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Diagnosed with UC at 60. Was in remission 4 months with max dose of oral mesalamine; developed acute pancreatitis and had to discontinue. Terrified of biologics, but may be only resort left? Please share experiences…
So sometimes when I go to the bathroom, I get blood in my stool, some days it’ll be a lot the point of where it drips into the toilet, otherdays it just shows on the bathroom tissue. And I dont know if it’s just because i push too much, or if it’s because I sit for too long. I also get constant bloating, pressure problems, as well as watery stools, and less frequently, hard stools. But the bloating and pressure have been ongoing for years now, sometimes it makes me think that it could be a cause due to constant anxiety that I suffer from. If anybody has any possible idea as to what it could be let me know. Thank You.
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@ejlouboutin16 I have a similar problem. I am not sure where the blood comes from but I have coincidentally come to realize very recently (as in the last few weeks) that I either have lactose intolerance or IBD (Inflammatory Bowel Disease). From what I have been able to determine, with just lactose intolerance there is not generally blood in a person's stools which is why I now wonder about IBD. I plan to try to isolate what else other than lactose containing foods may be causing problems for me, and then I plan to make an appointment with a gastroenterologist.
I too have bloating and pressure.
I suggest you make an appointment with a gastro and try to get to the bottom of it. If you do, and if you find anything out, please let me know and I will do the same if I make it to the doctor. The doctor I would like to see is scheduling in September or October so I may have to settle for someone else.
@contentandwell, I will try to see a doctor as soon I get health insurance back, so it could be at least a couple of months before I find anything. Inclusively, besides bloating, I tend to notice anal itching and even cramps in my case. So i personally hope that it’s just something as minor as IBD or fissure/hemorrhoids
@ejlouboutin16 That's too bad that you need to wait to see the doctor. I do not have itching, and not really cramps, more of an upset stomach frequently when after eating dairy and something else that I have not yet isolated.
You may be confusing IBS with IBD. They are not the same. If you google IBS vs IBD you will find more information about both of them, but frankly, I find it sort of confusing. That's why I think I do need to see a doctor about it, so that he or she can sort it out and suggest what might help.
@contentandwell I just hope, that it’s nothing cancerous, like I mean I’m just 21, but I just want to be sure
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@ejlouboutin16 I totally understand. That is a concern for me also, which is why it is important to get checked out by a gastroenterologist.
I have two different things that require an appointment with a gastro, but these days at the major medical centers the gastros specialize so much that I will need to go to two! One for my Barrett's Esophagus, and a different one for this.
Hi. When I posted this, I thought space was limited and didn’t provide many details. I am a 62 year old female, diagnosed with UC 2 years ago. I have been on oral mesalamine, which worked for 3 months until I developed acute pancreatitis. Prior to that, I had been prescribed Canasa (suppositories), Uceris rectal foam, hydrocortisone (oral and rectal). GI doc is pushing ENTYVIO and I am terrified of possible side effects. I am in good health, never smoked, do not drink, eat a healthy diet and exercise regularly. I am about to make an appointment with integrative medicine doctors to try acupuncture and herbal treatments like aloe vera and Boswellia? Has anyone been on Entyvio or more natural things and have they helped? The fact that I developed pancreatitis from 8.4 G of mesalamine daily was frightening and GI doc said that was a rare side effect. This is a horrible debilitating disease and I just want my life back. Has anyone had good or bad results with their UC treatment? Thank you so much!
I don't have UC, but you might find a separate forum on the Mayo site just for IBD. Might find more help there. Hopefully a moderator will jump in and direct you to the right place. Sorry you are having these problems.
Thank you for responding! I am searching a few sites to get information from people that have used the medicines out there for UC. It’s frustrating to say the least… So thank you for your input!
Best of luck to you!
Thanks so much! I see my GI doc on Tuesday and I am armed with a list of questions and several clinical trials. 🤞
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I am all too familiar with blood in my stool. I was diagnosed with ulcerative colitis almost 2 years ago. It was a shock, to say the least, because my health has always been good. As a result, I have learned so much about this disease. What I can tell you is that blood dripping into the toilet may very well be hemorrhoids or even a fissure, and both are very treatable! I had those things in my 20s and 30s because of anxiety and always rushing in the bathroom… My first UC flare, years later, was bloody stool, and the blood, frequency and abdominal pain became progressively worse over a period of weeks. Diarrhea increased until it was 8-12 bloody loose stools daily. I lost 22 pounds in 2 months, while I waited for an appointment with a specialist. I am fortunate to have found a GI doctor that specializes in IBD. The best thing to do is to make an appointment with a gastroenterologist as soon as possible; many of them have long waiting times, so you may want to get on a cancellation list, so that if someone cancels, you may be seen sooner. A colonoscopy is the best way to diagnose so many of these conditions, but there are also blood tests that will show certain "markers" to see if it may be ulcerative colitis or Crohns disease. They can also do a sigmoidoscopy, which is less invasive than a colonoscopy. UC is typically lots of bloody diarrhea and there is abdominal pain. There are different levels of severity from mild to severe and there are many different treatments, from oral mesalamine to biologics. Mine has progressed in less than 2 years and I have been on oral mesalamine, rectal mesalamine, rectal steroidal foams (budesonide), and since the flares continue, biologics are the next step. It is a process, and in the meantime, you can keep notes on your daily food intake, daily bowel movements and any other significant things that happen in your daily life. It will be very helpful to both you and your doctor. What I have found helpful is drinking LOTS of water so you don't dehydrate; it also helps you go to the bathroom more regularly. Get up and move around so you're not sitting for long periods of time; get enough sleep, and the hardest thing of all – try to ease your anxiety. I know that's easier said than done, and I have been anxious my entire life. Try to take just a few minutes whenever you think about it to just "breathe" or focus on something as simple as looking out the window and watching a bird or whatever you might see at that moment in time. I saw my GI doc yesterday and while I'm preparing for the biologics (updated vaccinations) I have also made an appointment with another group of doctors that do things more naturally with acupuncture and herbal remedies. My GI doc does not believe they will get the UC back into remission, but he said it can help with anxiety and ease some of the symptoms. I owe it to myself to do this and you owe it to yourself to see a doctor to find out what's wrong! I'm sure you're having anxiety just worrying about your symptoms. Once you know what's causing them, you can get a diagnosis and a treatment plan that works for YOU. Good luck to you! Do this for yourself!!
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