Hi; I'm new here. I'm 60 and live in central Virginia. Two and a half years ago I had my prostate removed by Da Vinci robotic laparoscopy surgery. Since then I have been recovering and with Levitra, I am pretty functional. Cialis doesn't work for me - I get bad muscle cramps. I had ED before the prostate surgery, but needed only a very low dose of Levitra - 5 mg was fine. After surgery I was very hit or miss even with a full 20 mg dose. When I did get an erection, it would have a short shelf life. If I didn't use it right away it would fade and not come back. Now I am much more reliable. I would like to get away from the pills, and have had some success without, but I just don,t feel that it will be reliable. I also developed Peyronies after the surgery, so now I curve up and to the left. That is strange looking, but does not present me any problems. I'm glad I found this site to discuss with people in a similar situation.
Lefty
Prostate Cancer Survivor
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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
Prostate Cancer Survivor
60 yrs old, robotic prostatectomy Nov. 2009
Re: Prostate Cancer Survivor
Welcome! This is a great place for support from understanding men!
Re: Prostate Cancer Survivor
Hi Lefty,
Similiar story. I am 49, with no history of ED, I had "the robot" 4.5 months ago. I am currently on a therapy of daily pumping (just to erection and release, no rings, yet) and daily Cialis (5 mg) Without the pump,i am no more than 60% hard, and that's only after some significant play time. I am still seeing some slow progress and am hopeful.
As to the Cialis, I found less side effects when I switched to mornings, rather than evenings.
We're all in this fight together, good luck.
Rich
Similiar story. I am 49, with no history of ED, I had "the robot" 4.5 months ago. I am currently on a therapy of daily pumping (just to erection and release, no rings, yet) and daily Cialis (5 mg) Without the pump,i am no more than 60% hard, and that's only after some significant play time. I am still seeing some slow progress and am hopeful.
As to the Cialis, I found less side effects when I switched to mornings, rather than evenings.
We're all in this fight together, good luck.
Rich
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anothernight
- Posts: 15
- Joined: Sun Mar 11, 2012 11:21 pm
Re: Prostate Cancer Survivor
Welcome. Contact me anytime...newby so don't expect much. I am glad you are here.
Re: Prostate Cancer Survivor
Welcome to FT Lefty,
I am a fellow PCa Survivor and developed ED Post-Prostatectomy in February 2004.
The "standard" ED Treatment Modalities (PDE5 Inhibitors, MUSE, VED, Injections) did not work satisfactorily for me.
In December 2007 I opted for an IPP (Inflatable Penile Prosthesis) which, thankfully, completely corrected my ED.
My wife and I have enjoyed my Titan Implant for the past 4+ years and counting.
There is a wealth of information in this Group --- ask questions and join the chats --- you are among friends here.
Hope to see you in the Chat Room.
Best of luck,
Bob
I am a fellow PCa Survivor and developed ED Post-Prostatectomy in February 2004.
The "standard" ED Treatment Modalities (PDE5 Inhibitors, MUSE, VED, Injections) did not work satisfactorily for me.
In December 2007 I opted for an IPP (Inflatable Penile Prosthesis) which, thankfully, completely corrected my ED.
My wife and I have enjoyed my Titan Implant for the past 4+ years and counting.
There is a wealth of information in this Group --- ask questions and join the chats --- you are among friends here.
Hope to see you in the Chat Room.
Best of luck,
Bob
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