The Association of Peyronie’s Disease Advocates (APDA) was incorporated as a 501c(3) for the purpose of providing unbiased education, a Support Forum, awareness and treatment options for the patients, partners and physicians seeking resources for Peyronie’s Disease (PD).  People with this condition have a certain type of immune cell marker, which indicates that it may be inherited. We are the first and only patient advocates dedicated in spotlighting the physical and psychological effects of PD.

Our core hope is that each man will equip himself to be his own advocate in making informed decisions regarding which treatment option will work best for him and his life. The better a man with Peyronie’s Disease understands how to deal with this condition, the sooner he will be able to move forward and live a fulfilling life.


1 thought on “Association of Peyronie’s Disease Advocates”

  1. Joe says:

    I’d like to ask anybody out there who can speak authoritatively (as a medical expert): Peyronie’s is a progressive disease, so does early treatment mitigate the physical damage secondary to Peyronie’s?

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