drink all of that water.
I have never heard of a hospital being selected for a patient. What state are you in? My transplant was at Mass General and from what I know the patient chooses the hospital where they want to be listed. There are four hospitals in MA that do adult liver transplants, two in Boston, one in Burlington, and one in Worcester.
JK

REPLY
@christinelouise

I am a transplant patient too and I too am interested in how you came to be in the hospital. I was in the hospital at Mayo for 6 months after my transplant with complications. Let me know about your transplant experience( all of you in this conversation.)
Christine
Christine

Jump to this post

@CHRSTINELOUISE, Six months in the the hospital must have been quite a trial and then afterwards as well. I hope you are doing well now. Transplant experiences are so different. It's hard to compare cases. I had a rejection scare three days after discharge that put me back in the hospital for three days on IV TACROLIMUS. I am currently 13 months +/- post OP. My Transplant clinic Nurse lowered my Magnesium to 200 mg. Twice a day, and wanted to discontinue Urso, but the doctor wanted to stay with the protocol. I wish you all the best. My hospital was selected for me on a first bed avialable protocol. I did how ever end up at my first choice.Tim

REPLY
@contentandwell

@benlam11 I am relieved for you that they found the root of your problems. Medications are such a double-edged sword -- they are good for certain things but can cause other problems. I was on Furosemide for a while, near the end of my pre-transplant time and it didn't cause me a problem but a number of other medications did, particularly one that if I remember correctly was for nausea.

That's great that Mayo has been so good for you. I feel the same way about Mass General. From what I have heard most of these transplant centers have really excellent teams and are very caring. There are a few that operate at less than expected but overall most are quite good. I know at this point that if I ever need hospitalization I will head right down to Boston to go to MGH.
JK

Jump to this post

I am a transplant patient too and I too am interested in how you came to be in the hospital. I was in the hospital at Mayo for 6 months after my transplant with complications. Let me know about your transplant experience( all of you in this conversation.)
Christine
Christine

REPLY
@benlam11

Rosemary, Volunteer Mentor @rosemarya This is Ben Lambert and I just spent a couple of days in the hospital and they discovered my medications 2 - 25 mg metoprolol and 2 - Furosemide pills were creating the problem. So now I'm free of all Blood Pressure Medications and feeling much better. Just in case someone else goes through the same episodes - call your coordinator nurse and get on top of it quickly - not like me who waited several days thinking it would go away. The Mayo has been incredible one of their home outside providers - not so much. So once you leave the Mayo orbit (even though Mayo allows these sales people in), be cautious.

Jump to this post

@benlam11 I am relieved for you that they found the root of your problems. Medications are such a double-edged sword -- they are good for certain things but can cause other problems. I was on Furosemide for a while, near the end of my pre-transplant time and it didn't cause me a problem but a number of other medications did, particularly one that if I remember correctly was for nausea.

That's great that Mayo has been so good for you. I feel the same way about Mass General. From what I have heard most of these transplant centers have really excellent teams and are very caring. There are a few that operate at less than expected but overall most are quite good. I know at this point that if I ever need hospitalization I will head right down to Boston to go to MGH.
JK

REPLY
Please sign in or register to post a reply.