Hello all.
I had some radical cancer surgery in April, the total pelvic exontoration left me with two stomas (colostomy and urostomy) and no anus, prostate or penile bulb.
I’m getting used to the stoma bags and am recovering really well overall. But I miss having a working dick. My husband is really supportive but we are both beginning to miss the intimacy of fucking.
I’ll be looking through this site for information on vacuum pump to maintain size and for help understanding implant options.
I saw a London specialist today (Prof Ralph) and am toying up between private surgery (£15k in Jan) or NHS (free in 9-12 months).
I’m looking forward to reading about your experiences.
London post cancer surgery
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For your security and privacy, FrankTalk will time you out after five minutes if it senses no activity. Posting on the forums may take longer than five minutes and the site does not sense your typing a post as activity. If you are submitting a post that might take a few minutes to write, please compose it in a word processing program and then cut and paste it into the discussion board. This will save a lot of frustration.
Thanks
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DoubleOstomate
- Posts: 1
- Joined: Mon Sep 08, 2025 4:58 pm
- Location: London UK
London post cancer surgery
Total pelvic exontoration (radical cancer surgery) in April. No prostate, penile bulb, bladder or anus but I do have two stomas (colostomy and urostomy). Considering implant to bring my cock back to life.
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