Campaign for Kalydeco

Signatures 17269 total

Page: « ‹ 1, ... 327, 328, 329, 330, 331, 332, 333, ... 346 › »

1. 16451
   Name: Rupert Pearce Gould on Nov 30, 2012

   Comments: I fully support

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2. 16452
   Name: Stuart Walters on Nov 30, 2012

   Comments:

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3. 16453
   Name: Becca Creighton on Nov 30, 2012

   Comments:

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4. 16454
   Name: Anne-Marie Ramsay on Nov 30, 2012

   Comments:

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5. 16455
   Name: Suzanne Sinclair on Nov 30, 2012

   Comments: please arrange this for all the kids who desperetly need it

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6. 16456
   Name: Pamela Bayliss on Nov 30, 2012

   Comments:

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7. 16457
   Name: Shelley King on Nov 30, 2012

   Comments:

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8. 16458
   Name: Lesley Andrews on Nov 30, 2012

   Comments:

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9. 16459
   Name: Lesley Andrews on Nov 30, 2012

   Comments:

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10. 16460
    Name: Catherine on Nov 30, 2012

    Comments:

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11. 16461
    Name: Julie Hendry on Nov 30, 2012

    Comments:

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12. 16462
    Name: Rachel Williams on Nov 30, 2012

    Comments:

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13. 16463
    Name: Brian And Justina Kennedy on Nov 30, 2012

    Comments:

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14. 16464
    Name: Danielle Watson on Nov 30, 2012

    Comments:

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15. 16465
    Name: Kathleen Dingwall on Nov 30, 2012

    Comments:

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16. 16466
    Name: Sheila Levi on Dec 1, 2012

    Comments:

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17. 16467
    Name: Kimberly A Cheevers on Dec 1, 2012

    Comments: I have 2 daughters thriving with CF because of Kalydeco---you cannot put a price tag on that.

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18. 16468
    Name: Jaime Anderson on Dec 1, 2012

    Comments: come on! let's get this done and dusted!!

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19. 16469
    Name: Kimberley on Dec 1, 2012

    Comments: I can't bare to see my sister suffer any longer! We need a cure!

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20. 16470
    Name: Nicola Mackay on Dec 1, 2012

    Comments:

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21. 16471
    Name: Anonymous on Dec 1, 2012

    Comments: I have a 5 year old boy with cystic fibrosis. We live in the United States. Although he does not carry the G551D mutation, I am beyond thrilled that this medecine has proven to help about 4% of the CF population. However, I am sad to hear that there are some with the mutation in the UK that are not able to benefit from this drug yet. Having to wait until January 2013 for a decision seems unbelievable to me. Please allow those with this mutation access to this drug!

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22. 16472
    Name: Lorraine Scott on Dec 1, 2012

    Comments:

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23. 16473
    Name: Robert Henderson on Dec 1, 2012

    Comments: Hope it all goes well for her. All the best

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24. 16474
    Name: Nikki Ross on Dec 1, 2012

    Comments:

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25. 16475
    Name: Chris Colkin on Dec 1, 2012

    Comments:

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26. 16476
    Name: Simon Valentine on Dec 1, 2012

    Comments:

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27. 16477
    Name: Martin Perrin on Dec 1, 2012

    Comments:

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28. 16478
    Name: Ann Hodgkiss on Dec 1, 2012

    Comments: Please don't delay this any longer, CF is a fast growing disease & thanks to new born screening it is being picked up just after birth. This allows earlier treatment & a better way of life for a child, but this drug could improve the prognosis so much, it must be allowed. Why should they suffer when we pay millions on none working none English speaking immigrants in our country. Charity begins at home, sort our your own problems first.

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29. 16479
    Name: Susan Doughty on Dec 1, 2012

    Comments:

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30. 16480
    Name: Genevieve Kiszczuk on Dec 1, 2012

    Comments:

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31. 16481
    Name: Genevieve Kiszczuk on Dec 1, 2012

    Comments:

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32. 16482
    Name: Naomi Beaman on Dec 1, 2012

    Comments: still can't believe it's not free already!!!

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33. 16483
    Name: Paul Sanchez on Dec 1, 2012

    Comments:

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34. 16484
    Name: Katie Anderson on Dec 1, 2012

    Comments:

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35. 16485
    Name: Lynn Robinson on Dec 1, 2012

    Comments:

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36. 16486
    Name: Christopher Robinson on Dec 1, 2012

    Comments:

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37. 16487
    Name: Gordon Cronin on Dec 1, 2012

    Comments:

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38. 16488
    Name: Jane Harris on Dec 1, 2012

    Comments: Please allow this life changing drug. Thankyou

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39. 16489
    Name: Andrew Harris on Dec 1, 2012

    Comments:

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40. 16490
    Name: Hannah Morris on Dec 1, 2012

    Comments: I have CF and hope the government realises that any drug with long ter.m benefits which will enable me to take less of the many other drugs I have to take is long term cost effective. Please help us

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41. 16491
    Name: C. Walker on Dec 1, 2012

    Comments: We have been waiting 23 years for such a breakthrough that will literally transform our son's life... It would be nothing short of catastrophic and inhumane if this treatment is not made quickly available to this particular group of CF sufferers. It would be mental torture to have this life transforming treatment denied to the CF community and their family and friends who daily live their lives with such courage, hope and inspiration.

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42. 16492
    Name: Penny Hilton on Dec 1, 2012

    Comments: EvEveryone with CF should have access to any medication that helps to prolong life expectancy and give a better quality of life.

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43. 16493
    Name: Norma Kalbraier on Dec 1, 2012

    Comments:

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44. 16494
    Name: Matt Lent on Dec 1, 2012

    Comments:

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45. 16495
    Name: Aaron Sanders-Symeon on Dec 1, 2012

    Comments:

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46. 16496
    Name: Anonymous on Dec 1, 2012

    Comments: I urge the nhs and vertex to reach an agreement because kalydeco treats the cause not the symptoms it will help slow down the inevitable decline in health and enable a good quality of life to be enjoyed for longer.

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47. 16497
    Name: Georgina Lesser on Dec 1, 2012

    Comments:

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48. 16498
    Name: Celia Charlton on Dec 1, 2012

    Comments: As a nurse working with children with CF , I know how extremely important it is that this drug be made available to this group of patients as soon as possible .

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49. 16499
    Name: Peter Humble on Dec 1, 2012

    Comments: The obvious comment is that treatment would lead to less need for national health care and hopefully lead to a more productive life.

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50. 16500
    Name: Sharon Stead on Dec 1, 2012

    Comments: PLEASE COME TO A REASONABLE CONCLUSION REGARDS THIS DRUG.IT IS VITAL CF SUFFERERS WITH THE C551D GENE HAVE THHIS AVAILABEL AT A COST THAT CAN BE MET.

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