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Signatures 908 total

Page: « 1, 2, 3, 4, 5, 6, 7, ... 19 »

  1. 151
    Name: Fsfs on Aug 12, 2008
    Comments:
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  2. 152
    Name: Tammy Ma on Aug 12, 2008
    Comments:
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  3. 153
    Name: Reta Clark on Aug 12, 2008
    Comments: Please consider the funding for this drug it is of value to the whole society. When we know we can make a difference it doesn't make sense not to. This is our YOUTH and future's we are working for.
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  4. 154
    Name: Sarah Mourtizen on Aug 12, 2008
    Comments:
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  5. 155
    Name: Anonymous on Aug 12, 2008
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  6. 156
    Name: Lisa Green on Aug 12, 2008
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  7. 157
    Name: Roland Semprie on Aug 12, 2008
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  8. 158
    Name: Shannon Drage on Aug 12, 2008
    Comments:
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  9. 159
    Name: Piper Gara on Aug 12, 2008
    Comments: It is unforgivable that this treatment is not covered in Ontario!
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  10. 160
    Name: Glynis Gilman on Aug 12, 2008
    Comments:
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  11. 161
    Name: Patricia Otero on Aug 12, 2008
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  12. 162
    Name: Oona Tiplady on Aug 12, 2008
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  13. 163
    Name: Matthew Levy on Aug 12, 2008
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  14. 164
    Name: Anil Sayani on Aug 12, 2008
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  15. 165
    Name: Anne De Silva on Aug 12, 2008
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  16. 166
    Name: Kerry Sharpe on Aug 12, 2008
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  17. 167
    Name: Marie Ibell on Aug 12, 2008
    Comments: A remarkable individual Simon is the victim of a government that would appear to be more concerned with votes over life. As a group with a rare disease they are rare in the number of votes. Hopefully the Ontario government is rare in its discriminatory approach .
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  18. 168
    Name: Louise Winter on Aug 12, 2008
    Comments:
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  19. 169
    Name: Patricia Noel on Aug 12, 2008
    Comments:
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  20. 170
    Name: Christine Kiss on Aug 12, 2008
    Comments:
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  21. 171
    Name: Lou Douillard on Aug 12, 2008
    Comments:
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  22. 172
    Name: Tracy Johns on Aug 12, 2008
    Comments:
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  23. 173
    Name: Tami Tate on Aug 12, 2008
    Comments:
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  24. 174
    Name: Lucas Riedl on Aug 12, 2008
    Comments:
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  25. 175
    Name: Rita Gara on Aug 12, 2008
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  26. 176
    Name: Brad Stevenson on Aug 12, 2008
    Comments:
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  27. 177
    Name: Suzanne Neumann on Aug 12, 2008
    Comments:
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  28. 178
    Name: Lauren Karst on Aug 12, 2008
    Comments:
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  29. 179
    Name: Rebecca Richardson on Aug 12, 2008
    Comments:
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  30. 180
    Name: Nicholas Schubert on Aug 12, 2008
    Comments:
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  31. 181
    Name: Jane Scurfield on Aug 12, 2008
    Comments:
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  32. 182
    Name: Derek Dolsen on Aug 12, 2008
    Comments:
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  33. 183
    Name: Kat Watson on Aug 12, 2008
    Comments:
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  34. 184
    Name: Andrew Moll on Aug 12, 2008
    Comments:
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  35. 185
    Name: Tracey MacLeod on Aug 12, 2008
    Comments:
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  36. 186
    Name: Anonymous on Aug 12, 2008
    Comments:
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  37. 187
    Name: Maureen Miller on Aug 12, 2008
    Comments:
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  38. 188
    Name: Maureen Miller on Aug 12, 2008
    Comments:
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  39. 189
    Name: Malcolm Adams on Aug 12, 2008
    Comments:
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  40. 190
    Name: Anonymous on Aug 12, 2008
    Comments:
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  41. 191
    Name: Anonymous on Aug 12, 2008
    Comments:
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  42. 192
    Name: Danuta Pascore on Aug 12, 2008
    Comments: Please provide funding for the approved treatment for people with Hunter Syndrome (MPS II).
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  43. 193
    Name: Gerry Barranda M.D. on Aug 12, 2008
    Comments:
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  44. 194
    Name: Julie French on Aug 12, 2008
    Comments: how evil and devastating our government has become... I am an RCA and let me tell you that these poor victims of this disease demand just as much care as everyone else.
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  45. 195
    Name: Cameron Gilbert on Aug 12, 2008
    Comments: Hopefully we can achieve this goal with the help of all our friends working together.
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  46. 196
    Name: Peter Weber on Aug 12, 2008
    Comments: I am very much in support of this petition
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  47. 197
    Name: Lea Harper on Aug 12, 2008
    Comments:
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  48. 198
    Name: Lesley Kroch on Aug 12, 2008
    Comments:
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  49. 199
    Name: Russell Wong on Aug 12, 2008
    Comments:
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  50. 200
    Name: Chris Davis Sr on Aug 12, 2008
    Comments:
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