Posted 3/10/2014 9:18 PM (GMT 0)
Hi tpmkn,
Welcome to the forum.
Sounds like you have your hands full at your house with Cirrhosis and HE! We were in your shoes in 2010 when Mike was in and out of the hospital before his transplant. He is amost 3 years post now and doing pretty well. His last hurdle is that he also has Hep C...and is getting treatment for that now.
I am wondering about your mealplan question. It is an issue as those very ill with Hep C become very picky eaters. Mike hated everything.
But with a young family, you need to feed yourself and the children nutritious meals and maybe think of him as someone you have to cook special for.
I often made soups from scratch that I knew he would eat...low fat, with chicken mostly, and not too many seasonings...with the veggies I knew he would eat. I made it my crock pot and froze it in freezer bags in single portions.
I supplemented his meals with Ensure or other of those type. He like the chocolate ensure and the vanilla Glulcerna. He would eat canned fruit, so I got the kind with juice not syrup...they need to avoid high fructose corn syrup.
He would eat eggs and we found a bread that wasn't too high in sodium...though that is hard..and one he would eat. He was pickier than he is any other time.
I am going to send a note to a veteran member of our team, A. Ziffle, who has alcoholic cirrhosis, but he came back from the brink several years ago with good diet, sobriety, and a lot of will power. They finally recommended a Tips procedure for the fluid as he was getting tapped way too often.
There is a quite a bit of good information in the Resources folder at the top of this forum.
I bet others will jump in with their meal ideas.
Hugs,
Mama Lama