What to expect from being told need transplant to having the transplant

[Guest guest]

My husband has completed evaluation at Baylor University in Dallas and

approved to be placed on transplant list. This happen so fast and I

feel lost and out of control. I don't understand how this dx came

about so fast and how can they be sure. He is jaudiance. His MELD is

only 15. His fatigue and confusion is getting worse. What can we

express regarding his physical and emotional health until a transplant

becomes available??? He has rare blood type and we have been told that

is a good thing and he would probably get his transplant faster. He

believes he will not get any worse and won't need a transplant but I

can see the fatigue getting worse. He has not lost his appetite if

anything he is eating more. Any info would be greatly appreciated.

Thanks,