Diverticulitis Support Group
Diverticulitis is a common disease of the bowel, in particular the large intestine. Diverticulitis develops from diverticulosis, which involves the formation of pouches on the outside of the colon. Diverticulitis results if one of these diverticula becomes inflamed. Diverticulitis most often affects middle-aged and elderly persons, though it can strike younger patients as...
Hello everyone,
This is my first post anywhere. I am hoping someone can help me figure out some things about my Diverticulitis. First (for the sake of saving reading time for people) my questions. Then I will post my experience.
1. I don't have "pain" per say. I always have a full, stitch, hard, bloated, uncomfortable feeling (trying to find words to describe it) on the upper left side of my stomach. Sometimes it is like a sharp-shooting twinge can happen more on the lower left side. Because of this, I have no idea if I should start to add-on more low-residue foods. I am afraid that if I add something, it will push me to an attack again. All of the articles I have read say, "Once you no longer feel pain, then you can advance to the next stage of eating (from liquid, to full-liquid, to low-residue, etc.)." It doesn't hurt- but it is uncomfortable and mostly scary. So do I stay on liquid until I don't have that feeling at all anymore? Or will I continue to feel something no matter what?
2. Other than having a colonoscopy, is there a way to flush out the diverticuli? I have not been able to find any information about this yet. Or once the diverticuli become infected, whatever stuff is stuck in them (foods, fecal matter, etc.). is stuck there?
3. I've read that things like grapefruit seed extract and giner are good for inflammation, but I have Silent Reflux- wouldn't these aggravate my reflux?
My experience:
I am a 39 y/o female. In November 2016 I cut out carbs (no bread, no soda, no potatoes, etc.), cut out all dairy (am lactose intolerant so I never really ate much anyway), drank only water (no coffee, teas, juices, etc. and I didn't really drink these anyway but was having soda often), and basically was following a Paleo-Low-carb-dairy free, acid free, diet. Daily my meals where a combination of the following: cooked with/ate only butter, chicken, ground beef, steak, salmon, raw carrots, raw broccoli, raw baby spinach, one to two avocados every day, one to two bananas a day, cooked asparagus, cooked brustle sprouts, bacon, eggs. I felt super great. Meals were super easy to prepare, I didn't have any cravings for starches anymore, I slept really well, had a ton of energy, lost 20 lbs., and was just super good. I started doing this because in the same month, I woke up choking and going to the ER. I was Dx with Silent Reflux. That was really scary and I didn't want that to happen again.
February 2nd I went to the doctor because two night before I was lying on my right side sleeping and woke up because I had a charlie-horse-like pain on my left side. The next day it got slowly worse and then finally I went to the doctor. I have no fever, no chills, no nausea, nothing other than the pain. They did blood work and had me come back the next day. WBCs were elevated and the pain was worse so they sent me right to the ER. ER did more blood work, WBCs still rising, pain worse, but still have no fever, nausea, etc. CT scan showed Diverticulitis, no perforation, no abscess. Was given 10 days of Flagyl and Levaquin (both generic). Pain started to get better but this feeling on the upper left side that I asked about above is still there and hasn't gone away.
The last night of my antibiotics, I had fever, chills, and felt super nasues, so I went back to doctor the next day. They did more blood work and supposedly my WBCs were coming down, but they extended the antibiotics for 7 more days. After 4 days I had pain and severe cramping in my legs and arms and went to the doctor who stopped the Levaquin (I was Dx with drug-induced neuropathy) and told that I could experience tendon rupture. I took the Flagyl for one more day and that made the cramping in my legs come back so I stopped that too.
Went back 3 days later and the cramping in my legs was gone, but until now the neuropathy remains and I am having all sorts of other things going on from the medication. Doctor said it was common and sometimes it can get worse over time and sometimes the body can heal. That wasn't helpful but she was very-matter-of-fact. Took some more lab work to test magnesium, B12, potassium, etc. She was supposed to call me this past Friday but didn't.
As far as the Diverticulitis, she said to try and start adding things like cooked carrots. That it was best for me to go to a high-fiber diet as soon as possible (even though I told her that is what I was doing since November and despite me reading so many places that high-fiber is actually not good for Diverticulitis). I told her about the "pain" I was having and described it as I did above in this post. She said that was normal because of the inflammation and it could take 6-8 weeks before that feeling went away. She explained that the area was so inflamed that tenderness is normal and with time, it should be better. Either way, I am still losing weight too fast and I needed to start adding food and it would be fine. I asked for a referral to a GI doctor but she said not at this time and all they would do was tell me the same thing- it takes time, I need to start adding more soft foods, and if it starts to really hurt- go to the ER.
