Eating Healthy with Crohn’s Disease 

Honestly it varies for each person so much...every time I meet a nutritionist for this they're not helpful and they recommend fruits and vegetables which are literally the problem!

The problem is that you have clueless people who have never experienced this condition firsthand who then want to advise those who have on what to eat. Here's my advice to my fellow Crohn's Disease sufferers: be your own doctor.

I tried to alleviate my crohns by eating as healthy as possible, but it only made it worse. Eating things like fresh fruit and vegetables or nuts just lead to a bowl obstruction. I've had to switch to basically meat and grains only, but it's helped me stay pain-free for over a year now. I've even had to go as far as biting off the ends of french fries to avoid the potato skin. But the lack of pain is absolutely worth it.

This is the thing they don’t tell you about Crohn’s disease, not all treatments works, in my case none and that not everybody goes into remissions. I’ve had Crohn’s 35 years and I’ve recently found out that in all these years, my disease has never gone into established remission and all the years I’ve beat myself up and thinking that I was some kind of a neurotic hypochondriac always in pain and in discomfort, the hospital knew it through regular blood tests and reading my inflammatory markers but didn’t care to tell me as some of those arrogant gastroenterologists do have their personal selective “guinea pigs” and I was one of them and still am. Crohn’s disease is an illness I wouldn’t wished on my worst enemy because it’s a nasty one that doesn’t entitled you any support from society, and sufferers of this vile illness aren’t completely informed and made aware of the numerous complications on the human body that Crohn’s causes. And the most important fact that aren’t addressed by doctors and nurses to their patients with the disease is the heavy toll it has on mental health. Twice I was made to feel guilty about being anorexic and on both occasions it wasn’t at all my fault but my mind was screaming to my body that all food caused pain, because unfortunately to this day, every time I eat, I will have to lay down as I experienced a lot of pain and discomfort until my abdomen settles, but those hospital outpatients appointments never tells you that, and they don’t make clear to their patients that everyone has individual experiences. For example, in the five years they thought I had cancer because I’ve never had atypical symptoms for Crohn’s disease. And no treatments has worked and now, the hospital is working on my terms and I’m on multiple medications for pain reliefs and strong vitamin supplements to make sure I remain healthy. However the most important part of my treatment is my mental health as my Crohn’s is very sensitive to my mental health. But that’s the thing, hospitals aren’t always on top of your mental health, hence why I feel sufferers of Crohn’s disease should always make sure that their health professions are including your mental health as part of your treatment programs, it is very important. Due to my Crohn’s and the complications of the disease, my eyes have been affected, complications from both uveitis and side effects from “wonder drugs” to calm down my arthritis. My liver and right kidney has been damaged by side effects of another “wonder drugs” to calm down my Crohn’s symptoms and I also have a blood disorder, something I was born with and for some strange reason the Crohn’s don’t get on with and as I get older, there’s a big list of food products that gut can’t tolerate, which has totally ruined my chances of becoming a vegan lol. However, my point is that people with Crohn’s or any ongoing health issues, please don’t just rely on the health professions that’s dealing with your health issues because they all don’t give you the whole truth. Become proactive and get yourself informed about your rights and the whole umbrella of complications surrounding your medical complaint/issue. Crohn’s disease is seriously the apex of the giant iceberg that is the disease, so personally get to know your illness, your pain and your mental health because only you truly know how you feel. You can read all texts and medical information about your disease but all those side effects and symptoms they mention, it doesn’t always mean you will experience them as your body operates by its own tempo and not by the rate medical journals states. For example, the most common drugs used to treat the symptoms of Crohn’s is steroids, however my body can’t tolerate the drug as it caused severe internal bleeding. Another drug common with treating the symptoms of Crohn’s is Azathioprine, however due to a supposedly mild blood disorder I was born with, I became violently ill within a few weeks and have permanent damage to my liver, which is under regular check to prevent liver disease. So, it’s very important to be proactive in your ongoing treatments and to ask for appropriate care, especially if you feel your mental health may be comprising your physical health

Recently been diagnosed. But also recently been under a high amount of stress and pressure for years and THAT is when it hurts most for me of course the ulcers suck and everything

It's impossible to advise anyone with this disease as everyone has different triggers and intolerences. I was diagnosed in 2005 and it's been tough finding my path and still feel healthy. Milk products are out ( and should be for everyone anyway ) and things like chocolat are killers as are Peppers and anything from the cabbage family. My diet is boring and means I Don't accept invitations to eat as often the restaurant hasn't anything I can handle and if I do eat for peace I pay the price. People say I am picky when I am not, just careful. I tell anyone who tries to force me to eat Something that it's like forcing a diabetic to eat sugar. When I do meet someone who has it we exchange notes but they usually are very different. Some people cannot give up the ' wrong' food like alcohol and meat and prefer to suffer or take meds. When I'm ill I feel like dying, when I'm not I am on top of the world, it is what it is.

