The Cancer Survivors Network (CSN) is a peer support community for cancer patients, survivors, caregivers, families, and friends! CSN is a safe place to connect with others who share your interests and experiences.

Thank you for being a part of the Cancer Survivor Network community. Survivors and caregivers like you have played a unique role in fostering an online environment that encourages connection among those needing support, community, and education. On May 28, the Network will be discontinued. More details are available here . If you have any questions, contact CSNSupportTeam@cancer.org. Thanks again for the support you’ve provided each other over the years. We remain committed to supporting you in other ways throughout your cancer journey.

new to ostomy

FlossiesBaby
FlossiesBaby CSN Member Posts: 1
edited March 2014 in Caregivers #1
my 86 year old mother underwent her second "emergency" surgery for colon cancer last month - and this time came out of the hospital with a permanent ostomy - as well as Xeloda chemo to reduce the 2 "very small" malignant nodules remaining on the colon. She seems to the coping with everything fairly well....except the apparently enormous amount of gas being created each day by her system - we're still trying to find the "right" ostomy bag combo for her needs, and the current set doesn't have a membrane that leaks the gas out, so she's having to "burp" her bag many times a day - is this normal in a new ostomy - or perhaps a side effect of the xeloda? any thoughts - and any thoughts on a good bag combo to use? I'd like to make htis a 'painless' as possible for her.

thanks