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New app for Peyronies self assessment - Details here



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realficker

October 05, 2020, 04:58:57 PM
Hello,
I am new and just want to introduce myself. I am now looking forward to being there and hopefully learn a lot. I am not a native speaker and I hope you will understand me. ;)
Have a nice day... :)
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Stabler

#1
October 05, 2020, 05:08:09 PM
Hello, can you tell us, do you have Peyronie's disease and if so what is your history with it. The forum can help more if we know why you are here.

Stabler
Moderator since 2015- Missouri- I work in the medical field and have strong knowledge of insurance and how to obtain coverage for medication and other treatments. Being a woman I do not have Peyronies but you can ask me anything. I am happy to help.

realficker

#2
October 05, 2020, 05:23:57 PM
I have ED oder PIED. I am not sure. That ist the reason. ;)
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peter123

#3
October 05, 2020, 05:57:36 PM
so many germans here
THIS USER HAS BEEN BANNED FROM FORUM FOR REPEATED RULE VIOLATIONS He never had Peyronies Disease but has body dysmorphia and his pastime was to attack all treatments, medical resources, and opinions.

TonySa

#4
October 05, 2020, 08:13:32 PM
Read the survival guide for info in Peyronies Disease.  https://www.peyroniesforum.net/index.php/topic,3180.msg44057.html#msg44057
PxD 2 yrs 9/16.  Failed all treatment. 9/11/18: excision, grafting & implant Dr Karpman MtnView Ca, AMS CX 18cm + 3-1cm RTEs.
Pump failed.  2/11/20 Dr Karpman installed Titan 22cm +1cm RTE.
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