Health Organization for Pudendal Education

The group I a secret group for those being treated for chronic uti, many women around 6 I've spoken too have reported pgad sensations completely gone after taking antibiotics for a chronic uti. Xx

Hi guys. Yes I have had an infection since around June 2015, it's been hiding under a bio film, the prof is James Malone Lee & I owe my life to the man tbh I am so much better than I was. I've took nitro, cefalexin & oxy and I am a lot better with bladder symptoms and being able to have sex....

Hi violet, In the UK a very well respected urologist professor has proved that dipstick tests and cultures can miss up to 50% of utis because they get hidden under biofilm, I went to Harley street London & he diagnosed my urine through a microscope and found a raging infection. He is now seeing ...

Hi everyone, I posted here before as I have been suffering this for nearly a year now. I have had periods where I felt I was cured of pgad. I am having an awful flare at the moment, my pgad has been caused by a chronic uti irritating the nerves in my pelvis. For me 600mg of lyrica and 50mg amitripty...

hi.. just thought I would post to leave some hop e :D - with seeing skilled pelvic floor specialists in Birmingham uk, seeing a urinary prof on Harley St London & with meditation, listening to nerve healing frequencies on youtube as I sleep a long with pregabalin & amitrip - I am 90% cured o...

Hi candice, I am also 21 & suffering from pgad - I have also been diagnosed with a chronic UTI meaning that my bladder wall is infected & most likely causing my pgad. At first I was unable to cope, then with help of pregabalin 600mg & amitrip 50mg I still had hypersensitivity but barely ...

Hi, I posted a few weeks back & I wanted to leave some positivity. I am no longer pregnant, unfortunately however I am now on 600mg pregabalin & 50mg amitriptyline.. I am wanting to wean off.. I have been in treatment with a professor who looked at my urine under a telescope & he said I ...

Hi Flor, I just thought I'd share some info with you, I listened to Dr echenberg on a radio station and he said the way he's realised and found most successful is to consult a urologist even if you have no urinany symptoms, get a knowledgeable PT and also find a Dr who is familiar with pudendal nerv...

Hi Violet,
I was just wondering if pt could make my pgad worse (by reading your comment you got pgad after pt)
I am going to explain all my symptoms to the pt. I have practically had a 90% symptom free day. So that's positive
Lily x