Hello, folks.
Back nearly 2 years ago (when I was 39 years old) I found this board while searching what to do for this wretched disease, all while getting depressed further because the reality set in that there is no "one size fits all" and everything seems to be based on "hope". However, reading about other people and their experience did help me. While I don't expect my experience to help others so much I figure I should get a little active on here to gather more information, my thinking through it all, and current thought process.
Nearly 2 years ago I found a very small, not even pea-sized lump in my penis. I did not think much of it and it had no affect on my life at all. A couple months later, I started having pain during erections and a very small bend to the right in my penis, not enough to affect my life still but I reached out to my doctor, who referred me to a urologist. The urologist confirmed that it was Peyronie's but said it was a mild case and likely toward the end because the pain had subsided by the time I got the appointment. She gave me the name of another urologist that specializes in Peyronie's should things get worse.
About 4 months later, it got much worse. The bend to the right was much more pronounced (couldn't guess on angle) but still no pain and really did not affect my life much still but I decided I should reach out to the other urologist to try to see what could be done. A few months later, I had my first appointment with him and said
Xiaflex might be a viable option for treatment. It took about 6 more months to have the first injection because of COVID starting and restrictions that had been put in in the spring, by that time the bend to the right was gone and the bend was significantly upward. Sex was impossible, I could not get a good erection let alone maintain one. I asked my PCP for cialis and he gave that, which helped but still not enough to successfully have sex.
So far, I have been through 3 rounds (2 shots in one week) of
Xiaflex and no real change at all. I did ask the urologist if it would be worth buying a
traction device (such as RestoreX) to use in conjunction with the cialis and
Xiaflex and he said there just wasn't enough evidence to warrant purchasing a device so I dropped. He is a very well-known urologist in the Peyronie's research community, hence why I am seeing him and trusting him.
But...of course, after every round of
Xiaflex, I have a little hope that something might change but end up being depressed when there is no change and end up keeping the appointments for the next round. I will likely go through all 8 rounds to see it to the end but have little hope that it will meet my goals. My goals are simple, same as the urologist, able to have stable erections without cialis and comfortable sex. I don't have high standards nor expect my penis to be 21 again. My guess is I will opt for any possible surgery to correct the issue, regardless of potential downsides since I cannot currently have sex now so....there wouldn't be much change if I had the surgery and still couldn't.