Signatures 754 total
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101
Name: Kimberly Morey on Jun 22, 2012Comments:Flag
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102
Name: Annette Lynch on Jun 22, 2012Comments: Please take this petition serously. As a pudendal/piriformis/sciatic pain sufferer I have lived in horrible pain for over 6 years while seeking answers and treatment from over 14 specialists, several chiropractors, and several PT's without much help. I had to travel 1600 miles across the country to get surgery for my condition because there are no specialists in the Boston area where I live. Please help educate those professionals so they will be better able to recognize and treat this disorder. Sincerely, Annette LynchFlag
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103
Name: Leslie Edens on Jun 22, 2012Comments: We need more doctors to understand how this condition effects not just the one who has it but also their family members. The pain that we have to endure every day of our lives with no help from the medical field. i have been to so many doctor's that have no clue what this condition is or even how to treat it.We need more research done we need help by the medical field more doctors who are fimliar with this condition please help us because we are suffering thank youFlag
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104
Name: Leslie Edens on Jun 22, 2012Comments: We need more doctors who can help with this condition there are many of us that suffer, Not enough doctors that can help us with this condition, this effects every aspect of your lifeFlag
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105
Name: Sara Barsted on Jun 22, 2012Comments:Flag
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106
Name: Scott Quintanilla on Jun 23, 2012Comments:Flag
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107
Name: Angela Giza on Jun 23, 2012Comments:Flag
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108
Name: Frank Devillers on Jun 23, 2012Comments:Flag
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109
Name: Judy Jackson on Jun 23, 2012Comments: I had decompression surgery in Houston in 2006 and it worked.Flag
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110
Name: Sharon Grau on Jun 23, 2012Comments:Flag
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111
Name: Kathy Doherty on Jun 23, 2012Comments: This condition deserves as much research and attention as cancer, or any other life-changing disorder. It is one of the most painful conditions imaginable.Please devote research to therapy and a cure!Flag
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112
Name: Karen Kennedy on Jun 23, 2012Comments:Flag
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113
Name: Karen Kennedy on Jun 23, 2012Comments:Flag
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114
Name: Dr. Robert G. Boyd on Jun 23, 2012Comments: I have piriformis syndrome. So I know that the medical community is not doing much to treat patients who have peripheral nerve entrapment. I have not yet found a local doctor who can help me.Flag
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115
Name: Bill Decker on Jun 23, 2012Comments:Flag
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116
Name: Patricia Lynch on Jun 23, 2012Comments: Please keep working to help these people.Flag
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117
Name: Kev Howey on Jun 23, 2012Comments: Needs further research asapFlag
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118
Name: Matt Carter on Jun 24, 2012Comments:Flag
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119
Name: Sharon G. DeVillers on Jun 24, 2012Comments: A family member of ours just went to Oklahoma, from Massachusetts, for this surgery at great expense to her family. Their was'nt any doctors in the area that have expertise to perform this proceedure. She is now on the mend after a very long battle to even prove there was something physically wrong with her, with most of her symptoms reduced after two weeks out, which proves the diagnosis of many doctor's she sought help from, ( that she seek psychological help) even that much harder to take.Flag
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120
Name: Denise Epperson on Jun 24, 2012Comments:Flag
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121
Name: Joseph Grau on Jun 24, 2012Comments: My daughter has suffered for 8 years from this painful condition and little has been done to help. This is a real medical and needs to be addressed.Flag
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122
Name: Silvia González on Jun 25, 2012Comments: I am a 48 years old woman who was diagnosed with pn 2 monhs ago. My syntoms started a few month ago and we do not have good doctors here in Mexico. HELP pleaseFlag
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123
Name: Domy89 on Jun 25, 2012Comments:Flag
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124
Name: Duncan O'Brien on Jun 25, 2012Comments:Flag
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125
Name: Anonymous on Jun 25, 2012Comments:Flag
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126
Name: Anonymous on Jun 25, 2012Comments:Flag
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127
Name: Ann Broussard on Jun 25, 2012Comments: We need more doctor who are a ware of this disabling disease so we can get help in adentifying This disease.Flag
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128
Name: DAVID JONES on Jun 26, 2012Comments: TRAIN DOCTORS TO DIAGNOSE PUDENDAL NUERALGIA. PLEASE. ITS WRONG TO LEAVE THESE PEOPLE IN MISERY AND THE SUICIDES RATESARE HIGH.Flag
