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hi i have diverticular disease of the upper and lower tract and a malrotated bowel possibly from hysterectomy operation for cancer im putting on weight but barely eating ,i feel nauseous all the time and my heads fuzzy constant pain currently waiting for surgery to fit a stoma but im more scared that it may not be duverticular disease but the cancer and wanted to know if its possible it could be cancer instead of dd what are the odds xx kind regards sorry for the essay ,lisa
I was diagnosed with diverticulitis around 2018 & followed ALL instructions from my Surgeon. Valentine Day 2020, after aneurysm surgery 5 February 2020, i ended up in hospital with a perforated colon. I had surgery & was placed in 7 week medically induced coma. When i came around i woke up to colostomy bag & the pandemic started 😮. 1 year later my bag was successfully reversed & i live with good quality life.🙏
My eldest son had speen removed emergency surgery and a colostomy bag introduced after the 6-9 month was rejected for reversal( during Obama health insurance period) being he was temp summer employee in tourist city after the year got ear infections the same er Dr did not apply anti biotic for the infection being without spleen which is your infection fighting organ and flushed his ear cracking ear drum pushing infection into area next to brain stem 30 hourslater he was taking helicopter ride to big city hosp and the infection destroyed his lower brain stem ending in total stoppage of liife functions
@@user-ef3nu1eh7z😢 I’m so so sorry. I’ve lost 4 of my 5 brothers. 3 due incompetence of doctors, and my mother died due to ER doc putting patch for high blood pressure on her back then writing a prescription for same. She took the meds with the patch…. She was gone in 3 weeks. In my state you cannot sue Dr or hospital for wrongful death.
I want to spread the word as someone who has had intensely bad flare ups of diverticulitis. My advice to anyone, no matter your diet. The most important change I’ve made to avoid flare ups is to drink a glass of water before anything first thing in the morning. The water aids digestion, stops blockages, encourages bowel movement. Obviously, drinking water after ever meal would also be ideal, but if you’re too busy just make sure the first thing you put to your lips when you wake up is water. Touchwood I haven’t had any flare ups.
Lemon water hydrates and prepares the stomach to digest….or lime water ot organic apple cider vinegar..not much per 8 ounce glass…like 2 tsp. To 2 Tablespoons. Also drink in silos as you eat…instead of plain water. Ask your integrative doctor to be sure your gut can handle it.
Thanks for mentioning that, I was diagnosed years ago, and I did take slippery elm. I’ve recently had an attack of diverticulitis, and this would have helped tremendously. Guess what I’m going to buy tomorrow 👌
I had my first colonoscopy last year and was diagnosed with diverticulitis. My doctor just said keep an eye out for it. I had no idea that the blockage and pain I feel on occasion could be attributed to this when I’ve even told my doctor my symptoms. I have learned two things from this video. 1. I need a new doctor and 2. It’s way more serious than I thought. Thank you for this. I now know why I feel the way I do, and how to help prevent future flare ups.
Seems to be harder and harder to find a doctor who cares and actively engages with their patients to help them heal. It's all about the money. How many patients can I get paid for today? And if they don't give us the proper diagnosis and remedies/ cure, that guarantees at LEAST one more visit/paycheck! It's sad what the world has come to. 😔
My mother had this. A super bad case. She was in the hospital for 2 weeks getting pumped with antibiotics. They even had to remove a foot of her intestines and put her on a colostomy. After a year it was reversed and now she’s good as new!
It was always planned to do the reversal after a year. After she went back for her year checkup they said everything healed perfectly. The scheduled her and went in and hooked her back up in other words. She had to drink stuff for two days before hand to clean her out.
I started with Diverticulitis in my mid 30’s. Excruciating pain in my lower left quadrant. My doctor thought it was atypical appendicitis but after having scans it was found to be Diverticulitis. I was regularly admitted to hospital with high fever, pain and sickness. I was put on an antibiotic intravenous drip and food was withheld for 4-5 days. This pattern carried on for years. I then started a food diary which pinpointed eating red meat to be the culprit. Reading more and more about food and digestion, I cut out red meat, then fowl,(and all the antibiotics and growth hormones associated with this food production) and then finally having read about micro plastics being found in ALL marine life, I became Vegan. I’ve been Whole food plant based eating for over 4yrs now and had not ONE twinge! I feel fitter, sleep better and have so much energy,it’s unbelievable. I’ll be 70 in a couple of months but feel like I did in my 40’s. Might be worth considering?
products are amazing these days!! Big hugs honey and stay healthy darling🙏❤ I myself am sensitive to micro plastics as well. You should start a channel or group because there's so many that don't know the journey of relief and that it's different for all of us. Big hugs!!
I'm 37 and started with all the egregious issues at 33😔 All of what you've been thru negatively as well as vomiting with blood with in minutes of drinking water or tea and while figuring out what foods affected me most it would happen in the morning and have me down for weeks . I can barely handle any food group so I went plant based and after eating such I actually cried. I'm very petite and the most I've weighed was 138 lbs. While not being able to eat I was down to 106 lbs within four months and it set off so many other problems . Plant based saved my life and the quality of the
Another sign is coughing hurts in area of infection and sitting up can hurt . Also can have feeling of incomplete bowel evacuation. I get diverticulitis twice a year and I starve for 2-3 days just water , then clear soup, boiled eggs , jelly , and it clears up every time , no need for antibiotics.
Nice you are able to clear it up. But, people can die from a perforated bowel which can happen with this. Nothing to mess around with. A guy at work let his go too long and died. He was only 47.
Also going over bumps while driving 😑 I can usually manage mine at home too. As long as there’s no fever and no dehydration…and no passing blood from where it shouldn’t be passed 😏
I’ve been told I have Diverticulitis. Most of the symptoms would indicate that. Interestingly since I started taking Milk Thistle Extract it hasn’t been a problem. If I ever get runny stools, taking Milk Thistle Extract clears it up overnight ! Why do you think the Scottish have it as as a National Emblem !
New evidence points to gluten intolerance. As I had diverticulosis 10 years ago, my GP wanted me to have another colonoscopy, which displayed I had now diverticulitis. I took out gluten, as per the Mayo clinic, and haven’t felt so good in my life: bloat is gone, I no longer have IBD, and other symptoms have disappeared (mouth ulcers, bad joint inflammation, anaemia, and skin problems). My diabetes is under far more control. To think I had Celiac Disease almost my whole life…….
Me too. I found out I was lactose intolerant and borderline fructose. A friend said the holy trinity is Gluten,lactose/fructose. Dive deep and you will see why they are related. Back to Diverticulitis. I had my first flare when first diagnosed with lactose. But I have been borderline gluten my whole life. Now when I eliminate it I feel great. Like you it makes a huge difference. Thanks for sharing as this now just confirms what I have been denying. It’s gluten. There goes my croissants. And I;m french so imagine how hard it is. 😊
My son has celiac. Gluten damages his gut lining, we are 100% gluten free and for the most part, low carb. Sugar is a trigger for all kinds of inflamation and his doc said avoid it to heal ibs as well. Even if gluten does not always cause outward symptoms it is still damaging the gut lining.
One thing to consider. Majority of things grown are sprayed with round up hence gmo. They have to genetically modify crops in order for it to accept pesticides and herbicides(such sweet names for weed and bug killer) without dying. Now, imagine that going into your body everyday. The real problem is not the food itself. It’s what’s allowed in it’s production. And this does not get enough attention. It’s like everyone’s heard the food has been GMO,d for 30 years but oh well. Or they don’t know why it’s modified. So we should really consider not trusting the people that produce the food because they are also the same people that make the weed killer and the same people that make the medicine, IE Monsanto better known in the states as Bayer(aspirin)
@@sreamingonline6160, in North America, that is so true. But not in Europe or other ares of the world. When I was in England in the summer, I didn’t react to their bread as badly as here.
I had very sharp pain on the left side when I would stand up. My Dr ordered a colonoscopy and found diviculitus. I never had a weight problem until the last couple years and this weight gain has caused all kinds of issues. I hit 60 and im falling apart.
Agree I'm 70 became a vegetarian at 62 started running did a couple of half marathons yes you are falling apart that's life just get on with it you know the answers. Good luck the hardest part for me is motivation
Cardfan, please don’t give up. I hit 62 and got hit by all sorts of issues. I researched, watched medical videos and partnered with my doctors to find root causes and change habit and lifestyle. I lost 30 pounds, changed my diet and it was so hard but worth it. Made all the difference. Now I stay diligent and the quality of my life/health are greatly improved. I hope to encourage you to keep at it and find the strength to make some changes that benefit you. We are all different and have to do different things, and I wish you well.
Ive have been hospitilized twice over 15 years with DV....and had multiple serious infections and flares up...just when I was consdiering facing surgery....I suddenly was without any symptons or infections. Why? for me...and Im no medical expert....mysteriously once I gave up working...and all the stress that went with it...I also changed my eating and water intake habits...I am sure the following changes to my daily habits have kept me flare up free now for over two years. 1) drink a tumbler of water with every meal and before I go to bed. When I eat: I sit at a table and only eat...no tv , no phone, no computer...I eat, and I chew....I realize over 5 decades Ive forgotton what my teeth are for...chew, chew and chew again.. no food goes down my esophagus without being pulverized first... and eat smaller but more often...no large meals, chew well and lots of water for flushing the system. Last summer I finally started re-introducing foods that I havent eaten for years. I ate half a tomato and waited a week . I was fine, Ive slowly re-introduced all foods except for small seeds, like sesame and poppy seeds...Ive been sympton free now for two years. Its worked for me....fingers crossed.
