Hi ostomates! I'm new here, so I hope I'm doing this right :)
I'm currently 7 weeks post-op from having a revised stoma and Barbie butt created. A couple of days ago, I went to a follow-up appointment where we discovered my wound had completely opened up and was not healing. I was immediately admitted and sent to the operating room to get a wound vac placed in my bottom.
A little history of my recovery from the beginning: the first two weeks went perfectly enough. I still had the dissolvable stitches in place and an abdominal JP drain at this point. At my two-week follow-up, my surgeon told me I was healing really well and having very little drainage from my bottom, so we decided to remove the JP drain.
The following day is when I started noticing more drainage from my bottom, which was expected because the drain was no longer collecting that fluid. At 3 weeks, I returned to work full time. I work remotely but am required to sit 8 hours a day. I didn't sit directly on my bum; instead, I alternated sitting on my sides as much as possible. Unfortunately, the draining just continued and worsened. At 5-6 weeks, my stitches were dissolved, I still had a lot of discomfort but not much pain at all. The only thing that concerned me was the drainage; I just thought I was healing very slowly at this point.
I'm back home today, two days after the vac was placed. I'm told the vac should help keep the area dry and promote healing. I'll also have to go back once a week for wound care and to have the dressing replaced for the next 6 weeks (under anesthesia in the OR). I've decided not to go back to work for the full 6 weeks this time. This has been very stressful for me.
I have a great deal of support from my husband and family, but I still would like to hear from anyone who has had this surgery and/or a wound vac. How was your healing process? Did the vac work for you? Did you have any leaking with the vac? Was it painful the entire time? How long did you take pain meds? I was given 28 pills of 5 mg oxy, but I don't like taking them for fear of becoming dependent. I also ordered Collagen Peptides protein supplements. Has anyone else tried this, and was it helpful?
If anyone has any advice on anything or questions, I would be grateful for them. Anything at all would be appreciated.
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Hi Hatlady and all,
I've had my ostomy for over 50 years, since I was a kid, and didn't think I really needed to be part of the ostomy site. But once active, I came to realize, that although I may not need help at the time, I was able to reach out and help others in need. Back in the day, before stoma therapists, I use to visit new patients in the hospital or homes ... While professionals are great, it is also good to be able to speak with people with personal experience. I was a free member for awhile, but after writing often, I was given free months. I then started paying, and decided to just take lifetime membership. After all, I was going to have my ostomy for the rest of my life. I'm one of those people who can disappear for a few months at a time, but I'm always glad that the site is here, I can return and reconnect with old friends, and make new ones. This is an excellent site ... Best regards to all ... and Best wishes for a Healthy and Happy New Year.
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