I have questions about Hepatic Encephalopathy
My husband has been diagnosed with stage 4 liver disease. We are waiting for an appointment to see if he can be put on the transplant list. Prior to his diagnosis and even after a hospitalization, he has signs of HE. Hallucinations, personality changes, irritability and impulsive behavior. He no longer has hallucinations but he still has the others on some level despite being on lactulose. Question about HE - Is there any other ways to treat this besides lactulose? After transplant (if he is eligible and if we get one) will these symptoms and changes go away? Is therapy helpful for HE? As a caregiver how do I handle the anger, moods, impulsivity?
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We are within 45 minutes of Mayo Clinic in Rochester, MN so that is a lucky break for us.
We are looking at having him enter a 30-day in-patient program soon as we know he has to have it completed before being put on a list.
Congratulations on your husband’s referral. It will be a bumpy road, but it’s good he has your support. The lactulose can be tricky to manage…most of us with late stage cirrhosis had to learn how best and how much to take. So, your husband will have some trial and error as he learns how his body does best. Ultimately it is key to helping him while he waits for his transplant.
Be sure to encourage him to walk and eat well so that he is as healthy as possible for his surgery. His transplant team will be a valuable resource for you and him.
Those of us on Connect are happy to help answer questions you both might have, of course, from our own journey and experience as liver disease patients and transplant recipients. I wish I had found Connect before my transplant…I had so many questions! I research everything, but reading medical journals doesn’t tell you about what we face as patients and caregivers.
My best to you both!
That’s kind of odd and certainly not informative! Remember, the jury is still out on what exactly it means to have have higher antibodies anyway. Being vaccinated, safe, and well protected with a good mask are the most important things.
@sharonagnes, I am thinking about you as you and your husband begin your journey into the future. I hope that you are soon to be busy with more appointments that will result in your husband being listed for a transplant.
How are you holding up with your new caregiver role? What questions about the liver transplant evaluation process would you like to ask?