I've been hospitalised 3 times and on antibiotics approx 3 times in less than a year with this. The first time I was admitted to hospital I also had Hydronephrosis of the kidney caused by the Ureter being completely constricted which caused them to think I had bowel cancer, but thankfully not. I was told to cut out/down on red meats/animal fats etc and increase fibre, fruit/veg. I told the consultant I've been a vegetarian for the past 8yrs and only eat fruit/veg/pulses etc don't drink or smoke, so who knows what causes it.
Thank you so much for a very clear explanation and description of this problem. I was diagnosed with diverticulitis when I was young, due to being fed white rice and white bread. I didn’t realize that this condition can cause frequent and urgent urination , but it makes complete sense. I feel as if you have provided me with vital help in your own calm and straightforward way. Having a vegan diet is a cure all, but remember to take B12 methylcobalamine NOT B12 CYANOCOBALAMIN
I haven’t been able to have this question answered, so maybe you can help? I have pernicious anemia, and have to inject myself every month with B12, and it is in fact cyanocobalamin. Is there any other injections that are safer, or any other way to get it if I can’t absorb orally?
Going back to when my problem began 35 years ago, I wasn’t even close to heavy set (145-160 lbs at almost 5’10”), I was extremely active (second job in the evening was teaching country dance 4 nights a week), but I did smoke about 5 cigarettes a day (basically it was from being at the bar teaching dance), and I have ended up with pockets in all 4 “quadrants”. I have constant flare ups. I am “old school”, so I stay away from hard seeds, nuts, anything with a seed top like broccoli (I say “old school” because most of my doctors over the years say there is NO diet restriction now). I still get flare ups and we joke at the hospital that I am a “frequent flyer” and “have now paid for my wing.” Funny thing: My mother, same thing. 2 of my mothers sisters, same thing. My grandmother, same thing, while she was alive. One of my brothers, same thing (so bad he was put out of the military after 20 years of service). I 100% believe there is a hereditary link that they just aren’t studying.
Actually it has been identified as a hereditary disorder, so you are right on! I think they haven’t identified which gene it’s on yet. See Mayo Clinic and NIH.
I have stage 4 metastatic breast cancer and due to treatments and opioids, I'm experiencing a majority of these symptoms. Thank you for a very informative video, as I feel I no longer understand my body and have to learn how to live with a body with cancer.
My husband has recently been diagnosed with breast cancer. I’m going to do what I can to help him deal with it naturally. A friend was telling me today that her father has had breast cancer for 4 years, but she’s been helping him with diet, juicing & using modalities like Bioresonance, and although there is still evidence of cancer a bit in blood tests, it’s ‘undetectable’ on scans. The Drs asked what they’d been doing. Cleansing the body is paramount. Giving it the tools to cleanse & eliminate toxins that are driving the cancer. My hub is nigh on 82 & set in his ways so whether he will be happy to have fresh juices & cut out sugar & refined carbs & adopt a strict whole food diet is yet to be seen. My friend’s father is older than my husband & he is happy to do it - she got him drinking juices when he was in hospital with sepsis some years back & that helped him recover - but Hub may not be so compliant.
I was diagnosed with this last year, I asked my doctor about the pain and what could be done. His answer was take panadol. I was shocked, because the pain gets so bad, I feel close to passing out.
If you want to lessen the inflammation, google high inflammatory foods and stop eating those foods. medication is a "bandaid"... stop cooking foods with seed oils (vegetable, corn, soybean, sunflower, etc.) choose butter or olive. Eliminate sugar completely so check ingredient list (sugar, fructose, sucrose, lactose, brown sugar, etc.)... start with this. Everytime there's a flare up, it's because you ate something that is high in inflammation.
@@iKeto_gal I have tried to eliminate sugar from my diet, but just about everything has sugar in it. I drink plenty of water to flush my system out, which I feel helps a little bit. I'm starting to think it's dairy products that upset me, I guess it's a case of trial and error as to what sets me off .
@@bettinafullerton6452 , yes keep a diary of all your foods/meals every day all day. Also, google "high oxalate foods"... that could be a source of your condition as well. Look up on UA-cam Sally Norton. She goes in depth about high oxalate foods. I'm not suggesting it and it's not for everyone, but if you ever get to the point where you want to be cured and are desperate, slowly go from low carb diet to healthy keto to carnivore diet. Carnivore is the strictest of the elimination diet but if you search here on UA-cam and watch Dr.'s speak about carnivore diet, you'll be amazed at how healthy not just physically but mentally too. Good luck and God bless you on this health journey 🌻
During an attack of diverticulitis does the pain cause you to sweat profusely, go very shaky, ringing in the ears and faint, i have to rest my head on cold tiles in an attempt not to pass out. Its one of the worst feelings ever. 🥵
My husband passed out and fell off a forklift. Thought his stomach was hurting from the fall. Colon ruptured, had surgery and colostomy bag. Tried to reverse it and remove bag but they couldn't so they then gave him an illiostomy bag and that was even more difficult. Had that for a while and lost weight. Wouldn't try surgery again until he gained some weight. Finally they removed the bag and he was fine. Then got a hernia in that spot. Had surgery for that. Later got a small bowel obstruction from scar tissue from all the prior surgeries and had surgery for that. My advice is to go get it checked out asap to avoid all that stuff!!!!! Don't wait.
So we found out my husband had diverticulitis (I don't think I explained that clearly) but we had no idea. He was mad at me and not talking to me (for some other unrelated stupid reason) so I had no clue that he was hurting or sick or anything. So this all went too long and he almost died. So please go to ER or call your doctor with any serious pain or you could end up with a poop bag or you could die from the infection imgoing into your blood. For real.
I ended up having all the symptoms mentioned, became critically ill with a blocked bowel and was given a colostomy. Had major flare-ups for several years, but fine now.
My sister takes oregano oil and it stops the pain after a few doses, 2x’s/day. Aloe Vera juice is also helpful. Both taken regularly can ward off attacks. Aloe Vera is daily and oregano oil once per day, usually 2-3 days/week for maintenance. She also avoids gluten.
Almost in tears reading these comments and watching this video. I feel so seen… it’s been multiple years of this. ESPECIALLY the UTI symptoms… no actual burning when I pee like a UTI, BUT my bladder area feels like knives when I stand back up. Or the stream is restricted and it’s harder to pee. Once ended up in the ER 2 years ago because I couldn’t pee at all but they said they found an ovarian cyst and that it had “ruptured” and that the “fluid/blood in the abdomen” was what caused it. Now I’m starting to doubt that’s what actually caused that and am wondering if it was part of this… because I was just checked again and was clear of ovarian cysts but still have symptoms. hoping to be seen by a GI soon. Very hard to find doctors that actually care. Left the doc in tears today feeling so unseen and like just a case. Given laxatives…
I have been having bladder symptoms since September and they keep ignoring it. We know our bodies. I know it’s from my Diverticulitis and finally seeing a new doctor in May
My doc prescribed miralax and miralax gummies cause my gut shut down. Ran a cycle of antibiotics. She said it could be a couple if months t clear up. It is debilitating. Soup and puddings help.
You are seen. This disease is a freaking nightmare. I was just diagnosed with this a couple of days ago, now 4 days of agony have gone by and I have the same exact UTI type symptoms you mention, but I’m a male and UTI are less common in men so that was weird. Been trying to educate myself on how I can get my flare up to subside. I’m usually not a complainer type but damn, this is a crazy type of pain and agony. Stay strong and I hope you stay flare-free.
Try a urologist. I went when the uti symptoms wouldn't go away and I didn't feel like everything was emptying, he performed a cystoscopy and found a diverticular outpouching had rubbed and irritated the bladder in one spot that it ended up connecting to the bladder and creating a hole. I am scheduled for surgery at the end of the month to remove 8-10 inches of my sigmoid colon and disconnect the colon from the bladder.
@@JUNIPERJ2001 wow thank you for sharing. I hope all goes well of course and if you can please keep this updated. I will add that the UTI type symptoms have subsided for me. However, I wouldn’t rule this out and I will seek a urologist just to make sure. Best of luck to you!
I’ve just had a colonoscopy that has confirmed diverticulitis and I’ve been suffering from symptoms like you describe with regard to it feeling like a UTI.
I had suffered from diverticulitis for a few years. The first 3 -4 years I was with a local hospital and doctors group. I would end up having a bad flare up and be admitted to the hospital for a few days until it resolved itself. Now, this was almost 20 years ago, and one day, after a particularly awful episode one of my doctors straight told me, "We're just country doctors out here. See something like this maybe once, twice a year." That very moment I decided I needed better medical support. I joined an insurance group which allowed me to access University of Davis medical Center in Sacramento, Ca. Had another flare up, and thi time we had surgery. Opened me from breast bone to pubis, arcing around the belly button. Approx 6 centimeters of large intestine was removed. Had a very good year and a half after that. Yes, it did require a diet modification; for me it was small seeds was the culprit. Well, a year and a half after surgery it hit again. And bad. Had an awful bowel obstruction. Surgeons went in again. Opened up along the same incision. I was told that I was open for over six hours; that, at one point my entire large intestine was outside of my body; the surgeon resolved things by excising nearly half my large intestine, from mid-line of the transverse colon to the anal vault, also because of scarification from the previous surgery I also lost approx. 75% of my liver. Since then have not had anything other than bad stomach aches.
So sorry you have been through so much. My mum has it and my aunt just died from bowel obstruction. I'm having a flare up this last 24 hrs..I will not eat for a few days, drink plenty of water & hope I don't need a hospital visit? I'm celiac. Stay well 😊
@@paulamonty5472 thank you... for me it's been and will be a process. Probably the worst on-going thing is a tendency o become dehydrated too easlily. And, once in dehydration it'll take IV fluids to get me back to better. Just can't drink enough to make a difference.
