Weird Symptoms of Diverticulitis | Atypical Clinical Features of Diverticulitis
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- เผยแพร่เมื่อ 31 พ.ค. 2024
- Weird Symptoms of Diverticulitis | Atypical Clinical Features of Diverticulitis
Diverticulitis is a gastrointestinal condition involving inflammation of diverticula, which are bulges in the large intestinal wall due to weakness of the large bowel wall. Diverticulitis causes several characteristic findings, including abdominal pain and changes in bowel habits (most commonly diarrhea). However, diverticulitis can lead to other atypical and rare findings that we discuss in this lesson.
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JJ
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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?
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..
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!
How we live as long as we do is an absolute miracle , there are so many things that ca go wrong.
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.
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. 😔
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
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.
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
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.
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'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.
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.
The one surest way of exascerbating your Diverticulitis symptoms -- watching videos about Diverticulitis!
To be serious though, I learned a lot here that I hadn't previously been aware of, Thanks.
I really appreciate all the informative medical content on TH-cam! I had attacks of diverticulitis starting in my 30’s, which is an early start - my family history of this is extensive. Now that I’m dealing with ongoing complications of diverticulitis, I’m having my sigmoid colon removed. It’s either that or another 40 years of non-stop abdominal pains and the antibiotics from hell (Flagyl).
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.
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 kind of you to explain this so clearly,many thanks.
Flare up felt like a bruise or soreness lower left quadrant. A little tender to touch, carried on a few weeks until I ran fever for no reason. I knew something was wrong. Gastroenterologist diagnosed and prescribed a regiment of antibiotics during Covid. Yes, scared me good.
Great video, can relate to this, living with an incurable disease is so hard, but you just have to live life day by day as it goes by (Cancer sucks)~
it is never the end of the world, i had HIV but when a friend of mine recommended a healer and caster for me, and she helped me out and i am NEGATIVE now, i was tested twice and i am free now
@@haynesatteh4463 wow, how can i get in touch with her? this healer, does she cure other sickness
@@ddirtdid yes, her name is MIRIAM CHAMANI DIETRICH, you can look her up online.
@@haynesatteh4463 wow, found her website, thank you very much for this.
@@ddirtdid Please think again before you involve your self with witchcraft, it might seem harmless but it leads down a very very dark path. Pray to the LORD GOD for guidance! Dr. Tullio Simoncini has been healing cancer patients with sodium bicarbonate injection treatments for a while now. No spells, no hocus pocus, no dark engergies. All TRUE scientific research with a 99+% success rate. Based in Italy I believe.
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 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
I've learned so much from this information you've shared on diverticulitis! Very thorough . I'm going through my first bout of this painful condition. One of the best videos or explanation I've seen on here. MY doctor barely touched on half of this info. I surely appreciate this.
Same here. It's a learning process
Not everyone's bodies respond the same so u need to keep trying to figure it out. No doctor can explain what they haven't experienced.
@@susanchilds1768 Yes this is true 100%!
Thanks for the information. I recently got diagnosed with diverticulitis. This video is very helpful.
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.
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
any studies blaming lack of fiber for anything should be taken with a grain of salt.
Excellent, thorough, and explicit.
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.
Great explanation. Many thanks.
Excellent explanation! Thanks so much!
Wow this is extremely enlightening. I’ve been blaming everything but the kitchen sink! Now I know.
Love this video. So much helpful information. Thank you!
What a great informative video i have so many of these symptoms the urinary problems bad urgency the bloating abdominal distension and gas, with a peculiar sensation on the very lower left side of my colon i guess that is the diverticula....I really do feel more informed now with having watched this video. Thank you.
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 TH-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 TH-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 🌻
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 hate to pour cold water on these theories of why some people have these diverticula, but I was diagnosed when I was about 12 with this condition and back in the day low fibre was never an issue, obviously age was not (for me anyway) and another one I read about was that it was cause by hard stools which is actually a bit of an engineering impossibility. I also never smoked and until I got into my 50's didn't carry excess weight. As a kid growing up in the country exercise was also never lacking. I would suggest these things might worsen or increase the likelihood of inflammation, but that the actual diverticula is a genetic defect that then results by normal mechanisms such as poor clearing of old material that lead to inflammation etc. Throughout my life I have simply had a high fibre diet with lots of greens and grains etc. and nuts and as a result had maybe 5 bouts of diverticulitis in 66 years. Still a good video, so thanks.
I’m confused. You said that fibre was never an issue for you (but you still got diverticulitis) but you finished by saying that you stuck with a high fibre diet (and still got diverticulitis 6 times)
Do you think the fibre might be part of the cause or the cure?
