Austin, thank you so much for giving some badly needed humor to this subject. I may be needing this procedure and I’m terrified. Was it actually painful as opposed to uncomfortable, cramping up, gas pains? I suffer from anxiety and I think I’d need some form of sedation. Thank you so much again! You are a very man! God bless you.

I’m applying it in 2025 and also my 9th grade board exams in 2025 I just hope that I got selected inshallah❤

I lost my colon to pancolitis

@almost Austin how you feel now ?

I had this done has I was experiencing some rectal bleeding found out it was no cancer detected but caused by haemorrhoids and also detected a inflamed bowel got a appointment next February to see a gastrologist

In the long run, this medication is worse than the disease itself. My lymph nodes swelled, I had a 40⁰ fever, sepsis twice, hair loss, and heart failure... Not to mention that it didn't reduce the Crohn's inflammation at all.

Actually your finger showcasing 4 annoyed me😂😂

I think this is for people who have an old Apple watch they upgraded from and want to still use it. $80 is high imo

Brilliant video. I can relate to this 😂😂😂

I think the moment you lie down it puts pressure on the colon. Also, the moment you decide it's bed time the body starts to flush remaining food waste in the bowels and this stimulates colon as well. (I think it has to do with getting ready to detox while you sleep)

Bandhanghan Vati for planet Ayurveda supporting healthy functioning of the intestine

HI AUSTIN MY MY NAME IS PAUL MY WIFE AS BEEN AND GOING THOUGH THE SAME AS YOU BUT SHE AS ALSO BEEN INFORMED THAT SHE AS CROHN,S AND WILL BE NEEDING A BAG AND SHE IS STARTING THE INFLIXIMAB INFUSIONS SHE IS IN SO MUCH PAIN AT THE MOMENT CAN YOU INFORM ME IF MY WIFE WIL BE HAVING STERODS AS WEL AS THE INFUSIONS THANK YOU PAUL

How are you feeling today man?

Does this also work for video?

This is great of you want your younger child to have a phone in the Apple ecosystem to communicate and track without connecting them to the entire internet. Looks like I found my kids Christmas present. Also helps I bought a new watch so I have an older one for them to use. Excited!

OK so I'm a FLEX semi-finalist and a very pessimistic person regarding my life and expectations, but a huge optimist in other people's lives, so although everyone is telling me that I shouldn't be stressed and that I am a guarenteed finalist I still have that one little crumble of insecurity in me. So my interview is in 2 weeks, and I already started preparing for it just to calm myself down and be sure that I've done everything that is in my power to be accepted in the program. This, and many different YT channels and videos helped me so much. THANK YOU❤

I started steroids today. Thank you for sharing your story.

I've had Crohn's for 33yrs and am going to get my 1st infusion in a few weeks. Can't wait! Good vid by the way, much appreciated.

I have my FLEX interview today. It's my second time being a semi-finalist, but I'm still very nervous❤❤

My 3rd round interview of FLEX is next week i am going to try my best THANKS!

it is 1 44 pm and my interview is on 2 40 pm for yes program wish me luck

I am semifinalist of flex programm and my interview soon, after 7(may) month results will be announced ,i will write my result😅

This product does NOT exist!

Getting that Pfizer shot will be the ‘cause of your health issues substantially taking a hit.

this video was one of the main reasons I applied to UNF, and now 4 years later I graduated :) so thank you! Love UNF ❤

Hey bonjour du Québec! We are octobrr 14th 2024. I am 37 yo and I began feeling weird with my intestinal bowel movements and bladder since 2004. At first it was just a tendancy to have diarhea. Then it was in university that suddently I bagan having emergencies with transport. All of a sudden having inflammation and pain in the rectum and being unable to empty my bladder. Inflammation while peeing. Pain in the intestinal. Then anything caused me diarhea. With inflammation..... I got urologist diagnostic of IC prostatitis. But in 2018 my situation worsen. And I got diagnosed with Ulcerative Colitisis. 6 years of trearment make it better. But I never was able to be confident enough to work since 2008.

