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DiscussionAnyone had plexus nerve block for cancer pain?
Pancreatic Cancer | Last Active: Feb 25 2:24pm | Replies (28)Comment receiving replies
Replies to "Has anyone been advised to use a celiac plexus nerve block for back and upper abdominal..."
@donnarushing55 and @tinerobison, I moved your questions about celiac plexus nerve block related to pancreatic NETs to this existing discussion:
- Anyone had plexus nerve block for cancer pain?
https://connect.mayoclinic.org/discussion/celiac-plexus-block-1/
I did this so you can read previous messages and connect easily with others like @lulusmom @granite @beatrixlee @lizduffey @joylynnlove @stageivsurvivor and others.
Interesting my husband supposably has a Pnet in his tail of his pancreas and has had different measurements but neither has measure up to greater than 2 for them to do surgery. They (Hopkins and Mayo in Minnesota) have offered no treatments but wait. He has extreme pain after eating seems like the pressure of food in his stomach puts pressure on nerve/tumor. They recommend a nerve Bloch as well at our local health system. He has had 2 TAP blocks but not celiac plexus from my understanding. The 1st one worked about a 1.5 weeks. The 2nd he had done on 1/23 and so far he has had 1 flare up but it seem to subside and then went away. He does still have constant indigestion. They claim his is non functioning but I am not 100% sure they are correct I feel like they just haven’t caught his active when they have tested him. I am curious what your history of symptoms and progression of your journey has been. Ours has been frustrating as my husband’s quality of life has been not good because of the constant pain and occasional diarrhea flare ups which can be bad.