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I have tried most household products when showering with my ileostomy.

I take showers at night and usually change my appliance right after. I change my appliance about every 3-4 days.

Does anyone know of any good prodcuts that can prevent the bag and wafer from getting wet somehow??

I feel like I ALWAYS have to change it after a shower because it gets wet and the seal loosens up.
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I used a Hollister 2-piece system. I would always empty and then unclip the bag when I took a shower, leaving just the wafer on. That also gave me a chance to rinse the bag. I would use a hairdryer to dry the bag wafer when I got out. On days when I changed the bag, I would shower with the entire thing off, to give my skin a break.

Maybe try unclipping the bag if you have a 2-piece. Water made the bag heavier and perhaps the extra weight is pulling down on the seal and weakening it.
A friend who taught me a lot about ostomy care (She has had hers 21 years) swears that the best thing is a newspaper plastic bag taped to you is the best.
I don't get the paper.
so I fold my bag to make it a little smaller and make me a square of plastic/Saran wrap and tape that over my bag. When I had the huge open wound, I wrapped my torso in saran wrap. That's what my nurse told me to do. (then sponge bath what the saran wrap covered when I got out of the shower)

LOVE my "naked" showers on change day. Smiler
I pop my bag off and place it on the top of the toilet next to the shower. I shower, dry off the area around my wafer, and pop the bag back on, then continue drying off. I use coloplast products and the wafer never comes loose from getting wet. Love my change days when I shower with the wafer...I'm freeeeee..... :-)
I have a phobia of showering "naked". I have never showered without my bag/wafer on. Even when I haven't eaten in awhile, my stoma is constantly active and I can't imagine having stool come out as I'm trying to shower. There are some high tech products out there that I've been looking into. I have tried Saran Wrap and tape and blow drying and all that. Just haven't found something I'm satisfied with. Maybe I never will. Who knows.

Thanks everyone
I came up with something for my daughter that works great! She uses aqua guard 9x9 dressing protectors. They can be expensive but our insurance pays for them with a prescription just like the ostomy supplies. They are a square sheet of plastic with adhesive around the edges. You just fold up the bag and peel and stick! They work amazingly well! I think the cheapest I found them online for about $8 for a pack of 5. But because insurance will pay for them we just order from edgepark and they bill insurance.
When I had an ostomy I just tried to not direct the shower over the bag area too much and then used a hairdryer immediately after to dry the area. I was changing the appliance every two days. My stoma was to active to shower 'naked'.
I did findgettign that bag wet was a problem and did not think of taping a plastic cover over the area but that seems like a very good idea.
I, too, showered without the bag which gave me a chance to rinse it out....although I was told it wasn't necessary. If my stoma became active during my shower, it didn't bother me. Since I showered in the a.m. before breakfast, it never was that active at that time of day. Every seven days when I changed my wafer, I showered without anything "glued" to me. What a pleasure!

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