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If you or a family member has been diagnosed with extramammary Paget's disease (EMPD) we would love to hear from you! While EMPD diagnosis is rare, this website has made it possible for EMPD patients to learn from each other. The myEMPD.com website is managed by EMPD patient volunteers. There is power in community and to date, over 700 people with EMPD, in many different countries, have been located.
There is also a private support group available, which includes female and male EMPD patients and family members from all around the world. For more information, inquire here.
This website is dedicated to assisting those that have been diagnosed with EMPD, along with the family members of those with EMPD. The website is paid for by many EMPD patients and has no affiliation with any doctor, hospital, medical center, or pharmaceutical company. The information contained on the website is believed to be accurate, however, all users should consult their own doctor for advice and treatment.
While we read and write English we are happy to translate your inquiry from any language. We usually respond within a few days.