Відео

They’re so many natural remedies you can do without any medication. I’ve seen several gastroenterologists and they didn’t help and just wanted to push all the drugs and/or remove my colon. Being disciplined and doing my own research has helped me tremendously to learn how to fix myself and stay into remission. Good luck to you 🙏

I am also suffering from the same issue but i just want to know can a lady conceive if she is having uc… if u have any knowledge about it pls share… can i conceive and will it effect to baby and what if all good but in between of the pregnancy if symptoms again flare up that what can i do ? Pls share if u have any knowledge about it plssss

A more natural and more effective long-term approach to Crohn's and Colitis than the standard medical treatment is presented in an excellent evidence-based book by Galina Kotlyar: Crohn’s and Colitis the Flare Stopper System: A Step-by-Step guide based on 30 years of Medical Research and Clinical Experience. Also see You Tube video: Full Cabbage Juice routine for ulcers by Dr Garnett Cheney

It is definitely possible to manage UC effectively and restore the quality of life. Planet Ayurveda's herbal medications will help a great deal to achieve this: Vatsakadi Choorna, Kutajghan Vati, Pitta Balance and Arjuna Capsules.

Many people said in comments under carnivore diet videos that their UC got better or healed. I would listen to them and give it a go

Try the carnivore elimination diet immediately!!!!!!!!!!!!!!!!!!!!!

Now my bleeding didn't stop doctor prescribed me azithioprine can this stop blood

I would say my UC is being managed because i have a Freedom Time Window in my day, usually in the afternoon when i can go out and do my shopping, meet friends.....etc where i am not worried about having to rush to the bathroom. There has never been Pain....and only in the beginning, B4 diagnosis that i was getting a lot of blood come out ! It is amazing Jacob how fit & strong you have become, despite this CRAZY disease. I am just thankful I haven't got bowel cancer !

I'm curious, what does your diet look like? Maybe you could make a video about it?

❤️🙏🙏🙏🙂😴

It does make me feel depressed sometimes but it's good to laugh about it and accept this condition.😊😂😢❤

Thanks, Jacob for this video. It is very relevant to my immediate situation.

Recently found your channel Jacob, hoping to watch all your content! If I can ask, what do you think about IBD and Cannabis? Have you ever had any experiences with it? Would you ever do a video about it? - Thanks!

Inflixmab

Funnily enough, my weight and muscle is more than it ever was pre-Crohns. I think having had weight that is barely even existing anymore, I really started loving food and my body fat afterwards

I've had UC for 27 years your information is great, keep going with it. thanks

Thank you so much. My flares are much milder than yours, but I understand a lot of the feelings you’ve had.

Why do you think that IBD is incurable when there are many who have recovered. They have been on remission for years. Diet along with exercise and a healthy lifestyle are the medicines. It may take a while but patience and consistency is the key. Keep fighting . A positive mindset can also accelerate healing.

My healthcare provider is a useless gastroenterologist. This is my fourth one!!!

I just made a donation. I hope Mihail can get the treatments he needs to recover. My hope is that Mihail will recover, and he will use the pictures of him in such a bad condition as motivation for other people to not give up. -Btw, I really like your channel Jacob. I agree with all of your advice!

It's tough to see when he couldn't even get a clear diagnosis to find a solution to his issues.

I agree with your point of getting enough sleep. I think it's one of the most important things to do for IBD. I sometimes get into a really deep sleep when I have a flare and feel very fatigued and when I wake up I usually feel loads better.

I just got out of hospital with full pancolitis and I am so scared of all of this. Thank you so much for this resource it really means a lot to me and my family (had my first son about 1 week before the hospitalization).

I m hope less you gave me hope

Bro i have alsarative colitis I'm 20 years old its been 2 months. When should i start gym and i am 5 feet 9 inches my weight is getting lesser day by day. How can i go at best in this joirney.

I’ve had Chrohns for almost 10 years now. Been in a flare the past 2 after prednisone stopped working. Appreciate you telling your story. Let me know if you ever want to podcast and talk about this or anything along those lines!

Thank you for sharing 🙏 i am also going through the same problem. Hope it will get better

Hi, Jacob.my child is suffer with uc she had taken pentasa that is mesamiline for a two month after she finished the pill she was get relief for two or three weeks,after a while she saw blood and begain the pain again .I don't know what to do ,now I am trying to help her by reading books focusing on best food for uc .Jacob will u advices me fo my child.she is nighteen yrs old.

