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.
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DoubleOstomate
- Posts: 3
- 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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LGXDownunder
- Posts: 466
- Joined: Fri Mar 07, 2025 7:59 am
- Location: Sydney, Australia
Re: London post cancer surgery
DoubleOstomate wrote: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.
Welcome DoubleOstomate
Yes, in my opinion do use a VED regularly pre-implant to maintain size and prevent penile atrophy/size loss.
Doing that should help with allowing implantation of the maximum sized cylinders that your anatomy can accept.
But please confirm this with your surgeon, especially considering the amount of work you have had done.
I'm not in the UK, so can't comment on the options there but there are other UK guys on here, and quite a few have gone through the NHS.
By all accounts that I've read Professor Ralph is probably the leading implant surgeon over there and very highly regarded.
Even my own uro surgeon in Sydney Australia is well aware of him, having studied in the UK.
I'm sure you will find plenty of relevant information on Franktalk. My own story to date is here if of any interest:
https://www.franktalk.org/phpBB3/viewtopic.php?t=26157#p248832
71, married, Sydney Oz. PC & nerve sparing RRP Mar 22, profound ED since. Tried pills, Trimix inj, focal shockwave, VED.
Finally implanted Mar 6 2025 AMS 700 LGX 21cm x 12mm, no RTEs, MS pump, Penoscrotal.
Recovery great so far but have a bend.
Finally implanted Mar 6 2025 AMS 700 LGX 21cm x 12mm, no RTEs, MS pump, Penoscrotal.
Recovery great so far but have a bend.
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