I am a college student and I would like to know more information about this subject in order to complete my assignment. I have been tasked to ask the community any ostomy related question in order to record my answers and pass down to my professor.
The answers may vary among ostomates. I have an ileostomy and I shower and exercise every day. Exercise for a colostomate can be a little more risky. But all ostomates have to be careful to not get a hernia. The older posts in the links below may be helpful.
I agree with Bain that the answers are likely to be different for each of us. They are also likely to be different depending upon timing and circumstances as exercise soon after the operation is going to be different to that which might be attemptedat a later date when things have had a chance to heal. There are no right or wrong answers to your question. I bath everyday, but then I irrigate and am not likely to have output to deal with in the bath. Other people have different circumstances so they will cater to them as they see fit.
I hope this helps
I've had an colostomy since 1976 (age 1. I never made any changes in how bathed other I didn't scrub my stoma, just regular bath soap. I do shave around my stomach as my appliance stays on better -,4/5 days between changing.
I never lifted heavy weight on a regular basis, that's just begging for trouble, - as ostomates we have a built in hernia. But water skiing, swimming, volleyball, rowing, horse back riding are all sports I have done competitively.
Hope this is helpful, if you have more questions, send me a note.
I am 71 yrs old and had surgery for an illistomey in Feb 2017. I exercise dailey ( almost) on the tread mill usually. Take a shower (all the guys accept my bag ) and I have not had any issues with it. I shower at night also and usually end up changing my bag (while in shower soI can scrub the adhesive off while showering)...makes things easier.I change the bag about every 3 days) If there is some poop leakage, it just washes down the drain.
If flying, I eat VERY light so as not to use athe airplane facilties. I do carry a card stating I have a medical issue that may require me using airplane facility at any time (unless they want to clean up the mess)
Ask me any thing else you may want to know
Feel free to e mail me at : ****
to take a bath you can leave the bag on or leave the whole thing off. I've never tried it off. you never know when your stoma is gonna start dong its thing. I normaly leave it everythng on. no problems. to exercise I'd tie that belt around me. they didn't just give it to me from the beginning. I had to ask about after reading about it. theres also other more protective belts that go over the bag. it depends on what your going to be doing.
I had my ostomy in 1986 aged 40, there is nothing I couldn't do up until recently, but I think it's now down to old age and the fact I have Parkinson's.
I used to work as a chef lifting very heavy pans and large joints of meats worked long hours too, I went swimming and to the gym, noi problems there either
My food never changed, I ate almost everything. I believe it's down to attitude think Oh poor me and that is how you will be, but think this is something that saved my life so I am going to live it and you will be fine
Hope this helps
Depending on the type of bag, some people like to shower with it covered (like with a plastic bag) because many of the bags now have a soft, cloth-like cover for comfort, but it gets wet and needs to be changed then. If you tie a plastic grocery bag over the pouch, it stays pretty dry. If you have the kind that doesn't have the cover, it's all waterproof and a shower doesn't cause any problems - same with swimming.
The food part is mainly an experiment to see if anything causes problems. I eat anything I want when I want - except for popcorn. For some reason, that causes me grief, so I just avoid it. You also figure out a diet that will adjust the texture of the output. If I overindulge in pasta and everything becomes too firm for comfort, then it's back to salads and more vegetable (read, more fiber) for a few days to thin it out so it passes easily through the stoma. Other than that, I have had very few problems since about 2 months after getting my ostomy when I figured things out.
Good luck on your project. I hope we have given you enough for your paper.
The same as usual......i.e. the same as before you had a colostomy. Cheers.
Two answers to this question.... when I shower, I place an inexpensive sandwich baggie over my pouch and tape it around the top and sides to protect the pouch from getting wet. I do not like a damp pouch against my skin. It also helps protect the seal of the wafer. When I bathe in the bathtub, I fill the tub to where it just touches the wafers edge. I will quickly rinse off and wet the wafer but I will not submerge for long periods of time and wet the pouch. I believe (but I am told this is not true by the manufacturers) wetting the wafer reduces wear time. I try not to wet the wafer or if I do, it is a quick rinse and I dry it off. Sincerely, LH
Hi ckaige. What's a bath?