@@whattha930 That's correct, I still got Diverticulitis 6 times, Would I have had it 12 times on a low fibre diet? Possibly, with extended diverticula you can still get stuff lodging in them if the conditions are right. All was saying is that the diverticula disease is surely not caused by low fibre or high fibre etc. Once you have the prerequisite extended diverticula the equation changes, anything that can find its way in there will have a harder time getting back out. The specialists suggest have a high fibre diet because it reduces inflammation and bowel cancer risk and when you get diverticulitis don't have anything gritty that can fill the pockets. Like most things in life they are a 2 edged sword.
@@etmax1
Aha, I see. Thanks for the info. 🙏
I’m glad you responded, first hand testimonials are my preferred source of info. 👍🏼
Thank you - very clear and concise information
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❤
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.
I describe the pain of a diverticulitis attack as "having a razor blade encrusted pine cone dragged through my bowel backwards". The pain can be so intense, you feel the edges of your vision begin to fade and become virtually semi conscious. You feel hot, sweaty and chilled and even pass out, as the pain can be almost as intense as childbirth. After the intense pain begins to pass, you'll have a series of massive cramps and diarrhea, leaving you utterly exhausted. Nowadays I know the buildup signs and have learned it is best not to eat at all for a few days.That way, I don't usually end up in hospital. An attack can leave your digestive system very fragile though and you often have to be so careful about what you eat for weeks and even months later. Raw or fibrous foods, too many carbs or sweet dairy can be a trigger for me, so I have to moderate their consumption. Nuts and seeds don't seem to bother me, but as several others have suggested, drinking water in the morning is a big help as are probiotics. I always have a drink after my meals, before bed and first thing each morning, and have found intermittent fasting can be helpful too.
That sounds pretty accurate. When I had colitis and diverticulitis, I was screaming in the bathroom. The dr said I’ll come back. I said oh no you won’t! He waited. It was excruciatingly painful and I needed an epidural. I have problems eating many foods due to allergies and other health issues. I was fairly young when this started. I’m glad someone described what I’ve been unable to. Obviously I have diverticulosis, I just eat a bland diet and pray an infection never comes back again.
This is a completely accurate description of the symptoms I have that diagnosed me with Diverticulitis a month ago, was treated, had a flare up last few days, awful!
Very accurate indeed!
This is what I've been dealing with for over 4 years debilitating pain literally makes my back and legs hurt . my ga GI doctor says diverticulosis but the CT scan says it's mild diverticulitis, and he refuses to give me antibiotics time to change doctors I think I hardly eat anything mostly fluids
Actually thought describing like I had glass or something in there was Overkill
but that's what I felt like..
and then you said the Pinecone thing
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
I have it and a flare up is so painful that vision is blurred all teeth feel like they are being pulled out at the same time and sweat and chills and fever and it feels like it’s never going to stop but when it finally does stop you feel so exhausted you can barely move for hours. I literally thought that I was going to die the first time it happened. It’s also linked to stress. Never eat sesame seeds or other seeds.
thank you
Thank you for this information.
Thank you for a clear presentation
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 🔥
I had a colonoscopy yesterday.i am 76. I was told I have diverticulosis
I have daily diarrhoea since I had a cholecystectomy 6 years ago. The surgeon yesterday said I have a flat duodenum and severe diverticulosis. I start medical treatment tomorrow.
Sorry to hear that. How are you now? Will be good to know your progress.
I have all those symptoms including knee pain and bladder problems.
What kind of bladder problems?
Thank you
so interesting....and well presented ...thank you....who knew leaking faeces could cause abscesses in upper leg.
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
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 have Diverticulutis and find that diet and fasting help when I feel a episode coming on.
I find the fasting is the only thing that helps … if I over do it or eat something that doesn’t agree with me … i feel sluggish and truly rotten …
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.
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.
Thank you this answers many of my problems. I was misdiagnosed for several years as having IBS but later it proved to be diverticulitis throughout my system and I have often wondered if this is linked to my constantly needing a pee.
Yes, once your gut is inflamed, it pushes or squeezes your internal organs.
The peeing thing could be your prostrate. Get it checked out.
Severely cut out sugar and carbs and you should get relief. Not 💯 but a lot.
I am glad mine is quite mild.
Thank you!💥
And to all a good night!
Thank you 🙏🏼
Ty great info.
I’m having a flare up right now, I haven’t passed out on the toilet yet but I am spotting blood. I am swollen to the point of looking 8 months pregnant and the flatulence could strip paint off at 50 yards. I’m also coeliac. I was diagnosed with IBS, then IBD and then diverticulitis, tbh I don’t think they could make their minds up, this was never the life I would have planned for myself, I’ve read that someone else said that it’s a miserable existence and it really is.
I am the same ..
Passed stools this morning but still incredible pain .
Awful.
Starving hungry. Don't know what to eat as there are foods I can't have regardless.
It's terrible pain .
Rather have a baby again.
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.
