Chronic Pain members - Welcome, please introduce yourself

Posted by Kelsey Mohring @kelseydm, Apr 27, 2016

Welcome to the new Chronic Pain group.

I’m Kelsey and I’m the moderator of the group. I look forwarding to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.

Why not take a minute and introduce yourself.

Interested in more discussions like this? Go to the Chronic Pain Support Group.

Profile picture for dixiekidd76 @dixiekidd76

@marcd2k
I had back surgery in February 2025. A Fusion! The Neurosurgeon says X-ray always looks good. He doesn’t know what is causing all this pain all over my body. My primary care has done a MRI, X-rays, blood work and Ct scans. All they have found is I have anemia and arthritis in my neck. My feet, toes legs hurt bad and my arms and hands.

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@dixiekidd76, I experience those symptoms as well. I have several autoimmune conditions. I also have CRPS, formerly known as RSD. It can move around like that. There is no cure that I’m aware of. Just a thought of something for you to check in to.
Best wishes.

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Profile picture for gypsyblue @gypsyblue

@heisenberg34, your post breaks my heart for you. You absolutely need a new primary. WOW! That is just terrible. I am blessed and grateful for my primary. He’s one of a kind for sure. He’s always there for me. I can text, email, call anytime and he will respond. He calls regularly to check on me and my father. Also his pcp. He even makes house calls. I don’t know what we would do without him. You deserve so much better!
Best wishes and never give up looking for the care you deserve.

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@gypsyblue Thank you! I am grateful for your kind words. I had a wonderful PM doctor back in PA. Then, he went and retired! I was so sad. He was kind, empathetic, and even encouraged me to get other opinions. I have an appointment with a new PM doc next month. The only caveat is that she is very busy and is about an hour away. I guess it will be worth it if she is willing to look deeper into my pain. Who knows? (The shadow knows, right?) Have a blessed rest of the week!

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Profile picture for wt1413wt @wt1413wt

Hello. In June 2019 I had a cholecystectomy or gallbladder removal surgery. The gallstone pain finally made me pursue surgery. Since I was moved to a hospital bed post-op, the new - and however possible, worse - pain began. I was in the ER twice in two months post-op. I have been to a University hospital more times than I can count, with so many X-rays, ultrasounds, etc. I finally gave up they would solve this pain issue after seven months and exhausting any money I had left. I partially work from home and hoped the worst spasms and mule-kick-to-the-diaphragm pain would happen at home, as the event would last up to 24 hours, and they still do today.

06/2019 Post-op: Spasms are ALWAYS happening, like rhythmic waves, and are very light. Few are still intensely painful, and come out of nowhere. Feels like a lightning strike inside from 3 cm right of the xiphoid process, down to half way point of the right quadrant. Like being punched hard in the diaphragm non-stop. Still can’t breathe deeply without the punched feeling. One of the worst was trying to pretend everything was fine when I was on a flight and the spasms began - I did not want to be on the news for an emergency flight diversion. That was intense.

Last week was suddenly the worst event I’ve experienced. I woke up, had a glass of water, began to prepare breakfast for the kids, and was hit hard. After 12 hours of writhing on the floor, cursing and praying, my resolve not to spend anymore money on a high medical deductible gave out. Pain became incapacitating and absolutely intolerable. Having a high Pain tolerance I can put up with a lot, and have had work injuries that caused excruciating pain - this was the limit of my tolerance. I Waited 12 hrs to go in but couldn’t handle anymore pain, thought this was going to end me (no fear of death but just wanted to get moving with it).

Could be they entrapped even the Vegas nerve during surgery, or some other nerve? Muscle at rib attachment was extremely rigid and inflamed, and is during these events. Bile is likely backing up from odid’s sphincter into stomach (?) - must have thrown up several cups of bile (not stomach acid). Doctors say it’s not possible but my body disagrees - this fluid was something I’ve never known before (and my stomach to my esophagus never ached or burned). This wasn’t an upset stomach and only right upper and right mid quadrant we’re ever in pain.

They released me after four days and said they couldn’t help any more. They put me on Amitriptyline and Gabapentin (again), and gave me a small amount of Ativan (‘just in case the worst spasms/pain occur‘, they said). They want me to go to a pain clinic for a nerve block shot in the abdomen. What will that cost and will it even work?

Does anyone at Mayo have experience with what appears to be chronic and intensely acute spasm and nerve pain or damage post-op cholecystectomy? I can’t support my family living moment-to-moment in fear of another attack.

I look forward to some idea in handling nerve and/or biliary pain. Thank you for this forum!

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@wt1413wt hello, I know this was posted several years ago with the neighbor picked her out what your pain was caused from? I had a long wedge resection about three years ago. Everything was going as normal until I started a medicine for my autoimmune disease, which gave me really bad stomach aches with acid reflux. I then developed what I thought was a hernia because I had these beer pains in my stomach out of the blue where it felt like somebody was squeezing my stomach so hard the pain was like a 10. I went to the gastroenterologist several times for an upper G.I. and they said I do not have a hernia. My PCP doesn’t really know what to do. The gastroenterologist said it could be a hernia. They could not find, but it also could be muscular like maybe a muscle spasm. Now, since stopping the medicine, it has gotten better, but if I sneeze or bend over too far , it will come back really hard. It won’t last that long, but the pain is intense. It almost sounds like you have something similar to what I have.

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Hi im Carol0229 new to this. A bunch wrong.Hope you can help

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Hello,
Although many years have passed the area around my incisions in the upper right quadrant remain triggered - always. The deep unbearable pain occurs much less often but will take me to the ground when it does happen.

I received a nerve block at OHSU in C3/C4, which nerves feed down into the rib attachment and right quadrant area. This was the first time I finally felt no pain or triggered tightness. However the block only lasted an hour or so.

The second time all pain was removed was when I went to the ER after about 12 hours of 10/10 pain and uncontrollable spasms, afraid to move if the pain would get worse, sobbing like a small child. They finally administered a strong does of ketamine. I finally had zero pain and felt normal again. This only lasted 15 minutes or so. A few days later I was released because they felt the pain was manageable. They also blamed an inflammation of the stomach lining, but only checked after several days, and was likely because of the pain and spasms feeding backwards. It's a mess.

Other research reflected this might be due to nicking the sphincter of odi near the stomach, and the procedure nicking nerves in order to inflate the abdomen with air to complete the surgery.

No other pain meds have worked other than high-dose ketamine and the nerve block in my spine. That procedure was quite painful as a newbie was attempting the procedure. They finally had the surgeon do the block, and there was no pain at all...

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I have been suffering from chronic migraine for many years, and have not been able to find a solution. My migraines are bearable in cold weather. Once the season changes and the barometric pressure rises, I am in pain 24/7. Summer is a disaster. I am now trying large doses of Gabapentin plus starting Botox injections, something which I have put off as I detest needles, but finally am trying as a last resort. None of the injection- type drugs have ever helped. I wish you luck.

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