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Signatures 17269 total

Page: « 1, ... 304, 305, 306, 307, 308, 309, 310, ... 346 »

  1. 15301
    Name: Daniel Adams on Oct 30, 2012
    Comments:
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  2. 15302
    Name: Anonymous on Oct 30, 2012
    Comments:
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  3. 15303
    Name: Anonymous on Oct 30, 2012
    Comments: See off CF!
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  4. 15304
    Name: Jayne Cott on Oct 30, 2012
    Comments:
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  5. 15305
    Name: Penny Gilbert on Oct 30, 2012
    Comments: please add my name to the signature list
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  6. 15306
    Name: Suzanne Jones on Oct 30, 2012
    Comments:
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  7. 15307
    Name: Rebecca O'Brien on Oct 30, 2012
    Comments:
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  8. 15308
    Name: Adele Phillips on Oct 30, 2012
    Comments:
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  9. 15309
    Name: Gordon Allen on Oct 30, 2012
    Comments:
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  10. 15310
    Name: Penny Evans on Oct 30, 2012
    Comments: Help Cystic Fibrosis
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  11. 15311
    Name: MRS MAUREEN REID on Oct 30, 2012
    Comments:
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  12. 15312
    Name: Neil Young on Oct 30, 2012
    Comments: i fully support this campaign
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  13. 15313
    Name: Hollie Donovan on Oct 30, 2012
    Comments:
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  14. 15314
    Name: Bethany Fox on Oct 30, 2012
    Comments:
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  15. 15315
    Name: Richard Tullett on Oct 30, 2012
    Comments:
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  16. 15316
    Name: Kenna Bannister on Oct 30, 2012
    Comments:
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  17. 15317
    Name: Nikky on Oct 30, 2012
    Comments:
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  18. 15318
    Name: Ian Minshull on Oct 30, 2012
    Comments:
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  19. 15319
    Name: Alexandra Petty on Oct 30, 2012
    Comments:
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  20. 15320
    Name: Andrew Nixon on Oct 30, 2012
    Comments:
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  21. 15321
    Name: Sophie Everett on Oct 30, 2012
    Comments:
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  22. 15322
    Name: Jodie Stagg on Oct 30, 2012
    Comments:
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  23. 15323
    Name: Ebonie on Oct 30, 2012
    Comments:
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  24. 15324
    Name: Lisa Jansen on Oct 31, 2012
    Comments: I know someone whose life has been transformed from 24-7 oxygen to a life transformed to independent living with Kalydeco. This is not just hope, it is the best there is as a cure for a significant amount of cf sufferers. A dream come true for those able to take it.
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  25. 15325
    Name: Sharon Vickers on Oct 31, 2012
    Comments:
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  26. 15326
    Name: Miss Abiagom on Oct 31, 2012
    Comments:
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  27. 15327
    Name: Andrew Heywood on Oct 31, 2012
    Comments:
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  28. 15328
    Name: Luke Miles on Oct 31, 2012
    Comments:
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  29. 15329
    Name: Luke Miles on Oct 31, 2012
    Comments:
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  30. 15330
    Name: Luke Miles on Oct 31, 2012
    Comments:
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  31. 15331
    Name: Luke Miles on Oct 31, 2012
    Comments:
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  32. 15332
    Name: Dawn Ellis-Jones on Oct 31, 2012
    Comments:
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  33. 15333
    Name: Anonymous on Oct 31, 2012
    Comments:
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  34. 15334
    Name: Lisa Beale on Oct 31, 2012
    Comments:
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  35. 15335
    Name: Anonymous on Oct 31, 2012
    Comments:
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  36. 15336
    Name: Suzanne Harding on Oct 31, 2012
    Comments: Several years ago my daughters fiance died as a result of this disease. I would not like for other families to go through this when there is a treatment available.
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  37. 15337
    Name: Stuart Baird on Oct 31, 2012
    Comments:
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  38. 15338
    Name: Angela Doherty on Oct 31, 2012
    Comments:
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  39. 15339
    Name: Steve Burghard on Oct 31, 2012
    Comments:
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  40. 15340
    Name: Pamela Mcnair on Oct 31, 2012
    Comments:
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  41. 15341
    Name: Ellen Willis on Oct 31, 2012
    Comments:
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  42. 15342
    Name: Angela Ciuraj on Oct 31, 2012
    Comments:
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  43. 15343
    Name: Cody on Oct 31, 2012
    Comments:
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  44. 15344
    Name: Stuart Browne on Oct 31, 2012
    Comments:
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  45. 15345
    Name: Karen Stanley on Oct 31, 2012
    Comments:
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  46. 15346
    Name: Tina Cantwell on Oct 31, 2012
    Comments:
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  47. 15347
    Name: Kevin James on Oct 31, 2012
    Comments: I wholly heartedly support this. My son Chris, now aged 21 was thought to have CF as a baby,thankfully he did not. However, I read up on the condition at the time and still feel that anything which is a breathrough in the fight against this terrible condition is very welcome.
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  48. 15348
    Name: Micheal Jones on Oct 31, 2012
    Comments:
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  49. 15349
    Name: Mrs Berenice Jackson on Oct 31, 2012
    Comments: I have a grandaughter with c.f. I don't know which gene mutation she has except it is most common one. Anyway I support the petetion to get the drug in this country for any one suffering for c.f. II always support the c.f. charity.withbn fund raiaing musical events.
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  50. 15350
    Name: Amanda Stulka on Oct 31, 2012
    Comments:
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