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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Thanks so much @sallyw133 for the migraine information for my aunt. She was told that her's is stress related too. She is retired so there is no job stress. I am going to share your post with her.
I have a :significant tortuous colon" according to the colonoscopy notes. I think that is what is causing my slow-motility. I take a daily Senokot S tablet. I don't know if that's the right thing to do because it's a stimulant, but it seems to be my only hope of going. What is your daily treatment for our slow-motility challenge?
Thanks so much for all your good information! 😊
Excellent post, Jacque. I agree 100% . Too many doctors slough this condition off as "no big deal" or "nothing to worry about". If you are very lucky , you will find a doctor that is actually helpful, and takes the time to help you find a solution.......even a partial one. I even had one GI Dr. suggest having my colon removed. Insanity. Everyone is different and what works for one will not work for all, (Miralax does nothing for me) so I keep trying different things in order to live a "normal" life. Right now that consists of Linzess, senna, prune juice, and coconut oil ,VERY early in the morning. Senna and colace at bedtime. Once it starts working, it takes several hours or longer before I can leave the house. Sometimes not until noon. jacque, if you don't mind me asking ...when do you take the prunelax and is that all you are taking ?
I take the Prunelax every evening at 7:30pm, or as near that time as possible, and it produces a result the following morning. I also use psyllium powder, mixed in my cereal or oatmeal. (8 mg) daily. I occasionally use Metamucil crackers also, one or two depending on my diet for the day, making sure I drink a full glass of water with it. The psyllium powder makes my oatmeal a slime and I've come to find it repulsive. It inflates the volume of the oatmeal, so I've divided it in half because I just couldn't "stomach" it anymore. On those days, I supplement with the Metamucil cracker, in addition to the oatmeal. It works for me and I don't feel like I'm going to vomit with the slimy oatmeal. I've been doing this for quite a few years. The cereal is much easier and palatable for me but I know some people have difficulty with milk. But as we discussed earlier, everyone is different and we all need to find what works for us as individuals. Medicine practices have changed. And my husband, who is a retired clinical pharmacist, is the first to make that statement. He worked in a hospital for over 30 years. A clinical pharmacist is much different than a retail pharmacist at a drug store. He dealt with life and death situations. He has commented numerous times that the treatment now has turned into a "herd treatment" vs focusing on the individual. So we have to be our own best advocate and not give up! Jacque
I’ve been working with a dietician for the past month. Very low fiber diet. No raw fruits and veggies other than my lunch smoothie bc they’re blended. No meat. Do feel better not having All that bulk but have had to add Miralax and mag oxide and still not really going. Think I still need something for motility. Trying not to use Motegrity . Too $$$
@sallyw133
Very interesting! I have been doing the exact opposite. I thought a high fiber diet would be more helpful for slow motility. Thank you for telling me about your low fiber diet and please keep me posted on how things are go and any success you have coming up with a combination of possible solutions. This process is definitely a constant trial and error. It seems that if I find something that works, it soon stops working and I need to try something else. Nothing seems to be "the answer" for long.
Well I’m another you can add to your list…my colon, I’m quoting from colonoscopy from 2018;
The colonoscopy was technically difficult and complex due to restricted mobility of colon, a redundant colon, significant looping & tortuous colon. Many
small & large mouthed diverticula found in sigmoid, descending & transverse colon. And of course, let’s not forget hemorrhoids (internal)…what am I supposed to do with all this info? They diagnose but don’t give any treatment, except “avoid constipation”.
Also, come back for another colonoscopy in 5 years..which I did, with the same results
Correction: I take 8 GM of psyllium, NOT 8mg.
I thought same. Gi only told me no fiber supplements. Dietician said high fiber and fibrous foods are difficult to digest so tend to move slowly and get caught up in kinks and loops. I’ve found I do feel less “packed”. However, still having problem getting things to move. Mineral oil does help but not sure about using it frequently. I’m trying to avoid using Motegrity as I have to
go on SS at the end of year and too expensive. So I’m experimenting to find alternatives before then. Have a virtual visit with dietician in morning, so hoping for more advice from her.
@hello1234 - Thinking it over, I think my problem was that because of osteoporosis and concern about heart disease, I have very little salt in my now mostly entirely home cooked plant diet. Plus I took the 1 - Senna S per day she recommended PLUS Miralax in addition. I hadn't even reached the 2 liter/day of water that she recommended.
Currently my doctor suggests I not use Miralax at all and up to 2 Senna-S and 2 - 100 mg docusate sodium stool softeners per day, as needed. I'm experimenting with just the stool softeners to see how it goes.
Do you you know what contributed to your need for your saline iv?
I had previously posted an incorrect dosage on the powdered psyllium. I take 8 gm daily, NOT 8mg.