Health Organization for Pudendal Education

Hi Violet,

I'm sorry it has taken me so long to respond to you.

This is the pelvic PT I treated with (Debbie Callif). She doesn't know of any support groups in this area (southeastern Wisconsin). She did introduce me to a fellow patient who has pudendal neuralgia and we have become friends so at least I have one person I can talk with on a regular basis who understands what it is like living with this condition. Thanks for the info, though.

Gwen Rubis

Hi Gwen,

That's good that you at least know one other person in the area. Maybe the two of you could start a support group. I think sometimes it's hard for people with PN to get out though so it's nice to have an online group too.

Take care,

Violet