You get a sense of humour doc ur blessed
I find this helpful for l have a lot of flare ups with diverticulitis thank you ❤
Wow learnt so much from this video.
Thank you so much for a very clear explanation and description of this problem.
I have all these symptoms. All quadrants will experience exactly what he says. I even get the urgency to pee.
Great I have this,thank you for your help
Abdominal pain can often manifest as referred pain that can even be felt in areas like the testicles, because of how the nervous system is wired.
Marshmallow root and slippery elm capsules....good quality from a healthfood store.
Good information, i suffer from it and have more constipation through it when it flares up. Sickness is horrible. I suffer from P.A D. also which doesnt help. The fever that come along with it is another thing
Same the constipation is awful…
I have diverticulitis but I was recently hospitalized for pancreatitis when i thought it was just my diverticulitis . They did a ct with contrast and told me i did have mild diverticulitis but the majority of my issues were being caused by pancreatitis. They still don't yet know why as I don't drink alcohol and never really was a heavy drinker .
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 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.
Ive got celiac disease and mild pain in my left lower abdomen. This video is the first time ive heard of this condition. Im already doing a liver and gut cleanse, gi tract repair regime with my naturopath. Hopefully this is the first and last i hear about this horrible condition 😅😅
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.
Have you done a video on sciatica?
Thank you!Good work
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.
Interesting that this complication has symptoms indistinguishable from prostate problems. I have all three symptoms that you showed plus my belly has swollen to a huge size but I only have a thin layer of fat on me everywhere.
I am the same, it's so annoying isn't it??! I'm not 100% sure that it's diverticular disease as I had scan and they haven't confirmed, but a lot seems to point to that. I'm working on trying to reduce these symptoms myself (trying gluten free and reduced dairy as much as possible and drink more water). I think I need more medical advice though as the swelling is so noticeable and now half my clothes don't fit! Plus of course the other symptoms are not great.
My mom had this. She didn't like to ever complain. I was told my mom was sick by my brother. She did smoke often and didn't eat that great. She was bloated a lot of the time, I have that now. I used to be so skinny and I'm still thin, but my stomach looks like I'm having a child soon! I hate it. I started to have a feeling of having to "go" every minute. A friend thought I should see the Dr. for a urinary tract infection. But it wasn't that. Eventually a Dr. did tests and told me I had Intercistial cystitis. A flare up around the wall of the bladder. I feel like I have to go all the time. It ruins my social life. Now I'm wondering if I have this diverticulitis. The first Dr. got it wrong when she said it was overactive bladder. Then the other one who was top in his field said Cystitis. Could it be diverticulitis? God I hope not.
Get to a GI doctor for diagnosis to be sure. IC and IBS often happen together, and since diverticulitis is an autoimmune disease it’s possible you could have that too or instead. Finding out is important so you are treated correctly. If a urologist diagnosed you with IC it’s unlikely he was wrong but knowing if you also have GI problems is important. From an IC/INS person +35 years.
I have Celiac disease, and like you have a very bloated stomach. Never had a bloated stomach when i was in my teens. Flat as a pancake. Now I look like I'm pregnant.
Celiac, too. No grains or dairy and I’m fine. Add them back and I’m a basket case, with dizziness, ataxia, brain fog, exhaustion, big puffy belly and just not myself.
Not worth it to go off the celiac diet.
Ask your GP to do a SIBO test. I was the same as you and worked out myself that it could be SIBO, I did 5he breath test and I was right! The doctors hadn't a clue! After a course of antibiotics I was fine and much more comfortable. Good luck xx
What is a SIBO test? I have a lot of the symptoms in this video, and the bloating is an absolute pain...looking about 4 months pregnant, and more swollen on the left hand side. It doesn't matter what I do! I'm trying gluten free and reduced dairy, plus more water. I had a CT scan but they've not given any information about my stomach yet. I'm having to just 'carry on' when bending or even driving is difficult and I can't fit in my work clothes any more. I'm wondering if I am Celiac, and I've got no idea what to eat, so confusing! 😮
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!
Hi doctor, I was diagnosed with diverticulosis and Erosions in my stomach, but my pain is in right part of stomach but my gobbler was removed 20 years ago.
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.
If you get painful cramps during an attack, try drinking peppermint tea
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.
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
Very informative. I'm unfortunately blessed with bad genes and diverticulitis runs in the family. It's occurred twice in a year and the docs are worried, so they're going in to remove part of the colon in a few weeks.
Hope all goes well with your surgery 🙏🏻
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 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…
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
For many years, I thought my diverticulitis issues were IBS. Best to educate and see your medical specialists for proper evaluations. Another symptom suffered is decending colon constriction.
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 had a ct scan with contrast and it was clear but I'm still having this burning sensation in my left side lower abdomen.
This was a terrific presentation!
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!
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
If diabetic, keep the blood sugar in check. Too high will cause flare ups.