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129
Name: Maddie Abrams on Jun 27, 2012Comments:Flag
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130
Name: Maddie on Jun 27, 2012Comments:Flag
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131
Name: Mark R. Sartin on Jun 29, 2012Comments: My wife suffers from this every day.....Everyone should sign this petition.Flag
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132
Name: Mary Marshman on Jun 29, 2012Comments: PN sufferer since Nov. 09. Probably caused by chronic constipation with a couple of impactions. Having to travel 2200 miles to see a qualified physician is ridiculous!!!!! We need many more trained doctors.Flag
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133
Name: Anonymous on Jun 29, 2012Comments:Flag
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134
Name: Nancy Gavenda on Jun 29, 2012Comments:Flag
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135
Name: Joseph Rasel on Jun 30, 2012Comments:Flag
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136
Name: Anonymous on Jun 30, 2012Comments: please help us find a cure for pudendal nerve entrapment. It controls our lives and ruins our lives. we want to be productive in society.Flag
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137
Name: Erich Ortlieb on Jun 30, 2012Comments: People like my mother would significantly benefit. thx.Flag
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138
Name: Bruce Sartin on Jun 30, 2012Comments:Flag
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139
Name: Karen Wiesner on Jun 30, 2012Comments: Having lived through the pain of this condition and the TEN years it took to get it diagnosed and treated, I do know that this research is imperative!!!!Flag
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140
Name: Lisette on Jul 1, 2012Comments: Raphael, je ne suis pas contre un autre son de chocle mais celui-ci je l'entends souvent. L'argument du choix et de l'e9coute de la population est celui que j'entends le plus.Et c'est merveilleux, c'est Walt Disney, c'est les bons sentiments e0 la louche. Et le politique se re9fugie derrie8re, ne fait rien. Pas d'ide9e alors celles des autres (les habitants de9sarme9s) sont les bienvenus. Et pan ! voile0 le re9el !Et dans la gueule le re9el !Mais j'entends bien votre de9sir de pluralisme. Reste que oui, vraiment, la voix patrimoniale est toujours la dernie8re entendue. Contribuez autant que vous voulez, c'est gentil mais ne vous e9tonnez pas que je mode8re. Ce blog n'est pas une agora. Il y en une gigantesque sur les ruines de la Cite9 des poe8tes. Elle est e0 vous maintenant.Flag
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141
Name: Andrea on Jul 1, 2012Comments: Je n'ai pas prononce9 cette pasrhe mais je n'ai fait que relayer un autre son de cloche.J'aime beaucoup votre blog et j'aime beaucoup les be2timents que vous pre9sentez mais je trouvais plus sain de donner un autre son de cloche dans cette affaire.J'entends bien que les urbanistes ont aussi une marmite e0 faire bouillir mais c'est un peu facile de sortir l'argument de cette manie8re non ? et en profiter pour ne pas publier ma contribution.Flag
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142
Name: Avril Jones on Jul 1, 2012Comments: I give my wholehearted support to this very distressing condition from which I suffer. What is happenning to our NHS. Noone seems to care anymore.Flag
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143
Name: Jane Fahys on Jul 1, 2012Comments: please do not share my name or email address. thank you.Flag
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144
Name: Avinash on Jul 1, 2012Comments: Seulement, c'est toujours sur les loetmengs des domine9s qu'on tente des expe9rimentations.Si cette phrase a vraiment e9te9 prononce9e, Raphael anonyme, elle est d'un populisme comique. J'aime votre humour. Et les urbanistes comme les autres, cherchent des marche9s et les gagnent avec des mots.Chacun ses mots, Raphael.Flag
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145
Name: Suzanne Mansur on Jul 2, 2012Comments: I suffer from Pudendal Neuralgia & it has drastically affected my life....I'm only 43 yrs old & I am now considered disabled. I have been dealing with this condition for 5 1/2 yrs & I have yet to find a successful pain management program. I have been so shocked at how many physicians have either no or limited knowledge of the Pudendal Nerve and/or how to treat the issue or who to even refer a patient to with this kind of issue!! Those of us who suffer with a Pudendal Nerve condition and those of us who know &/or love someone who suffers from a Pudencal Nerve condition plea in desperation for more knowledge given to, assistance from and treatments available from the healthcare professionals!!!!!Flag
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146
Name: Lisa Carter on Jul 2, 2012Comments:Flag
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147
Name: Charlotte Jansen on Jul 2, 2012Comments:Flag
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148
Name: Annabel Croucher on Jul 2, 2012Comments:Flag
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149
Name: Ekaterina on Jul 3, 2012Comments: Cathy- omg, I can imagine! That's often how I feel about medcail stuff. Especially shifter stories where heroines give birth to litters. Um there are reasons humans don't have litters. >.Flag
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150
Name: Antonia Forsyth on Jul 3, 2012Comments:Flag