Imagine my consultant in Purley war memorial hospital Croydon London Uk said: you can eat, smoke, drink alcohol, doesn't matter

Yogurt everyday, and green tea with benfibre, every day, have really helped me. Ive tried everything over the years, sometimes I can eat anything, and others I cant eat at all, but yogurt and green tea have definitely curbed the frequency of attacks.

Avoid sugar and milk helps massively, I went from going to the toilet 25 times a day to around 8 times.

If you have digestive problems, try eliminating bread from your diet. I was diagnosed with IBS three years ago, and it's gone now because I quit eating bread. The symptoms went away as a result of eliminating bread from my diet. Give that a try first before anything else. If that doesn't work, try to reduce inflammatory foods like sugar and vegetable oils. Vegetable oils are man made(except for coconut oil, olive oil, avocado oil and a few others) and can cause severe inflammation. Sugar, of course is inflammatory as well. My thoughts are that you should only eat natural foods. We evolved to eat natural foods, and man made foods like vegetable oils and super pure foods like sugar can cause all kinds of inflammatory responses. Crohn's disease and IBS are inflammatory conditions and may be reduced or eliminated by not eating sugar, bread or vegetable oils.

Crohn's Disease is a type of inflammatory bowel disease. It can occur anywhere along the digestive tract. If Crohn's Disease is located in the small intestine, this has an impact to interfere with how we digest and how we absorb our nutrients from our food. They can also lead to symptoms of diarrhea, because we are not able to digest and absorb nutrients from our food. It can lead to other symptoms, such as gas, (and) bloating, and pain, because undigested food (s), once it leaves the small intestine and enters the large intestine, it can be fermented upon the bacteria there, leading to gas and bloating and other symptoms along that line. In order to cope with the nutritional implications that Crohn's Disease inflicts upon us, there's a couple of tips that we can try. There's no need to avoid any food, unless you are bothered by that food. So, as an example, if you have a problem with digesting fat well, because that is digested in the small intestine. There's no need to go fat-free, but can we choose low-fat food options, such as baked or grilled, or steamed fish, or perhaps using a broth-based soup versus a cream-based soup. Another thing is how much you eat at one given time can play a role on how well you feel after eating that certain food. As another example, lactose, the milk sugar, it may not be digested well in Crohn's Disease, because Crohn's Disease may interfere with the enzyme's ability to digest lactose. So, eat less dairy. Spread out your dairy. Treat dairy like a garnish or a small snack, versus the main entrée, to help you feel better after eating dairy.

My little brother has this, makes me feel awful. I’m so sorry to everyone that there’s just seemingly no attempt at finding real dietary solutions. You’re just being recommended the same old 1980’s low fat, high veg, bread based diet nonsense that never worked for anyone. It’s just that or different conflicting opinions all over the place and nobody you can trust, it’s sucks, this is what I hate most about researching important things. Medical and science fields have trends like any other and aren’t nearly as thorough or knowledgeable as they want us to think. Most things will never be researched, the boundaries of knowledge are close enough for even a layman to butt up against. It simply isn’t satisfactory.

Thank you guys so much for the information. This is a great starting point for me to begin to feel human again.

Coconut has helped me with my intestinal problems...coconut oil...3 Tbls a day...., I add lots organic shredded coconut to my cooking...make homemade macaroons...yummy!, and I drink light coconut milk.

My son has been struggling with this since April of 2023 and Loma Linda hospital cannot figure things out. He is 9 years old and he keeps having issues who do you guys recommend in California??

Why is it that nutritionists never mention the inflammatory effects of some foods? I understand that animal products are pro inflammatory and plant products are anti inflammatory so surely this should at least be mentioned.

This is oversimplified and unrealistic and unhelpful.

For me personally, I’m vegetarian (for unrelated reasons) and try to avoid fatty or greasy foods, or soda. I also eat more carbs and fibers that are easy to digest. But that’s just me, everyone with Crohn’s is different

Thank you 😊! I have crohns in issues through large and small ! Just misserable !

I too just had a flair up in my chrons and I need to not eat dairy as often as I was!

