Let me start by correcting one misconception, that we don't like to listen to you complain about
your side effects. That's what we do here. It's most of what we are about
. You can get better advice on treatments other places but this forum is one of the best venues on the planet for complaining about
the side effects. So complain away; we can take it.
In a previous post I think you mentioned that you are using a pump. That's good -- they are somewhat helpful -- but if you are not getting any response from pills at 7 months it might be time to think about
trimix. If you haven't tried them injections are easier than you think -- but they'd have to be, wouldn't they? Like you said, it is not uncommon for it to take a year or two for the nerves to recover (if they recover, of which there is no guarantee) but it's important to keep the tissues in good shape while you wait and trimix can help with that.
If you haven't already watched Dr. Mulhall's videos this might be a good time. Gedman has a recent post and he has a link to the videos in his signature. ( See Ready for a new home: ED pump and Peyronie's book
) The links to the videos are in his signature as "( I, II, III )". The takeaway for you should be that 1) ED often gets worse before it gets better, and 2) it's best to keep working the problem while you wait for your hydraulics to come back online.
65 Slow PSA rise 2007-2012: 1.4=>8
4 bxs 2010-2012: 1&2 neg, 3 pos 1/14 6(3+3) 3-4% (2nd
opn. 7(3+4)), 4 neg
DaVinci 6/14/12. "some" nerve sparing on left
Path: pT3a pN0 R1 GS9(4+5)
Pos margins on rt
24 mo ADT3 7/12 - 7/14
Adj IMRT 66.6 Gy 10/17/12-12/13/12
8/2012-3/2015: Incont., Trimix, VED, PSA<0.015.
AUS & IPP installed 3/5/2015Forum Moderator - Not a medical professional