Thanks for documenting your experiences it makes me feel normal 😅I was also worried about catching colds and virus’ but I haven’t had one yet. It’s my 1 year anniversary of starting Infliximab. I was so poorly, this time last year I was 49kg I’m now 60kg. I lift weights and lost all of my muscle when poorly 💪🏻 I was in a bad way from the illness and also the IV and oral steroids which have horrific sides. I’ve been watching a lot of IBD content lately just remembering the trauma that was last year 😂 I’m so grateful and lucky that the Infliximab has worked for me

I just got diagnosed with UC a month and a half ago still in my 1st flare..thanks you im feeling so validated in what has been going on with me physically and mentally... ....And you've managed to make me laugh about it. 😅 Subscribed!! Peace & blessings from the USA

Hi Jake - thank you for your great work and time taken to explain more about the condition. It’s good to know that it’s possible to change meds if needed in order to reduce the side effects. We have been told that people with UC are unable to join the army - our son was actually pleased to hear this! He stated that the UC may save his life in this instance 😂 he was dreading the idea of conscription as threatened recently. God works in mysterious ways ❤😂

Everybody suffering from ulcerative colitis needs to see your account of your experiences. You've described exactly how I felt and thought before and after I was diagnosed recently. I'm 74 and have been pretty free of illness all my life. You're right - it's tough. Thanks, Mate.

Have you tried carnivore diet? How long did you eat only meat for?

Hi thank you very much for your excellent explanation your of IBD, I have just been diagnosed with the same problem I am 72 years old, Healthy all my life suddenly after my wife died I have the same symptoms you describe and I did not understand what was going on, fearing the worst I had the sense to go to the doctors who sent me for the camera up the rear, She explained why, but not in laymen’s terms. I found your experience and the way you explained it (in understandable English) in a weird way a comfort I now know its not the end just an obstacle and containable. Thank you again

Hi Jacob, I was diagnosed with ulcerative colitis 3 months ago. It’s nice to know I’m not alone in this. I’ve just come out of hospital the last week. I took myself to A&E, I was kept in for week. I’m now on steroids and mesalazine. Thankfully the bleeding has stopped, it feels like I have to keep my gut calm and quiet. Sorry to ramble on but thank you

Thank you Jake for sharing your ulcerative colitis story. My story was similar to yours in many ways. I also received inflectra while in the hospital, and within 12 hours I started to feel dramatically better. Two months later I was hiking and playing basketball again. But after the stressful Christmas Holidays, I experienced a minor flare. I haven't produced antibodies to inflectra, so I'm still receiving inflectra infusions. Thankfully, prednisone pills and mesalamine enemas put me back in remission. I'm a big fan of the liquid mesalamine enemas because they work directly on the inflammed tissue. My long term hope is to eventually replace inflectra with occasional hyperbaric oxygen treatments, and continue to use a maintenance treatment of mesalamine enemas. I think this would most safely treat the body both locally with the enemas, and entirely with the hyperbaric oxygen. We'll see! Anyway, I wish you continued good health!

Ahh brilliantly said Jake. Thank you so much for putting your experience with UC out there. You really don’t know how much you are appreciated here😅 Everything that you have described is what our son has been experiencing. The blood… oh my goodness… the blood and trying to provide a stool sample when it’s just liquid! Also the fear of not knowing what is causing the pain. So glad that you are doing well on the meds and healthy lifestyle. You look really well! Our son is being weaned from the prednisone by tapering down and has started a routine of Pentasa and Aza meds. He’s also been lifting weights and has gone back to playing tennis for the first time since last October 👍 Quite a journey!

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Another booty-full video😂 very cheeky indeed 😂 you are cracking us up 😅 ❤

Better out than in!

Hi, Jacob. You’re awful young. I’m sure this disease is very scary for you, as it is progressive. I’m 56 now. I had IBS in my 20’s and 30’s and progressed to IBD/colitis is my late 30’s early 40’s after getting a bout of altitude sickness that took well over a year to clear up. That’s when I got my first colonoscopy. I think at 36. I was officially diagnosed with colitis at 46. It is getting worse. I started on rectal Lialda, progressing to additional oral once a day to four times a day with steroids. Injected Humira didn’t work for me - after fistula diagnosis. I’m now on Renvoq. Been on this two weeks, so it’s undetermined if it’ll work. Honestly, I don’t know if people are really healing themselves. If they are, I don’t think it’s the same disease. I’ve tried everything. Not taking meds is risking further disease and cancer. I think best to take the meds - even tho I too would like to get off them. Biologics are scary. Maybe they’ll find a cure. Thanks for the videos. It’s nice to know what someone else is thinking/feeling.

So, what has helped you?

Just done 12 days in the hospital, second time this year. Refused pred this time, that really is the bloody devil. did accept. Bude, at least I can sleep on this one. I’ve done all the diets in the world to fix it, vegan, flexitarian, fasting, fruitarian,,, fruitarian had the biggest success, but not sustainable going into the winter especially. But now on animal-based diet, which is basically fruit and meat. Getting great results, think I’ll be able to stick at this one. But it’s different for everybody, finding your own answer with this disease is a nightmare. good luck.

I've been on remicade/inflectra since March 2023. This medicine worked miraculously on me, and saved my colon. I recently flared, but I have not developed antibodies to inflectra. My gastroenterologist said that sometimes inflectra doesn't reach the rectum. I share your concerns about the long term risks of staying on inflectra. As long as you're feeling healthy, perhaps its best to assess your inflectra routine on a yearly basis, or even every five years. And try not to worry too far into the future... And certainly try not to worry on a daily basis. (But of course stay as healthy as you can, which I know you will do!) Good luck!