Letter for help

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Sergey070907

June 20, 2024, 11:44:37 PM
Has anyone tried to write to one of the famous and rich people? For example Elon Musk, maybe he would donate one of his millions for the development of a medicine?Or maybe he'll be personally interested in it.Of course, all this looks crazy and I don't believe it, but...
34 years old,onset of illness at age 22,injury, loss of length and girth, loss of sensitivity, erection preserved.Ultrasound showed thickening of the tunica.Treatment at the onset of the disease: electrophoresis with longidase.No major changes.

sammysosa17

#1
June 21, 2024, 01:35:50 AM
someone that might take particular interest is Bryan Johnson from Blueprint
Mid 20s
Single
Congenital curve since youth, injury in 2021
43 degree downward curve, 12 degree left curve
Starting RestoreX, 900mg Propolis, 300mg CoQ10

Sergey070907

#2
June 21, 2024, 02:42:09 AM
I would write this personally, but I do not have access to foreign social networks and it would be better if someone from the community did this with a link to the community. To make it official.
34 years old,onset of illness at age 22,injury, loss of length and girth, loss of sensitivity, erection preserved.Ultrasound showed thickening of the tunica.Treatment at the onset of the disease: electrophoresis with longidase.No major changes.

Mikel7

#3
June 21, 2024, 05:25:33 AM
Remember that in the world of big pharma the money makers are what they focus on. High blood pressure, diabtetes, etc.... Peyronies is not a big deal to them. It only affects men and then not every man so it is not that important to them $$$ wise.
Lump 4/2020, age 63 , Dr Levine 6-26-20, Dors Curve 11/2020, Peyronies
Vit E400mg, COQ10, Heat Therapy, Penimaster, Pentox, Cialis, Restorex
SNHL 7/2020 - Stopped all Meds because ototoxicity  Heat/traction/VED are working. CPPS Diagnosis - Stable :)

Sergey070907

#4
June 21, 2024, 06:41:48 AM
I understand all this, but need to take every chance.
34 years old,onset of illness at age 22,injury, loss of length and girth, loss of sensitivity, erection preserved.Ultrasound showed thickening of the tunica.Treatment at the onset of the disease: electrophoresis with longidase.No major changes.

Pfract

#5
June 22, 2024, 04:20:59 PM
Although I sympathize with you, I don't think this would get anywhere like it was said here. I feel like a donation to a foundation like https://peyronies.org/ would be more beneficial.

 

Axel_PD_Workbook

#6
August 28, 2024, 05:25:24 AM
Maybe this could help?
If you would like to support my work, I´ll set up a Patreon account in Sept 24. Here anyone can financially support valuable work. Since I have been working on the Peyronies Disease-workbooks around the clock for many months and will continue to do so in the future (with pleasure) and since a maximum of 1$ per book reaches the author when sold in bookstores, a small financial cushion could help.

Especially because I would like to use this and my own funds to financially support Peyronie's sufferers who cannot afford, for example, 300 bucks for a suitable medical aid. 1000 thanks in advance.
Diagnosis in early 2023 - cure (hopefully) in mid-2024. I have written a book about my experiences. Axel Westerwelle
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