Implant with nerve damage (HF or Peyronie's most likely)

[GBDS22206]

Hello everyone! I'm 19 and been having erection issues for awhile but they didn't bother me much until it got to the point of me being unable to penetrate. I'm not sure yet what's the reason but my issues look either like Peyronie's or hard flaccid, here's the symptoms:

1. Lower sensitivity and DE, some numbness (can't orgasm at all during sex), gotten worse with time

2. Chronic pains, they go away sometimes and usually get worse after masturbating

3. Can get hard but can't stay hard, sometimes instantly get down from 100% to 60-70% rigidity after stopping stimulation and slowly go down from there

4. Lowered libido which I've heard can come from Peyronie's or HF

5. Bottleneck shape, it's thinner under the glans but seems to even out when I get fully hard, also have a curve and it's a bit askew at the base.

6. Difficult to get aroused without physical stimulation, at best I get to 20-40%

7. Morning woods present but not fully hard, they look like an inflated implanted dick without engorgement I think

I'm not entirely sure what could've caused it, but my main suspicions are either rough masturbation (although I wasn't squeezing that hard) or sexual injury (my ex almost broke it twice when riding me, it was painful and after the second time I think everything started to get worse). Might be something else but still... Did anyone else had such issues and got implanted? I worry mostly about sensitivity, sure I can get engorgement and won't go flaccid thanks to it, but what if I barely feel anything still? Is it worth it?

[Kodixx]

GBDS22206, my symptoms leading into ED were very different than yours, but I wanted to say that I'm very sorry to hear about yours and wish you the best in getting diagnosed and getting successful treatment. The members of FrankTalk have a wealth of experience and knowledge, and are a great sounding board for all of these topics and symptoms. That said, nothing replaces a complete Dr's evaluation -- and even a 2nd or 3rd opinion if the treatment(s) are invasive (such as surgery). Do you have access to a urologist and/or neurologist ?

- Chuck

Did anyone else had such issues and got implanted? I worry mostly about sensitivity, sure I can get engorgement and won't go flaccid thanks to it, but what if I barely feel anything still? Is it worth it?

[fucked0ne]

I doubt it’s Peyronies. Can’t guys with Peyronies still get it up despite the curvature? Also, when you do manage to get it up, is it curved? HF often has a flaccid curve that straightens out with tumescence (as pathetic as it is); also, “hour glassing.”

[fucked0ne]

(Deleted) Posted twice.

[GBDS22206]

I doubt it’s Peyronies. Can’t guys with Peyronies still get it up despite the curvature? Also, when you do manage to get it up, is it curved? HF often has a flaccid curve that straightens out with tumescence (as pathetic as it is); also, “hour glassing.”

Yeah, it sounds more like HF. I have some natural curvature but lately it's been looking way worse when not fully hard, when it is it pretty much looks the same as before, although it's somewhat askew now at the base.

There's no hourglassing but there is bottlenecking which disappears as well when I get hard, but there's also something that looks like a plaque where the narrowing starts. I pretty much can get to 100% each time I masturbate, but the more I do it the less sensation I have and lately it's been harder to cum. I plan to not touch it for a week or too, just booked an appointment with my new uro, hope there's no permanent nerve damage...

[GBDS22206]

In fact I'm sitting right now with it semi-rigid and firm to the touch.

[fucked0ne]

I doubt it’s Peyronies. Can’t guys with Peyronies still get it up despite the curvature? Also, when you do manage to get it up, is it curved? HF often has a flaccid curve that straightens out with tumescence (as pathetic as it is); also, “hour glassing.”

Yeah, it sounds more like HF. I have some natural curvature but lately it's been looking way worse when not fully hard, when it is it pretty much looks the same as before, although it's somewhat askew now at the base.

There's no hourglassing but there is bottlenecking which disappears as well when I get hard, but there's also something that looks like a plaque where the narrowing starts. I pretty much can get to 100% each time I masturbate, but the more I do it the less sensation I have and lately it's been harder to cum. I plan to not touch it for a week or too, just booked an appointment with my new uro, hope there's no permanent nerve damage...

Well, if you have something that looks like a plaque, then you should be checked for Peyronies. You may not need surgery. There’s a study, easily found with a Google, which showed chronic intake of antioxidants (vitamin e, bilberry, etc) cured Peyronies over three years in volunteers.

[GBDS22206]

I doubt it’s Peyronies. Can’t guys with Peyronies still get it up despite the curvature? Also, when you do manage to get it up, is it curved? HF often has a flaccid curve that straightens out with tumescence (as pathetic as it is); also, “hour glassing.”

Yeah, it sounds more like HF. I have some natural curvature but lately it's been looking way worse when not fully hard, when it is it pretty much looks the same as before, although it's somewhat askew now at the base.

There's no hourglassing but there is bottlenecking which disappears as well when I get hard, but there's also something that looks like a plaque where the narrowing starts. I pretty much can get to 100% each time I masturbate, but the more I do it the less sensation I have and lately it's been harder to cum. I plan to not touch it for a week or too, just booked an appointment with my new uro, hope there's no permanent nerve damage...

Well, if you have something that looks like a plaque, then you should be checked for Peyronies. You may not need surgery. There’s a study, easily found with a Google, which showed chronic intake of antioxidants (vitamin e, bilberry, etc) cured Peyronies over three years in volunteers.

Idk, having full blown ED and loss of sensation at 19 and hoping that it gets better in a few years... I have an appointment in a week and we'll see what's what, but going the medication way doesn't seem like a viable option especially where I live.