Against advice from some people on this forum I have started the
nerveblock process.You go 3 times and the 3rd one is the real thing.
First they have to see if that nerve plexes is involved in your pain at
all and if this will help your pain.I'm having the 3rd one the real one
on Nov. 16th. I had to try something. I'm hoping this is a different
type of block than others have had that did not work. The 1st 2 only
last 2-3 days and in that time you have to see in what degree it
decreased your pelvic pain. The last one took about 60% of my pelvic
pain away but my legs ached terrible like withdrawing off drugs. I have
a call into doc about that. This block is 4 needles 5 inches long,
guided by a xray machine. They go into back to th front where your
Hypergastric nerve plexes is and inject steriods and some kind of
lidocane. It should last 6-8 months. In that time my body will have
time to heal properly by decreasing inflammation. Read "Interceeds"
pages and pictures on adhesions. They make it sound like an autoimmune
disease. Our bodies do not finish heaing process for some reason.
Hopefully this block will help it to finish heaalling process. I
suppose what adhesions I have will stll be there? Good question to ask
doc. I hate doctors. Just when you think there caring and not just out
for your insurances money they are unkind. I was crying in the room to
get my last block and all she could say was "I HAVEN'T DONE ANY THING
YET" Like I'm a big baby. I don't think they stop to think about all
we've been through. I asked for a valim or something before going in
lie they did last time and the %^$#@#$ NURSE LAUGHED AT ME and left the
room. BIZARRE !!! Anyway I have typed this twice ad lost it I think so
if you get it twice you know why. Please responed with warnings or
questions. Otherwise here I go. JJ