I was recently diagnosed with diverticulitis, the major health incident that occurred to me which led to me being given a colonoscopy and diagnosis was a sudden and very rapid swelling between my leg and penis, also alarmingly my scrotum swelled enormously, and so rapidly that the skin split and bled, I didn't see this mentioned in your excellent video.
Last year I had at least 6 flare-ups in just a few months time which were debilitating. I had to make changes in my life. I'm not sure which one change made the biggest difference, but I haven't had a flare-up in about 10 months, and I was getting one right after the other before I made these changes. 1) I eat about 30 grams of fiber daily without fail. 2) I walk 2 miles every day 3) These changes resulted in me losing 65 pounds and still doing well with weight loss. The antibiotics my doctor gave me never helped. No one told me how to get rid of my suffering. I just read a lot and this strategy is what worked for me and maybe it will help you. Diverticulitis is extremely painful and I couldn't live like that anymore. Good luck.
Benefiber, kefir, home made fermented cabbage, homemade (see Dr. William Davis) SIBO yogurt apple cider vinegar tablets and probiotics like Digestive Advantage have pretty much gotten rid of it for me. I still get a minor twinge here and there but not painful. I still have overactive bladder however. Have to get up at night to pee at least 4 times (on a good night). 7 or 8 times a night most nights.
Thank you thank you ! No one not 1 doctor explained the different types of pain from this issue …. I have had pain all around the abdomen’ so well said ! I know now ! ❤
Amazing explanation! thank you, for years I confused my diverticulitis with prostate problems, now I see the difference, and understand why my prostate test results were ok. My next visit to my doctor I will tell about diverticulitis and the symptoms I have.
This video is very helpful. I've been having flare-ups every 2-3 mos, and my surgeon seriously recommends surgery sooner than later. I'm on the fence about it, but if resectioning the colon with removal of infected areas makes my life a bit more dealable, I will make that decision sooner than later.
I am 76 years old & had 12 inches of my Sigmoid colon removed about 25 years ago. Get your surgery as soon as you can. The surgery is not that bad. Listen to your surgeon.
My last flare-up (3rd one) was in my upper left quadrant, which surprisingly isn't shown here . I would pinch under the left ribcage with my thumb and index fingers and feel pain from front to back . Even tapping in the back would hurt EXACTLY like kidney stone pain (which I had 2) . Went to ER, told them I have history of both, kidney stones and diverticulitis, but was 90 percent sure it was stones , since my first 2 diverticulitis flare-ups were in the lower left quadrant. Was about to be discharged from NYU in NYC without any imaging, under the premise it was kidney stones . I insisted to receive imaging because I was about to go on a 1 month vacation to Europe and wanted to know how big the stone was and where it actually was. They finally put me in a CT scan and it was diverticulitis in the descending colon . I am 49 years old, regular body , otherwise healthy and somewhat fit . I drive for a living , so I guess sitting down all day could be an issue , although I exercise 3 times a week and walk as much as I can . I realized I wasn't eating enough fiber and not drinking enough water and I changed both 180° . This is scary stuff , the idea of colon perforation and surgery and colostomy bags at this age is extremely scary to me . Pls let me know if this helped somewhat or share ideas by contacting me at ionroata at g mail. Good luck with this !
I have just been diagnosed with Diverticular Disease. I was wondering why upper left quadrant was excluded as I have exact pain as you describe going through to my back. Doc says it's trapped wind but it's extremely painful and not letting up.
Thank you for this...I've had back pain that I thought was kidney failure but all my blood panel levels were perfect. Diverticulitis is my guess being the culprit of all my stomach issues. Scheduled for a colonoscopy and heard horror stories that the camera could poke a hole in your lining is this true?
Recently had an episode. over the last year, I have had some symptoms, but not as bad as last week. It was so unbearable so I drove to the ER. I had a CT scan and had uncomplicated Diverticulitis. 7 days of Cipro and 1 other antibiotic. 2 more days left of pills, and I am feeling wayyyy better.
Doctors are idiots . I would get a second opinion or third . Then they treat you like a drug addict because you are in pain and they can’t figure it out
I have diverticulitis. The first bad flair up, I drove myself to the ER. It felt like labor pains. I thought I would never feel that pain again lol. I never have constipation only diarrhea & I run a low grade fever . I stay bloated , like I'm pregnant. It's like it never gets better, unless I have antibiotics.
@@franwebb7756 just feel I need to tell you not to take Aloe Vera long term as an ingredient in it causes your colon to look like a cheetah inside full of yellow with black spots, seen in a colonoscopy, which makes it difficult to detect polyps.
I had meckel's diverticulum as a toddler. I’m missing a decent amount of both intestines and stomach. I suffer with some of these symptoms today . I’m almost 50.
I have been told for years that I have IBS. Finally found a new doctor who ordered a CT to find out what’s going on. CT/contrast found diverticulitis. I thought that the pain in my lower abdomen would go away after Aunt Flo left town for good, I was wrong. Pain so bad it felt like I was in labor, I couldn’t take it any longer. Make that appointment today and find out what is going on with you don’t wait like I did. IBS my *SS.
about three years ago, my small intestine burst from Diverticulities. No pain, just felt weird. Called an ambulance, passed out in ER, and woke up after an emergency operation and woke u9p with a stoma. This sounds different from what you talk about here. The surgeon told me I would have died if I didn't get there when I did. Now I'm confused.
I had the same outcome, stoma for over 12 months then another op to reverse the stoma . That was 7 years ago , so far so good , no further issues. Have you had the stoma removed yet ?
It probably caused bowel obstruction which could cause a perforation that can cause death. I've known several people this has happened to. Glad you are still here to tell your story!
I’m glad you’re ok but how on earth did you not feel it??? I had colitis and diverticulitis and thought I was giving birth without an epidural. It was horrible!!! I know we’re just stranger on YT but I’m glad the surgeon was able to save you. God bless.
I don’t know if info presented is accurate. But it makes absolute sense and is presented clearly and concisely. I expect you have an excellent understanding of the situation. Thank you for the excellent work and effort.
I have Diverticulitis with frequent flair ups, recently had blood passing instead of anything else so went to ER, got CT Scan which was first in the 8 years I've suffered from this that they caught an active flair up on CT. Confirmed it was diverticulitis and my bowel was so inflamed and swollen that it was not even letting gas through without massage from out side to help it. I was in extreme pain because of the gas more so than the inflammation itself as that had been chronic for years. I am planning to have my sigmoid colon removed to lessen the frequency and severity of my attacks if not eliminate them outright.
@@trendingvideostowatch6670sorry,Im only seeing this now! I found nothing that helped the pain. It came and went. It was very painful. It’s been a long time since I’ve had it. Very mysterious…
As someone who works outside, water is key to digestion and functions in the gut. Working outside you will need to drink more water than normal due to sweating. Summer is hell for me.
Been dealing with this for about 15 years. I'm blocked and bloated most of the time. When I'm really bad, Milk of Magnesia, fiber, stool softeners usually clean and open me up quickly. fiber and apples are my normal remedy. I also have frequent anxiety attacks in my sleep after sleeping on my side. It makes for an unpleasant existence most of the time.
My savoir is Ole Vera juice - but has to be pure 100% no other ingredient. I get mine at local supermarket. It softens my stools and i don’t get side effects like nausea from other ‘fiber’ powders (won’t name them) that my specialist recommended. And its all natural. Just half a glass each morning. I have also started no red meat, no alcohol, low gluten, no lactose and even sugar - so yeah life is difficult when eating out. Good luck!
This is my 2 nd year with it. Omg…it’s the pits ! If I run into any trouble it’s weeks of STUMBLING after that. Soups, no fibre, pain, and I can only sleep on my right side now! Crazy stuff but NO OP for me…
I was having bad flare ups every month and a couple of times I had to drive myself to the ER because I couldn't get the pain under control. My new symptom is bladder pain along with incontinence occasionally and I'm not even 60 yet. Last Doc visit prior to the incontinence my Doc thought I had interstitial cystitis and gave me antibiotics which did help but the pain never really went away. Now with this new symptom I'm at a loss but I guess I'll have to go back and advise him of my new symptom. As a side note I haven't had a flare up in 2 months since adding more fruit to my diet but my bladder hurts quite frequently.
I have all those symptoms except vomiting and leg pain, one thing I get that was not mentioned is I occasionally get bloody diarrhea, sometimes mild and sometimes severe
I put honey on the spoon 4 drops of oregano then more honey to cover it take it and if you can hold it under your tongue for as long as you can 15 to 30 seconds, then swallow it.
Had a male UTI going on for nearly 2 years on and off.Treated with anti-biotics Clears for a month and returns.2 horrible cystocopys later and a scan, diagnosed with Diverticulitis.
@@lindalamb7512 Me too, that's why I'm sorry to see that after 3 weeks the topic starter still hasn't replied, I'm in pain there too and the "doctors" I'm dealing with don't know what it is , it's like being stabbed with a knife, it's such a sharp pain, fortunately sporadic but still painful, get well soon
@@FreeYourMind-FP mine is right below left breast. I have chrons in recession but recent afib issues. Was recently diagnosed w hiatal hernia and diverticulosis. Plus cardiologist said it’s not heart related. Gi wants to do colonoscopy to be sure. But I’m worried. See if u can get colonoscopy w GI to check out too. Thanks for raising the question. You be well too, friend!!
I got diagnosed in the summer of 2021. I was in absolute agony and felt like I’d been kicked in the groin by a horse. I feared the worse, but an MRI scan proved it to be diverticulitis, thankfully. A course of antibiotics sent it away. My Dr recommended taking Metamucil everyday, which I did for a while but now I take it intermittently.
