You making everything I love. Wow cheese too but haven't been having it. 😊

I thought I was the only one going through all the crap and felt so alone. So good to know uou❤

I've done really well on Keto, then Ketovore. I lost 75 lbs. and all my issues went away for years My problems started up when I quit smoking three years ago. I developed a sweet tooth, and my IBS showed back up. I've lost most of my senses of taste and smell with COVID. I have gained so much weight back. I swear the food we eat is being tampered with. There are less and less things I can eat, so I'm going full Carnivore or Lion diets. I felt the best then, lost weight, and healed for years. Things are just so expensive right now!!! Thanx for posting! Very helpful! Btw...I'm 72 years old.

This will sure irritate ur gut!!

Holy shit, dude. I'm only like a minute and a half in, but I'm in tears. I am in a very similar position to you in this video; early twenty-something girl who got diagnosed with Crohn's at 19 after I began experiencing a flare-up during my second year in college, and I had no idea what it was in the moment I was being diagnosed (just that it was bad because my mom immediately broke down into tears next to me after the call with my PA ended). Since then, I've been trying to wrangle the same flare-up by trying out different medications, which have been somewhat successful since addressing it in some way is better than leaving it to fester, but man, it's been an exhausting process. I graduated college in 3 years, which was one of my goals going into college, but I am someone who's very hard on myself, so I got really down on myself when my body couldn't keep up with my academics and activity (I was also on a club sports team all 3 years). My fatigue got to a point where I couldn't even wake up to my alarms for practice in the morning during the months leading up to my diagnosis. Almost a year after my diagnosis, I had my first two fistulatic abscesses form and got them drained, then had to get surgery on them when the drainage hole closed and one of them got septic. I was totally fine besides fever symptoms, but that was the beginning of the fistulas and abscesses for me. I've had 2 more abscesses form that I had to go to the hospital for since then and another surgery to tend to that first abscess pair that we've had to have an open wound for until I find the optimal medicine. Less than a month before my graduation, I was also diagnosed with psoriasis as a symptom/companion to my Crohn's (which is apparently the most linked skin disease to Crohn's). I was very lucky to receive swift treatment so that my skin issues (which are on my scalp) cleared up by the time it came. Luckily, I am receiving much better care now than I was during college, but I just wanted to say THANK YOU for normalizing this because it's so hard to explain to people, especially those who believe it's my work ethic having declined and not my body.

i just got diagnosed in July at 20 not sure how to feel, glad I found your channel

I hope stelara always works for you 🙏🙏

I hate crohns. EVERY FOOD makes me sick.

Video should be called what DO NOT eat while flare lol

I have had a tummy issue since 2020 but haven’t been able to get in with a primary until next month, I’m hoping it’s not crohns, but family members have it. After waiting years for a doctor I just want to get some help and hopefully a diagnosis 😅

BRAT/CRAM diet.

Hey I have crohns and I have so many questions What are some foods that don’t cause flares? and how do you keep energy? I am constantly tired pretty much I tried to go on a guts to glory diet but I’m not constant and it’s hard for me to figure out what foods actually cause flares 😅 please help!

Feel better ❤ i inject in my stomach feel no pain. Good luck! 🍀

How did you get diagnosed? Ive really been struggling. My sister and father have Crohn's and for the last year i have been having "flares" almost constantly, ive lost 40 pounds, cant eat most days, extremely fatigues, swelling and pain in the stomach, arthritis, etc. ive been to the hospital multipe times and a GI soecialist with no luck because they jepe pushing me away. Any tips would be amazing! ❤

You can’t have caffeine? I’m watching videos about what other ppl eat during flare ups, and I know everyone is different but I think my bf has struggled with this so badly. He’ll have a flare of for a day or so and then he will go eat takeout foods and I can’t help but feel that’s a recipe for disaster. Somehow he doesn’t learn what works for him or not and he will stay sick for longer. He drinks a ton of caffeine products and still had a lot of dairy despite saying he is a bit lactose intolerant… it seems a big amount of oats domt sit well with him like it doesn’t digest but I’m trying to see what others do. He also just doesn’t eat all day and stuffs himself like a holiday Turkey at night 🤦🏻‍♀️ it’s so hard to watch this idk how to help him.

