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Mesh less repair after 8 month : disaster
Hi everyone,
I’m reaching out because I’m dealing with some unexpected complications following a hernia repair, and I could really use some advice or similar experiences.
Last February, I underwent a meshless repair (using the Minimal Repair Technique) for a small, asymptomatic right-side indirect inguinal hernia. The recovery was pretty rough, with significant pain initially.
About a month post-surgery, I started experiencing digestive issues – narrow stools, constipation, flaring. Now, eight months out, while the repair itself seems solid (I’ve had it checked multiple times), and I only have mild discomfort after activities like yoga, these digestive problems persist and are seriously impacting my quality of life.
Things came to a head about a month ago when I had a major flare-up: fever, severe constipation, and what felt like a compromised immune system. This led me to consult a gastroenterologist, who ordered a colonoscopy, blood work, and stool analysis.
The results were puzzling:
– Colonoscopy showed localized inflammation without an apparent cause
– Blood tests revealed slightly elevated C-reactive protein levels
– Stool sample indicated mildly increased calprotectin
The gastroenterologist’s take? An inflammatory process of unknown origin, thankfully not malignant. His theory is that the surgery, despite being minimally invasive and mesh-free, somehow triggered an autoimmune response that he believes could be long-term.
I’ve lost weight due to relying on laxatives, and I’m dealing with near-constant abdominal pain. My surgeon is baffled, saying he’s never encountered this in thousands of procedures. He’s suggested a nerve block to see if it helps, even though pain isn’t my primary issue.
In my search for answers, I’ve only found one similar account – someone who developed IBD after hernia surgery with mesh. However, their procedure was much more extensive than mine, involving mesh placement within the peritoneum, which wasn’t the case for me.
I’m at my wit’s end here. This situation isn’t sustainable, and I feel like I’m on a wild goose chase for medical answers. If anyone has gone through something similar or has any insights to offer, I’d be incredibly grateful.
Thanks for reading, and I appreciate any help you can provide.
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