Same here, metamusil has helped me tons, but i think I'm having antiehd episode and this time not sure what triggered, i think is gluten or cheese, i need to be gluten sugar corn free, and noticed the change when i go back to the old delicious bad habits ....specially after Christmas 😭😭
From someone who has experienced diverticulitis, the pain is horrible. When you can’t stand straight or walk without severe pain in the pelvis that is a sure sign something is wrong. Mine started in the right side and I am not Asian, I was misdiagnosed several times until it got very painful. Low grade fever as well. All these other symptoms you mention it is very vague because all the other symptoms can be so many other things. Basically the only way you will get a true sense of what it going on is a CT scan with contrast.
@@juliebryant3968 yes it can be found that way too, however if you are in an active flare infection a CT scan is what will be done as a colonoscopy in an active flare is not recommended.
Can diverticulitis be missed, even with a CT with contrast? They were 99% sure that’s what I had, because of my symptoms, which have still not gotten better. I’m struggling every day, with every single possible symptom of it, but they said they couldn’t find anything. Colonoscopy will be next month, but curious if it could have been missed?
Yes, mine was missed. They sent me home, still in agony, with some opioids which incidentally barely touched the pain and made me vomit. Next few days were really awful. Could barely stand upright. Applied heat on my lower abdomen and rested for about 5 days. Eventually it subsided. Later diagnosed during a follow up colonoscopy.
The only thing that helps me is regular water fasts 3-5 days, NO fiber, just red meat, chicken, fish, shrimp, eggs, and bone broth. Carnivore. NO sugar or white flour products. The worst for me is walnuts( even chewed carefully into mush ) and vegetables/ fiber. I have no flare ups since starting this protocol, and if I feel the slightest twinge of pain, from eating something I shouldn't have, I drink lots of water, take oil of oregano and grapefruit seed extract, 1 tablespoon of olive oil daily, and the little twinge of pain stops within a day or two. Stomach massage daily and walking also helps to keep things moving, and the pockets clean... Carnivore and water fasting has been a game-changer for me!
For some reason potatoes are my trigger foods to a flare up. I wish I understood what properties in potatoes make this happen. I eat homemade lentil or barley broth soup everyday and avoid potatoes, seems to stop most of the inflammation for me.
JJ Medicine have you heard of such cases: my aunt had DV, and one day the DV explode and affected the bledder and from there when you go to toilet and you want to urinate, with the urine it came out s*it? My father now has DV (brother of my aunt) and he feels some leg pain, but we've been to the doctor, they made colonoscopy and didn't find any leak and only the DV was found and a polyp which was removed and it was "good" not canceric. Should I worry about the leg pain (not leg pain but pelvis pain)? Tomorrow we are going to see the doctor and will talk with him again about it. Thank you for all the explanation and good video.
I had an instance with lower right quadrant pain and it ended up being epiploic appendagitis... not long after that I was diagnosed with diverticular disease and crohns.
Diagnosis with Diverticulitis in 2016 not had flare ups until now Feb 2023 whilst away on hols in Spain any ideas,? does anyone else get a (fever and headaches,)? besides bloating and discomfort sometimes I feel slightly sick , but always constipation, burping and farting , feels similar to Flue coming on
Ive had it for 10years, am 63. Extreme fatigue, slight fever, lower left pain. Now has turned into pain at touch lower left and right when attacked. Refused surgery 3 times. Once had a bad attack, ended in sepsis due to ecoli. Very dangerous. I take 50k vit d now when severe attack, and in between when i feel twinges, i take boswellia serrata which i swear really does the trick. Regular Probiotics, vit d, psyllium, 5dl warm water first thing in morning. I try to limit red meat, dairy, eggs and sugar. My crp was always above 10 (up to 300 when attack), now for first time in 10 years? under 5...
Can diverticulitis be missed during a colonoscopy? If someone has a colonoscopy and is told their bowels are healthy, could they still have diverticulitis that wasn’t noticed during the procedure?
I’ve been told I have Diverticulitis. Most of the symptoms would indicate that. Interestingly since I started taking Milk Thistle Extract it hasn’t been a problem. If I ever get runny stools, taking Milk Thistle Extract clears it up overnight ! Why do you think the Scottish have it as as a National Emblem !
Milk Thistle isn't Scotland's Natioanal Flower, the Cirsium Vulgare is Scotland's National Flower, the Milk Thistle is Onopordum Acanthium, they are easily mistaken for one another
If you have severe pain - do not let it go! I had perforation in 3 places….almost died. Lost 13 inches of my sigmoid colon, had colostomy, then a colostomy takedown. Two 6 hour surgeries. Now when get pain, i immediately go on a liquid diet! No red meat! No bread! No grease! Ever! It took me over a year to get my health back.
Don’t estimate STRESS, I have been in Hospital on 4 occasions in the last 5 years and have had many flares. My job and management was extremely stressful, changed jobs and for 6 months I have had no issues, flares and have postponed my colon surgery in January.
Very informative video. I was diagnosed with diverticulitis about 15 years ago, and they said it was IBS until I had a a camera put in. Recently I had an ultrasound scan and they noticed that I have an enlarged Spleen too, so I wonder if that is anything to do with it too?
I had the diverticulitis but no pain. They did found a small cancer and they take it out, no chemotherapy. I do think I check it, it was during the virus.
Hi everyone! I hope you all found this lesson helpful :)
Please check out my other lessons, including my *Most Popular* videos:
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hi i have diverticular disease of the upper and lower tract and a malrotated bowel possibly from hysterectomy operation for cancer im putting on weight but barely eating ,i feel nauseous all the time and my heads fuzzy constant pain currently waiting for surgery to fit a stoma but im more scared that it may not be duverticular disease but the cancer and wanted to know if its possible it could be cancer instead of dd what are the odds xx kind regards sorry for the essay ,lisa
Hi could you please do a video on diverticulosis?
It scared me a lot.
I was diagnosed with diverticulitis around 2018 & followed ALL instructions from my Surgeon. Valentine Day 2020, after aneurysm surgery 5 February 2020, i ended up in hospital with a perforated colon. I had surgery & was placed in 7 week medically induced coma. When i came around i woke up to colostomy bag & the pandemic started 😮. 1 year later my bag was successfully reversed & i live with good quality life.🙏
I'm so sorry to hear and hope you are feeling better. God bless❤
Glad u r better!
A few drops of peppermint oil in water helps with symptoms of diverticulitis
My eldest son had speen removed emergency surgery and a colostomy bag introduced after the 6-9 month was rejected for reversal( during Obama health insurance period) being he was temp summer employee in tourist city after the year got ear infections the same er Dr did not apply anti biotic for the infection being without spleen which is your infection fighting organ and flushed his ear cracking ear drum pushing infection into area next to brain stem 30 hourslater he was taking helicopter ride to big city hosp and the infection destroyed his lower brain stem ending in total stoppage of liife functions
@@user-ef3nu1eh7z😢 I’m so so sorry. I’ve lost 4 of my 5 brothers. 3 due incompetence of doctors, and my mother died due to ER doc putting patch for high blood pressure on her back then writing a prescription for same. She took the meds with the patch…. She was gone in 3 weeks. In my state you cannot sue Dr or hospital for wrongful death.
I want to spread the word as someone who has had intensely bad flare ups of diverticulitis. My advice to anyone, no matter your diet. The most important change I’ve made to avoid flare ups is to drink a glass of water before anything first thing in the morning. The water aids digestion, stops blockages, encourages bowel movement. Obviously, drinking water after ever meal would also be ideal, but if you’re too busy just make sure the first thing you put to your lips when you wake up is water. Touchwood I haven’t had any flare ups.
Hi apparently drinking water after eating is not good. It will dilute the stomach acids and you will not digest completely
@@Nissa55574 what about first thing onan empty stomach?
2 cups of water Evian water is ph balanced not acidic
Lemon water hydrates and prepares the stomach to digest….or lime water ot organic apple cider vinegar..not much per 8 ounce glass…like 2 tsp. To 2 Tablespoons. Also drink in silos as you eat…instead of plain water. Ask your integrative doctor to be sure your gut can handle it.
Thank you so much, I will faithfully do this each morning!
I suffered with diverticulitis for a few years, until a mate from Japan mentioned Slippery Elm. One capsule a day and I've not had it since..
What is that? A vitamin?
Thank u 🙏
Thanks for mentioning that, I was diagnosed years ago, and I did take slippery elm. I’ve recently had an attack of diverticulitis, and this would have helped tremendously. Guess what I’m going to buy tomorrow 👌
It was in powder form and pretty ordinary to take, but it works wonders.
If it’s still in powder form you could buy empty capsules. They probably have a tablet now, I’d be inclined to buy the powder.
I had my first colonoscopy last year and was diagnosed with diverticulitis. My doctor just said keep an eye out for it. I had no idea that the blockage and pain I feel on occasion could be attributed to this when I’ve even told my doctor my symptoms. I have learned two things from this video. 1. I need a new doctor and 2. It’s way more serious than I thought. Thank you for this. I now know why I feel the way I do, and how to help prevent future flare ups.
Seems to be harder and harder to find a doctor who cares and actively engages with their patients to help them heal.
It's all about the money. How many patients can I get paid for today? And if they don't give us the proper diagnosis and remedies/ cure, that guarantees at LEAST one more visit/paycheck!
It's sad what the world has come to. 😔
My mother had this. A super bad case. She was in the hospital for 2 weeks getting pumped with antibiotics. They even had to remove a foot of her intestines and put her on a colostomy. After a year it was reversed and now she’s good as new!
What did she do to reverse? Diet?