Plz research what you are putting in yiur body when you eat chicken nuggets, eapecially processed...not good!!

When I was on entyvio for my crohns It caused hair loss. The emotions you feel from this are so normal. You’re channel is so relatable thank you so much for being so REAL. I am starting a new biologic called skyrizi and I’m so nervous. You make me not feel so alone, I thought I was the only one who is scared of treatments.

Du ernährst dich sehr, sehr ungesund. Zu mir wurde gesagt, dass ich währed der Schübe nur leicht bekömmlich es gedünstetes oder gekochtes Gemüse essen darf mit wenig Öl (Raps- oder Olivenöl) . Ansonsten viel Gemüse, fettarmes Geflügelfleisch, Kefir, Joghurt. Kein Weißbrot, keine Süßigkeiten, höchstens zwei zuckerarme Früchte am Tag, nichts Frittiertes, Gebratenes, Paniertes, keine künstlichen Zusatzstoffe. Gesunde Fette sind sehr wichtig, leicht lösliche Ballaststoffe (so viel wie möglich), Probiotika (das fehlt bei dir komplett).

Wow I finish watching your video..like you I have all the symptoms except of tummy pain I have burning sensation on my lower right tummy .I'm still watching for the result of my MRI but in my blood confirm that I have already Crohn's desease

Thanks for sharing your story, also, bread is bad it has gluten and fiber, instead eat rice and potatoes and chicken that is not breaded, go for gluten free cereals as well.

Videos like this make me feel less alone ..

I have the opposite problem. Im diagnosed with crohn , but i never had problem exept last week and so i dont know if its really true

Here in 2024, this is happening to me 3 months after major weight loss due to a flare and I feel so disheartened and anxious :(

raw vegetables really upset my stomach. it’s crazy how food triggers are different for everyone.

Thanks for your video I get my results on Thursday hoping that I don’t have this disease while feeling bloated after each meal and being scared to eat I still have faith

My mother was diagnosed with crohns disease in 1984.She was 79lbs before they finally came up with a reason why, she was losing so much weight.My mother had part of her intestines removed.She got better after a couple of months.She is.now 80 years old❤

thank you for this

hello, I was recently diagnosed with Crohn’s and was wondering what do you get from Chick fil a? I couldn’t imagine not eating lol

Wouldn't egg, cheese and gluten in the toast be an issue?

I was diagnosed at the age of 2-3 and it's still so hard to manage and to know what I can tolerate because it changes for me but I know for sure a gluten free diet does help. Also same with the lactose intolerance I can't have milky stuff bit cheese is ok

I wasn't anorexic but I lost 25 lbs in 3 weeks when I had my 1st serious flare up and my family thought it was stress due to my parent's divorce, years later after dealing with disability fatigue while being a mother of 3, I am finally getting the correct diagnosis

I was diagnosis also colitis when I was 15 and it's been hard

Thanks for the video!

My boyfriend has crohn's so I am here trying to learn more about what types of things I can make him or should stay away from.

Thanks for this, I relate so much to the bloating day after day. I'm a 23 yo and waiting for my colonoscopy/endoscopy in January to see if I have Crohn's. Been in a flare for over three months at this point hoping it ends soon

hi! I rlly like ur videos as someone else with an autoimmune disease (celiac) its just so relatable to see someone else kinda like me. I hope ur having a great day!!

