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Thank you

Thank you

I am a new ostomate and yesterday I had a huge likage OMG! Didn’t know What I did wrong and went to a panik state! Forgot how to put the pouch I just knew to take a shower and dry off.!!! I dried myself out the powder for the skin then the spray then again the powder finishing with then with the epray I put the ring on the stoma!!! Of course was wet! Was waiting to dry off if course it was not drying so I put it far from the le Stoma and put the pouch And the ring before the pouch sommmmmmmm

Bless you. Thank you for sharing.

I've always wanted to do this but I just couldn't do that to my stoma ,I can't bare the thought of touching it

How to avoid bad smell from your otoscope bag

How old were you when you had to use that bag? Thanks for valuable information 🙏and if you were to go through all that experience at the age of 65?

Does gas go into your bag after surgery ? Normally, it would release through the rectum. And, if it does go into your bag, how do you handle it? Also, do you really have to stay off work or driving for weeks just for the colonoscopy? Thanks for your help.

Hi Brother, love your vids Did they pump you full of gas like they do when we had a working bum? Or do they do it without inflating your colon? I am having mine this month as well through my stoma.

Thank you! I’m going in Friday for mine…you’ve relieved my anxiety immensely 😊 I’m in Canada, so I’ll be awake, but sedated

I completely relate with all of this. I had so many abcesses and fistulas too and it was horrible. Trying to work long hours at work really stinks. I had my stoma surgery 5 years ago and it was the best thing. Thank you for this video.

I believe I have this and every 1 to 2 months I have extremely bad pain but the hospital who told me I got slow transition sent to another one and they’ve said I’ve just got a bad tummy and guess this is what I have for the rest of my life

Hi Sydney, thanks for your valuable and helpful videos. I had my stoma surgery (colostomy) back in Aug 2021 due to colorectal cancer which was very low so entire rectum had to be removed and in that process there is a high chance veins which supply blood to the organ gets damaged or cut. I was not explained in detail about ED but that would not have changed my decision. I have this issue and unfortunately Viagra has not helped at all. Not tried any other options and don't know if there are any trusted and proven options out there. Waiting for an appointment with urologist for last 10 months. Thanks to you again and everyone who has contributed. if I can be of any help, please feel free to reach out.

This is really helpful. So many videos are from the USA which has different practices, so it's good to hear what goes on in the UK. I had my colectomy and permanent ileostomy in 2015 after ulcerative colitis leading to colon cancer, and they left a rectal stump. I have had 2 parastomal hernia repairs which both failed (the last one in 2018 led to sepsis and further hospitalisation). I was then referred to a different hospital in another town at the end of 2018. Since then it's been a comedy of errors and I've been waiting over 5 1/2 years for my operation to correct a complex parastomal hernia which is now spreading to my midline incision. They have decided that I need Barbie Butt surgery because there is still inflammation in the rectal stump which continues to put me at greater risk of developing another cancer. Your description of the aftercare in the UK is extremely useful. The next step in my journey is the pre-assessment with the anaesthetist, having seen the surgeon last week, and hopefully I will get a date soon, although I'm not holding my breath as we've been here before. You've given me some pointers to put on my list of things to discuss with the anaesthetist. Many thanks! Good to hear how well you have done, and that you have good quality of life now. IBDs are the pits, aren't they!

Thank you so much for sharing.🫶🏾

I have a colonoscopy bag i go for my appointment in 2 days they found a tumor in my ct scan so have to get a colonoscopy ..

I have ibs, nothing else, and I've never had to consider this surgery for myself or anything scary like that, but your video was so comforting and informative that I felt reassured should that ever happen, there's your content to soothe the nerves! So thank you for making this info available to those that need it and those that were just learning! I'm so glad your quality of life is better now post op~ from South Africa

@sydneystoma385 Thanks for posting this. I have started stoma irrigation and it has made a huge difference. One thing is that my lower back muscles have been sore since I've started. Did this happen to you?

I've dealt with diverticulitis for 12yrs...3 months ago I went into emergency surgery because it perforated into my body I was in MAJOR PAIN not really knowing if it was from my diverticulitis or something else...long story short it was from my diverticulitis..the pain going through this procedure was pretty real..I was going through social media and the internet to search for answers and help on questions and found your story on what you went through and it's answering pretty much what I need to know and do to carry on with my life...Mahalo for sharing your experience and story to everyone who is dealing with a stoma and tryna move on with a sort of productive life 👍🤙

A very informative and reassuring demonstration. Thanks so much for sharing. So glad you're enjoying the benefits.

