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I have suffering hemorrhoids from last 10 years.i lost my childhood to this disease .now it has become more dangerous. And due to this i have lost 15 kg weight.now my will to live has ended.i am not

Baldurs Gate 3 also helps me besides the 7 steps that are clearly excellent advice😝

Nice brother from India

Knowledge is important and knowing the negative effects in a real way can really change the way you live - it's a complicated topic and upbringing has a huge influence but it's not always so possible for the parents or children to lead healthy lives even if they know how to.

Do eat meat, fish, eggs and butter.

Hey Jacob, just got diagnosed with crohns in the last year, been super sick, unable to work out till just recently, it’s been harder than before, need more time between workouts to recover, muscles are sore longer, any suggestions? I eat super healthy, take a lot of supplements, I don’t overdo my workouts but still try to push myself..

amazing video thank you

Have you tried getting in touch with Josh Dech?

I got a mild moderate form mayo 2 just a little bit blood and mucus not a pool not so much to the toilet just 3 4 times and the feeling i cannot hold it is almost gone i dont need to poo when im always outside it is at the last 20 centimeters of my colon but i dont feel pain cramps stuff like that just sometimes leaky gut but just little drops but i stopped eating fatty proces stuff spicy stuff diary i can sleep trough the night just the morning i wake up i go 1 or 2 times to the toilet but i just got diagnosed recently and soon gonna be on mesalazine just keep a eye on your health see what foods make you feel good and stick to it talk with your friends family try to get support from everyone dont feel sad and sorry god gives everything for a reason i never smoked drinked alcohol just ate unhealthy once in a while. One thing i do have but hopefully the doctors will sort it out is that my poo is kinda yellow.

Great video, thank you 😊

can you make a video on training/working out with UC?

Have you got heart palpitations? I have been getting these since Remicade. Also what dose are you on? They upped mine to 10kg/MG every 4 weeks :(

Thanks for sharing

Hey mate. Have you been alright lately? Hope you’re all good bro. I enjoy your videos as they are educative and provide quality information into the life of having UC. It’s definitely a journey to live with UC but as long as it’s under control then everything will be fine.🙏🏼

btw I am not saying I had stopped biologicals deliberately, they have kept me going for many years. I will most probably continue to use another when needed. As well as grass fed meat, that I eat when I can, I had slippery elm recommended to me and this I like.

perhaps a 'whiteboard' about sleep, insomnia, sleep hygiene, importance of sleep etc you may have already touched on this unsure. Socialising and managing friends and family who don't understand. Hidden illness and issues with this. just some ideas, you may have already done all of this

I hope you feel better soon. Ulcerative colitis is rubbish, I have referred pain, but I think SIBO or bile acid malabsorption explains it. No one really has any idea, just trial and error all the time to get through. UC for over 20 years, several biologicals, recent Ustekinumab; made me feel unwell for three years. Started other medications made me feel stressed and anxious. Stopped biologicals for a couple of months and feeling more like myself first time for years. I know it is risky. Your whiteboards are really good and informative. oh I have gone carnivore, vegetable and fruits I am having trouble with.

Jacob you are a fantastic communicator, I have microscopic colitis, recently started Budesonide, not instant improvement, but promising. This Saturday, I felt best for ages, but then schoolboy error, I let my guard down and made some bad food choices, Sunday as well. Today really bad flare!!

Bro how many months your remission may last. Can you tell me how much time before your flare

This is a great reminder, thank you Jacob :)

I have smoked vaped daily for the past 45 plus years. Five days ago I quit so far lol. I do believe there is a correlation between blood in stool and the weed. To day no blood. Don't know I might have my head up my hoop. Been flaring for one month now. I am trying to heal with the Gaps diet, I have healed with the gaps diet before. If not I will be going for the biological drugs. Been on heavy prednisone dose four times in the last fourteen months. Being disciplined with my food choices is difficult for me but have been on track this time and seeing improvement. Thanks for giving me a space to unload.

Hiya Jacob, Do you have any suggestions for drinks? Flare & remission. I don't drink alcohol, never have really, or fizzy drinks, haven't for years, (or Dairy. I'm allergic unfortunately) but I do drink squash. Silly I know because they're full of crap. I do try to drink water, boring though isn't it 🥴😂 Any suggestions that I can replace the squash with? Love the channel mate. Thank you!

Bro please reply , does person with uc get UTI ??

