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
New Support Group for PN and or PGAD
Re: New Support Group for PN and or PGAD
Hi Hope,
I tried to join your group (I made an account with the name "April May"). I realize now, though, that I didn't answer your screening questions in a way that would clearly indicate that I am who I am. So, I'm just letting you know here that that is me!
April
I tried to join your group (I made an account with the name "April May"). I realize now, though, that I didn't answer your screening questions in a way that would clearly indicate that I am who I am. So, I'm just letting you know here that that is me!
April
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- Posts: 148
- Joined: Tue Sep 05, 2017 2:12 am
Re: New Support Group for PN and or PGAD
Thank you for joining the group April!