About gall stones

Hi All,
I have gastroparesis (vagal nerve damage to stomach) as a result of getting
my gall bladder out. I also have sphincter of oddi dysfunction - my last
ERCP w/sphincterotomy (both biliary & pancreatic sphincters were cut) and
placement of a pancreatic stent left me with pancreatitis.
I’ve been having problems keeping food & water down, let alone pain pills
or antinasea pills. My stomach gi thinks it’s either the gp getting worse
or maybe it’s chronic pancreatitis (my pancreatic & liver enzymes are all
normal) - so I’m scheduled for a gastric emptying scan on the 8th to see
if it’s the stomach that’s been acting up.
GP is one form of neuropathy (it’s autonomic), and I have peripheral neuropathy
in my right leg (which started about a year or two after the gp).
Since the pancreatitis, I’ve had trouble urinating - meaning I can’t go all
the way - it’s like I can’t empty my bladder completely, so I go all the time -
at least 3 times a nite I wake up to go.

I wound up at the ER on Fri - w/severe upper abdominal pain - they said it’s
not pancreatitis since my levels were normal (yet I know they don’t have
to be “off” to have pancreatitis - and my stomach gi dr agrees). They said it
was the SOD, gave me IV painkillers and sent me home. I told them about
the urination problem, and they said I should mention it to my stomach gi.
I searched on the internet to see if underactive bladder can be related to
neuropathy - and it appears it can. I’m worried that the neuropathies I already
have are just going to get worse and that I’m going to wind up with more of them
affecting more organs/body parts. What can I do to help prevent this from
happening?
Does anyone else have this bladder symptom? What do you do about it?
I’m drinking lots of water and lots of blueberry - juice, tea - to make
sure I’m flushing the urinary system as best I can, and I’m taking
Uva Ursi hoping that’ll help too.
Any advice/input would be greatly apprectiated.
Cathie in PA