@loungingsofa70, Welcome to Mayo Connect and Congratulations on your recent livertransplant! I requested that your question be moved to this discussion because this is where other new transplant recipients will be more apt to see and to relate to your situation. I encourage you to read thru what has been posted so far by other members.
My transplant was 11 years ago, and I remember that I got tired easlily, and napped daily.

I want to invite other newly transplanted members to this conversation.
@btwest6, @gphetteplace, @tjgisewhite, @jsw, @michaelswaim, - Have you had an experience similar to @loungingsofa70 that you would like to share?
How are you doing since your transplants? Any updates?

Hi, @loungingsofa70 Welcome to Connect.
I am about 3.5 years post-liver transplant. I do remember being very tired initially but I think I started feeling less tired at around the 3-month mark. I am presuming that to be so because I know that is when I returned to my health club for water aerobics.

What I have found from other liver transplant patients with whom I have connected online is that everyone seems to have different experiences. Some people recover amazingly well in a very short amount of time, some people take a year or more to feel like themselves. For me, being positive helps.

Have you spoken to your transplant team about the right-sided back pain? If not I would at least mention that to them. It's always good to let them know anything that's going on. I found out just how much symptoms that seem unrelated can be indications of other things that you would never think of, when I was pre-transplant so now I try to be conscious of everything. Still, I have trouble with that though. Right now for instance, I am having a problem that I never imagined would be caused by a medication, and I just discovered that it is.
JK

@loungingsofa70 hi there! I am 18 months post transplant (liver). It took me a year to start to feel relatively "normal". I joined a gym at 13 months post transplant as that is when I felt able to do more. Prior to that I had fatigue, loss of appetite, insomnia and sore joints. I'm now stronger and much more confident. I thought I would never get better. If I had not been proactive and just waited I may not have had any progression. My mantra..You can do this...and I did. After all we've been through we must continue to fight for our well being. I still have complications (I'm due for surgery ERCP again June 15). But I'll go into this prepared. It takes everyone to know their own bodies and what they're capable of. We all recover at our own pace in our own time. Chin up!!

Hi! I had my LT the week after yours. I’m feeling about the same. I’ve had pain under/below my ribs on my left side (front and back) that feels like a pulled muscle. They confirmed it wasn’t a hernia. I’ve also had episodes of fast heart rate (185 BPM) which were accompanied by shortness of breath, so I’m keeping an eye on my vitals. The doctor said my heart muscle is fine (my EF is 70, great for a 61year old) and it was probably just that I was deconditioned, which makes sense because I was very sick and very sedentary before the transplant. It has improved over the last few weeks. Hopefully we just need to keep working on our endurance! I feel sooo much better with the new liver I’m impatient to start some aerobic exercises. I’d love to hear your progress!

My husband had his transplant (liver) on 2/9/2020. We have found that bike riding is a good activity for us. It seems like his stamina is greater for that than walking, but still gets us out and moving. I feel like the key is to remember that recovery comes more quickly for some than others and that patience with yourself having just come through major surgery is important. Some days are great and others are fair. All are better than before transplant.