New Support Group for PN and or PGAD
Posted: Sat Mar 24, 2018 3:00 pm
Hi,
I created a new support group named Pudendal Neuralgia and PGAD Warriors. Here is the entry request link https://www.facebook.com/groups/129664091204848/ . Since this group is a secret group you will be prompted to ask a few questions before I approve your request and add you to the group. This is to protect everyone's privacy and a way for me to ensure members have PN and or PGAD. If the link does not work you can send me a Facebook friend request. My name on Facebook is Hope Smith and I have a gray puppy as my profile picture. No one can search for the group on Facebook, so don't bother to try. All you will find is the entry request link that I posted above.
The mission of this group is to provide a supportive atmosphere to share experiences and knowledge between each other and to foster a community of support and hope.
Hope
I created a new support group named Pudendal Neuralgia and PGAD Warriors. Here is the entry request link https://www.facebook.com/groups/129664091204848/ . Since this group is a secret group you will be prompted to ask a few questions before I approve your request and add you to the group. This is to protect everyone's privacy and a way for me to ensure members have PN and or PGAD. If the link does not work you can send me a Facebook friend request. My name on Facebook is Hope Smith and I have a gray puppy as my profile picture. No one can search for the group on Facebook, so don't bother to try. All you will find is the entry request link that I posted above.
The mission of this group is to provide a supportive atmosphere to share experiences and knowledge between each other and to foster a community of support and hope.
Hope