Signatures 746 total
-
1
Name: Shawn Ellis on Jun 1, 2012Comments: Chronic Pelvic Pain is Frequently Caused by PNE and more research and better surgical approaches, research, and studies need to be done in order to help thousands of people misdiagnosed and underdiagnosed each year.Flag
-
2
Name: Donald Soles on Jun 1, 2012Comments: Physician and fellow-sufferer since 2008Flag
-
3
Name:
Trish Wolfe Mazeika on Jun 1, 2012
Comments:Flag -
4
Name: Clinton Radenbaugh on Jun 1, 2012Comments: The morbidity rate including suicide is VERY significant. Patients with this disease are inevitably outcasted, isolated, and mistakenly labeled as hypochondriacs because of the extreme nature of their seemingly invisible symptoms and the lack of understanding of this obscure condition.Flag
-
5
Name: Brittany Carter on Jun 1, 2012Comments:Flag
-
6
Name:
Karen Napoli on Jun 1, 2012
Comments:Flag -
7
Name: Lillian Crow on Jun 1, 2012Comments: I suffer from this horrible, painful condition. We really need help with this terrible pain.Flag
-
8
Name: Clinton Radenbaugh on Jun 1, 2012Comments: The morbidity rate including suicide is VERY significant. Patients with this disease are inevitably outcasted, isolated, and mistakenly labeled as hypochondriacs because of the extreme nature of their seemingly invisible symptoms and the lack of understanding of this obscure condition.Flag
-
9
Name: Gary Stratton on Jun 1, 2012Comments: I suffer with this horrific illness. It has changed me and my life considerably. More understanding and research is desperately needed. Thank YouFlag
-
10
Name: Alisa Milewski on Jun 1, 2012Comments: I got this from a hysterectomy in 2009, i have been fighting this since than, numerous nerve blocks have made me worse. This has cost me my marriage of 20 years. I have lost alot because of this. We need help, and we need alot. People have thought of suicide because if this. The pain is inhumane . Please help us.Flag
-
11
Name: Deborah Wagner on Jun 1, 2012Comments: PNE is so misunderstood by the medical community. The cost of this is immense is so many ways. We are desperate for new options and treatments. Please help. Thank you.Flag
-
12
Name: Anne Marie Tyre on Jun 1, 2012Comments:Flag
-
13
Name: Lemuel Tyre on Jun 1, 2012Comments:Flag
-
14
Name: Anonymous Facebook user on Jun 1, 2012Comments:Flag
-
15
Name: Donna Ellis on Jun 1, 2012Comments:Flag
-
16
Name: David C. Rich on Jun 1, 2012Comments:Flag
-
17
Name: Skip Bowdenzki on Jun 1, 2012Comments:Flag
-
18
Name: Nancy Hopkins on Jun 1, 2012Comments: It is especially important that urologists recognize PN, so that they don't permanently entrap the PN by doing a hydrodistention of the bladder (which is contraindicated for diagnosing interstitial cystitis).Flag
-
19
Name: Anonymous on Jun 1, 2012Comments:Flag
-
20
Name: Ray Paquette on Jun 1, 2012Comments:Flag
-
21
Name: Angela Williams on Jun 1, 2012Comments:Flag
-
22
Name: Atara Schimmel on Jun 1, 2012Comments: Many of us attempt suicide and want to die because the torture of this condition is inhuman. Our humsn minds and being cannot survive this type of nerve damage. Please help us.Flag
-
23
Name: Atara Schimmel on Jun 1, 2012Comments:Flag
-
24
Name: Scott Ellis on Jun 2, 2012Comments:Flag
-
25
Name: Arlene Jones on Jun 2, 2012Comments: This is miserable. No doctors know what it is. I was treated like a mental case. Considered suicide until a doctor finally came though for me. We need help.Recognition. Empathy. Awareness. Research. Cure.Flag
-
26
Name: Laura Russell on Jun 4, 2012Comments:Flag
-
27
Name: Janet McElvaney on Jun 4, 2012Comments:Flag
-
28
Name: Gary Henderson on Jun 5, 2012Comments: Went to pain doc for wife after eliminating all other possible diagnosis and doc says agrees with pudendal nearve problems but you just sive with itFlag
-
29
Name: Rhonda Sartin on Jun 5, 2012Comments: When I finally found a doctor who knew about pudendal neuralgia it was like being lost in a foreign land and stumbling onto someone who spoke my language. The worse part was the mental health speech from my doctor after several specialist referrals/treatments did nothing for the constant pain. Finally someone with a degree confirmed what I knew all along.Flag
-
30
Name: Joan Flyte on Jun 5, 2012Comments:Flag
-
31
Name: Julie Schoenberg on Jun 5, 2012Comments: Please, please give us more research and awareness. So many of us are suffering terribly with no hope in sight.Flag
-
32
Name: Heather Geldhof on Jun 5, 2012Comments:Flag
-
33
Name: Billie Fitzsimons on Jun 6, 2012Comments:Flag
-
34
Name: Helen Hindson on Jun 6, 2012Comments: thanks for all of your hard workFlag
-
35
Name: Christine Lacerenza on Jun 6, 2012Comments:Flag
-
36
Name: Clive Jacobs on Jun 6, 2012Comments:Flag
-
37
Name: Anonymous on Jun 6, 2012Comments:Flag
-
38
Name: Sonia Saxena on Jun 6, 2012Comments:Flag
-
39
Name: Anonymous on Jun 6, 2012Comments:Flag
-
40
Name: Solomon Schimmel on Jun 6, 2012Comments:Flag
-
41
Name: Melinda Mann on Jun 6, 2012Comments:Flag
-
42
Name:
Sheena Patrick on Jun 7, 2012
Comments:Flag -
43
Name: Judy Park on Jun 7, 2012Comments: By training medical staff to look for problems relating to the pudendal nerve, it can only bring about wider education for them, and broaden the base of resources for patients dealing with disorders relating to PN and PNE. Currently there are far too few medical professionals well-versed in the many disorders associated with the pudendal nerve, leaving many patients desperate for answers.Flag
-
44
Name: Mimi Yasgur on Jun 7, 2012Comments:Flag
-
45
Name: Jessica on Jun 7, 2012Comments: Thank you for creating this petition. It is indeed a very disabling condition and more awareness is needed.Flag
-
46
Name: Anonymous on Jun 8, 2012Comments:Flag
-
47
Name: Matej Jasso on Jun 12, 2012Comments:Flag
-
48
Name: Alec The Science Kid on Jun 16, 2012Comments: www.flydoodlescience.comFlag
-
49
Name: Anonymous on Jun 20, 2012Comments:Flag
-
50
Name: Melissa Tinnin on Jun 20, 2012Comments:Flag