Today I asked my gastroenterologist about hyperbaric oxygen + mesalamine enemas as a long term maintenance therapy. -I've been on inflectra for 1.5 yrs. I received inflectra during my 2nd hospitalization for severe UC. I was just skin and bones when I received inflectra. Also, I had a minor flare earlier this year, but I've been in remission from this flare for the past 6 months. Like you, inflectra worked miraculously for me too. Within hours after my infusion, I felt like a dark cloud that had been keeping me down just floated away... Anyway, my doctor said that he has only treated Crohn's Disease patients with hyperbaric oxygen. These patients tend to improve with hyperbaric oxygen treatments, but the treatments need to be sustained for a long period of time. And when the treatments stop, the disease tends to return. My doctor is not aware of any clinical trials of hyperbaric oxygen as a maintenance therapy for UC. I've seen some clinical trials that use hyperbaric oxygen for severe UC as an additional therapy to standard treatments. HOWEVER, my doctor isn't opposed to hyperbaric oxygen as part of a maintenance therapy if I can remain free of a flare for the next couple of years. That sounded very reasonable to me. I hope this info helps! -I'm feeling very healthy these days. I'm playing basketball most Sunday mornings, and I hiked Mt Whitney last month. This is the highest mountain in the continental USA, 14,495 ft!

I have a disability card now. Called in German. ( Behinderte Ausweis 80%)

This is more than disability to me..Because any health problems that makes. One not able to go out . Not having a rest yourself. Always in pain. Going to hospital everytime" is a disability Because you can't keep a job. Here in Germany the government will care for you" your rent . Monthly allowance. And health insurance. Everything will be paid by them. And those who also need a care give help. Will got it

Nice analysis man

Hiya, I haven’t been on infliximab for 10 years but I have been on it for 6 years, firstly I was diagnosed with crohns disease at 13 and was put on a 6 week diet of modulen ibd formula that worked like a charm as I was severely underweight,after the 6 weeks I was prescribed azathioprine and been on it ever since, when I was 15, I had a bad flare that caused an infection and my bowel was restricting and closing up, at first surgery was put on the table but I refused so they gave me an alternative to choose from, which was either infliximab or adalimumab, I chose infliximab. I can tell you the first time I had it it help with symptoms a few days later,then my bowel started to unrestricted itself over time, it’s a miracle drug and after being on it for 6 years and I’m going on to my 7th I can easily say that not only have I not developed antibodies as I respond to it very well like you, the only side effects that I have ever had was fatigue and sometimes nausea which is completely normal. Though not all people are lucky with the treatment, I do think a massive majority of people who receive it have continuously responded well too it. Of course there are risks, and recently I did come into a flare that has lasted for a while but it was due to a stomach bug I caught. I had my infusion again last week and I’m starting to feel relatively normal. So it’s still working after all these years.Hope this helps you and thank you for spreading awareness and helping people understand this invisible illness.

Jacob, I've had the same quick response with this med. Hours later I felt better,, AMAZING!!! I did get the major side effects of Lupus and bad body aches. Had to get off the meds,, but wow. This one did help the fastest so far for me. Been on a variety of biologics and immunotherapy meds and I would recommend this to anyone in a major flare and was in HOSPITAL condition. Thanks for all the Videos brother. Stay well my friend.

hi Jacob, have you tried going full carnivore or full plant-based? I've heard from both sides conflicting claims that going one or the other is the cure, what is your opinion on this? thanks!

Very informative and thank you for sharing your stories.❤

Am passing out mucus 24 hours. Sit in the toilet all day. Everyday. Am really suffering😭. My anus is itching so bad. Because of the mucus. I cant even sleep.

Thanks very much

Thanks so much. I was just listening to you all day. Am suffering from intestinal problem too. My result is out. After a long time of suffering. Going to my doctor tomorrow morning to get it. Then we can discuss way forward. Because am at my breaking point already😪

brother do you have h pylori

Ian is 5’10-1/2” tall and is now only 123 lbs! :( Everything in this video is what he’s been through. He is now anemic and weak. They want him to start iron infusions. He is eating heavy carnivore.

Is Mince Lamb? Thank you.

This was very helpful indeed! Thank you for all these great updates. Ian is on 80mg of Prednisone/day and Mesalamine they doubled his dose. His insurance is really bad/cheap from work. He is still at the high point of his initial flare that started in July (his first diagnosis) and was getting better after 40mg of Prednisone + Mesalamine. Then a member of his family upset him and the flare came on 100x worse! So stress definitely plays a part in this Ulcerative Pancolitis of his. Thank you again, Cheers. IAN and ANN from Chicago. :)

The comments in the forum would select for those who have done well, because those who had a poor outcome or died would not be around to comment. -Remicade/Inflectra saved my colon, and I've been on it for 1.5 yrs. I'm very grateful for this medicine. Nevertheless, I eventually want to get off of biologics because I'm concerned about the long term increased risk of cancer and liver disease. I'm going to see my gastroenterologist this week for a routine appointment. I'm going to ask him if there are any clinical trials that offer a maintenance therapy of hyperbaric oxygen and mesalamine enemas. I'm not in a rush to try something different, but I do want to eventually switch to something that is safer long term.

Do you still take pentasa as well?

Thank you this is helpful. I will forward to Ian (my bf) who has Ulcerative Pancolitis.

What is your camera setup? Does it rotate, or is it a 360 camera and software focusing/rotating?

Unfortunately this is not quick by any means - for kids and busy parents, something quick from the shop is essential for day to day life, it should be different but convenience wins and life is a struggle. Maybe Huel or another alternative is better for them?