I would also like to know how she reversed it please 🙏
It was always planned to do the reversal after a year. After she went back for her year checkup they said everything healed perfectly. The scheduled her and went in and hooked her back up in other words. She had to drink stuff for two days before hand to clean her out.
@@JustSpeakingFacts_
Gotcha. Thanks for the info 👍🏼
My mother had this also. The flare ups were very painful for her
I started with Diverticulitis in my mid 30’s. Excruciating pain in my lower left quadrant. My doctor thought it was atypical appendicitis but after having scans it was found to be Diverticulitis.
I was regularly admitted to hospital with high fever, pain and sickness. I was put on an antibiotic intravenous drip and food was withheld for 4-5 days.
This pattern carried on for years. I then started a food diary which pinpointed eating red meat to be the culprit. Reading more and more about food and digestion, I cut out red meat, then fowl,(and all the antibiotics and growth hormones associated with this food production) and then finally having read about micro plastics being found in ALL marine life, I became Vegan.
I’ve been Whole food plant based eating for over 4yrs now and had not ONE twinge!
I feel fitter, sleep better and have so much energy,it’s unbelievable.
I’ll be 70 in a couple of months but feel like I did in my 40’s.
Might be worth considering?
products are amazing these days!! Big hugs honey and stay healthy darling🙏❤ I myself am sensitive to micro plastics as well. You should start a channel or group because there's so many that don't know the journey of relief and that it's different for all of us. Big hugs!!
I'm 37 and started with all the egregious issues at 33😔 All of what you've been thru negatively as well as vomiting with blood with in minutes of drinking water or tea and while figuring out what foods affected me most it would happen in the morning and have me down for weeks . I can barely handle any food group so I went plant based and after eating such I actually cried. I'm very petite and the most I've weighed was 138 lbs. While not being able to eat I was down to 106 lbs within four months and it set off so many other problems . Plant based saved my life and the quality of the
Wow I am petite too. St my biggest I was 141 pounds. I am down toe around 129 pounds and I am 5 foot.
Some people thrive on carnivore and keto diet interestingly.
@@underated17 Me 3. 5' tall. Heaviest was146. Now 110.
Another sign is coughing hurts in area of infection and sitting up can hurt . Also can have feeling of incomplete bowel evacuation. I get diverticulitis twice a year and I starve for 2-3 days just water , then clear soup, boiled eggs , jelly , and it clears up every time , no need for antibiotics.
Nice you are able to clear it up. But, people can die from a perforated bowel which can happen with this. Nothing to mess around with. A guy at work let his go too long and died. He was only 47.
Also going over bumps while driving 😑 I can usually manage mine at home too. As long as there’s no fever and no dehydration…and no passing blood from where it shouldn’t be passed 😏
I’ve been told I have Diverticulitis. Most of the symptoms would indicate that. Interestingly since I started taking Milk Thistle Extract it hasn’t been a problem. If I ever get runny stools, taking Milk Thistle Extract clears it up overnight ! Why do you think the Scottish have it as as a National Emblem !
Keto intermittent fasting
Your condition is not normal if it keeps repeating and the major cause in the western world is gastric overload
New evidence points to gluten intolerance. As I had diverticulosis 10 years ago, my GP wanted me to have another colonoscopy, which displayed I had now diverticulitis. I took out gluten, as per the Mayo clinic, and haven’t felt so good in my life: bloat is gone, I no longer have IBD, and other symptoms have disappeared (mouth ulcers, bad joint inflammation, anaemia, and skin problems). My diabetes is under far more control. To think I had Celiac Disease almost my whole life…….
Me too. I found out I was lactose intolerant and borderline fructose. A friend said the holy trinity is Gluten,lactose/fructose. Dive deep and you will see why they are related. Back to Diverticulitis. I had my first flare when first diagnosed with lactose. But I have been borderline gluten my whole life. Now when I eliminate it I feel great. Like you it makes a huge difference. Thanks for sharing as this now just confirms what I have been denying. It’s gluten. There goes my croissants. And I;m french so imagine how hard it is. 😊
My son has celiac. Gluten damages his gut lining, we are 100% gluten free and for the most part, low carb. Sugar is a trigger for all kinds of inflamation and his doc said avoid it to heal ibs as well. Even if gluten does not always cause outward symptoms it is still damaging the gut lining.
One thing to consider. Majority of things grown are sprayed with round up hence gmo. They have to genetically modify crops in order for it to accept pesticides and herbicides(such sweet names for weed and bug killer) without dying. Now, imagine that going into your body everyday. The real problem is not the food itself. It’s what’s allowed in it’s production. And this does not get enough attention. It’s like everyone’s heard the food has been GMO,d for 30 years but oh well. Or they don’t know why it’s modified. So we should really consider not trusting the people that produce the food because they are also the same people that make the weed killer and the same people that make the medicine, IE Monsanto better known in the states as Bayer(aspirin)
@@sreamingonline6160, in North America, that is so true. But not in Europe or other ares of the world. When I was in England in the summer, I didn’t react to their bread as badly as here.
@@lizzyfolks9116 right! That’s why half the world doesn’t accept imports of our food
I had very sharp pain on the left side when I would stand up. My Dr ordered a colonoscopy and found diviculitus. I never had a weight problem until the last couple years and this weight gain has caused all kinds of issues. I hit 60 and im falling apart.
I have all the symptoms in this video lol , plus cold , can't wait till I die , peace perfect peace ,
i drink a glass of water with one teaspoon of baking soda after every meal and feel great doing it religiously changed my life
Agree I'm 70 became a vegetarian at 62 started running did a couple of half marathons yes you are falling apart that's life just get on with it you know the answers. Good luck the hardest part for me is motivation
Cardfan, please don’t give up. I hit 62 and got hit by all sorts of issues. I researched, watched medical videos and partnered with my doctors to find root causes and change habit and lifestyle. I lost 30 pounds, changed my diet and it was so hard but worth it. Made all the difference. Now I stay diligent and the quality of my life/health are greatly improved. I hope to encourage you to keep at it and find the strength to make some changes that benefit you. We are all different and have to do different things, and I wish you well.
Laugh a lot
Ive have been hospitilized twice over 15 years with DV....and had multiple serious infections and flares up...just when I was consdiering facing surgery....I suddenly was without any symptons or infections. Why? for me...and Im no medical expert....mysteriously once I gave up working...and all the stress that went with it...I also changed my eating and water intake habits...I am sure the following changes to my daily habits have kept me flare up free now for over two years. 1) drink a tumbler of water with every meal and before I go to bed. When I eat: I sit at a table and only eat...no tv , no phone, no computer...I eat, and I chew....I realize over 5 decades Ive forgotton what my teeth are for...chew, chew and chew again.. no food goes down my esophagus without being pulverized first... and eat smaller but more often...no large meals, chew well and lots of water for flushing the system. Last summer I finally started re-introducing foods that I havent eaten for years. I ate half a tomato and waited a week . I was fine, Ive slowly re-introduced all foods except for small seeds, like sesame and poppy seeds...Ive been sympton free now for two years. Its worked for me....fingers crossed.
I've been hospitalised 3 times and on antibiotics approx 3 times in less than a year with this. The first time I was admitted to hospital I also had Hydronephrosis of the kidney caused by the Ureter being completely constricted which caused them to think I had bowel cancer, but thankfully not. I was told to cut out/down on red meats/animal fats etc and increase fibre, fruit/veg. I told the consultant I've been a vegetarian for the past 8yrs and only eat fruit/veg/pulses etc don't drink or smoke, so who knows what causes it.
Thank you so much for a very clear explanation and description of this problem. I was diagnosed with diverticulitis when I was young, due to being fed white rice and white bread.
I didn’t realize that this condition can cause frequent and urgent urination , but it makes complete sense. I feel as if you have provided me with vital help in your own calm and straightforward way.
Having a vegan diet is a cure all, but remember to take B12 methylcobalamine NOT B12 CYANOCOBALAMIN
I haven’t been able to have this question answered, so maybe you can help? I have pernicious anemia, and have to inject myself every month with B12, and it is in fact cyanocobalamin. Is there any other injections that are safer, or any other way to get it if I can’t absorb orally?
@@Youngone78 Here is the name of the natural injectable B12….Hydroxocobalamin
@@anthonyzoldork8557 Oxalates in vegetables seeds, and nuts.
Going back to when my problem began 35 years ago, I wasn’t even close to heavy set (145-160 lbs at almost 5’10”), I was extremely active (second job in the evening was teaching country dance 4 nights a week), but I did smoke about 5 cigarettes a day (basically it was from being at the bar teaching dance), and I have ended up with pockets in all 4 “quadrants”. I have constant flare ups. I am “old school”, so I stay away from hard seeds, nuts, anything with a seed top like broccoli (I say “old school” because most of my doctors over the years say there is NO diet restriction now). I still get flare ups and we joke at the hospital that I am a “frequent flyer” and “have now paid for my wing.” Funny thing: My mother, same thing. 2 of my mothers sisters, same thing. My grandmother, same thing, while she was alive. One of my brothers, same thing (so bad he was put out of the military after 20 years of service). I 100% believe there is a hereditary link that they just aren’t studying.
I think most disorders are a combination of hereditary and environmental factors
Actually it has been identified as a hereditary disorder, so you are right on! I think they haven’t identified which gene it’s on yet. See Mayo Clinic and NIH.
Family members share the same foods, eating habits. Even when we grow up and live separately, our favorite foods from childhood remain with us.
I have stage 4 metastatic breast cancer and due to treatments and opioids, I'm experiencing a majority of these symptoms. Thank you for a very informative video, as I feel I no longer understand my body and have to learn how to live with a body with cancer.
