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  1. 501
    Name: Anonymous on Nov 23, 2012
    Comments: Nice read, I just passed this onto a colleague who was doing some research on that. And he actually bought me lunch because I found it for him smile Thus let me rephrase that: Thanks for lunch! "We have two ears and only one tongue in order that we may hear more and speak less." by Laertius Diogenes. アグ ブーツ http://www.bootscheapsalejp.com/
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  2. 502
    Name: Anonymous on Nov 23, 2012
    Comments: Somebody necessarily help to make significantly posts I would state. This is the first time I frequented your web page and thus far? I surprised with the research you made to make this actual submit extraordinary. Wonderful activity! Christian Louboutin mens http://www.myclsale.com/christian-louboutin-mens-c-6.html
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  3. 503
    Name: Myrtle Jackson on Nov 24, 2012
    Comments: to our physicians and specialists, our caregivers, I was unaware that pudendal Nerve could bring on such suffering. my own son, who was big and strong, healthly. after a postrate operation, ended up with it now, his previous life was just a dream, the reality is he is bedridden and in pain. somewhere. somehow, someway, there is an answer. is there an answer? please, please, in your research, find an answer if possible his mom M. Jackson
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  4. 504
    Name: Colin Phillips on Nov 25, 2012
    Comments: My Pudendal Neuropathy was caused by Bortezomib treatment for Myeloma. It took 14 months for me to get a clear, named diagnosis. I hope some relief can now be achieved with pulsed radio frequency treatment.
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  5. 505
    Name: Anonymous on Nov 26, 2012
    Comments: I went over this website and I conceive you have a lot of wonderful info, saved to fav (:. moncler online http://www.monclercoatonline.com.es
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  6. 506
    Name: Annette L Clements on Nov 29, 2012
    Comments: I have been having trouble sitting, standing and lying down due to the pain in my tail bone! I am so tired. I need relief to be able to get comfortable and to get some rest... Please help.
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  7. 507
    Name: Hauda Antoinette on Dec 1, 2012
    Comments:
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  8. 508
    Name: Isabella Ghisi on Dec 2, 2012
    Comments:
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  9. 509
    Name: Anna Reid on Dec 5, 2012
    Comments:
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  10. 510
    Name: Paul Lewis on Dec 10, 2012
    Comments: please there is no worse of a condition that effects many aspects of ones life
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  11. 511
    Name: Safwnuwmow on Dec 10, 2012
    Comments: KAJeqI nuokvqkczjua, jygjtizerqon, bizilwglrbzc, http://lsgbzghvdgmp.com/
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  12. 512
    Name: Nichole Tremel on Dec 11, 2012
    Comments: i was diagnosed with PNE. I know the hard times that fall on us and there is nobody that can help us. I was accused of doctor hopping and then found out my nerve was entrapped in 2 separate locations! It's sad how we have no doctors that seem to want to help us!
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  13. 513
    Name: Anonymous on Dec 11, 2012
    Comments: You are my breathing in, I possess few blogs and sometimes run out from post :). "He who controls the past commands the future. He who commands the future conquers the past." by George Orwell. moncler online http://2012monclerdownjacket.webs.com/
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  14. 514
    Name: Anonymous on Dec 12, 2012
    Comments:
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  15. 515
    Name: Simon Dennis on Dec 13, 2012
    Comments: As a sufferer I would like to see this debilitating condition fully researched.
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  16. 516
    Name: Anonymous on Dec 13, 2012
    Comments:
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  17. 517
    Name: Joanna Putman on Dec 14, 2012
    Comments:
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  18. 518
    Name: Bernadette Olean on Dec 14, 2012
    Comments: i have a friend with this
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  19. 519
    Name: Loretta Holscher on Dec 14, 2012
    Comments: Recently diagnosed, suffered for 2 years before self diagnosing on line and confirmed by physician that I also found online.
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  20. 520
    Name: Marion Jones on Dec 14, 2012
    Comments: An extremely worthwhile petition. I am a sufferer and my life has been dramatically curtailed since a gyne operation 16 months ago.
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  21. 521
    Name: Ronald Holscher on Dec 14, 2012
    Comments:
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  22. 522
    Name: Thomas Brown on Dec 15, 2012
    Comments:
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  23. 523
    Name: Soula Mantalvanos on Dec 18, 2012
    Comments: right there with you! this is my story: pudendalnerve.com.au
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  24. 524
    Name: Anonymous on Dec 18, 2012
    Comments:
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  25. 525
    Name: Katerina Nestorovska on Dec 19, 2012
    Comments:
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  26. 526
    Name: Will Reve on Dec 19, 2012
    Comments:
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  27. 527
    Name: Kim Brown on Dec 20, 2012
    Comments: After 3 yrs of seeing numerous health care providers all over Mississippi, on to Texas, Tennessee, New York, and finally to Istanbul, Turkey to be able to have laproscopic pudendal nerve decompression surgery. It was very disheartening when doctors didn't know what was wrong with me, didn't know how to treat me & tried to convience me that I was imagining the pain. I would love for doctors to learn more about Pudendal nerve pain/entrapment to be able to help with this life threatening condition. As many untreated patients turn to suicide.