How r u Austin. U r not on Instagram now. Please update how r you doing.❤

Tim Redmond “power to create” 2011

Hi Austin, hope you are still at quite good health. I've been following your videos for several years now, and I always especially liked your open minded appraoch to new countries and the style of life and habits of the people there, and your reflective way of commenting. Would be happy to get an update of your life now after studying is finished. Back to Germany some time? ;-)

I sent my 72 year old brother some research about how to turn the UC off.Basically research and you will find that people are using the science of D3 3,000 to 5,000 .Build up your D3 levels with blood tests to get to 72 to 105.NOW, you will need 400 mgs of magnessium to stop any calsification and importantly us K2-100 mgs. High stress lowers D3 so a person may have breakthrough and need to go up to 6,000 units daily or 7,000 for a month or two. Study: Vitamin D3 alleviates inflammation in ulcerative colitis by activating the VDR-NLRP6 signaling pathway. Inflammation is a key factor in the development of ulcerative colitis (UC).Feb 8, 2023 I can tell you how D3 worked for me 15 years ago when I was 50 and I had severe allergies, colds and flues since childhood. 3,500 mgs of D3 ,400 mgs and K2 100 mgs and I have been perfectly healthy for 15 years when my immune system had the D3 to modulate my immune ......IT WORKS BUDDY .....now heal and back to school. Here is a patient that used D3 for the UC immune modulation. " I started taking 3000 IU a day after a flare up of UC in Dec 2019, when I found out it was an immunoregulatory (good timing for the pandemic too, gave me a bit of a head start). Since then, I've had 3 Vitamin D blood tests, incrementally increasing my dose finally to 10,000IU (+K2), and getting where I wanted to be >50ng/mL, (actually at 70ng/mL). Since taking the Vitamin D, in the 2 years, not only have I not had any UC flare ups, I've not had any flu or colds, unless you count a minor sniffle that lasted about a day. What did surprise me was that the occasional aching back and joints I had also disappeared. I regularly tell my friends the importance of Vitamin D, and some take it, but often forget for weeks at a time, some still think it's a coincidence, and some saw Hancock in Parliament say tests showed it was ineffective (he lied, there were no official tests). It's very frustrating when it's such low hanging fruit."

In a group opinion can you drive two hours after the infusion....anyone anyone lol?

I know this was made 3 years ago but I am due to start my first infliximab (remicade) infusion next week. I am going through a pretty rough flare at the moment but It’s next line of treatment. I am nervous about side effects. Did you have any long term side effects while on this drug? Thanks for the videos it did help cheer me up. I hope you are doing well and feeling better.

That's a great way of putting it! Obviously a cement company could not offset their carbon because they'd end up spending more than the price they'd get for the cement planting trees etc!

KEEP A STRAIGHT FORWARD ANSWER

The more you think of it the more you get scared of it. Just stay normal and calm. Eat diet which can help you with your UC. do exercise everyday. And stay happy. Forgive everyone. Ask God for recovery. Amin.

I can relate to everything you say. I'm in my 60s and having it tough too. It is a crazy condition that just makes life uncomfortable. But please hang in there. You are very inspiring ❤

Is public transportation easily available to commute to campus?

The most idiotic idea they came up with for a crisis they started at least 70 years ago😊.

Yes, I was waiting for acid rains.... the trees, crops, animals, etc probably too. What a clever, innocently looking nerd. 😊 I wonder if he has kids or is a tree lover 🤔 Naaa, definitively not.

Try health carb course for ulcerative colitis

My son was diagnosed with UC at the age of 19..😢nightmare for a mother.

Hope ur doing good now dude! Would love another update. Thing about ibd is their really isnt alot of people sharing experience with it, whether afraid coz of the stigma or what not so these videos of ur experience with uc have been great! Maybe just me but nobody talks about anxiety with uc but since getting ill i get afraid to go to public spaces nowadays🙃 wish their was an ibd group chat or something sharing tips and experiences 😅 sounds stupid but idk maybe it would help🤦‍♂️

So if im just trying to post one photo only if I archive and wait 2 days it won’t post on feed? Wish I had the option like some ppl do to just post on my profile without the world seeing it

Change your diet right away! You may still have time.

Just failed remicade. I’ve had hair loss and the texture of my hair has changed. It only helped the first infusion then stopped working for me.

Hey Austin, how are you doing now? I've just stumbled across your channel when searching Sigmoidoscopy. I was diagnosed with UC 29 years ago and actually ended up having a total colectomy 21 years ago. Back then we didn't have youtube videos and people sharing experiences it was all very scary. That said, my life is way way better post surgery than it was before. I have a J pouch and it changed my life!!! I love that you have shared your journey here and grateful for the real life experiences and information available to people suffering with IBD these days. I wish i had this 30yrs ago. Your sigmoidoscopy video really helped me as despite many colonoscopy's and major surgery i've never had a sigmoidoscopy so bit nervous lol. I hope you're really well and healthy and thank you for sharing ❤

Matt’s got good joke premises. He just can’t deliver it and doesn’t know when to turn it off. Also he’s starts at a disadvantage with a nonsense stage name.

Bring back the vortex game and I’m in

Hang in there mate, it’s hard but keep trying and looking after yourself.

I’m polish and I live in Germany and I’m going on Erasmus to Barcelona. My Spanish level is a C1, do you think I might have a higher chance to befriend locals? I mean im going there to improve my Spanish