Crohn's disease is hard. Yogurt, Cottage Cheese, and Aged Cheddar Cheese are foods I can eat and not trigger my Crohn's. Adding dairy back to my diet also eliminated reoccurring bouts with kidney stones. High Fiber is also a trigger for me....

I have crohns boy its hard to live with cant eat hardly anything that will cause flare ups also i feel tired most of the time.

Currently i am going through a flare up and found this useful.

For me I find stay away from nuts, whole grains because it's harder to digest. Still to plain white bread, banana, pasta. Anything that's easy to digest and gives me some nutrients.

From my experience (5years of crohn) Medications are much important than diet because crohn is immune-related disease so keep in mind to try couple of types(described by physician ofc) before changing diet, Im taking Humera anti-TNF for about 2 years and I can barely feel any symptoms, and my diet isn’t quite healthy. Also I find fibers causes diarrhea more than any food.

Hello, I am learning (trying) about Crohn’s Disease as a friend of mine has just been diagnosed. I practice fasting, I am sure fasting could help very well? But conducting research online I am not having much luck? I would appreciate anyone who could tell me how good or bad fasting maybe for Crohn’s Disease? Thank you.

Recent i was diagnosed with crohn and had got that bad that i had to be operated an lost 30cm of small intestine. No i am trying to recover and learn about how to live with it.

Just got diagnosed yesterday with it, I was suffering 5-6 months before that🙏😭

You can contact him 🙏

So after removing causative agent ibuprofen (impeding mucosa secretion), and providing fiber for gut bacteria to produce short chain fatty acids that are critical energy sources for colonic cells, is there anything that could still lead to Crohns?

It could be that your diet can only control the symptoms, but really does not affect the condition at all.

Nutritionist only tell you to try everything and listen to your body... Everytime. This is what she literally said in this video. What worked for me: Humira or a comparable treatment.. (don't be afraid of it..) Smoke weed when your stomach hurts. Take Cholestyramine twice a day to stop from going to the restroom nonstop. I had a foot of my small intestine removed and caused me to go non stop... Started Cholestyramine once at lunch and once at night. This made me stabilize be able to gain weight, absorb nutrients and go to the restroom normally. Eat in moderation, don't have Mexican 3 days in a row, or red meat 3 days in a row. NO SOUP Don't eat tons of salad and fruit. Moderation is key. Don't eat tons of spicy. Again moderation is essential.. Stay away from Preservatives. Don't eat frozen foods Breads are great. Smoke weed when your stomach hurts again. minimize the alcohol (if you can stop do it). If you do drink take 6+ imodiums to put a plug in you... Emergencies if weed doesn't stop the pain and its excruciating... Go to the ER and get Diladden.. This i would only suggest if your in agony. What didn't work for me: Green juices Vegan/Vegetarian Diet Clinical Trials (Stomach Parasite treatment didn't work) Weed only trials (done in netherlands). I did this in my own experiment, not with doctors. Good luck all Nico

Let me tell you about my experience: I am not good with English😅 Anyway :I am 17years old, I knew that I have crohn disease when I was15,after trying a lot of traitement ,now I take humira(adalumimab) , and I feel better,okay for the food , don't eat nor drink: Milk🍼,cheese🧀,coffee☕,juice🍹,soda, fried food🍳 ,anything made with sugar (all the sweets)🍩🍨🍧🍪🍦🍡🍥🍰🎂🍫🍬🍭🍮🍯,spicy food🍲🌶, or(those you use to make a flaver to the food like black peper..😂 Vegetables(you can cook them on evapor ,or boild them and make a soup) Don't eat the food when it's hot,don't eat fruits:(only banana,) Hmmm,what else?😅 You can eat pasta,soup,boiled eggs,rice,(you'll be a zombie like this😂) Okay every thing makes you feel pain stop it, Drink a lot of water,ask your doctor for some vitamines, If you have crohn You'll feel tired and dizzy all the day,but you'll used to this ,with some vitaminrs you'll be better. This is only my experince, 😁It dosen't suit everyone. Thanks a lot for reading.

I'm new chrons disease patient can I get any advice about what should I eat

Recently diagnosed here. 3 meals a day puts me in sheer agony. I'm losing it. Seriously. Does it get better?

I have chrohns disease I eat wtf I want I'm always bloated and constipated n I'm trying to loose weight I try sticking to my diet but I can't I can only eat twice a day anything more my belly well hurt

Pitta Balance for planet ayurveda t has a very great result in balancing the pitta dosha in the body.