Just joking. The adhesives work well for me so I have no need to cover my bag when washing. After showering and toweling dry, I make use of my hair dryer to remove all/most of the moisture - especially, as others have noted, on the back side where the covering is a felt-like material. Diet hasn't changed all that much. Just can't eat like a "New Yorker" anymore (meaning now I chew my food before swallowing). And I drink a lot more plain and carbonated water. I'm cautious with exercise due to the possibility of a hernia. However, I doubt the weight of our remote will cause much damage...
i have a colostomy this is my 3rd one in my life time lots of problems in past hoping most are all gone been good for past year, with the new one. i go to the gym 2 hours 6 days a week,i lift weight on the machines,i walk on the stair stepper and i use the tread mill. i am also into archery we have 4 course to walk up and down hills to shoot targets. plus i hunt when weather permits. some the biggest problems i have is heat i sweat it off then have to change, when it rains and i am soaken wet i have to change cause of the humdity i come apart or when taking a bath in hot water it does not stick very long after, i pat dry the waffer still doesnt stick to long afterwards so i just change. i also have to shave my belly mine is located up past my used to located belly button. i have not tried any of the sport tapes do to when the wax ring starts to swell it starts to leak, so i have to change anyways. if i dont use a wax ring i will leak in an hour of moving around and doing things.
I read where you said you eat salads. Do you eat lettuce and tomato as well?? I had my surgery on July 12th and I used to eat salad all the time. Is there some salad items that you do not eat?? I am struggling with putting together meals that I can eat. What happens if you get a blocked stoma?
What we eat is a very personal thing and different foods affect our systems in different ways. It's all about experimenting to see what you can and cannot eat comfortably. Personally, I like salads and eat them regularly although I gave up on lettuce because it gave me severe wind. I now eat watercress as a substitute, which I am led to believe has more iron content which is good from my point of view because I need to supplement this.
I believe that problems do not just arise because of the food but the way it's prepared, served and the way it's eaten. Small portions,spread over the day rather than in one go, well chewed (or reduced into small pieces) and plenty of liquid. Anything that causes a problem - stop eating, at least temporarily until the stoma settles into a routine, then you might try again, with caution.
There are a few past posts on this subject so you might like to browse through the 'collections' section.
As for blockages, I used to get them regularly but then I started irrigating and no longer have this problem.
Hi, Freedancer! Welcome to the club (although it is a club none of us was thrilled to join)! I noticed you just had your surgery in July, so everything is still very new to you. First, I want to reassure you that dietary issues you may be having right now will not necessarily be issues 6 months or a year from now. Your system is literally still in shock from the surgery and everything it is having to adjust to. Hold that thought firmly!
For the first couple of months, the ostomy nurses, doctor, and the dietician at the hospital all told me the same thing - stay on a low-reidue diet until your system gets readjusted. It will be very boring, and not the very best thing for your overall health LONG TERM, but is what you need RIGHT NOW. Then start adding back other foods a little at a time until you are back on a healthier diet. As you go along, you may still find a few foods that cause you problems - for me, popcorn is an issue and I just don't eat popcorn any more. I do miss it sometimes, especially when I go to the movies and the smell surrounds me, but I am much happier when I just don't eat it.
Second, you did not say whether you had a colonostomy or ileostomy, and that really does make a difference, from everything I have read here on this site. Apparently, with a colonostomy, you can eat more variety of foods without distress, due to there being more of the intestine remaining. PLEASE have a discussion with a registered dietician who has experience with ostomy patients. They can help set you on a path to healthy eating without long-term effects.
And please remember to have patience - it all will eventually settle down to the point where you will look back and think, "What was I so worried about?" I know it doesn't seem so right now, but I promise you, it WILL happen!