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Milk is worse for that.try black coffee love

Gross😂😂

I switched to oatmilk so no i don't have to play this game anymore lol

😂😂😂

This is not an IBD friendly diet

I was told to stay away from oats since I have Crohn's disease.

How can we eat oats? It’s contain gluten?!

Thank you for sending me this link through Instagram, this is what I need . My BMI hasn’t been normal since 2017 and it’s 16 now and I have osteoporosis and I’m 50 1/2 years old and it’s so important for me to gain muscle and weight. I understand there is no one diet . I have been gluten free, dairy free, soy free , preservative and artificial free, very little sugar , caffeine and alcohol free for many many years . I eat mostly organic and grass fed meat for a little meat but mixed with plant protein. So that’s a bit about me - I was diagnosed about 18 years ago . Although I had it a lot longer looking back . Mine is illoceical valve and right and left . Mostly mine is microscopic based on biopsies . Only one time at initial diagnosis did they see it . I’ve had 6 colonoscopies during this journey . Despite all my exclusions I’m flared and in pain and again can’t gain weight 🥲. Which is important because of 2 types cancer history and always checking for reoccurrence.

I went 100% Carnivore for 3 months as a last ditch effort to gain remission. I have Crohn's and UC. It was brilliant at first and loads of symptoms disappeared: asthma, acid reflux, restless legs etc. However, I ended up in hospital with a severe gallbladder infection, on IV antibiotics for a week. Now I have to avoid meat and fat so I'm back on vegetables.....

Any info about turmeric therapy. And psyllium

Thanks - over restricting is an issue - a great approach

Yes. Thank you. Dumped with this. Thx.

Good job. New diagnosis - I’m 60 now.

is there s way to still purchase your june webinars on what to eat? i just found you! thank you

You need to get together with a chef so we can all learn what to eat, and how to make it taste good.

What about microscopic colitis?

CZcams

Want additional support or to ask a personalized question? Join us starting on October 6th for What to Eat with IBD & Reduce Symptoms! Get all the details and sign up here: LINK In this mini nutrition program, you’ll get: ✔ Three live and recorded webinars with Q&A (watch whenever is most convenient for you!) ⁠ ✔ ALL the answers to your question of “What to Eat for IBD” ✔ Tools that will help you have fewer flares, induce remission, and reduce IBD symptoms WITHOUT over-restriction ✔ Knowledge of how to use nutrition to reduce your risk of flare up long term BONUS: We will have extra time set aside for individualized coaching with the group during each webinar so you can ensure the advice is relevant to you. Ask us any and all questions on your mind right now so you can stop guessing or feeling confused by conflicting advice and instead feel confident you know exactly what to eat (and what to avoid) to reduce your symptoms and have fewer flares. Learn more and sign up here: crohnsandcolitisdietitians.com/what-to-eat-with-ibd-webinar/?et_fb=1&PageSpeed=off

How can I find out more about your shakes?

How can I communicate you? Actually I am struggling with UC for exactly 3years.It's ruining my life.

Carnivore diet works for me.

Please tells us what we can or cannot eat.

Quit sugar and all processed foods eat real food.

I have also had covid twice and not vaccinated that's when I started having inflamtion symptoms

I have a question I did a colonoscopy 2 years ago and there was no colitis or crohns and I did a celiac test none was found I just recently had a endo scope and biopsy done with no chrons or colitis found but gastroduodentis was found now 2 days ago I went to the hospital with extream stomach pain and had a cat scan done it it came back as left side colitis I'm now taking 2 types of antibiotics metronidazole and ciprofloxacin I also have ibs my question is I'm not sure what type of colitis I have because my test showed just colitis not ultracerative colitis I notice I have alot of right hip pain bothers me to stand up some times so any help would be appreciated

I just got out of the hospital because of my ulcerative colitis, their food is horrible, I didn’t eat for a week there, even the doctor that was taken care of me and told me I could eat sugar🤦🏼‍♀️

Why you didn't say clearly what to eat and just talked in general ??👎👎

I have UC, A2 raw milk and yogurt has really helped me so much.. lots of grass fed butter, tallow , liver, no Grain organic eggs and lots of grass finished red meat 🙌🏻I have also started eating chia seed with coconut milk with organic stevia also has done a lot of good ❤

The medicines the Physicians prescribe have some major side effects. Diet is key. A poor diet probably has a lot to do with the diagnosis to begin with. We are what we eat. Prayers for those who suffer with all ailments and diseases. 🙏🏼

want to consult you

I find that keto/LCHF works for me (colitis)

I have Crohns and a stricture and I switched to red meat, eggs, raw milk and honey and fell amazing. You cant eat high fiber with a stricture unless you like extreme pain

Google

Thank you for the information. Recently diagnosed and still trying to figure out how to change up my diet to live a normal life. Appreciate you taking the time

Chatting 3 weeks later! Thanks

OMG! thanks you guys! this was so my experience when I was diagnosed back in 2016 at 50 years of age. I was ignorant, dismissive and didn't have a clue. My GI also said diet doesn't mater. I was in and out of flare's until I got really sick in the late winter of 2021. As a grown man I lost 40lbs from 180lbs and they nearly removed my Colon. Med's were not working other than Prednisone. However, while I was very sick I was able to figure out on my own after endless research what would work for me. Specifically dietary. I really focused on this aspect. I modeled mine at first around Specific Carbohydrate Diet. Everything you guys mention is spot on and so true. I now keep within my therapeutic diet 80-90% of the time along with a maintenance med. I include a high amounts of raw fermented foods daily. Home cooking as much as possible. No processed foods. No Caffeine, added sugar or very little alcohol. I also learned that your body tries to tell you what you need. The minute I tried raw, unpasteurized Sauerkraut It hit me. This is what I was missing as I think my body was trying to tell me but I didn't realize! Gut-brain connection. This dietary awakening combined with a maintenance Biologic and a wellness plan is working for me. I just had a full colonoscopy after 2 years yesterday and it was totally normal! I do wish my GI sent me to see someone like you folks the day I was diagnosed!

Seems am tolerating dairy products better, is it a bad thing? Won't they aggreviate inflammation and trigger a flare up?

I am 99% sure I have Crohns of UC :(. awaiting colonoscopy to confirm. One of my problems is HIGH cholesterol inherited. My LDL's hover at over 200 if I eat grains. On keto I can keep it under 100! So to get fiber now with my major gut issues I do not really want to add in grains and have my LDL's go nuts again. Just adding in oats got it back up over 200 my last blood test. Any suggestions?

I am also suffering from the same disease.

can you please mention your Instagram id

mam I am colities patient my fecal calprotectin range 2300 please diet and medicine share me i waiting for your answer

thanks for this video, quick question, do you consider coconut oil and coconut milk with the same effect? Thanks

It's a very terrible disease, my 15 years old boy has had it for 8 years. His doctor just said that the medication that he is on will be his last hope, after that, only surgery and I said No, surgery is not on the plate at this point. So I started a strong diet and fasting with him, yes he lost weight, but let me tell you, it worked and I believe he is in remission, no more going to the bathroom in the middle of the night, and dropping from 10 trips to 1, he uses the bathroom before going school, I guess a precaution. I think I will make a video and post it, I just don't know how that works.

p̶r̶o̶m̶o̶s̶m̶ 😅

Mam how i decrease my fecal calprotin plz share deit plan