Thank you for sharing your experience with us.. i'm student nurse of asian country .... i had never seen this procedure practice our hospital settings ... i learnt lot of things ..and i again thank you to ..god bless

I'm sure there must be different programmes, I was told to specifically avoid milk, so no coffee or tea unless black. Also instructed to drink at least 250mls per hour of other drinks to prevent dehydration then nothing at all 2 hrs before procedure.I still have a rectal stump so have to have a sigmoidoscopy at same appointment. Booked in for this monday, 22nd Ju!y....not looking forward to it!!🙁🇬🇧

NOT peristalis but peristaLSis

I hope all is well with you, Chris. Cheers from Down Under. 😊

You sir are an absolute savage. I can only hope to one day have my situation in check the way you do. My ilyostomy makes it a little tougher. I wouldnt imagine in all my days of having to do a car change. That in itself just made you like an ostomate john wick to me lol. Great job God Bless

I'm hoping the pain isn't going to be as much as it is now 😢.... I have to wait 18 months to 2 years to have the operation on the NHS 😢

How long did it take you to heal?

Had a perianal abcess year and ahalf ago and just got one again a few weeks ago went to doctor and it already drained on its own and they prescribed me antibiotics and now i think its forming into a fistula but i dont have any pain going to thw doctor again soon 😢

Thank you. This has been extremely helpful. My sons recently had surgery for abscesses and has three setons. He was diagnosed 10 years ago with undetermined ibd. The surgeon said 100% crohns now. This has helped me to understand more on what is going on. I look forward to watching your other videos. Thank you for doing these videos!

hi , great info,i have uc, ive given up drinking and have noticed a considerable improvement in gut health,i was a moderate drinker and drank most nights it has to be a personal choice ,but just wanted to add that in thanks ,ps lagers really did leave me bloated to

i said this so often to my wife, i cant remember this or that this is the first time i learned about the name fibromylagia

It feels sore and uncomfortable all of the time.

Thanks for this good information had a stoma for 16 years now the rectums had it so painful need the Barbie butt that packing sounds bad. can’t take the pain of the stump no more might have to do it this year I get on with the bag fine my stumps never been great after the first surgery all them years ago tbh.

Sir God bless you for such an informative and well done video. Your casualness and relaxed manner really put people at ease to those unfamiliar with this. My new partner has had a colostomy due to cancer and I am understanding how this all works. Many thanks.

Thanks for sharing

My wife is divorcing me because of my colostomy. No sex in 4 years since my operation. I have a parastomal hernia a year after the op. Now she's decided she can't handle it anymore and is leaving me after 15 years. This stoma ruined my life.

Chris, I'm curious if you've heard of this product being available in the U.S.? I've got a permanent colostomy. Like you, I've had difficult with Coloplast Mio product as it doesn't adhere well for me. I typically go through 1 or 2 a day and can't get in the pool and swim laps like I'm used to. I'm relatively thin but have a problem getting it to stick in the 9:00 position. It appears that the Pelican Modavi has a superior sticking ability and I'd really like to try it. Any knowledge of how to get it in the U.S.?

You commented that you took a medication that caused you to virtually flood your stoma bag, could you tell me what that medications name was. I'm heading in a direction of having my colon removed and I'm using multiple enemas to try to empty material out of my colon, but they haven't given me any medication that would promote peristalsis. I would like to have this medication in my medical arsenal if you know what I mean. Thank you for this video, I've subscribed, and will be going through your other videos to get your experiences and wisdom.

Hola qué función cumplen las Irrigaciones en Ostomas?? Soy de Argentina y tengo una Ileostomia definitiva y la verdad es la primera vez q escucho de este procedimiento en Ostomas!! Graciaas y espero respuesta? Desde ya agradecida!!

I use Gas tablets they are ok in Australia blue tablets doesnt help all the time but better than nothing

How do I get the convex bag ? Please give me the can you give me the address

Does your stoma make loud farting sounds and how loud is it?

Sydney stoma, are the coloplast bags lacking? Is this why you use pelican as well?

Sydney stoma, do the filters on the coloplast bags cause pancaking?

Is this a colostomy or an ileostomy?

I have a ileostomy for profound slow transit and it has changed my life ❤. I was on all the medication going from my Consultant and daily irrigation. I put up with it for 10 years and now I’m living. Good luck 🤞

Thanks Sid I noticed you are wearing a convex bag with a belt which is what I do. However, yours looks like it has stickers or something at each side with the belt. Mine just attaches. Does this help it not become unattached? 👍

Thankyou so much, I will try these on my father-in-laws bags

Not many positives

Chris. Thankyou so much for sharing the 3 vids. I am booked in for the same soon and I am very anxious. Also the info I have been sent is all describing a rectal procedure. You have really helped. Thanks so much