My husband has recently been diagnosed with breast cancer. I’m going to do what I can to help him deal with it naturally. A friend was telling me today that her father has had breast cancer for 4 years, but she’s been helping him with diet, juicing & using modalities like Bioresonance, and although there is still evidence of cancer a bit in blood tests, it’s ‘undetectable’ on scans. The Drs asked what they’d been doing.
Cleansing the body is paramount. Giving it the tools to cleanse & eliminate toxins that are driving the cancer. My hub is nigh on 82 & set in his ways so whether he will be happy to have fresh juices & cut out sugar & refined carbs & adopt a strict whole food diet is yet to be seen. My friend’s father is older than my husband & he is happy to do it - she got him drinking juices when he was in hospital with sepsis some years back & that helped him recover - but Hub may not be so compliant.
Hoping you are doing ok❤
I was diagnosed with this last year, I asked my doctor about the pain and what could be done. His answer was take panadol. I was shocked, because the pain gets so bad, I feel close to passing out.
Oh it hurts alright. My last round I had colitis as well. 🤦🏻♀️
If you want to lessen the inflammation, google high inflammatory foods and stop eating those foods. medication is a "bandaid"... stop cooking foods with seed oils (vegetable, corn, soybean, sunflower, etc.) choose butter or olive. Eliminate sugar completely so check ingredient list (sugar, fructose, sucrose, lactose, brown sugar, etc.)... start with this. Everytime there's a flare up, it's because you ate something that is high in inflammation.
@@iKeto_gal I have tried to eliminate sugar from my diet, but just about everything has sugar in it. I drink plenty of water to flush my system out, which I feel helps a little bit. I'm starting to think it's dairy products that upset me, I guess it's a case of trial and error as to what sets me off .
@@bettinafullerton6452 , yes keep a diary of all your foods/meals every day all day. Also, google "high oxalate foods"... that could be a source of your condition as well. Look up on UA-cam Sally Norton. She goes in depth about high oxalate foods. I'm not suggesting it and it's not for everyone, but if you ever get to the point where you want to be cured and are desperate, slowly go from low carb diet to healthy keto to carnivore diet. Carnivore is the strictest of the elimination diet but if you search here on UA-cam and watch Dr.'s speak about carnivore diet, you'll be amazed at how healthy not just physically but mentally too. Good luck and God bless you on this health journey 🌻
During an attack of diverticulitis does the pain cause you to sweat profusely, go very shaky, ringing in the ears and faint, i have to rest my head on cold tiles in an attempt not to pass out. Its one of the worst feelings ever. 🥵
My husband passed out and fell off a forklift. Thought his stomach was hurting from the fall. Colon ruptured, had surgery and colostomy bag. Tried to reverse it and remove bag but they couldn't so they then gave him an illiostomy bag and that was even more difficult. Had that for a while and lost weight. Wouldn't try surgery again until he gained some weight. Finally they removed the bag and he was fine. Then got a hernia in that spot. Had surgery for that. Later got a small bowel obstruction from scar tissue from all the prior surgeries and had surgery for that. My advice is to go get it checked out asap to avoid all that stuff!!!!! Don't wait.
Iam experiencing this at the moment.
So we found out my husband had diverticulitis (I don't think I explained that clearly) but we had no idea. He was mad at me and not talking to me (for some other unrelated stupid reason) so I had no clue that he was hurting or sick or anything. So this all went too long and he almost died. So please go to ER or call your doctor with any serious pain or you could end up with a poop bag or you could die from the infection imgoing into your blood. For real.
@@sophiaodero4018Go to the ER
Yes. Profuse sweating. Also fever.
I ended up having all the symptoms mentioned, became critically ill with a blocked bowel and was given a colostomy. Had major flare-ups for several years, but fine now.
Glad u are fine champ 🔥
My sister takes oregano oil and it stops the pain after a few doses, 2x’s/day. Aloe Vera juice is also helpful. Both taken regularly can ward off attacks. Aloe Vera is daily and oregano oil once per day, usually 2-3 days/week for maintenance. She also avoids gluten.
Also very good to alternative the Oregano oil with is Grapefruit seed extract in water!!
How many drops of oregano?
Amazion oil of oregano tabs
Almost in tears reading these comments and watching this video. I feel so seen… it’s been multiple years of this. ESPECIALLY the UTI symptoms… no actual burning when I pee like a UTI, BUT my bladder area feels like knives when I stand back up. Or the stream is restricted and it’s harder to pee. Once ended up in the ER 2 years ago because I couldn’t pee at all but they said they found an ovarian cyst and that it had “ruptured” and that the “fluid/blood in the abdomen” was what caused it. Now I’m starting to doubt that’s what actually caused that and am wondering if it was part of this… because I was just checked again and was clear of ovarian cysts but still have symptoms. hoping to be seen by a GI soon. Very hard to find doctors that actually care. Left the doc in tears today feeling so unseen and like just a case. Given laxatives…
I have been having bladder symptoms since September and they keep ignoring it. We know our bodies. I know it’s from my Diverticulitis and finally seeing a new doctor in May
My doc prescribed miralax and miralax gummies cause my gut shut down. Ran a cycle of antibiotics. She said it could be a couple if months t clear up. It is debilitating. Soup and puddings help.
You are seen.
This disease is a freaking nightmare. I was just diagnosed with this a couple of days ago, now 4 days of agony have gone by and I have the same exact UTI type symptoms you mention, but I’m a male and UTI are less common in men so that was weird.
Been trying to educate myself on how I can get my flare up to subside. I’m usually not a complainer type but damn, this is a crazy type of pain and agony.
Stay strong and I hope you stay flare-free.
Try a urologist.
I went when the uti symptoms wouldn't go away and I didn't feel like everything was emptying, he performed a cystoscopy and found a diverticular outpouching had rubbed and irritated the bladder in one spot that it ended up connecting to the bladder and creating a hole.
I am scheduled for surgery at the end of the month to remove 8-10 inches of my sigmoid colon and disconnect the colon from the bladder.
@@JUNIPERJ2001 wow thank you for sharing. I hope all goes well of course and if you can please keep this updated.
I will add that the UTI type symptoms have subsided for me. However, I wouldn’t rule this out and I will seek a urologist just to make sure.
Best of luck to you!
How kind of you to explain this so clearly,many thanks.
I’ve just had a colonoscopy that has confirmed diverticulitis and I’ve been suffering from symptoms like you describe with regard to it feeling like a UTI.
Same it feels like a UTI
Yess i was diagnosed with diverticulitis 3years ago i was 18 😢.
It was very painful.
I just got ct scan today. I think this is what I have
Yea the pain in my d*ck was the worst part about this
My mum was misdiagnosed with diverticulitis, but it was advanced ovarian cancer.
I had suffered from diverticulitis for a few years. The first 3 -4 years I was with a local hospital and doctors group. I would end up having a bad flare up and be admitted to the hospital for a few days until it resolved itself. Now, this was almost 20 years ago, and one day, after a particularly awful episode one of my doctors straight told me, "We're just country doctors out here. See something like this maybe once, twice a year." That very moment I decided I needed better medical support.
I joined an insurance group which allowed me to access University of Davis medical Center in Sacramento, Ca. Had another flare up, and thi time we had surgery. Opened me from breast bone to pubis, arcing around the belly button. Approx 6 centimeters of large intestine was removed. Had a very good year and a half after that. Yes, it did require a diet modification; for me it was small seeds was the culprit.
Well, a year and a half after surgery it hit again. And bad. Had an awful bowel obstruction. Surgeons went in again. Opened up along the same incision. I was told that I was open for over six hours; that, at one point my entire large intestine was outside of my body; the surgeon resolved things by excising nearly half my large intestine, from mid-line of the transverse colon to the anal vault, also because of scarification from the previous surgery I also lost approx. 75% of my liver.
Since then have not had anything other than bad stomach aches.
You’ve been through a lot. I’m so sorry.
@@imaamericangirl1406 thank you. I appreciate that. Thje divertic is an insidious disease that can be difficult to diagnose.
😮 holy shlit ... glad you're doing better. I hope mine doesn't get that bad, ugh.
So sorry you have been through so much. My mum has it and my aunt just died from bowel obstruction. I'm having a flare up this last 24 hrs..I will not eat for a few days, drink plenty of water & hope I don't need a hospital visit? I'm celiac. Stay well 😊
@@paulamonty5472 thank you... for me it's been and will be a process. Probably the worst on-going thing is a tendency o become dehydrated too easlily. And, once in dehydration it'll take IV fluids to get me back to better. Just can't drink enough to make a difference.
How we live as long as we do is an absolute miracle , there are so many things that ca go wrong.
I've just had a bout of Diverticulitis. My 3 bout. Lucky my GP immediately diagnosed it, and antibiotics for a week. I had severe constipation also
You need more fiber...2 plums or 4-5 Prunes per day. Water first thing morning and after every meal
I was recently diagnosed with diverticulitis, the major health incident that occurred to me which led to me being given a colonoscopy and diagnosis was a sudden and very rapid swelling between my leg and penis, also alarmingly my scrotum swelled enormously, and so rapidly that the skin split and bled, I didn't see this mentioned in your excellent video.
Oh my gosh! Hope you're feeling better.
Oh hell nah
He did. Leg abscess caused by fecal matter
Last year I had at least 6 flare-ups in just a few months time which were debilitating. I had to make changes in my life. I'm not sure which one change made the biggest difference, but I haven't had a flare-up in about 10 months, and I was getting one right after the other before I made these changes. 1) I eat about 30 grams of fiber daily without fail. 2) I walk 2 miles every day 3) These changes resulted in me losing 65 pounds and still doing well with weight loss. The antibiotics my doctor gave me never helped. No one told me how to get rid of my suffering. I just read a lot and this strategy is what worked for me and maybe it will help you. Diverticulitis is extremely painful and I couldn't live like that anymore. Good luck.
