Interesting article on sharks blood and how scientists have discovered a way to prevent fibrosis from it's use.
I can't copy the link here as I am on my phone overseas. But the article is on the Herald Sun website from Australia.
Google search shark blood drug testing in humans - herald sun
If someone finds the link and can post for other then thanks.
Not sure if it's helps us but at least it's a good discovery on the scar tissue topic and will be able to treat life threatening scarring of vital organs.
Treeza.
Sounds cool. Please post some more info. I'm still waiting for bull shark testosterone to be availanle too, like in gta v xD
http://www.heraldsun.com.au/news/victoria/drug-based-on-antibody-discovered-in-sharks-blood-to-be-tested-in-humans/news-story/c042fb20f83ca4a9ee524451aa1ea502
James
Thanks James, what did you think? Seems like scientist are just going to stumble across an effective treatment in the future. Only a matter of when, not if.
OK Jack, you win, deleted my post :)
James
25.. Come on mate, give me some sort of hope!
Im 25 years I'm dead too.who the F~@< can live trough this for 25 years?
I'm about to turn 27 and I have never had an usable penis, despite how much hard I try to have my thing fixed. Nonetheless, I don't spend most of the time here spreading pessimism and bringing people down (even if I'm in constant and lingering pain...). On the other hand, it looks like some people see it as some kind of hobby and it's beyond me why..
OK Jack, you win again, deleted my post :)
James
Be real, xiaflex is nowhere near a solution for most guys. The treatments you mention are tractiom ved supplements and pentox, right? You can do something, but really not that much you gotta admit that. Those treatments are very very old and not even recommended by lots of urologists. Most still advice to wait amd see because obviously thry can't do much. I'm not pessimistic, just being real and yes I do think 25 years is too fuckimg lomg considering the time we live in and the importance of the issue. But too bad only sufferers see it that way.
I still see your behavior unacceptable, you are an experienced member so people in here rely on what you say..if you take hope away, what's left then? I tried everything and, more than once, surgery..if I stuck with your words I should kill myself...and I'm not the only one
So when I log in to keep me informed I need to see this? Everyone is realistic in here, stop with this. No one goes out and sings his happiness out once read some news..we are all very cautious and that's all.
Gentlemen, let's all try and be upbeat in our attempts defeating Peyronie's, that is to say, persistence, perseverance, stubbornness, determination, relentlessness and drive in any protocol we have chosen to take.
I live in hope that someone out there has our backs and is doing the research and treatment/s which surely must come from it
Stay hopeful :)
No, I don't feel like I'm taking your hopes away, and I don't tell you what to do I'm just saiying Idon't like the attetiude of trying a lot of stuff in vain an telling yourself it will work. Been there done that.. some things work, but seriously.. we need more treatments. It doesn't mean we shouldn't do anything. It means we shouldn't tell ourselves some unproven techniques/treatments will help us even tho they don't do mucj at all. Instead I think we should raise awereness, tell our urologists what's going on, tell your GP you cannot live like this andjust do whatever to make people hear your story no matter how embarassing it is because thry should know we're here and NOT happy with dealing with this stuff with barely any hope at all. It's not takingyour hope away, it's being realistic and not willing to experiment with bs and wanting to ACTUALLY cure this stuff.
I wasn't talking to you. I'm with you popooo
Lol, ok then sorry for my rant. xD