Debilitating multisystem dysfunction from diverticulitis surgery

Posted by Devin @djfilipiak, Dec 22, 2025

I am a 35-year-old male with a decade-long history of progressively debilitating multisystem dysfunction originating from catastrophic diverticulitis surgeries in 2016. I am currently in a state of assumed acute decompensation, characterized by rapid weight loss: Loss of +/- 30 lbs. in 4 months., functional urinary obstruction, and systemic inflammation (CRP 20 mg/L toward the end of an episode).
Recent imaging (MRE, Nov 2025) confirmed bowel loops tethered to the ventral abdominal wall. However, local General Surgery declined intervention (Dec 2025) due to the complexity of the "hostile abdomen," leaving me with an "inoperable" mechanical defect that requires tertiary-level reconstruction. This complex presentation is further complicated by a 'Double Crush' phenomenon, involving confirmed L4-L5 spinal nerve root compression (2020) exacerbating the pelvic neuropathic pain.
This period established the "Hostile Abdomen" and deep pelvic scarring.
Event: Severe Diverticulitis complicated by Colovesical Fistulas (Bowel connected to Bladder).
1. The Surgical Series (4 Surgeries in 2016):
• Laparoscopic Sigmoidectomy (Attempted): Planned ahead of time
(General Surgeon/DO). Procedure failed/converted.
2. Emergency Open Sigmoidectomy (Ileostomy):
• Performed by General/Trauma MD because original Dr.
was unavailable.
• Outcome: Sigmoid colon removed, temporary ileostomy bag placed.
3. Failed Ileostomy Reversal:
• Attempted by original Dr. (and Partner).
4. Final Colorectal Anastomosis:
• Successful reversal 8 weeks later.
5. Key Provider:
• Urology:
i. Managed the fistulas during this crisis (2016). Significance: He knows the deep pelvic anatomy was compromised early on. Even though this was the first person to dismiss my issues and my theories which are now coming true.
I am currently experiencing the following functional deficits:
1. Failure to Thrive (Nutritional Crisis)
• Rapid Weight Loss: Loss of ~30 lbs. in 4 months (230 lbs./199.4 lbs.).
• Early Satiety & Nausea: Eating triggers immediate nausea and "fullness" due to mechanical restriction. Diet is limited to soft/liquids (mashed potatoes, broth).
• Documentation: Primary Care confirmed "unhealthy weight loss due to lack of appetite" (Oct 2025).
2. Mechanical Tethering (Ventral Abdominal Wall)
• "Stuck" Sensation: Specific, localized pulling sensation at the 2023 Hernia Mesh site (periumbilical).
• Positional Obstruction: Acute episodes where bowel seemingly "locks up," requiring physical maneuvering (kneeling) to release the bowel loop (e.g., event on Dec 7, 2025).
• Correlation: Matches MRE finding of "small bowel loops closely opposed to ventral wall."
3. "Double Crush" Pelvic Dysfunction
• Urinary Retention: Inability to initiate voiding unless the rectum is empty ("Can't pee until I poop"). The struggle to urinate is constant. It is exacerbated by any gas or fullness in the colon. It is also worse during the cold or if I am physically cold, anxious, or shivering at all.
• Neuropathy: Retrograde burning in urethra ("flames gone backwards") and chronic left-sided testicular pain.
4. Systemic Inflammation
• Elevated CRP: 20 mg/L. Indicates active tissue trauma/inflammation (Autoimmune/Infectious causes ruled out).
• Hyperhidrosis: Profuse sweating secondary to sympathetic upregulation/pain.
• Fatigue: "Crash cycles" rendering the patient physically unable to work. Gabapentin has helped relieve this.
5. Symptom Classification Guide
• ZONE 1: ABDOMINAL WALL & BOWEL (The Mechanical Zone)
▪ Status: NO GENERALIZED PAIN.
▪ Clinical Definition: Mechanical Obstruction / Ventral Tethering.
▪ Patient Experience:
• Restriction: A sensation of being physically "stuck" or "tethered"
to the abdominal wall.
• Cramping: Intense muscular contractions attempting to push past
a blockage.
• Distension/Bloating: Hard, physical fullness immediately after
intake.
• Positional Lock: Bowel loops feel "caught," requiring physical
movement to release.
▪ Incorrect Documentation: Do NOT write "Stomach Pain," "Abdominal Tenderness," or "IBS-type pain." Pain is too quickly dismissed. This is not a simple pain issue!
▪ Etiology: Physical Adhesions (Confirmed on Nov 2025 MRE).
• ZONE 2: PELVIS, PUBIC & URETHRA (The Neuropathic Zone)
▪ Status: ACTIVE NEUROPATHIC PAIN PRESENT.
▪ Clinical Definition: Double Crush Neuropathy / Radiculopathy.
• Patient Experience:
• Urethra: Retrograde BURNING ("Flames gone backwards") specifically when retention occurs.
• Testicle (Left): Chronic ACHING and sharp neuralgic zaps.
• Pubic Symphysis: Radiating nerve pain connected to spinal
history.
▪ Correct Documentation: "Pelvic Neuropathy," Pudendal/Genitofemoral Neuralgia," "Radicular Pain."
▪ Etiology: Nerve Entrapment & Confirmed Radiculopathy.
▪ Documentation: Diagnosed with "Radiculopathy, lumbosacral region (M54.17)" and "Low back pain (M54.50)" (March 2022).
• Mechanism: L4-L5 spinal nerve root compression compounding
with pelvic adhesions.
I have hit roadblock after roadblock over the years and having to self-advocate. Which has earned me the term of combative. How many other "combative" patients are in this forum? Hopefully lots, so I know I am not the only obsessive one on making sure my care isn't just how someone else wants it.
Has anyone else dealt with similar issues? Any advice? Currently I have submitted my info to Mayo, Penn Presbyterian, and trying to with Johns Hopkins. I am 35 years old and have not been able to sustain or even settle myself. I am in mass debt, school, etc. I am lost without actual direct guidance from someone who believes me and accepts I am not stupid or just Dr. Google.
*Parts of this summary (which is now considered my Patient Bio and Dossier) was produced via assistance with Google Gemini which utilized every one of my care documents, discs, images, dr notes, and my own input to compile this description of what I am dealing with in words that make it more understandable to a provider, and those self-advocates who have spent years, hours, days, researching legitimate information, like I have.