I’ve had four bouts from oct to feb. Started taking meta-mucil, probiotics and four apple cider supplements daily and all my troubles are gone.
Benefiber, kefir, home made fermented cabbage, homemade (see Dr. William Davis) SIBO yogurt apple cider vinegar tablets and probiotics like Digestive Advantage have pretty much gotten rid of it for me. I still get a minor twinge here and there but not painful. I still have overactive bladder however. Have to get up at night to pee at least 4 times (on a good night). 7 or 8 times a night most nights.
Thank you thank you ! No one not 1 doctor explained the different types of pain from this issue …. I have had pain all around the abdomen’ so well said ! I know now ! ❤
Same! I was diagnosed, then forgotten.
Amazing explanation! thank you, for years I confused my diverticulitis with prostate problems, now I see the difference, and understand why my prostate test results were ok. My next visit to my doctor I will tell about diverticulitis and the symptoms I have.
This video is very helpful. I've been having flare-ups every 2-3 mos, and my surgeon seriously recommends surgery sooner than later. I'm on the fence about it, but if resectioning the colon with removal of infected areas makes my life a bit more dealable, I will make that decision sooner than later.
@@Th3_Colony thank you, good to know!
@@ovehlu there's always risks with surgery. Surgeons get paid no matter your results so think long & hard before you go ahead.
@@katiekane5247 absolutely, 💯!
I am 76 years old & had 12 inches of my Sigmoid colon removed about 25 years ago. Get your surgery as soon as you can. The surgery is not that bad. Listen to your surgeon.
@@helmijohnson5079 thank you!
Wow this is extremely enlightening. I’ve been blaming everything but the kitchen sink! Now I know.
My last flare-up (3rd one) was in my upper left quadrant, which surprisingly isn't shown here . I would pinch under the left ribcage with my thumb and index fingers and feel pain from front to back . Even tapping in the back would hurt EXACTLY like kidney stone pain (which I had 2) .
Went to ER, told them I have history of both, kidney stones and diverticulitis, but was 90 percent sure it was stones , since my first 2 diverticulitis flare-ups were in the lower left quadrant. Was about to be discharged from NYU in NYC without any imaging, under the premise it was kidney stones .
I insisted to receive imaging because I was about to go on a 1 month vacation to Europe and wanted to know how big the stone was and where it actually was.
They finally put me in a CT scan and it was diverticulitis in the descending colon .
I am 49 years old, regular body , otherwise healthy and somewhat fit .
I drive for a living , so I guess sitting down all day could be an issue , although I exercise 3 times a week and walk as much as I can .
I realized I wasn't eating enough fiber and not drinking enough water and I changed both 180° .
This is scary stuff , the idea of colon perforation and surgery and colostomy bags at this age is extremely scary to me .
Pls let me know if this helped somewhat or share ideas by contacting me at ionroata at g mail.
Good luck with this !
I have just been diagnosed with Diverticular Disease. I was wondering why upper left quadrant was excluded as I have exact pain as you describe going through to my back. Doc says it's trapped wind but it's extremely painful and not letting up.
@@nosila444same , and the back pain 2... im glad to hear there's more people like me
Thank you for this...I've had back pain that I thought was kidney failure but all my blood panel levels were perfect. Diverticulitis is my guess being the culprit of all my stomach issues. Scheduled for a colonoscopy and heard horror stories that the camera could poke a hole in your lining is this true?
@@nosila444 Same here.
Recently had an episode. over the last year, I have had some symptoms, but not as bad as last week. It was so unbearable so I drove to the ER. I had a CT scan and had uncomplicated Diverticulitis. 7 days of Cipro and 1 other antibiotic. 2 more days left of pills, and I am feeling wayyyy better.
This was so very helpful. I’m having surgery next week and feel I have many of these symptoms that my doctor never mentioned.
Doctors are idiots . I would get a second opinion or third . Then they treat you like a drug addict because you are in pain and they can’t figure it out
I have diverticulitis. The first bad flair up, I drove myself to the ER. It felt like labor pains. I thought I would never feel that pain again lol.
I never have constipation only diarrhea & I run a low grade fever . I stay bloated , like I'm pregnant. It's like it never gets better, unless I have antibiotics.
Try adding aloe vera water or gel caps to your routine especially if you notice a symptom of a flare up.
Thank you Fran, I will try this for sure.
@@franwebb7756 just feel I need to tell you not to take Aloe Vera long term as an ingredient in it causes your colon to look like a cheetah inside full of yellow with black spots, seen in a colonoscopy, which makes it difficult to detect polyps.
I had meckel's diverticulum as a toddler. I’m missing a decent amount of both intestines and stomach. I suffer with some of these symptoms today . I’m almost 50.
High fiber diet (I finish every meal with a fiber bar and 5 to ten prunes) exercise and no flares 🤞🏻.
BTW it’s called diverticulosis. It’s only diverticulitis when having inflammation from an attack.
Excellent, thorough, and explicit.
I have been told for years that I have IBS. Finally found a new doctor who ordered a CT to find out what’s going on. CT/contrast found diverticulitis. I thought that the pain in my lower abdomen would go away after Aunt Flo left town for good, I was wrong. Pain so bad it felt like I was in labor, I couldn’t take it any longer. Make that appointment today and find out what is going on with you don’t wait like I did. IBS my *SS.
about three years ago, my small intestine burst from Diverticulities. No pain, just felt weird. Called an ambulance, passed out in ER, and woke up after an emergency operation and woke u9p with a stoma. This sounds different from what you talk about here. The surgeon told me I would have died if I didn't get there when I did. Now I'm confused.
I had the same outcome, stoma for over 12 months then another op to reverse the stoma . That was 7 years ago , so far so good , no further issues. Have you had the stoma removed yet ?
It probably caused bowel obstruction which could cause a perforation that can cause death. I've known several people this has happened to. Glad you are still here to tell your story!
I’m glad you’re ok but how on earth did you not feel it??? I had colitis and diverticulitis and thought I was giving birth without an epidural. It was horrible!!! I know we’re just stranger on YT but I’m glad the surgeon was able to save you. God bless.
I don’t know if info presented is accurate. But it makes absolute sense and is presented clearly and concisely. I expect you have an excellent understanding of the situation. Thank you for the excellent work and effort.
Thanks for the information. I recently got diagnosed with diverticulitis. This video is very helpful.
I have Diverticulitis with frequent flair ups, recently had blood passing instead of anything else so went to ER, got CT Scan which was first in the 8 years I've suffered from this that they caught an active flair up on CT. Confirmed it was diverticulitis and my bowel was so inflamed and swollen that it was not even letting gas through without massage from out side to help it. I was in extreme pain because of the gas more so than the inflammation itself as that had been chronic for years. I am planning to have my sigmoid colon removed to lessen the frequency and severity of my attacks if not eliminate them outright.
I had the leg abscess…it was horrible. Had no idea it could come from diverticulitis! Wow
Hi! What medication did you take? I also have leg pain and I think its abscess 😢
hi
still waiting for your answer .
thank you
@@trendingvideostowatch6670sorry,Im only seeing this now! I found nothing that helped the pain. It came and went. It was very painful.
It’s been a long time since I’ve had it. Very mysterious…
As someone who works outside, water is key to digestion and functions in the gut. Working outside you will need to drink more water than normal due to sweating. Summer is hell for me.
I notice when it gets hot and humid I have to eat very little because I will have diarrhea.
Been dealing with this for about 15 years. I'm blocked and bloated most of the time. When I'm really bad, Milk of Magnesia, fiber, stool softeners usually clean and open me up quickly. fiber and apples are my normal remedy. I also have frequent anxiety attacks in my sleep after sleeping on my side. It makes for an unpleasant existence most of the time.
My savoir is Ole Vera juice - but has to be pure 100% no other ingredient. I get mine at local supermarket. It softens my stools and i don’t get side effects like nausea from other ‘fiber’ powders (won’t name them) that my specialist recommended. And its all natural. Just half a glass each morning. I have also started no red meat, no alcohol, low gluten, no lactose and even sugar - so yeah life is difficult when eating out. Good luck!
@@lizisler9415 Are you saying Aloe vera juice?
Sorry to hear that Jeffrey, are you drinking plenty of water?
Stool softeners will make it worse. Avoid them. Eat fiber. Take magnesium.
This is my 2 nd year with it. Omg…it’s the pits ! If I run into any trouble it’s weeks of STUMBLING after that. Soups, no fibre, pain, and I can only sleep on my right side now! Crazy stuff but NO OP for me…
Great explanation. Many thanks.
I was having bad flare ups every month and a couple of times I had to drive myself to the ER because I couldn't get the pain under control. My new symptom is bladder pain along with incontinence occasionally and I'm not even 60 yet. Last Doc visit prior to the incontinence my Doc thought I had interstitial cystitis and gave me antibiotics which did help but the pain never really went away. Now with this new symptom I'm at a loss but I guess I'll have to go back and advise him of my new symptom. As a side note I haven't had a flare up in 2 months since adding more fruit to my diet but my bladder hurts quite frequently.
Thank you for a clear presentation
I have all those symptoms except vomiting and leg pain, one thing I get that was not mentioned is I occasionally get bloody diarrhea, sometimes mild and sometimes severe
I heard in the cases with blood in poop you need to see a Dr ASAP and have a Colonoscopy as soon as possible
Oil of oregano works wonders!
I keep this on hand always. And for me activated charcoal helps but not all can tolerate it. Need to drink plenty of water with it.
How do you take it and how many drops please thanks
Do you dilute it ?