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  28. 528
    Name: Leslie Edens on Dec 22, 2012
    Comments: It's time doctors take this serious and no it is not in our heads the pain we endure ,It robs us of our independence ,it destroys relations ,we can not sit imagine a day where you can not sit because of the pain ,There are not enough doctors who treat this or even know any thing about it.It is time we take a stand for we are human and we suffer in silence.You doctors need to open your eye's and insurance company need to also they will not even pay for a surgery and who has the money to pay the price they are asking.I bet if one of your loved ones suffered with this you guys would step up to the plate or better yet if you had it you would be doing research on a cure,as I write this I am in pain and in tears because I have no life unless you call live laying in bed because that is the only relief some of us get,others don't
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  29. 529
    Name: Alex on Dec 23, 2012
    Comments: This painful condition is a living hell a torture. I have had this for 8 years and it has ruined my life. No one can understand the pain and there needs to be more research worldwide, more attention worldwide given to this on every level medically for all of us who suffer so that something anything can be found to take away this inhuman pain!! we all want this pain to just go away.
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  30. 530
    Name: Gil Weinstein on Dec 23, 2012
    Comments:
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  31. 531
    Name: Anonymous on Dec 24, 2012
    Comments: There are countless individuals suffering from PN/PNE with virutally no assistance from the medical community as they are not trained in this area. I pray to God that in the very near future more training will occur. I am one of those sufferers who cannot get a correct diagnosis due to the above. PLEASE - train the physicians!
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  32. 532
    Name: Brian T Lloyd on Dec 29, 2012
    Comments: I have suffered PNE for 4 years . I am now 68 years old . Gabapentin/Neurontin at least helps me function .
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  33. 533
    Name: T. Cornish on Dec 31, 2012
    Comments:
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  34. 534
    Name: Anonymous on Jan 4, 2013
    Comments: Please let everyone know about this, we need some help and need it soon!!!!
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  35. 535
    Name: Clint Radenbaugh on Jan 4, 2013
    Comments:
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  36. 536
    Name: Mary Schor on Jan 5, 2013
    Comments:
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  37. 537
    Name: Kathleen Keyes on Jan 5, 2013
    Comments: Please help....I am one of many who have suffered with the pain of pudendal neuralgia for 3 years now. Very few doctors even know what it is!
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  38. 538
    Name: Arlene Jone on Jan 5, 2013
    Comments:
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  39. 539
    Name: Cathryn Gould on Jan 5, 2013
    Comments:
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  40. 540
    Name: Anonymous on Jan 7, 2013
    Comments: Believe in Believe in PN. Stop suicides. These people need help.
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  41. 541
    Name: Myrtle Jackson on Jan 7, 2013
    Comments: thank you for drawing attention to this terrible affliction. please accept my gratitude for anything you can do for these people who have never hurt anyone and now must suffer for the rest of their life with up to now...no hope
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  42. 542
    Name: Christie Scott-Swentko on Jan 7, 2013
    Comments: Please help bring awareness of this horrible and painful disease that we suffer from every single day. Pudendal neuropathy has stole my young life away from me, being a wife, a mother, a happy person, my health, my hobbies, everything! I suffer never ending disabling pain that has turned me into a person I never wanted to be. In the Chicago area where I live I have no one to turn to for help, please help us!
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  43. 543
    Name: Missy Dawson on Jan 8, 2013
    Comments:
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  44. 544
    Name: Allan Buxton on Jan 8, 2013
    Comments:
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  45. 545
    Name: Anonymous on Jan 9, 2013
    Comments:
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  46. 546
    Name: Marion Jones on Jan 9, 2013
    Comments:
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  47. 547
    Name: Richard Hornby on Jan 9, 2013
    Comments:
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  48. 548
    Name: Domnique Zeiler on Jan 9, 2013
    Comments: This illness needs to be recognized and people need to stop ignoring it or telling the sufferers that its all in their heads!
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  49. 549
    Name: Tina Jaray on Jan 9, 2013
    Comments:
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  50. 550
    Name: Tina Jaray on Jan 9, 2013
    Comments:
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