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Profile picture for alishome281 @alishome281

@djfilipiak I can understand your frustration about finding some one to help you. I had a modified multivisceral transplant due to total gut failure. Very few hospitals offer this transplant, I had to go to Indianapolis. I went to IU Health and saw Dr Mangus. He is phenomenal in all things gut and gut failure. Have you considered traveling to get the help you need? He's definitely worth traveling, but you may set up a telehealth call do discuss your case with him. I have a friend that just had bowel surgery after she got so many no's from local providers.

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@alishome281 I am in Buffalo NY. I have no qualms travelling. I've even looked international

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Profile picture for linda82 @linda82

Wow, so sorry to hear all of this. So many complications at one time and trying to figure all of it out!
After my surgery (robotic and open) my main issue is feeling full so quickly and weight loss. My biggest fear is adhesions and what is happening inside my belly. I have done well and no diverticulitis episodes or IBS since surgery.
Never stop being your own advocate and never give up. Hopefully you will get more insight from others on this site.
Hugs

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@linda82 How long hasbit been since your surgery? Did they remove a portion of your Sigmoid Colon?

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Profile picture for Devin @djfilipiak

One of the worst parts??
Being visibly a healthy 35 year old male. In today's world of assumptions, and mass media hypersensalization of common societal normal, makes the struggle extra difficult. Now everything portrayed is in my mind making me feel insecure or insufficient or weak. There's people out there who have it worse, right? Yes. Absolutely. But I'm not living their life 😔 I'm barely able to live my own.

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@djfilipiak forget media, your life belongs to you and there are some things that have nothing to do with you, and others that you can do something about and be in the ‘driver’s seat’…your choice ! forget comparisons !

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Devin @djfilipiak your case sounds complicated to say the least! I have a history of gastroparesis due to autonomic neuropathy complications of diabetes and I have also been diagnosed with diverticulosis/ diverticulitis that seems to be genetic. Both my dad and grandfather had it. From a dietary standpoint the two conditions respond best to different & opposite things. Gastroparesis does well with small, frequent, low fiber snack like meals. Diverticulosis/ diverticulitis does better with high fiber. So the balancing act can become frustrating. But my situation has never involved surgery and for that I am thankful. It sounds as though you have endured several unsuccessful surgeries. It is very disappointing that Mayo “denied your case”. I think the world of them and thought they would be the ones to help if no one else could. I’ve always had the impression that Mayo enjoys a challenge and I would be inclined to keep asking if I were you. However I’ve personally experienced that they don’t like to be the ones to have to fix others’ mistakes so maybe there’s that. Whatever you do I would look to a large teaching facility for your care and further treatment.

