A Call for Stories
Posted: Mon Apr 09, 2012 7:02 pm
Hello,
I am a person who knows the pain the nerve pudendal presents. There is more written knowledge today about the complexities of this nerve and the host of problems it presents than ever before; due in part by doctors trying to find solutions, and from patient advocates.... but there is still more knowledge that needs to be reached.
I would like to contribute your pudendal stories in collaberation with knowledgable medical doctors in the realm of the nerve pudendal. I believe it is important to have first hand stories voiced through pudendal patient's themselves. These stories will further educate health professionals, the public, and the general pelvic pain population, to bring about an acute awareness of a very real illness.
I can't guarentee publishing, but I'd like to try by establishing true account stories. Your names will not be used in order to protect identities. You can email them directly at reneew@sleepyeyetel.net. In this way your stories remain confidential. Tell me your gender, present age, and the state ( no city) or country where you live. The published stories will "not" contain your names, but please sign your real names at the bottom of your story along with: I grant permission to publish my story in any form.
Tell me at what age your symptoms began and if you know how you aquired pudendal neuropathy. Tell me what you have dealt with and are now dealing with. Have you had surgery, what type, was it helpful? Anything...just tell your story.
Thank-you!
I am a person who knows the pain the nerve pudendal presents. There is more written knowledge today about the complexities of this nerve and the host of problems it presents than ever before; due in part by doctors trying to find solutions, and from patient advocates.... but there is still more knowledge that needs to be reached.
I would like to contribute your pudendal stories in collaberation with knowledgable medical doctors in the realm of the nerve pudendal. I believe it is important to have first hand stories voiced through pudendal patient's themselves. These stories will further educate health professionals, the public, and the general pelvic pain population, to bring about an acute awareness of a very real illness.
I can't guarentee publishing, but I'd like to try by establishing true account stories. Your names will not be used in order to protect identities. You can email them directly at reneew@sleepyeyetel.net. In this way your stories remain confidential. Tell me your gender, present age, and the state ( no city) or country where you live. The published stories will "not" contain your names, but please sign your real names at the bottom of your story along with: I grant permission to publish my story in any form.
Tell me at what age your symptoms began and if you know how you aquired pudendal neuropathy. Tell me what you have dealt with and are now dealing with. Have you had surgery, what type, was it helpful? Anything...just tell your story.
Thank-you!