I put honey on the spoon 4 drops of oregano then more honey to cover it take it and if you can hold it under your tongue for as long as you can 15 to 30 seconds, then swallow it.
Had a male UTI going on for nearly 2 years on and off.Treated with anti-biotics
Clears for a month and returns.2 horrible cystocopys later and a scan, diagnosed with Diverticulitis.
hi there what scan diagnosed ur divertculitis pls??
What about the upper left quadrant?
Hi, what about the Left Upper Quadrant?
Thank you in advance
That area was where I had most of ulcerative colitis attacks at. There and the transversing.
great video
Amatoellaahbintmk. I have pain there.
@@lindalamb7512
Me too, that's why I'm sorry to see that after 3 weeks the topic starter still hasn't replied, I'm in pain there too and the "doctors" I'm dealing with don't know what it is , it's like being stabbed with a knife, it's such a sharp pain, fortunately sporadic but still painful, get well soon
@@FreeYourMind-FP mine is right below left breast. I have chrons in recession but recent afib issues. Was recently diagnosed w hiatal hernia and diverticulosis. Plus cardiologist said it’s not heart related. Gi wants to do colonoscopy to be sure. But I’m worried. See if u can get colonoscopy w GI to check out too. Thanks for raising the question. You be well too, friend!!
I got diagnosed in the summer of 2021. I was in absolute agony and felt like I’d been kicked in the groin by a horse. I feared the worse, but an MRI scan proved it to be diverticulitis, thankfully. A course of antibiotics sent it away. My Dr recommended taking Metamucil everyday, which I did for a while but now I take it intermittently.
Same here, metamusil has helped me tons, but i think I'm having antiehd episode and this time not sure what triggered, i think is gluten or cheese, i need to be gluten sugar corn free, and noticed the change when i go back to the old delicious bad habits ....specially after Christmas 😭😭
Kellogg's bran buds daily with milk half cup. Does the trick
Thank you - very clear and concise information
From someone who has experienced diverticulitis, the pain is horrible. When you can’t stand straight or walk without severe pain in the pelvis that is a sure sign something is wrong. Mine started in the right side and I am not Asian, I was misdiagnosed several times until it got very painful. Low grade fever as well. All these other symptoms you mention it is very vague because all the other symptoms can be so many other things. Basically the only way you will get a true sense of what it going on is a CT scan with contrast.
I got mine diagnosed with colonoscopy
@@juliebryant3968 yes it can be found that way too, however if you are in an active flare infection a CT scan is what will be done as a colonoscopy in an active flare is not recommended.
Ew
Mine felt like I had gravel in my gut. It's been years and now I know how to treat it early to avoid hospitals. Diet very important. Avoid triggers.
Have you ever had anyone miss it in a CT scan? I had one in the ER but that hospital is known for missing things. I have most of these symptoms.
Yep had a flare up and has been causing all sorts of other problems.
Can diverticulitis be missed, even with a CT with contrast? They were 99% sure that’s what I had, because of my symptoms, which have still not gotten better. I’m struggling every day, with every single possible symptom of it, but they said they couldn’t find anything. Colonoscopy will be next month, but curious if it could have been missed?
Yes, mine was missed. They sent me home, still in agony, with some opioids which incidentally barely touched the pain and made me vomit. Next few days were really awful. Could barely stand upright. Applied heat on my lower abdomen and rested for about 5 days. Eventually it subsided. Later diagnosed during a follow up colonoscopy.
What really helps to avoid flare ups is half a cup of Kellogg's bran buds cereal with milk everyday. Keeps poop moving through ok.
Good for fiber, but very high in sugar which is not helpful!
@@hearme119 it's a trade off. Keeps the attacks away which only gets worse for the colon with every attack.
My colon pain presents as back pain...,bad back pain!!
I have all these symptoms. All quadrants will experience exactly what he says. I even get the urgency to pee.
The only thing that helps me is regular water fasts 3-5 days, NO fiber, just red meat, chicken, fish, shrimp, eggs, and bone broth. Carnivore. NO sugar or white flour products. The worst for me is walnuts( even chewed carefully into mush ) and vegetables/ fiber. I have no flare ups since starting this protocol, and if I feel the slightest twinge of pain, from eating something I shouldn't have, I drink lots of water, take oil of oregano and grapefruit seed extract, 1 tablespoon of olive oil daily, and the little twinge of pain stops within a day or two. Stomach massage daily and walking also helps to keep things moving, and the pockets clean... Carnivore and water fasting has been a game-changer for me!
so interesting....and well presented ...thank you....who knew leaking faeces could cause abscesses in upper leg.
Love this video. So much helpful information. Thank you!
If diabetic, keep the blood sugar in check. Too high will cause flare ups.
For some reason potatoes are my trigger foods to a flare up. I wish I understood what properties in potatoes make this happen.
I eat homemade lentil or barley broth soup everyday and avoid potatoes, seems to stop most of the inflammation for me.
I’m good with potatoes but not lentils, strange how it differs from one person to another
Barley works for me and also cornmeal.
Me too! Potatoes just do not sit well with me ever, even if I am not flaring up. I have a hard time digesting potatoes in any form.
I've had diverticulitis for several years and I get infections alot so did my Mom but she had colon cancer as well
JJ Medicine have you heard of such cases: my aunt had DV, and one day the DV explode and affected the bledder and from there when you go to toilet and you want to urinate, with the urine it came out s*it? My father now has DV (brother of my aunt) and he feels some leg pain, but we've been to the doctor, they made colonoscopy and didn't find any leak and only the DV was found and a polyp which was removed and it was "good" not canceric. Should I worry about the leg pain (not leg pain but pelvis pain)? Tomorrow we are going to see the doctor and will talk with him again about it.
Thank you for all the explanation and good video.
Is an mri a better way to see this?
I had an instance with lower right quadrant pain and it ended up being epiploic appendagitis... not long after that I was diagnosed with diverticular disease and crohns.
any studies blaming lack of fiber for anything should be taken with a grain of salt.
I had it in the RUQ mainly but would flare up in the epigastric area. I was admitted due to drs thinking I had gallstones. CT revealed diverticulitis
THANK YOU !!😅
Thank you!💥
I had a colonoscopy and I was told that I had severe diverticulitis and yet I’ve hardly had any pain.
You're lucky then .
The pain is terrible .
Thank you so much for a very clear explanation and description of this problem.
Diagnosis with Diverticulitis in 2016 not had flare ups until now Feb 2023 whilst away on hols in Spain any ideas,? does anyone else get a (fever and headaches,)? besides bloating and discomfort sometimes I feel slightly sick , but always constipation, burping and farting , feels similar to Flue coming on
IS IT POSSIBLE to clean out the diverticulum and then Lazer it closed?
Ive had it for 10years, am 63. Extreme fatigue, slight fever, lower left pain. Now has turned into pain at touch lower left and right when attacked. Refused surgery 3 times. Once had a bad attack, ended in sepsis due to ecoli. Very dangerous. I take 50k vit d now when severe attack, and in between when i feel twinges, i take boswellia serrata which i swear really does the trick. Regular Probiotics, vit d, psyllium, 5dl warm water first thing in morning. I try to limit red meat, dairy, eggs and sugar. My crp was always above 10 (up to 300 when attack), now for first time in 10 years? under 5...
Interesting. That's a lot of vitamin D!
Can diverticulitis be missed during a colonoscopy? If someone has a colonoscopy and is told their bowels are healthy, could they still have diverticulitis that wasn’t noticed during the procedure?
I’ve been told I have Diverticulitis. Most of the symptoms would indicate that. Interestingly since I started taking Milk Thistle Extract it hasn’t been a problem. If I ever get runny stools, taking Milk Thistle Extract clears it up overnight ! Why do you think the Scottish have it as as a National Emblem !
Milk Thistle isn't Scotland's Natioanal Flower, the Cirsium Vulgare is Scotland's National Flower, the Milk Thistle is Onopordum Acanthium, they are easily mistaken for one another
@@richardpeddie2060 but it is also a Milk Thistle
Does anyone know if it also gives you insomnia?
Could be. I have insomnia for the first time and also have diverticulitis at times.
I have it and suffer from severe insomina to the point I have to take meds or I will stay up for days until I hallucinate.
You get a sense of humour doc ur blessed
Excellent information. 👍
Thank you for your information I will try it ,end hope that it will works
If you have severe pain - do not let it go! I had perforation in 3 places….almost died. Lost 13 inches of my sigmoid colon, had colostomy, then a colostomy takedown. Two 6 hour surgeries. Now when get pain, i immediately go on a liquid diet! No red meat! No bread! No grease! Ever! It took me over a year to get my health back.
Thank you!Good work
Thank you for this information.
Had diverticulitis for over 8 years annual hospital stay for last 3 years now 4 years with a stoma life is far better
Don’t estimate STRESS, I have been in Hospital on 4 occasions in the last 5 years and have had many flares. My job and management was extremely stressful, changed jobs and for 6 months I have had no issues, flares and have postponed my colon surgery in January.
Very informative video.
I was diagnosed with diverticulitis about 15 years ago, and they said it was IBS until I had a a camera put in.
Recently I had an ultrasound scan and they noticed that I have an enlarged Spleen too, so I wonder if that is anything to do with it too?
Did they check your liver? Enlarged spleen is often seen with Fatty Liver Disease.
Marshmallow root and slippery elm capsules....good quality from a healthfood store.
I had the diverticulitis but no pain. They did found a small cancer and they take it out, no chemotherapy. I do think I check it, it was during the virus.
The best diet for diverticulitis before and after flares
Great I have this,thank you for your help
Thank you
Has Anyone Had Dark Diarrhea With Mucus ? Very Painful . I Don't Wish This On Anyone !