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.
My HE episodes included confusion, lack of awareness (time, place, situation) dizziness (including falling or fainting), irritability, and fatigue. Combined they made me one hot mess lol...When I had my most severe HE episodes I also lost consciencesness. (sp?).
I just had an he episode last friday and was in hospital 4 days. Im dont remember friday or Saturday very much. Its not the first that happened a year ago in October when i slept for days and woke up in a different hospital
This has been a fantastic conversation and I want to expand upon it.
For anyone not familiar with hepatic encephalopathy (HE)), it is a buildup of toxins in the brain.
"A liver damaged by cirrhosis isn't able to clear toxins from the blood as well as a healthy liver can. These toxins can then build up in the brain and cause mental confusion and difficulty concentrating. With time, hepatic encephalopathy can progress to unresponsiveness or coma.
Cirrhosis often has no signs or symptoms until liver damage is extensive. When signs and symptoms do occur, they may include:
Fatigue
Easily bleeding or bruising
Loss of appetite
Nausea
Swelling in your legs, feet or ankles (edema)
Weight loss
Itchy skin
Yellow discoloration in the skin and eyes (jaundice)
Fluid accumulation in your abdomen (ascites)
Spiderlike blood vessels on your skin
Redness in the palms of the hands
For women, absent or loss of periods not related to menopause
For men, loss of sex drive, breast enlargement (gynecomastia) or testicular atrophy
Confusion, drowsiness and slurred speech (hepatic encephalopathy) "
https://www.mayoclinic.org/diseases-conditions/cirrhosis/symptoms-causes/syc-20351487
-Were you told about the signs of HE to look for when you were diagnosed with liver disease?
-Were you monitored in any way by your medical care provider?
-What do you wish you would have known then, that you know now?
- What kind of hope and/or encouragement would you share with someone who is new to this conversatioin.
@racing212, @gaylea1, @wildcat, @contentandwell, @jeanne5009, @rowdyramsey, @flagal22, @mostlybill, @tgshomes, and anyone I missed: I hand the mike to you.
Well a year ago is when started going to the hospital for weeks and that's when they started lactoluse and xifaxin. I was getting fluid drained from abnomen every week for over a year. I haven't been drained since January of 2019. Im monitored every 3 months by a dr at rochester mayo in minnesota
@racing212 I had some similar but I think my maximum hospital stay was 3 day, and I never lost consciousness.
I was out this afternoon and I was thinking about all of this while driving home. I almost got tears in my eyes. To me, HE episodes that made me irrational were the worst thing that ever happened. It was especially disturbing when I realized that I was being irrational.
JK
Last fall the Dr. Told a friend that he didn't expect me to live until april. I fooled him its a year later and im still going strong. My meld score went up back in September.
I understand how u feel about HE. I feel the same way. Scariest thing that’s ever happened to me
@racing212 I found out after my transplant that my husband and sister didn’t think I was going to make it. When I discovered that I wondered if the hepatologist and her NP that I had prior to transplant thought that too because when they visited me in the hospital they were both so excited!
JK
I had all these symptoms (regarding women) except the ascites.. It was brutal.
I was in Las Vegas Hospitals for a month Last Year before they finally correctly diagnosed me with ammonia in the liver. I also was given Lactulose and xifaxan. I went to the Mayo in Phoenix and they looked at my past year of tests and determined I needed a Liver and Kidney transplant. For me it was a 9 month process of testing if I was healthy enough to qualify (I was 68). Last June again the ammonia caught up with me, and after calling the MAYO, they insisted I go to a local hospital and they would monitor me. Five days later I woke up and was told I was at the MAYO in Phoenix. After being stabilized, I had one additional test, which I fortunately passed and was placed on the transplant list that day and incredibly received the transplants the next day. Look at the success rate of each hospital and the five year survival rate. Do not skimp on this research. Be suspicious of low volume hospitals. The Transplant for me were not easy with major pain until we finally (2 weeks) discovered I cannot tolerate "OXY" drugs, however now, 5 months out (while I still have some problems) my overall health is better than it was 10 years ago. Get on the list ASAP, the sooner it happens the better, It will be based on your MELD score not first come first served. You will also need to be within a few hours of the transplant center and you will need to remain within a few minutes of the center for 6 weeks after discharge. Also price out the medications you need (some are quite expensive) and you will possibly need to hunt for help.
Good Luck, and I hope hearing from someone who has just been through it helps.