Best Products to Conceal an Ostomy Bag

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lanabana
Aug 23, 2012 4:00 pm
Hi, I have read several different posts in which people reccomend different yummie tummie products, spanx products, and other things such as this. I am not sure which one to get or which one works best and these are things I dont think you can try on. My main issue is that when my bag starts to fill up its all at the bottom area and getting fatter and fatter. also when I wear jeans the surgeon and wcon said to make sure the stoma is above the jeans which is fine but Sometimes it doesnt work as well and different people have suggest wearing a spanx tank (longer one) does anyone have more specific advice or more suggestions, even if you have told me before?

Thanks Elena
Msj
Aug 23, 2012 6:32 pm
Hello I am new to the forum,
But I have had a ileostomy for over 30 years and 1/2 of those years I had urinary koch pouch, but just 6 weeks ago had to go back to a urostomy. But through it all I have experienced and learned a lot as far as how to cover up this or that. I know what work for me was girdles, they held my ileostomy bag in firm, but know that I have my urosotomy bag back I will have to get the longer girdles. But that still will not stop the bottom from getting fatter. I am just going to change the way I dress a little, more skirts, dresses, etc.. I just do what I have to do. and still be beautiful and fashionable. I have practically had these bags all my life. I am 45 and the wonderful thing is I have been doing fashion modeling for 15 years..I will be slowing down a lot now with having a urostomy bag, but I had a great time doing it..
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Msj
Posted by: Karen & Stella
Fay,

I am one of those few people who still have a lot of output at night. However, I suffer from short gut syndrome after seven bowel surgeries that led to the loss of much of my small intestine as well as my large intestine from the initial bowel cancer surgery. It does get better over time as your system adjusts, but an ileostomy can be a challenging adjustment. It's important to connect with a good Enterostomal Nurse - ET nurses who can help you problem-solve over time. It's been five years since my initial surgery, and I had a great visit with a new ET nurse in December. He really helped me with the problem of high output at night. I had been getting up every 90-120 minutes to empty my high output bag because of filling. If I slept for three hours without emptying, I would have problems. My ET nurse helped my husband and me make a nighttime collection system using a Rubbermaid juice container with a handle and my old CPAP hose. This is connected to one of my two-piece high output bags and allows for continual drainage. It isn't pretty, but it has been a real lifesaver. I guess the real message I want to share is to stick with it, find a nurse who you can work with, and together you will find solutions to whatever challenges you face. This website is also an important support for me and others. There is nothing you will go through that others haven't already faced and figured out. There is so much wisdom here. Read the materials they've put together for newbies. There are a lot of great suggestions to use. I hope things get better quickly for you.
Karen
Past Member
Feb 10, 2013 8:49 pm
Hi there,
I am currently on my 2nd ostomy (1 ile, colo) and what I wear any time I leave the house is the Phoenix Ostomy Support System. It only works with a 2-piece. You rotate your bag so it is horizontal and it sits right in a pouch. The pouch cover snaps so it is very easy to access when you need to empty. Check them out at www.ostomysupportsystem.com