Campaign for Kalydeco

Signatures 17271 total

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1. 151
   Name: Claire Hickes on Oct 4, 2012

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2. 152
   Name: Kirsty Ann Bridges on Oct 4, 2012

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3. 153
   Name: J SCHMITT on Oct 4, 2012

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4. 154
   Name: Deborah Cogan on Oct 4, 2012

   Comments: I think this should be allowed. My son has CF and I'd hope my NHS would do everything they could.

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5. 155
   Name: Syanne Agius on Oct 4, 2012

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6. 156
   Name: Cathy Jorgensen on Oct 4, 2012

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7. 157
   Name: Anonymous on Oct 4, 2012

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8. 158
   Name: Douglas Forbes on Oct 4, 2012

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9. 159
   Name: Patricia Shreve on Oct 4, 2012

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10. 160
    Name: Mr Lyward on Oct 4, 2012

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11. 161
    Name: Anonymous on Oct 4, 2012

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12. 162
    Name: Lana Russell on Oct 4, 2012

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13. 163
    Name: Allison Button on Oct 4, 2012

    Comments: why oh why do people have to put a price on those that are sick, it's not fair. the CF kids and adults need this treatment my daughter needs thus treatment

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14. 164
    Name: Jeremy Hull on Oct 4, 2012

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15. 165
    Name: Bianca Nicholas on Oct 4, 2012

    Comments: Please sign this petition to urge NHS to ensure a new drug that can transform the lives of people over six years old with the G551D mutation of cystic fibrosis is made available as soon as possible.

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16. 166
    Name: Alex Hall Taylor on Oct 4, 2012

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17. 167
    Name: Daniella on Oct 4, 2012

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18. 168
    Name: Natalie Parody on Oct 4, 2012

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19. 169
    Name: Karl Haymer on Oct 4, 2012

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20. 170
    Name: Hayley Ball on Oct 4, 2012

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21. 171
    Name: Amanda Sorce on Oct 4, 2012

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22. 172
    Name: Alice Mayhew on Oct 4, 2012

    Comments: Please don't let money stop this treatment being rolled out.

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23. 173
    Name: Remo Smith on Oct 4, 2012

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24. 174
    Name: Alana on Oct 4, 2012

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25. 175
    Name: Gary Burkill on Oct 4, 2012

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26. 176
    Name: Thomas Bull on Oct 4, 2012

    Comments: i am a sufferer, if its there then why cant we have it?

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27. 177
    Name: J Sanders on Oct 4, 2012

    Comments: Please help improve lives with this treatment.

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28. 178
    Name: Roland Nopper on Oct 4, 2012

    Comments: Make this happen! Please!

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29. 179
    Name: Anonymous on Oct 4, 2012

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30. 180
    Name: Yvonne Hughes on Oct 4, 2012

    Comments: Please consider that if this drug does not become available in the UK then you are halting the progress and development of potentially life changing drugs for all of the cf community. Please Vertex and the wonderful NHS, listen to us, hear what we are saying - we never ask for anything - but need drugs like this now. Thanks

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31. 181
    Name: Kate Prosser on Oct 4, 2012

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32. 182
    Name: Tracy Jones on Oct 4, 2012

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33. 183
    Name: David McConnochie on Oct 4, 2012

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34. 184
    Name: Theresa Silva on Oct 4, 2012

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35. 185
    Name: Warren Lenney on Oct 4, 2012

    Comments: This medication could transform the lives of some patients with CF

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36. 186
    Name: Christine Bond on Oct 4, 2012

    Comments: This is so important for sufferers of CF. Our dear Angel DAWN would have been 33 this year. Instead she only had 3 short years with us. This can Prevent the same happening to so many more families.

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37. 187
    Name: Karen Haagman on Oct 4, 2012

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38. 188
    Name: Beverley Dyas on Oct 4, 2012

    Comments: PLEASE...desperate mother whos son has cf

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39. 189
    Name: Kristel Nicol on Oct 4, 2012

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40. 190
    Name: Kirsty Stuart on Oct 4, 2012

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41. 191
    Name: Kurtis Graves on Oct 4, 2012

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42. 192
    Name: Gary Prior on Oct 4, 2012

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43. 193
    Name: Anonymous on Oct 4, 2012

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44. 194
    Name: Rachel Jones on Oct 4, 2012

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45. 195
    Name: Denise Murphy on Oct 4, 2012

    Comments: we have already collected 12,000 signatures for our epetition! can we add them to this total? those who signed previously

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46. 196
    Name: Mary Allen on Oct 4, 2012

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47. 197
    Name: Jenny Morgan on Oct 4, 2012

    Comments: please

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48. 198
    Name: Francesca Trinidad on Oct 4, 2012

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49. 199
    Name: Matthew Stone on Oct 4, 2012

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50. 200
    Name: Anjali Soneji on Oct 4, 2012

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