Multimodal antioxidant therapy

[too-young-for-this-noo-XD]

I'd love to get some feedback from the community. I'm 29 years old (yes, ouch).
My andrologist specialist urged me to surgery. But since the surgery itself freaks me out more than the disease, I did a research deep-dive and I'm now on week 2 of testing my own therapeutic approach modeled after publications from Prof. Paulis, who achieved complete plaque (+calcification) regression.
My specific presentation is extremely rare. I have no pain, 29, no plaque, no calcification, but 7 months stable, and the location is within the parynchem of the entire left corpora. It was caused systemic and I will heal it system. But since I'm by far not the only one in that situation and many of you have had to walk those dark paths alone and gained immeasurable experience that I could never research on my own, I would love to get any form of feedback, it can be roasting, additions, removal requests and entire sections, it can be contributing something from the wishlist or data, whatever, it's open source and the repo on github.

https://ipp-treatment.fyi

With this I want to democratize how we approach something like multimodal treatment that hits into all pathological routes, be able to share feedback in individualizations of such year long individualized treatments, have an initial calculator to go to your doctor with a list, regarding contraindications and risks and how to monitor. I believe this approach rules supreme over everything previously done in Peyronie's treatment, because there is nothing that has shown as promising results as this one and it has near zero risks if monitored. Generally it aims to restore entire systemic function and cellular redux-homeostasis, something that improves overall health. So the way I see it is as long as someone doesn't have pain or other indications that make this therapy a total no-go, it should be considered the first-in-line treatment, as often the active and chronic phase are blurry and this protocol is proven effective in inhibiting progression in active stage, so there is nothing to even think about. Operation or vitamins lol. At least that's what its in my individual specific case.

And thank you to whoever founded this community.

[Mikel7]

You have a long post and I did read it and wondered did AI help you out with this? It is educational and I do understand the various treatments and possible outcomes. The one thing with peyronies is that it is a mysterious disease and unpredictable as to how it affects each man. You have to find what works for you and then work the treatment.