🙏💜

Your videos actually make me so happy! I was diagnosed 2 years ago at 13 and it makes me feel so good to know what other people do with Crohn’s

Hi, I’m glad I came upon this video. I’ve been doing a bunch of research in regards to my pain. Let me state that I’ve have had issues with Canker Sores and strep throat growing up as well. (I currently have 3 Canker Sores as I’m typing this now lol) I’m 22 years old and I’ve been dealing with belly button pain for YEARS. Sometimes if I were to move, I would get tightness dead center of my belly button with is HORRIBLE pain…. I can’t breath, can’t move. Sometimes it would make me laugh cause it’s ridiculous how often this happens. Of course it’s hard to laugh because the pain clearly gets worse. It’s sudden and severe pain that I have to wait out 30secs to 1 minute for it to go away. Now mind you I’ve had abdominal surgery at a very young age at the age of 10 to have an ovary removed. So my doctor assumed it may be abdominal adhesion and didn’t really address what to do next. Fast forward a few weeks later I started having suspected gallbladder pain. I had an ultrasound done for this and no gallstones were found so they are referring me to a GI doctor because there’s obviously something deeper in there going on. All of a sudden to “gallbladder pain” has gone away and now I have general discomfort and radiating, intermittent pain in the are right of my lower belly button followed by the current belly button pain. It’s sad to say, but I am honestly hoping it’s Crohns. I was tested for it when I was 4 because I was showing symptoms of it at the time as well, but of course since I was so young nothing was actually found. I’m always tried and genuinely do not feel good and the discomfort is getting worse by the day. ☹️ Hoping I can find a diagnosis soon! Thank you for this video!

Some doctors say Crohn Disease is caused by LEAKY GUT and leaky gut is curable, but doctors said you MUST change your diet. Do NOT eat FOOD CHEMICALS ! Please try Visbiome (Medical Food/powder, probiotic) ! 1 packet Visbiome= 450 billion good bacteria I know someone who was diagnosed with Crohn Disease a few years ago. She was in remission for the last two years, but after using IV medicine, she had recurrent infection (side effect) and had to take antibiotics. After using antibiotics 4~5 times in a short period of time, she had inflammation again. Her doctor said Visbiome will not help anything, but she took the medical food anyway (5 packets of Visbiome per day). Within two months, her blood test and fecal exam came out NORMAL (This means she DOESN'T have inflammation anymore). Probiotics die when they come in contact with stomach acid, so you must take it with EMPTY STOMACH (ex) right after you wake up in the morning). I think capsules have some food chemicals in it, so take POWDER PROBIOTIC. Even if there are a lot of good bacteria in the intestines, if there is no food (for good bacteria), they will starve to death. Salmon, garlic, onion, sweet potato, kale, cabbage, broccoli, banana, apple(with peel), plant root (plant root inulin feeds good bacteria All THE WAY TO RECTUM)...etc. I pray for your good health ! Jesus Loves You !

Am i going to die if I have this illness I think I have it for 9months til now. 😢 I didn't visit a doctor also because I already did that but they just give me laxatives😢

I found that when I cut out all gluten my symptoms improved a lot. Maybe you can try swapping the bread with a gluten-free alternative

I get you about feeling alone. I’m the only one in my family with crohns as of rn 🥹 I got diagnosed when I was 17. Now I’m 23. It’s been definitely hard especially since I have no one close to me to relate to. But seeing your KZbin videos and others have definitely helped 💕

Watching this on June 14 because I’m nervous for my colonoscopy

I only wish I could eat eggs and having this disease 😍

Why do they always tell sick females that it's in their heads? It's so misogynistic !!

Generic over the counter…..Vitamin supplements helping me a lot in dealing with Crohn’s, the supplements I take right now have; Calcium, Zinc, magnesium, B12 and D3. You can give it a try. As a probiotic I also drink Kefir made from Raw milk.. helps.

I got diagnosed when i was 24, im now almost 40 and i will say this disease definitely progesses w age. I just filed for disability last year. Almost died in 2015 of bowel obstruction spent 13 days on life support but 5 major surgeries and an illieostomy laster i was released, had a reversal 10 months later and in the last 3 months, havent been able to eat much, very bad mornings, and lots of pain. Making a doc appointment today for sure. Tired of not feeling good. I just want to have one good day. Anyone else ever feel hopeless w this. I wouldn't wish this on my worst enemy!!! It is absoltely HORRIBLE!!! Sending so much love and good vibes!❤

8 month flare up i didnt know flare ups could last that long

'Promo sm'