These forums contain all the announcements we've made about Ostomyland. This includes: announcements for community matters; notification of new features/services; maintenance alerts; known technical issues and more.
Please post petitions, board-run polls, sponsorships etc in this section (and not elsewhere on the board - thanks).
We do not allow surveys about product research, or which are intended for business purposes. We're a support board, not a flyer catcher for business adverts.
Want to tell everyone the latest news on your health? Here's where you can tell us about tests or operations you're having, waiting for and the results. Maybe you want to let us know a member is in hospital? If it's health-related it belongs in here!
Everyone has a story about their health which lead to them being here on this board. So why not tell us your health story? Good or bad. You may find people who have through the exact same experience as you, and you never knew it!
If you have excess products you would like to offer to your fellow ostomates, or if you are after some more supplies for free or a knock down price then this is the forum for you! Please note:Any and ALL transactions are direct between the two parties involved and are at your own risk. Ostomyland accepts no liability for any loss or damages as a result of using our Ostomy Trades forums.
I have a question about Ostomyland on fb, which was suggested I join by someone on this site. I surmise a lot of people here also belong to that fb group. My question is this: If I post anything will other fb friends who know nothing about my iliostomy see those posts? Same question goes for if I comment on another's post, will my unenlightened fb friends see them?
I have many "friends" who are nothing more than people I used to share coins with through games, whom I have never met, and are not personally involved in any way with my life. I think my question is one of not knowing how "closed" the group is.
This is my first time posting anything. I have had my colostomy for almost 4 years and I have held on to the hope for reversal through it all. Denial? Maybe. Anyway, my stoma prolapsed and was revised twice. No more will be considered unless I agree for permanent status so I endure. Because the stoma is prolapsed, it gets in the way and stems flow which is often painful. I am also prone to diarrhea and that hurts more because it burns. I can't seem to figure out which foods will hurt and suck at it so I avoid eating and eat when I'm starving. Generally miserable. It often feels like my intestines are churning and twisting itself in knots. I know it sounds strange but that's what it feels like to me. Foods that are binding like potatoes hurt because the prolapsed stoma gets in the way and other foods cause watery stools that burn. I need help finding food that won't hurt. Thanks.
Glad to see you got the first problem solved.
As for the second issue, I'm not totally sure what is recommended! But if I was going for OTC products I would use a natural vegetable oil based capsule to swallow with meals (Senna is the product I'm thinking of in the states.). Probably start with twice a day and then increase or decrease as the need warrants.