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Profile picture for Cheryl, Volunteer Mentor @cehunt57

Devin @djfilipiak your case sounds complicated to say the least! I have a history of gastroparesis due to autonomic neuropathy complications of diabetes and I have also been diagnosed with diverticulosis/ diverticulitis that seems to be genetic. Both my dad and grandfather had it. From a dietary standpoint the two conditions respond best to different & opposite things. Gastroparesis does well with small, frequent, low fiber snack like meals. Diverticulosis/ diverticulitis does better with high fiber. So the balancing act can become frustrating. But my situation has never involved surgery and for that I am thankful. It sounds as though you have endured several unsuccessful surgeries. It is very disappointing that Mayo “denied your case”. I think the world of them and thought they would be the ones to help if no one else could. I’ve always had the impression that Mayo enjoys a challenge and I would be inclined to keep asking if I were you. However I’ve personally experienced that they don’t like to be the ones to have to fix others’ mistakes so maybe there’s that. Whatever you do I would look to a large teaching facility for your care and further treatment.

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@cehunt57 ugh that all sounds frustrating and you are very lucky to have no had to deal with surgery. I will say, my diverticulitis surgeries, as bad as they were at the time, gave me 5 pretty decent years I wouldn't have had otherwise. Unfortunately, it's the next 5 that I started feeling the effects of the first 5 years of healing! Lol. And more university type clinics or study clinics is my plan. But unfortunately, now I am also finding limitations on NYS Managed Medicaid. So, that adds another layer/filter on selections, even if I wanted to consider self pay options. We'll see how long my energy can last this time around 😔

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Profile picture for anniegk @anniegk

@linda82 How long hasbit been since your surgery? Did they remove a portion of your Sigmoid Colon?

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@anniegk Mar 23 and they removed 12 inches of my sigmoid.

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Profile picture for linda82 @linda82

@anniegk Mar 23 and they removed 12 inches of my sigmoid.

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@linda82 #NoSigmoidCrew #StraightToTheDescent 🤣

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Profile picture for Devin @djfilipiak

@colleenyoung yes. I never really considered AI until I got bored recently. Then it was providing me things I already had confirmed and done. It's only recently that I've integrated it but I've been putting it as much to the test as possible.
Unfortunately Mayo clinic denied my case, so here I go navigating another brick wall 😔
Merry Christmas.

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I'm sorry for what you're going through but I'm glad you have the brain power to research. Some doctors don't like to hear patients have consulted Dr. Google. It is important to verify AI. Maybe you've already read a lot of medical journal articles before consulting AI but it should also give you sources.
With your complex case, you've done the right thing by trying to get into one of the major medical institutions. Not a doctor, but sounds like you need a skilled surgeon at a minimum.
The immediate issue sounds like nutrition while you wait to see a doctor. Since you research, I assume you are working on that with all your strength.
Finding a dr who listens is a challenge because our system means they don't have much time.
That's assuming you're in the US.
Condensing your issues into some bullet points, similar to what you posted, could be helpful. Make those points about what has been diagnosed and who gave the diagnosis. Then make some points about the issues that have not been diagnosed. That's where your research comes in, or you can ask about your theories.
Some doctors are surprised and dismissive by patients who have done research. It's unfortunate. you've been labeled as combative.
You may want to tell a doctor upfront that you have been labeled that. They may see it in your records anyway.
You could say something like: "Unfortunately, I've been labeled as a combative patient. I did not intend to be combative, but I'm trying to advocate for myself in a very difficult situation. I hope you will see me as a pleasant patient who has tried their best to learn how to be healthy.." Tnat's top of my head and it needs to sound like you! That's another issue with AI. It may not sound like you.
Make sure that what you sent to different institutions actually got there. It's amazing how things can go astray.
You may want to take a look at Reddit. You may have to separate your issues for search purposes.
A counselor could be an enormous help because you're coping with so much. They might be able to help you with communication suggestions too.
next
I don't know how you can do this but doctors usually want to know the main reason you're there. You've got a lot of reasons. You may have gone through that exercise when you submitted your info to those different places.
Again, I'm sorry for this and I hope you have some luck getting in somewhere you can be helped. I hope you have a good support system.

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What happened in the catastrophic diverticulitis surgeries in 2016 to cause all of your current conditions?

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Profile picture for bc321 @bc321

What happened in the catastrophic diverticulitis surgeries in 2016 to cause all of your current conditions?

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@bc321 the scarring and constant reopening and healing of old wounds so quickly.
More specific breakdown (updated but similar as original Post):
• Surgery 1 (Attempted): Laparoscopic Sigmoidectomy.
Procedure failed/converted.
• Surgery 2 (Emergency): Open Sigmoidectomy with Ileostomy.
Performed because original surgeon was unavailable.
• Surgery 3 (Failed Reversal): Attempted Ileostomy Reversal. Failed.
• Surgery 4 (Final): Successful Colorectal Anastomosis (Descending-to-Rectal).
• Complication History (2016): Renal Ultrasound (March 8, 2016) showed "mild degree
of dilatation of the left renal pelvis," indicating early evidence of pelvic
compression/obstruction affecting the urinary tract. Caused sepsis, near fatal.

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