Is there anyone else out there that has used or is using Cymed products? I have both a urostomy and an ileostomy. I used to use both Hollister and Coloplast but would have constant leaks even when I doubled up on the barrier rings. Plus, I could always smell the odor from my ileostomy. My life was miserable, and I didn't think I was ever going to leave the house. So, I heard about an ostomy group at my local hospital, at the time I was living in AZ, and I went. Of course, being 27 years old, I was the youngest one there and felt very out of place. Going to that meeting was the best thing I had ever done, and to this day, I thank God for giving me that push out of my comfort zone, which at that time was my bed due to severe depression after my surgery. Anyways, the wound/ostomy nurse introduced me to Cymed products for both my ostomies. My life was literally changed from that point on! They are the best products ever! They move with and conform to your body! They have a charcoal filter that absolutely eliminates any odor. Because I have 2 ostomies and want to be discreet, I use the pediatric size bag for my ileostomy (probably because I never allow stool to remain in there. As soon as I can get to a restroom, I eliminate the stool so my bag is always empty). For my urostomy, I use the 9" pouch. They have bigger and smaller, but for me, I feel that is the perfect size for a female. Another bag that I always empty when I get the chance! I believe you can wear the barrier rings for added protection with Cymed, but I'm telling you, you don't! You cut them to size. I use skin tac wipes before I put on the bags, but you don't have to. I will also use Nystatin powder (prescription) if I have a sore by my stoma, then I will lightly dab the skin tac wipes on over the Nystatin, let it dry, then hurry and place the bags on before urine starts to come out. I have absolutely no affiliation with Cymed, but I'm amazed at how many people know absolutely nothing about their products. Even hospitals are amazed at how great they are when I show them. If you have any questions, please feel free to ask me! 😊
MeetAnOstoMate is a remarkable community of 41,453 members.
“Every morning with my coffee, I read here and feel wrapped in warmth - I hardly post, but it still feels like family.”
“Our oncologist literally wrote down the link; they said more patients need this website.”
“This place pulled me out of the dark. I went from lurking to living again.”
“At 3am, someone’s awake somewhere in the world. I’m never alone here.”
Hubz had a regular checkup with the oncologist on Friday (his numbers are improving), and as they were asking how he's feeling since surgery, they became curious about how he's doing so well with his ostomy, both physically and mentally. He credited doing research online, trying different things, and especially the support from this group. They were asking because they see so many patients struggling to adjust.
We described this group as folks with every kind of ostomy, some for days while others for decades, but all willing to share what's worked for them with the caveat that every individual is different.
We described the most valuable element as feeling like you're not alone in this. That really piqued their interest, and they wrote down the link. It seems they had a few people in mind that might benefit from the community and thanked us for telling them about it.
You know, we can't remember exactly who we learned about this group from, but we're grateful for it every day! Thank you all! 🌻
Learn more about ostomy accessories, and when to use them.


