Anyone else have a Redundant / Tortuous Colon?
Hello. Anyone else out there that has a redundant/ tortured colon? I was diagnosed with this a few years ago. I’m usually ok, but if I get constipated, I get sick for a week or two. Last year my gastroenterologist referred me to a surgeon for urgent surgery to remove some of my colon. The surgeon I ended up seeing (not on the recommended list by my gastro doc due to others not available for a long time) said he believed I could live with the redundant colon if I followed a low FODMAP diet. I tried the diet religiously, scientifically (I’m a scientist), and I found it’s not the food I eat that causes these bouts of constipation. The only item I’ve found that might cause the bouts is coffee every day. An occasional coffee seems fine. What has helped me stay regular in a big way is Benefiber (or any pure wheat dextrose generic) three times per day. Lots of fluid.
My gastro doc was upset with the surgeon and said I’d regret not having the surgery. He fears I will end up in an emergency situation. I have searched the Mayo site and don’t find anything about redundant/ tortured colon. Are any Mayo docs doing research or treat this condition? Anyone else suffer from this too?
Thank you! -Jayne
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Thank you so much for replying. I'm going to try this asap. ❤
Just a few questions. Wondered with all “soft” foods, is there enough “bulk” to keep things moving? Also, I don’t see any carbs. Is there a reason for that?
Well, I am so disappointed and frustrated. I waited months for the apt with the new gi motility specialist on Friday. I even sent a two-page synopsis ahead of my apt detailing my history, my recent struggles with managing my constipation meds and what I hoped to achieve with my apt. with her. It was an almost 4 hour drive. I was hopeful at first as she was nice, not arrogant as some, but not long before my frustration started. I also have had chronic, almost daily migraines, for nearly 30 years, and she quickly jumped on that. I am well aware of the brain-gut connection and my neurologist and I have spoken of it often. Also the role serotonin plays. But, in 30 years I have also tried and failed virtually every migraine drug and treatment there is. So, she says she doesn’t think my bowels will get better until my head does and visa-versa, all tied together. My nervous system is on overdrive. So what do I want from her, she asks? I want to know what to take and how to take it so I can poop regularly and what to do when everything stops and I just cannot go at all and how to recognize if X-ray or something is needed? Nothing. I asked same questions three different times, becoming more and more agitated as I wasn’t getting any answers. So, she does exam and tells me I have very rapid heart rate! Also, abdomen is really tender. Ya, because I’m hardly pooping! Gets beeped that her next patient has arrived so she has to wrap things up. So, I ask again. Finally says that she thinks previous dr has me on good meds, nothing new she can suggest from that end. As far as when I feel like I’m all backed-up, am I really or am I just perceiving it to be that way? How do you just perceive that you’re not pooping? She feels the real key is getting my migraines better. At this point I want to ask if she has a magic wand but I restrain
myself. So, the one thing she offers up is citalopram which she thinks could calm down my over-active nervous system. When I bring up severely tortuous colon. She says she saw that in records. She also referred me to a cognitive behavioral therapist who she thinks could be very helpful. First apt is in Sept! So, I left with pretty much nothing. Actually less, because I now have no one. My previous doctor has turned me over to her so I can’t call him as they’re all part of the same system. When things just stop moving, he will usually order an X-ray and then something strong to clean things out. She didn’t appear to even believe me about that. To even find someone else and get an apt will take months to get in and I have no idea who to even go to. I literally just cried myself to sleep last night.
Does the emphasis on soft and blended foods (except for the oatmeal) mean that bms are easier with a low fiber diet? I have read that blending veggies reduces their fiber value considerably.
I certainly understand why you’re ready for answers and help! I’m going through something similar right now with my health. It can be frustrating to be patient dealing with our medical system. So much has changed since Covid. And I’ve had to wait months to get an appointment with a specialist. In February I found myself at the emergency dept one night after 11 days without a BM. It took 9 weeks to get into see my gastroenterologist then a week for the colonoscopy. I was diagnosed with Tortuous colon in May. I’ve had IBS for years also.
What is happening with your colonoscopy prep that you’re not clear for your colonoscopy? I know that’s really necessary for a look at your colon. Does your Dr have any idea why your bleeding? Are you waiting to get those questions answered?
I’m just now figuring out what to do for Tortuous colon. I’ve been reading about it online. This is a great place for information and support. I’ve been reading about food and natural ways to keep things moving! I’ve increased my water intake. I’m taking softeners every evening right now. My stomach is pretty bloated and some days I’m not as comfortable as others, that’s for sure!
Personally, I would call my drs office if I’ve waited several days for them to call me. If you need an appointment, kindly remind them you’d like to schedule it. I consider it advocating for myself! Unless there is a reason for the wait?
I’m glad you reached out! It really helped me to share my concerns about this diagnosis!
I completely understand your frustration, mostly because we are in the same boat with the redundant colon. I also have a side order of Crohn's disease, which makes things interesting. I too have had experience with certain "expert" doctors who don't seem to have a clue, sometimes the one we've waited the longest to see. It's especially infuriating when they treat you like you don't know what your own body is telling you, isn't it ? Many of us have had that same experience, and It's easy to feel like we've somehow slipped through the cracks of the medical system. There are many days that I feel like I am treating myself with the help of Dr. Google and an occasional tele-med visit with my GI doctor, who is in another city. He's pretty good, but he doesn't have all the answers either. I wish I had some words of wisdom for you other than "hang in there" or "thoughts and prayers" and that kind of stuff. I will say that I have learned a lot from forums such as this one. Some of it worked for me and some of it didn't. But it's hard to separate the good from the not so good. So I keep plugging away. My current strategy is a combination of things I've learned from other people, along with an Rx from my GI doc. Mostly it works, but it seems like I'm always tweaking it. Don't give up. And don't give up on finding the right doctor for you. There are some out there.......
They did get me cleared out enough for the 2nd attempt at a colonoscopy, they just can't see the whole thing because of all of the loops.
During the barium enema, the Dr. still couldn't see that much of it and I literally heard him say "I don't what to do."
There has been a lot of time between these appointments. Nobody knows yet exactly why there's still blood in my stool.
It's almost like the whole tortuous colon is a rather unusual issue and nobody really knows exactly what to do with us, ya know?
May I ask what kind of softeners you use?
Thank you so much for your input!
-Kathy
Thank you for your kind words. Was very despondent last night. Feeling a little better about everything today. Realized after talking with my husband that I basically have been managing this on my own anyway, so nothing really is any different. I guess I was just hoping this dr was going to be the one that would be more “hands on” with helping with that. I’m going to take some ideas I’ve gotten from this site and try adding them in a little at a time. I did find a new dr I’m going to call in am. Thanks again for your supportive words words. Means so much coming from those who truly get it!
Can you tell me how much magnesium chloride you are taking? I’ve been using mag oxide. Never heard of chloride.
Sorry, I wasn’t specific enough. I do eat carbs, pasta, potatoes and bread, etc. Colonoscopy showed lactose so had to cut cheeses, etc, Most of my foods are pretty soft, veggies, fruits, chicken, I find beef constipating..
Also, my Gastro had put me on a stool softener. But I no longer need it so I cut it out. Now I take a laxative stimulant, because of incomplete evacuation. IBS complicates life too.
Trial and error.