Bringing Awareness of Pudendal Nerve Entrapment to Peripheral Nerve Surgeons

Signatures 480 total

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1. 1
   Name: Laura Stonier on Jan 2, 2012

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2. 2
   Name: Anonymous on Jan 2, 2012

   Comments: This is a very serious health issue!

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3. 3
   Name: Anne Marie Hanson on Jan 2, 2012

   Comments: There are lives being/that have been destroyed by this and we need your help in banding together and building your expertise and providing us with a solution to regain some quality of life. Please!

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4. 4
   Name: Lemuel Tyre on Jan 2, 2012

   Comments: Please do something! I am watching my wife leave this planet day by day as she has been suffering for years now with pain 24 x 7!!

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5. 5
   Name: Christie Swentko on Jan 2, 2012

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6. 6
   Name: Leslie Carol Martin on Jan 2, 2012

   Comments: WE NEED HELP AND RESEARCH!! THIS IS DISABLING FOR US THE PATIENT AND OUR FAMILIES!!!

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7. 7
   Name: Mary Lee Frye Marshman on Jan 2, 2012

   Comments: I am a PNE sufferer. I have had an endless number of tests in my city but I have no access to a specialist. PNE patients should be able to see an experienced specialist within a reasonable travel time from their home...especially if there is a major university medical school in the area. I need help! You and your members have the ability to help me and others to have happy and productive lives, free of this horrendous pain.

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8. 8
   Name: Lisa Richter on Jan 2, 2012

   Comments: I have been suffering for almost 5 years, with severe adverse (damaging) reactions to medicines and injections. After losing my husband and family due to misconceptions, gross misunderstanding of this condition, and subsequent harsh judgments, I also lost my medical insurance coverage. Still I fight every day, all naturally, waiting for opportunities to pursue treatment/surgery that will do more help than damage. It's a difficult existence.. I have been bedridden for years. THANK YOU for helping us with a cure, by seeing the urgency and real devastation of this horrific condition, pudendal neuralgia.

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9. 9
   Name: Robert Marshman on Jan 2, 2012

   Comments: My wife suffers constantly, without a specialist that knows how to treat her. We need more attention given to pudendal nerve entrapment sufferers. Please help her.

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10. 10
    Name: Marie Urbach on Jan 2, 2012

    Comments: I am watching PN kill my daughter with every pain-filled minute. I know there are so many others. Please do something!!

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11. 11
    Name: Alisa Milewski on Jan 2, 2012

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12. 12
    Name: Jason Tomsic, DO on Jan 2, 2012

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13. 13
    Name: Jonathan Harrar on Jan 2, 2012

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14. 14
    Name: Helen Lee on Jan 2, 2012

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15. 15
    Name: Cathryn Gould on Jan 2, 2012

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16. 16
    Name: Jonathan Haag on Jan 2, 2012

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17. 17
    Name: Jennifer Gray-Heffern on Jan 2, 2012

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18. 18
    Name: Diane Lacroix on Jan 2, 2012

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19. 19
    Name: Anonymous on Jan 2, 2012

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20. 20
    Name: Ali Elahi on Jan 2, 2012

    Comments: I am a 37 year old male from Dallas with a failed Trans-ischia-rectal decompression procedure from Dr. Eric Bautrant in February,2010 in Aix En Provence,France and dorsal Nerve decompression surgery from Professor Oskar Aszmann in Vienna in April,2011.Symptoms include,E.D,bilateral sitting pain at ischial tuberosity,Urinary burning,Post ejaculation burning,Rectal spasms.

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21. 21
    Name: Ted Bartholdi IV on Jan 2, 2012

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22. 22
    Name: Michaela Zastera on Jan 2, 2012

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23. 23
    Name: Donald Coleman on Jan 2, 2012

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24. 24
    Name: LaVerne McCombs Legg on Jan 3, 2012

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25. 25
    Name: Ben Carlson on Jan 3, 2012

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26. 26
    Name: William Kain on Jan 3, 2012

    Comments: we have the tech, the brains, the willpower, let's do it.

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27. 27
    Name: Jessica Mariotti Tomsic on Jan 3, 2012

    Comments: I am a young mother who had a traumatic nerve crush injury during childbirth. I have suffered for over 3 years now. I have traveled all over the country numerous times, and even abroad for treatment. This injury has consumed every bit of my existence from the day my child was born. Not all are as fortunate as I was to travel abroad for surgical treatment. PNE NEEDS TO BE ADDRESSED IN THE UNITED STATES OF AMERICA, for the sake of patients everywhere.

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28. 28
    Name: Jill Rhoades on Jan 3, 2012

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29. 29
    Name: Atara Schimmel on Jan 3, 2012

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30. 30
    Name: Penny Wood on Jan 3, 2012

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31. 31
    Name: Noam Schimmel on Jan 3, 2012

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32. 32
    Name: Candy VanBriggle on Jan 3, 2012

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33. 33
    Name: Anne Trautman on Jan 3, 2012

    Comments: One of the most painful conditions known to women!!!!!

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34. 34
    Name: Rebecca Mullins on Jan 3, 2012

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35. 35
    Name: Larissa Canales Rubio on Jan 3, 2012

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36. 36
    Name: Solomon Schimmel on Jan 3, 2012

    Comments: Please read my daughters blog. She writes with passion and she will give you a deep and poignant understanding of how devastating this condition is.

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37. 37
    Name: Veronica Brown Lane on Jan 3, 2012

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38. 38
    Name: Sandra Conte on Jan 3, 2012

    Comments: I suffer from RSD/CRPS, and support this petition.

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39. 39
    Name: Cindy Smith on Jan 3, 2012

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40. 40
    Name: Krista M Roberts on Jan 3, 2012

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41. 41
    Name: Chrstine Annunziato on Jan 3, 2012

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42. 42
    Name: Brandi Brown Roth on Jan 3, 2012

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43. 43
    Name: Samie Leavitt on Jan 3, 2012

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44. 44
    Name: Yvonne Tallini on Jan 3, 2012

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45. 45
    Name: Barb Bussell on Jan 3, 2012

    Comments: Please give this the attention it so deserves!

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46. 46
    Name: Anonymous on Jan 3, 2012

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47. 47
    Name: Carolyn Merlina on Jan 3, 2012

    Comments: I am a 40 year old mother of 2 young children. I live in Colorado, and used to be very active: I've climbed 14ers, backpacked through fields of wildflowers and traveled the world. I have been a nurse for 19 years. My life took a turn for the worse when I picked up a pickaxe to help with yardwork. Now I cannot walk my dog, let alone lift my children. I cannot work. I have wanted to end my life. This has been devastating. Please help us.

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48. 48
    Name: Peggy A. Hnath RN on Jan 3, 2012

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49. 49
    Name: Valerie Goldberg on Jan 3, 2012

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50. 50
    Name: Mikki Gerlak on Jan 3, 2012

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