Yesterday I had diagnosed with chrons I need any advice because I have stricture in my intestine and I don't know what should I eat

In India Crohn's disease is relatively rare than the West, I have been diagnosed with Crohn's, can't eat wheat or oats, Or anything that has a lot of fiber. Can't go for a fiber free diet for too long, that would cause risk of getting diabetes, as it runs in my family. Can anyone suggest anything, talked with multiple doctors online, they wasn't much of help. I have been diagnosed with Crohn's in May this year, since then I cannot risk myself to get a physical check up much, due to the rampant spread of COVID-19 in my city, can I get suggestions about what foods should I try. Lastly, my affected part is small intestine (Terminal illeal ulcers). THANKS.

I heard if you chew your food more before swallowing works even better.

Hi, I have done surgery for right ingunal hernia 6 month ago and left hernia 2 months ago but still I am feeling pain over the area . This pain happens because intestinal ??

My doctors diagnosed me as IBS but IBS ttt didn't improve my problem so I think it is crohn disease I want to confirm the diagnosis but it is very difficult for me to do an endoscopy , are there any other ways to diagnose it?? Are there any symptoms that can differentiate IBS from crohn disease because I really get exhausted and depressed. I can't afford any more

incredibly bad advice through the whole video

What is the music name ?

After 2 months with IAFA Ayurveda, my Crohn's disease has significantly improved. Their holistic approach, including personalized herbal remedies and dietary guidance, has alleviated my symptoms and boosted my overall well-being. I highly recommend IAFA Ayurveda for their effective and compassionate care.

Thanks for this video! If you liked this video, you may also be interested in knowing the indicators of a healthy gut! They include: colon transit time of 12-24 hours, type 4 stool on the Bristol stool chart, not having diarrhea or constipation, having 1-3 bowel movements per day, and light-dark brown colored stools!

I have constipation like every time i need to go number 2. Sometimes its so bad i tear down there and i bleed because of the bad constipation :(

Do Carnivore diet people… meat, eggs and seafood

Really!

I was diagnosed with ileitis, but I have none of the symptoms. My issue is constipation and a bulging pain that started after C-section they always said it was ibs. I honestly feel like my bowels are twisted on the left side. Not one doctor has palpated my stomach to assess the bulge. It feels like my organs are stuck to my bowels when I bear down for a bm. This is so nerve wrecking because if I have Crohns I think it’s caused by constant constipation. Ik they will say that’s not possible but Ik my body. This just came out of nowhere. I am scared to eat anything at the moment. It’s very scary that I have multiple test but I feel I need an exploratory laparoscopic exam. But nobody will listen to me😢

GET HUMIRA CASe it feels like you don’t have it anymore take humaira

Recently diagnosed with crohns disease I had anal fistula first time in 2015 but dr didn't identify the cause now every year recurrent fistula formation then I change my dr and find out I am suffering from crohn's

Hot water with Chicken bolion in it is my savior... it’s the only thing I can stomach most times. Even straight water hurts my stomach.

crohn's moves around and goes into remission, so how do you target the location?

proper solution need to improve

Lol I really gotta stop eating crap food

Hey everyone! I was diagnosed with Crohn’s disease about 3 years ago. Since then I’ve been in and out of remission, but as of right now I feel amazing. I made a couple videos on my channel about my story if you wanna check it out!

Nice video but gender biased} I ama male adolescent who has had Crohn-s for 7 years (since I was ten(. It is not pleasant and rgough I have had this onlz for 7 years, this is forlife! Please in the future show some MALE patients as well, this is NOT a gender specific disease} Thanks}

Diettission is who I need to talk to .

Why can't I gain weight?

Useless video. What about fiber? Prednisone?

Hi people. My daughter who is 28 has been diagnosed with crohn's disease. Now my question is. The doctor has given her 8 tablets a day to take which has so many side effects. I want to ask does she have to take these tablets or can it be controlled with a diet???

Pizza makes it worse

Learn how to make kefir

Ulcerative Colitis is a serious problem. one of my friends facing this from the last 5 years. he tried lots of medicines but no effects and no relaxation but after Planet Ayurveda Ulcerative Colitis care pack. now he is feeling he can overcome from Ulcerative Colitis

Mam I am suffering from symptoms: motions with blood, weight lose,right leg joint is swealled,no hunger Help me to cure from it

😭

Here from mr beast

Worthless

Crohns disease ka ilaj key hai

Lmao its so funny.

She’s beautiful