Logo for MeetAnOstoMate
Support | Friendship | Relationships
26,891 members

Salts stoma bags

Wed May 18, 2022 12:34 pm
"This is the best website for people with an Ostomy, hands down. So much understanding. Everyone should join."

Black bags or any non see through  bags would be awesome !!!! But then again how many insurance would cover them 🤔

Wed May 18, 2022 1:15 pm


Abefroman1969 wrote:

I will have to look into it, having never heard of them I’m inclined to say no we don’t but it’s worth looking into, thanks for the tip Meadow, good looking out for us ungrateful colonists! 

You’re welcome Abe 😊

MeetAnOstoMate - 26,891 members
Wed May 18, 2022 2:54 pm

Rosebud 🌹

My blue cross insurance does cover opaque appliances in nude and gray, I absolutely loathe the transparent appliances and only use those in an emergency, I just feel unclean wearing a transparent pouch. Of the companies available to us in the US I prefer the coloplast gray, hollister I have ballooning issues and the pouches pill up and look like and old pair of sweats after a day or two and for some reason I just can’t stand convatec pouches, ballooning is a major reason but it’s not something I can put my finger on, I just don’t like them. It’s all about what works for the individual, I know several that can’t stand my preferred coloplast 🤷‍♂️. I do know that lots of us Yanks want to try the Salts Confidence BE® and now that we are aware of it the Pelican ModaVi platinum with vitamin E. The black appliances just look so sleek I may even want to try a white one to see if I can keep it clean. 

Wed May 18, 2022 3:45 pm

Thanks for the info i have that insurance too but because im not able to go back to work its state insurance for right now.I also use the convatec bags and i have problems with ballooning mostly at night and after a day or two they also look like there wrinkled right out the dryer...have no idea if its because its a 2piece the Hollister bags I used to use  when I 1st got outta the hospital but were a 1 piece and I had way too many problems.So I'll look into seeing if I can get a sample and go from there I had no idea it was available.  THANKS

Thu May 19, 2022 3:15 am

OK, so update: I’m no longer liking the Salts bags for me because when my output is more watery, it starts leaking from the outlet. The Salts bags will be good if your output is always more formed, such as with a colostomy. With my higher output ileo, however, I’m gonna have to regrettably say no. My output always goes more watery at least once a day, usually overnight when I’m only drinking water/juice, so by the end of the night it started staining my knickers. So I’m currently wearing the sometimes-itchy Coloplast bag, this one is convex again. I’m gonna look into trying Pelican, I’ll see if I can order come of their ModaVi samples. 

Thu May 19, 2022 6:36 am


Meadow Snow wrote:

OK, so update: I’m no longer liking the Salts bags for me because when my output is more watery, it starts leaking from the outlet. The Salts bags will be good if your output is always more forme...

Meadow,

😯 Oh no I am so sorry ...

I am a coloplast user too..I can't remember if you said you have tried the skin protective sheet?  The irritated skin is right around the stoma like a red ring or on the rest of the skin ?

Thu May 19, 2022 9:11 am


Beth22 wrote:

Meadow,

😯 Oh no I am so sorry ...

I am a coloplast user too..I can't remember if you said you have tried the skin protective sheet?  The irritated skin is right around the stoma like a red ri...

The skin in general, it feels more like an allergy-to-the-glue itch rather than an output-hitting-the-skin itch. Although I do get the latter occasionally as well, hence trying the convex bags. I’ve now ordered some samples from Pelican, so we’ll see how that goes. Once I be tried the pelican bags, I’ll talk with my stoma nurse and start thinking about what other products I can use alongside the bag

Sun Jun 26, 2022 4:24 pm

Sun Jun 26, 2022 9:18 pm
Hi Meadow Snow, I know how you feel, but I had an ileostomy back in 2013 for emergency reasons and are currently waiting for a reversal, but in the beginning my surgeon did not tell me much. I had to find out for myself by experimenting, but one thing my stoma nurse told me in the first few months is make sure I eat one thing every day with salt in it as you will be losing salt from your stoma and this will make you feel lethargic if not replace. I started eating one pack of ready salted crisps everyday because of this and this made a major difference to my energy levels. If you are now facing the prospect of endless products to use; Here is something I hope will help Ok :>

To prevent leaks, why not order flange extenders by Brava who also do the powder and spray that is in your video. I use them and I have not had a leak since, so try them and see how you go. I forgot to mention that if you see your Dr, you can get a Medical Card so that all your stoma equipment as well as your prescriptions are FREE and this lasts for 5 YEARS and then they send you a new one and so on as long as you have your stoma every 5 years.  I also know that Brava also have wipes that help when you have sore skin called cleansing wipes and they help cool the skin around your stoma and that you get 3 packets in a box and also ask your delivery company if they have mattress protectors for your bed in case of leaks in the night and also if they have complimentary bed protector sheets as I use these when I change my bag. I tuck one end just inside my underwear and let the remaining rest on my bed with all the other bits I need around when changing, and then when finished, I wrap the sheet tight with the old bag inside and then put it in the disposable bags that go in the bin. Also, if your seals are no good, then try Hollister's "CERA RINGS" as I have just started to use them and I have found that they are better than any other seal that I have used, which is why I told I no longer suffer from leaks. Hope this helps:> P.S. The Flange extenders by Brava are actually called "Brava Tape". I only have an occasional leak but nothing major, but I was told by a Fellow Ostomate which is what they call us people with Stomas, that always try new products and not to rely on one product because over time there is always something better if you develop problems later down the line. 

This is what I do now, as I have a parastomal hernia alongside my stoma therefore I have to alternate between two types of bag, one which has the biggest baseplate you can get for the two-piece and then I have my standard size baseplate, and this works as I do not get used to one type. If you want a reliable delivery company then I would recommend Securicare, who are based in Hertfordshire and I have never had a problem with delivery and if you forget to ring them to order supplies, they will ring you and ask what you require. They will ring at least once a month to check. I was with a Company called "Bullen" and I made and order one day, but never received it and I phoned for a new order and had the same problem so went with Securicare and have never looked back. They are very friendly and caring, and if you need to change products, then they will inform your local Gp.

Anyway, I hope this helps and just take it easy. It took me seven months to get back to normal. Keep a diary, so that you can see what foods make your output thick/thin and also what reacts with your bowel that will cause you pain. This way it will help you avoid foods that cause you grief. Take Care Sister Ostomate. :>

* Please, do not post contact information, personal information or advertising.
All times are GMT - 5 Hours