Health Organization for Pudendal Education

Good morning

I am in France and I have had a PGAD for about 2 years.

Unfortunately it is not always easy to find the right doctors/Specialists who know this syndrome well, but good news, this Pgad syndrome is better known by the medical world!

I did a lot of exams to try to find the cause of my syndrome: Pelvic MRI imaging, spinal cord MRI of the dorsal spine, brain MRI and a very useful exam => an EMG (Electromyogram) Pudendal/Perineal electrophysiology. Doppler venous ultrasound of the legs.

Apart from the psychological causes, if you want information to know the different neurological or venous or hormonal causes of PGAD and the examinations and specialists to consult, I remain at your disposal to talk about it.

see you soon

Hi Summer,

Sorry to hear you are going through this. What were your results for the diagnostic tests you had? Are you any closer to figuring out a cause of your PGAD?

So, I traveled to your country for treatment and I am pretty much cured of PGAD now, thanks to Dr. Bautrant. What physician are you seeing there?

Violet