questions about liver or bone mets symptoms

I have a question for those of you with liver involvement - in particular if you had a recurrence or progression that moved to the liver. Or if you had bone mets.

Did any of you have the following:
►Nausea - a lot like morning sickness - worse in the AM and popping up here and there throughout the day - but also worse with exertion and/or abdominal pain (sometimes it just hits out of the blue, along with sweats and worry that I will vomit)
►Fatigue
►Itching - gets worse at night - scalp, arms, trunk, legs, feet, back and often the worst is my butt! Hands don't itch much, but kind of get a tingle/burning pain now and then - a bit like neuropathy, but not quite - no numbness.
►Pain - above belly button by a few inches - center upper abdominal
►Pain - right shoulder (severe), and right back shoulder blade (mild) and right kidney area (comes and goes)
►Feeling bloated and pressure in abdomen - (feels a little like when a baby is growing, especially under right at the bottom of the ribcage)
►Upper abdominal pain if I strain a lot to move my bowels. Not like anything I've ever had before - not the same as when I had an obstructing sigmoid tumor. Not cramping pain, and much higher.

All of these have gotten slowly worse during the last 2 months - barely an issue 2 months ago, but affecting quality of life now - to the point I can't ignore them anymore. I can't stop scratching all the time, and feel overall crappy between the nausea and abdominal pain and bloating.

After my labs, I researched and found that when ALP is elevated, some symptoms can be fatigue & weakness, nausea, vomiting (so far no vomiting, but I've been close), itching, dark urine and light color stool. (Cloudy, but not dark urine for me, and floaters in my stool, but seem normal in color.)

My numbers are not that high above normal, but they are very high for me. It is a huge increase over my normal, but only slightly over guideline. My oncologist says that my itching and other problems are only found in people with much higher levels than mine, and with bilirubin elevated too. I never suspected anything to do with my liver until finding out my ALP, researching and reading the symptoms I've been complaining about for a while now. With my rising CEA, I expected a few more distant node mets in my whack-a-mole game. (To be truthful, I'd prefer one little resectable liver met - so it can actually be cut out, and the liver can regenerate, over multiple distant nodes again.)

Now the weird thing is my bilirubin, AST and ALT are normal. Generally with mets to the liver the others are elevated too - especially bilirubin. The only conditions I've found where that applies is with a bone issue - Paget's or cancer spread to bones. But if GGT is elevated too, it is usually liver disease. I don't know what my GGT is. The only bone that really hurts is my right shoulder - it is awful. It hurts all the time, whether I am using it or not. The chiropractor was able to assist me with mobility for the shoulder and many other areas of my body, but nothing has helped the pain. Weird, weird, weird... I didn't do anything to injure it either.

I know I'll have more answers after my scan next week, but I hadn't remembered anyone posting any symptoms they had with liver involvement - just our symptoms of initial colon or rectal cancer mostly. And the only thing I remember of anyone with bone involvement was bone pain. Anyone with bone involvement have elevated ALP with these symptoms?

I'm not realistically holding out hope for pancreatitis - not with all the other issues on top of the abdominal pain...

At least maybe I can lose some of the guilt I've had this summer over not getting big projects done that I meant to do, if there turns out to be a medical explanation. I've been getting more and more fatigued and just can't summon the energy to get things started. I have to really push myself to do anything at all. That is not normal for me. Pre-cancer I was the energizer bunny, so this drives me INSANE! I sleep 10 hours a night instead of my old 4-6. And I am still tired. If I sleep less than 8-10, I can barely function the next day and want to nap (I am not a napper). I've been beating myself up mentally every day over not getting more done - especially because I've been on a treatment break, and this is my chance to get everything caught up and in order. I had more energy last winter than I have this summer, and I was expecting to slowly get better, not worse.