Ostomy: Adapting to life after colostomy, ileostomy or urostomy
It takes time to become comfortable with an ostomy — a surgically created opening in your abdomen that allows waste or urine to leave your body.
Many questions may run through your mind as you practice good ostomy care and live your life. It can help to talk to others who have been there. Perhaps you'd like to ask others questions like: What can I eat? What about leaks? Can I go back to work after colostomy? Can I ride a bike with an ileostomy? Will everyone figure out I've had urostomy surgery just by looking at me? What about intimacy?
Welcome ostomates. Let's talk frankly about living with an ostomy. Why not start by introducing yourself? What type of ostomy do you have? How's it going?
Interested in more discussions like this? Go to the Ostomy Support Group.
Haven't heard of Platypus Bottle. Will check. Emptying away from home is challenging. My output is like diarrhea all the time. Need experiences of others. My ileostomy as 3 yrs ago due to dismobility.
Thanks for sharing.
Cynthia
@angievaz29, you've been through a lot. It sounds like you've faced many different emotions and have arrived at a point of acceptance and embracing life. Have you been able to connect with anyone else in your age group who lives with an ostomy?
I hope you're enjoying the long weekend. How is the return to work going?
Definitely has been challenging for me and no I haven’t but I’m not really open about publicly and work was alright
Did you have to ask for any accommodations at work?
It looks like my ileostomy will soon become a permanent part of my identity. Going from a loop to an end with total proctocolectomy at to remove the unhealthy parts. Crohn's continues to attack and we continue to fight back, and every battle has its scars. I am so thankful that my friends, my family and Mayo Clinic are with me every step of the way 🙏🙏🙏
Thanks. Followed a suggestion of standing to empty bag. Much easier. The output on toilet easier to clean.. Need to add clip to my bag for holding dress.
Smiles
cyngirl
I had a colostomy on 6/1/2023. I’m doing fairly well. The difficulties I’m having are constipation and pancaking. Living in an independent living facility so am limited by food choices and taste changes from radiation and chemo following dx of throat cancer. Am trying stool softeners that I don’t think is working very well. Other issue is the ostomy pouch and adhesive laying on stitches from surgery. I’m told it may take 6-9 months before they dissolve. The pressure of the bag is enough to cause the pouch to be uncomfortable. Has anyone dealt with that issue? Thanks. Nancy
Gail Garrepy here. I have had my Urostomy now for six months. I also have a left ureteral stent due to a blockage in that ureter. I will need that forever. It will be changed out every few months. It drains into my urostomy pouch. I’ve adjusted quite well to it all. I bought a stealth belt and I’m back to my aqua classes and finally getting my strength back.
@a009507, I wanted to check in to see how you are doing. Have you managed to find a way to make the pouch more comfortable? Have you found a stool softener that helps?
Thanks for asking. I’m now taking Miralax everyday. It’s working and has no taste which is even better. Also, am using water to clean my pouch. It really helps to clean out the pouch. I continue to have problems putting on my pouch so it sticks due to stomach roll in the area.
The stitches still present an issue but it seems I’ve become more accustomed to the discomfort.