Welcome to HOPE - www.pudendalhope.org

[Mod4]

The Directors of HOPE would like to welcome you to our new forum.
As we are in our infancy we would ask that you bear with us, we will provide you with a full explanation as to why we have had to take this step.
We just want you to know that we are a dedicated TEAM of people from many continents Worldwide who have been working very hard to form and secure this Organisation for many years.
We will do our level best to build this site to be the very best one available for HOPE and Help for information regarding Pudendal Neuralgia.

Thank you for your patience.

The Board of Directors of HOPE

[GraceUnderFire]

Looking forward to the explanation. Thank you Wouldn't want to go anywhere that Violet wasn't around to give her amazing information and wonderful support

Blessings,
Grace

[Amanda]

Grace Welcome to pudendalhope.org

Violet is here to offer her valued and experienced opinions and thoughts....she is a veteran of PNE and we value her very much.

Amanda

[Emily B]

Hello. I'm here too. Looking forward to understanding what happened. I don't know much about moderators and such. I just hope that we'll all still have access to the wonderful information we have in the past. The forum is my lifeline for information and support. Thanks for working to put this new one together and not just leaving us all in the dust.

Emily B.

[Celeste]

Anxiously waiting to understand what just happened.

[Violet M]

Hi, Violet checking in here.

Without all of the PN community posting information our organization is nothing. Thanks to all of you for hanging around and being there for all of our new members. We couldn't do it without you.

[HerMajesty]

Hey you guys definitely have my loyalty; guess you were running the nonprofit message board off of somebody else's domain name?
I hope this works out and grows. Whole thing is kind of a bummer.
Meanwhile, I just checked on the other site oo and it is "off-line temporarily"...to be continued, or not???

[Quilter 2]

Hi Guys;
Thank-you all for being there. Most of the time, I don't understand "threads" and all the other computer lingo, but someone is always there to help set me straight
The work you have all done is amazing and I bet, has kept a lot of us from just throwing in the towel. That alone, deserves a major THANK-you.
Doreen

[Karyn]

To the Directors and Moderaters of HOPE (past and present):
THANK YOU SO VERY MUCH for providing us a safe, informative and supportive place to come to. I sincerely appreciate all the hard work you've done to keep this going. I'll admit to being devasted when I tried to access the pundendal.info site the other day, but I'm so grateful that you didn't just leave us hanging. The forum has been a life line and a wealth of information for me. The work you've done and are continuing to do is so very important! Thank you! Thank you!
I'd also like to throw out a special HUGE thank you to Violet and Celeste (not a moderator, I know!) Violet and Celeste are not only major contributors with veteran status, but also continue to provide support and insight to all, even though they've had remarkable recoveries from PN. With that in mind, I think it's remarkable and selfless of both of you to stick around in an effort to help others.
Group hug to all members of the pudendal.info forum! You're all very brave and I hope to be able to reconnect with you here at HOPE.
With the utmost respect,
Karyn

[A's Mommy]

I also want to send a heartfelt thank you to the creators and moderators of HOPE.

I just got off the phone with a fellow forum member and this thought crossed my mind so many times: WE NEED TO STICK TOGETHER. We are all here for the same reason: we want cured of this horrible disease/illness that affects us so much in EVERY aspect of our lives; our work, our finances, our marriages/relationships, our children, even our faith.

I admire and THANK those of you who have been helped/cured by the PNE treatments and/or surgeries who are STICKING around to help us who are still on our journey to recovery.

To all: continue to post, lets get the word out on PNE, and make all the difference we possibly can. One thing that PNE hasn't stolen is our MOUTHS or our PENS. We can speak and we can write about it. Let's do it.

All the best to my dear friends on this forum,

A's Mommy