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Signatures 4445 total

Page: « 1, 2, 3, 4, 5, 6, 7, 8, ... 89 »

  1. 201
    Name: Chandler Whitley on Oct 11, 2012
    Comments:
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  2. 202
    Name: Chandler Whitley on Oct 11, 2012
    Comments:
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  3. 203
    Name: Shirley & Dale Block on Oct 11, 2012
    Comments:
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  4. 204
    Name: Del Sel on Oct 11, 2012
    Comments:
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  5. 205
    Name: Krista Rea on Oct 11, 2012
    Comments:
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  6. 206
    Name: Robin Hardy-Groce on Oct 11, 2012
    Comments: Thanks for the support!
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  7. 207
    Name: Cyndi Myers on Oct 11, 2012
    Comments:
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  8. 208
    Name: Margaret Ann Farrell-Keaveny on Oct 11, 2012
    Comments: This is the 5th Year Anniversary of the end of my life as I once knew it because of Trigeminal Neuralgia. We need public awareness for this disease & should not have to fight to be heard! We are being treated unjustly by the court system since this is a debilitating disease that eats away at us. We need a cure! Will someone hear our cries? Living with TN sucks!
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  9. 209
    Name: Jennifer Blackley on Oct 11, 2012
    Comments: It is one of the worst pains known to man!
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  10. 210
    Name: Anne Ball on Oct 11, 2012
    Comments: Great idea!
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  11. 211
    Name: Delia Voelsing on Oct 11, 2012
    Comments:
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  12. 212
    Name: Diane Katofsky on Oct 11, 2012
    Comments:
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  13. 213
    Name: Anonymous on Oct 11, 2012
    Comments: After a completely unnecessary nasal operation, my mom had to diagnose herself on the internet in which she discovered she had Trigeminal Neuralgia that led to an MRI which showed a benign brain tumor that had to be removed. Years later she is ok, but more education & awareness is needed!
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  14. 214
    Name: Jean Galloway on Oct 11, 2012
    Comments:
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  15. 215
    Name: Jeanette Cole on Oct 11, 2012
    Comments:
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  16. 216
    Name: Valorie Jean Shearer on Oct 11, 2012
    Comments: I have been suffering from this monster for over 35 years now. I had a microvascular decompression in 2007 but "it" came back less than 2 years later.. Yes, a cure would be lovely but I am not very hopeful at this point in my life.
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  17. 217
    Name: Mark Molter on Oct 11, 2012
    Comments: Awful disease, my surgery was successful.
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  18. 218
    Name: Jacqueline Kendrick on Oct 11, 2012
    Comments:
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  19. 219
    Name: Rachael Knight on Oct 11, 2012
    Comments:
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  20. 220
    Name: Christine Rice on Oct 11, 2012
    Comments: this is fantastic
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  21. 221
    Name: Connie Hall on Oct 11, 2012
    Comments: This is a wonderful idea. We need to educate so many people
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  22. 222
    Name: Shelly Key on Oct 11, 2012
    Comments:
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  23. 223
    Name: DAPHNE DRENNEN on Oct 11, 2012
    Comments:
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  24. 224
    Name: Charles Wickwire, Jr. on Oct 11, 2012
    Comments:
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  25. 225
    Name: Lisa Winston on Oct 11, 2012
    Comments:
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  26. 226
    Name: Jeffrey Bae on Oct 11, 2012
    Comments:
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  27. 227
    Name: Sue McGee on Oct 11, 2012
    Comments: The public needs to be aware of this!
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  28. 228
    Name: Brian Anastas on Oct 11, 2012
    Comments:
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  29. 229
    Name: Margaret Cameron on Oct 11, 2012
    Comments: Good idea
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  30. 230
    Name: Jeffrey Lord on Oct 11, 2012
    Comments:
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  31. 231
    Name: Ella Burakowski on Oct 11, 2012
    Comments:
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  32. 232
    Name: Toni Mims on Oct 11, 2012
    Comments:
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  33. 233
    Name: Susan Bolin on Oct 11, 2012
    Comments: Wonderful. It is so difficult to explain TN to other people.
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  34. 234
    Name: Gilly Cannon on Oct 11, 2012
    Comments:
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  35. 235
    Name: CECIL PERERA on Oct 11, 2012
    Comments: In layman's terms it is known as the " SUICIDE DISEASE " and it is accepted as the " WORST PAIN KNOWN TO MANKIND." Yet it is shocking that so little is done to bring relief to sufferers !
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  36. 236
    Name: Sandra Sahagian on Oct 11, 2012
    Comments: I think this is a great idea and beign that I suffer from TN, I would love for it to get attention that would eventually lead to targeted treatment and a cure.
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  37. 237
    Name: Melissa EL-Banna on Oct 11, 2012
    Comments: Help remove feelings of pain induced isolation. Get aware, support one another.
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  38. 238
    Name: Karen Russell on Oct 11, 2012
    Comments:
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  39. 239
    Name: Lisa Malecha on Oct 11, 2012
    Comments: This is a condition that NEEDS some awareness. So many suffer from this and other atypical facial pain and we NEED hope. Every day we hope that this will be the day that someone finds a cure.
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  40. 240
    Name: Catherine Graham on Oct 11, 2012
    Comments:
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  41. 241
    Name: Anonymous on Oct 11, 2012
    Comments:
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  42. 242
    Name: Anonymous on Oct 11, 2012
    Comments:
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  43. 243
    Name: Anonymous on Oct 11, 2012
    Comments:
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  44. 244
    Name: Suzette Tanen on Oct 11, 2012
    Comments:
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  45. 245
    Name: Anonymous on Oct 11, 2012
    Comments:
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  46. 246
    Name: Kim Warren on Oct 11, 2012
    Comments:
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  47. 247
    Name: Liz Dunphy-Bartlett on Oct 11, 2012
    Comments:
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  48. 248
    Name: John Heaney on Oct 11, 2012
    Comments: Very good cause
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  49. 249
    Name: Ken Buck on Oct 11, 2012
    Comments: I live every day with someone who has TN. A cure needs to be found.
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  50. 250
    Name: Barbara Benson on Oct 11, 2012
    Comments:
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