So I have been eating two eggs, avocado, 1-2 vanilla pudding cups, Ancient Nutrition Bone Broth Collagen (heard it was good for gut health and also for repair and am dealing with the side effects of the meds so I figured I'd try). Sometimes I will add a piece of white bread or a piece of sourdough bread or english muffin. I've tried bits of watermelon once (didn't seem to upset anything). The weird feeling in my stomach is always there but like today, I was so starving I ate english muffin plan, the weird sharp twinge happens more towards the lower left side, but still that other feeling on my left upper side is always there. There has been a few times that I have super bad gas pain and I don't know what to do about it so I just try and sleep with a heating pad over my stomach.
I feel super bad from the meds (the fatigue is awful and the burning and pain sucks too and depression and anxiety hit me from one day to the next), but I also feel bad from not eating but I am afraid to eat.
I am also considering switching over to Kaiser hoping that they will be able to refer me, help me in some better way because I am not happy with how these doctors have treated my concerns with such a matter-of-fact way. I kind of just want to have surgery because living with not knowing if I will have another attack, or not fully healing, and then having to take more antibiotics, is such poor quality of life. I don't want that but right now I don't have a clue when or how I will feel better.
I am really mad that by eating healthy, this happened. How does that even happen? It is like a cruel joke or Karma or something. If I had just kept on, I would've been fine. I am pretty sure trying to do high fiber will just mess me up again, and I have read that for some with Diverticulitis, high-fiber doesn't work. However, I now hate eating carbs because it does give me cravings and it makes me feel drowsy (you know that carb feeling).
Thanks for listening.
I feel your pain. I too am at my wits end with this condition. I can relate to a lot of the things you have described and your fears. I am writing this now because I can't sleep. Sticking pains, worry, losing weight too because I can't eat enough calories of the foods my gut will tolerate to even maintain the weight I am at presently. I even see a registered dietician. She can only help so much. I spend most of my day trying to figure out what to eat that won't cause distress. I can't tell you how much food I've thrown in the trash or if unopened, taken back to the store. Like you, I ate a healthy diet before with lots of raw and cooked veggies, fruit, no red meat (only an occasional lamb chop), but mainly fish and chicken, then I get this disease. My bowels were always regular until this thing. Now on a low fiber diet, it is a struggle with constipation which doesn't make you feel comfortable at all, even if you didn't have diverticulitis. I had to stop my Ester C cause now it gives me heartburn. Tried Boost at the suggestion of my dietician, but that too gave me heartburn. My GI track is really messed up. My plan for tomorrow is to look back at my food diaries, pick some less pain filled days, and eat what is written down for those day. When I try to add high fiber foods, even in tiny quantities, I have increased pain. Your dr. said it takes about 8 weeks to heal the inflammation, so if I just count from my date of diagnosis, that takes me to March 5th. But really, this really began before Christmas and got progressively worse.
Well, I'm going to go to bed, listen to my relaxation CD and fall asleep. At least when I'm asleep, I don't feel uncomfortable. Thanks for listening to me too. Write back and let me know how you are doing. I care.
Regards Rowe
I went back to the doctor because my stomach (colon) would not stop spasming and I was having really bad diarrhea. All she said was it was probably my stomach dealing with everything that was going on but that I should start adding more things, like cooked carrots.
So I did that this past week. I had like 3 bites. On another day I tried chicken and yesterday I tried a baked potato. The spasms and diarrhea did stop by adding a few things and I had regular bowel movements for the first time in a month but then...
Friday night I was at work, standing, and I had a crazy sharp pain on the right side. Then I started sweating but I am not sure if the sweating was from anxiety (because I was at work). I took my temp and it was fine. Last night I got a sharp pain on the left (the original spot) and on the right out of nowhere and then again on the right. Right now as I am sitting here typing I am getting sharp pain on my right side right underneath my rib cage. Now I am worried infection is coming back. Last time I didn't have a fever, just the cramps, but this pain is sharp and I hadn't felt like that before so I have no idea if I should go back to the doctor/ER or wait a few days and see if it get's better/worse. I went back to just liquids starting today to see if that helps.
When people say they have an attack, what does that mean? Could this sharp sudden pains I am feeling be an attack? Or is it more likely that the infection is still there and flaring up again?
The problem and fear I have with waiting to see what happens is that it gets really bad and I can't work. I can't afford that at all, so I don't know what to do about this in this moment. I have no idea what kinds of pain and discomfort are okay and normal vs. those that are serious. Again waiting around to see if I get a fever seems like a bad plan.
This is so frustrating. I finally cried about all of this today out of nowhere pretty much as soon as I woke up. I know that happened because this is so overwhelming but wow, I surprised myself when I cried.