I am on my 3rd day starting this treatment. Below is a link to a single study showing this treatment resolved peyronies disease completely in 8 months. Only one study to go off of and the cyclophosphamide has extreme side effects including hair loss. I have nothing to lose at this point so I am giving it a shot and will keep you updated if this actually works at all. Cyclophosphamide has been shown to break down and stop scar tissue from forming in a few different diseases including pulmonary fibrosis.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037975/
Man ill be folowing your updates ad if even remotely helps i will consider using it, i would care less abaout the hair, thank you very much! Btw there are so manny treatmants in development like peptides and stuff who promote angiogenesis etc that i dont know where to look for.....and why arent they on market...
Please keep us all updated. And stay safe. Those drugs sound like serious stuff.
Is this being monitored by a doctor?
How did you get these things prescribed?
Was it a urologist?
In my participation in this thread I hope it is not mistaken that I advocate taking this course of action. Without doctor supervision this is very dangerous. All I meant to say was, stay safe. Nobody on this forum would recommend doing this without the supervision of a physician.
To be quite honest it is not from the supervision of a doctor. I called a pharmacy in another country and ordered it. Then confirmed with a friend that is a pharmacist that I got legitimate cyclophosphamide.
I also am taking the dexamethasone twice a week
Pharmacists don't tend to have the equipment or skill to identify unknown substances... H-NMR, HPLC, Mass spec?
To be clear, I think this is a very bad idea. Dose is VERY important with cyclophosphamide, equally important is close monitoring.
Any updates for us Michiganguy? We all hope you are o.k. Please check in.
13 days in, no change. Cyclophosphamide supposedly takes 6 weeks to begin working in the body. So I will update then.
Saw the best urologist supposedly in the state of Michigan for Peyronies, Dana Ohl at U of M. Said even though I'm as bad as I am he won't consider surgery until my penis is half the size it was before. I was 7.2 before now 6.1. That seems ridiculous to me cause flaccid I am embarrassingly f'~c<+d now. Said he's seen worse at count myself lucky I was the most mild case of the day. And he said to stay off this forum cause people give wrong info and he hates this forum it's just a bad idea lol
Yeah because most of them see surgery as the only option. Sad truth, they have a hammer so all they see is nails.
Really interested in this. Keep us updated.
Urologist are the dumbest of all sadly. I have a theory that they take in only the ones that performed worst overall in medicine masters test. Dont go to urologists, find yourself a smart rheumatologist. That is my experience 13/15. I found only two decent urologists both of whom offered me nothing instead of acting like the c*nts the other 13 urologists are
Quote from: Hontas on August 15, 2019, 09:14:16 PM
Urologist are the dumbest of all sadly. I have a theory that they take in only the ones that performed worst overall in medicine masters test. Dont go to urologists, find yourself a smart rheumatologist. That is my experience 13/15. I found only two decent urologists both of whom offered me nothing instead of acting like the c*nts the other 13 urologists are
What did the rheumatologist do for you?
Any updates Michigan? Worried about you. Please check in and let us know.
Really interested in any update and what the side effects are like?
I'm also interested in trying this.
Quote from: Michiganguy19 on August 13, 2019, 02:10:56 AM
Saw the best urologist supposedly in the state of Michigan for Peyronies, Dana Ohl at U of M. Said even though I'm as bad as I am he won't consider surgery until my penis is half the size it was before. I was 7.2 before now 6.1. That seems ridiculous to me cause flaccid I am embarrassingly f'~c<+d now. Said he's seen worse at count myself lucky I was the most mild case of the day. And he said to stay off this forum cause people give wrong info and he hates this forum it's just a bad idea lol
why do you make up so much crap? who would believe that a dr saud sucj a ridiculud thibg?
Any update Michiganguy19?
Very curious to hear how the rather experimental treatment went! Or if anyone else has tried something similar with either of the two drugs?
How come no one is trying this out? This is the first time I've seen Peyronie's getting cured
Because there's barely any logic. And it's difficult to get your hands on it.
I'd say almost impossible to get your hands on...
But there's definitely a huge amount of logic in taking oral steroids such as dexamethasone during the acute phase to reduce inflammation. Whether it works for Peyronie's or not is another question entirely!
Any results @michiganguy??
@Michiganguy19 did you get any results? please update whether good or bad.
Hey, brother!
Any updates on the treatment?