Viagra Usage And Impotence

Ive spent and hour or so thinking back to the first time I used viagra im pretty sure i had a similar scenario to yours I Could go at it for a few hours if I wanted as my penis was had lost 90% of feeling and afterwards would be the skin would be saggy for a couple of days maybe even upto 4 days .
Ive been using viagra for around 14 years now some of the sensation has returned to my penis i would say around 20% max which is something ive learnt to accept the strange is its always cold to touch which always makes me wonder as I was told it should be the warmest part of your body. Masturbation is a thing of the past as finasteride has taken away the ability without chemical assistance which in itself removes the desire to be honest this doesn’t really bother me I didn’t really bother with masturbation anyhow as ive always lived in busy houses with very little privacy since i left home when i was 20.
My advice would be stick with viagra but talk your doctor keep pushing things along.
Above all support is vital at this point keep in touch with guys on this board and maybe talk to the misses .

Hello everyone,

Thank you for your advices, I’m sure something has changed in my penis and I don’t know what’s going to happen. Maybe it will be getting better in following days, I’m trying to not focus on it. Hope I’ll do it.

I’ve read a study that Viagra can boost up our reproductive hormone as well, my problem is at this moment, I cannot get a libido without it, that’s what made me angry.

https://news.wisc.edu/study-finds-viagra-increases-release-of-key-reproductive-hormone/

I’ve sent over an email to one of the best professors for Urology and Andrology in Europe. Waiting their reply for this.

I won’t give up! I can spend million of Euros for a cure or study as well. I’ve made my mind. I’ll go for it. Because at this week, I was at the deepest point that I can be! I was thinking some bad things as well, like giving up! But I won’t. I can demand a budget from government as well, we need to make a community for this. This is our life and we came to this world for once. And please, everyone in here let’s make a step. We can have a committee in Europe and gather together in order to deliver our message in Brussels.

Like Rumi says, “It’s your road and yours alone. Others may walk it with you, but no one can walk it for you.”

No one can walk for you! I’ve made the same mistake and have waited for a cure for a long time since 2009. It was a mistake, this is something that we need to deal with.

I’m so serious about this issue. Raise your heads! I’ve seen that there are some donation programs in here made by this community but those are so weak, it’s good to see anyway but the amounts are not good.

We can apply for funding from EU. We need millions of Euros for study and rather than the amount of money, we need to make our sound to be heard from EU Parliamentary.

Guys, we will survive and get over this sh.t somehow. We did not lose our limbs, we just spoiled and we can fix it.

Let’s not stay behind our screens, let’s go for a solution, at least let’s accelerate the path of solution.

Stop believing that is permanent, it’s only seems persistent and can be cured.

Let’s take action!

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Am I right in assuming from what you are saying that you are not short of funds and also may have connections with European government? I would encourage you strongly to donate to the PFS foundation as they have pretty much single handedly spearheaded the research into finding out what has happened to us and thereafter to pursue treatment options. Without our support none of this would be possible: https://www.pfsfoundation.org/donate/. If pursuing answers yourself from various medical experts, it would be a good idea to point them in the direction of the research the pfs foundation is carrying out to give them the best grasp of the current position. I really love your ideas at the end of your last post and am really keen on knowing more and whether any of us can help out. The European Medicines Agency could be a body worth targeting if you have an idea how to approach this. Thanks for your rallying cry. I definitely feel that apportioning part of our survival tactics to justice, without being driven mad about the overwhelming injustice of it all, is a positive approach to living with this as it can take us out of our own personal suffering and try and help right a wrong and do something for humanity and hopefully somewhat redress the worst inclinations that humans are demonstrably capable of.

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Have you heard anything back from J.vanzeeland

Ive tried messaging him the forum but he hasn’t replied which is out of character for this guy.
It would be a shame not to hear back from him to find out how’s hes doing also he did have plans to take our issues right to the government and health authorities.

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I was just roaming the forums and stumbled upon this thread. Has anyone heard back j.vanzeeland?

Last seen November 20th.

If anyone does get a reply from him, and he is able to fund something, please direct him to @Awor.

Hi Pete
I did speak to this guy alot initially as he was in a state of shock so i did my best to calm his fears.
He was very angry with the side effects hitting him sexually he had spoke of taking things as far as he could with the medical community etc.
The last time we spoke was around 2 months ago but since then I haven’t received a reply to my messages i sent him and he hasn’t returned to the forum he just vanished.

cialis doesnt work for me unfortunatelly

Have you tried viagra ?
Cialis didn’t work for me but viagra works
If you talk to your doctor he may have a better solution long term but worse case scenario he will prescribe you viagra to try.
Prescription pharmaceutical drugs are the only way to really test anything as they are guaranteed to be genuine.

I was moreso wondering about his whereabouts and well being. Hope he is alright. Point in case of the fellow above, if you have the slightest bit of sensitivity left, or are able to maintain even the slightest erection for masturbation I probably wouldn’t recommend use of PDE-5 inhibitors. @Baz44uk I know your case was on the extreme end of the spectrum in terms of how you were affected sexually, but this isn’t the first time I’ve heard of men with PFS left with an even deeper physical state of sexual dysfunction after using Viagra. I’d be curious to know how many members on here used or still use Viagra/Cialis, and how many have had success, how many were unchanged after discontinuing, and how many got worse. That being said, I also understand it’s just as bad to deprive your member of an erection over a long period of time, so I guess there are cases where it’s necessary.

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Hi pete
Just to clarify you’ve heard of guys left in a worse case of sexual dysfunction due to the use of viagra Cialis ?
This has crossed my mind in the past but after reading so many posts in hairloss forums regarding the use of viagra to combat the sexual issues due to Finasteride it seems common practice.
Doctors have given me prescriptions for viagra so i assume it is fairly safe and looking at studies it seems very well tolerated.
Do you suspect it could cause further long term issues ?

Hey Baz

Not so much the long term issues, but actually the short term immediate response to quite the contrary. Obviously in your case it worked fine, but Ive also seen some men get immediately worse. And for whatever it reason it seems to happen more with Viagra then it does Cialis

I use Siladenfil 50mgs and it’s effective for me and sometimes even increases libido which I know it’s not technically supposed to do. I notice my erections are better for days after taking it as well. Psychologically it helps me as it makes me feel more like my old self for a little while.

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